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Longer titles found: Max Planck Institute for Molecular Genetics (view), Human Molecular Genetics (view), Molecular Genetics and Metabolism (view), Somatic Cell and Molecular Genetics (view)

searching for Molecular genetics 223 found (3835 total)

alternate case: molecular genetics

Amgen (7,935 words) [view diff] case mismatch in snippet view article find links to article

Amgen Inc. (formerly Applied Molecular Genetics Inc.) is an American multinational biopharmaceutical company headquartered in Thousand Oaks, California

Annual plant (1,389 words) [view diff] no match in snippet view article find links to article

An annual plant is a plant that completes its life cycle, from germination to the production of seeds, within one growing season, and then dies. Globally

Selank (676 words) [view diff] case mismatch in snippet view article find links to article

nootropic, anxiolytic peptide based drug developed by the Institute of Molecular Genetics of the Russian Academy of Sciences. Selank is a heptapeptide with

Usha Vijayaraghavan (628 words) [view diff] case mismatch in snippet view article find links to article

the Indian Institute of Science. Her major research interests are Molecular Genetics, Plant Development. She has been featured in Women in Science. Usha

Yangochiroptera (578 words) [view diff] exact match in snippet view article find links to article

The rationale for the Yangochiroptera taxon is primarily based on molecular genetics data. The Yangochiroptera/ Yinpterochiroptera classification remains

Endothelin receptor type B (1,733 words) [view diff] case mismatch in snippet view article find links to article

syndrome (LWFS); a horse variant of Hirschsprung disease". Human Molecular Genetics. 7 (6): 1047–52. doi:10.1093/hmg/7.6.1047. PMID 9580670. AG mutation

Genetic divergence (809 words) [view diff] exact match in snippet view article find links to article

drift, and is the principal mechanism underlying speciation. On a molecular genetics level, genetic divergence is due to changes in a small number of genes

Fraser syndrome (1,464 words) [view diff] case mismatch in snippet view article find links to article

"The genetics of Fraser syndrome and the blebs mouse mutants". Human Molecular Genetics. 14 Spec No. 2: R269–R274. doi:10.1093/hmg/ddi262. PMID 16244325.

Outline of biochemistry (703 words) [view diff] no match in snippet view article find links to article

The following outline is provided as an overview of and topical guide to biochemistry: Biochemistry – study of chemical processes in living organisms,

Jeffrey V. Ravetch (580 words) [view diff] case mismatch in snippet view article find links to article

Ravetch (born 1951) is a professor and head of the Laboratory of Molecular Genetics and Immunology at The Rockefeller University. Ravetch earned his B

Ramamirtha Jayaraman (344 words) [view diff] case mismatch in snippet view article find links to article

He authored the reference manual, Jayaraman Laboratory Manual in Molecular Genetics and several pamphlets and articles; PubMed, an online repository of

Coproporphyrinogen III oxidase (2,088 words) [view diff] case mismatch in snippet view article find links to article

harderoporphyria, a variant form of hereditary coproporphyria". Human Molecular Genetics. 4 (2): 275–8. doi:10.1093/hmg/4.2.275. PMID 7757079. Kohno H, Furukawa

TSC1 (2,369 words) [view diff] case mismatch in snippet view article find links to article

polo-like kinase 1 in a phosphorylation-dependent manner". Human Molecular Genetics. 15 (2): 287–97. doi:10.1093/hmg/ddi444. PMID 16339216. Hodges AK

Battenin (1,268 words) [view diff] case mismatch in snippet view article find links to article

targeting of the CLN3 protein defective in Batten disease". Human Molecular Genetics. 7 (1): 85–90. doi:10.1093/hmg/7.1.85. PMID 9384607. Wisniewski KE

Rajesh Thakker (1,253 words) [view diff] case mismatch in snippet view article find links to article

including Genetic and Molecular Biological Aspects of Endocrine Disease, Molecular Genetics of Endocrine Disorders, and Genetics of Bone Biology and Skeletal

SMN1 (1,274 words) [view diff] case mismatch in snippet view article find links to article

further evidence for SMN as the primary SMA-determining gene". Human Molecular Genetics. 5 (11): 1727–32. doi:10.1093/hmg/5.11.1727. PMID 8922999. Talbot

Janet Rossant (1,125 words) [view diff] exact match in snippet view article find links to article

developmental biology. Her current research interests focus on stem cells, molecular genetics, and developmental biology. Specifically, she uses cellular and genetic

Yinpterochiroptera (631 words) [view diff] exact match in snippet view article find links to article

Craseonycteridae, and Megadermatidae. This suborder is primarily based on molecular genetics data. This proposal challenged the traditional view that megabats

Yinpterochiroptera (631 words) [view diff] exact match in snippet view article find links to article

Craseonycteridae, and Megadermatidae. This suborder is primarily based on molecular genetics data. This proposal challenged the traditional view that megabats

Twist-related protein 1 (2,365 words) [view diff] case mismatch in snippet view article find links to article

cause TWIST protein degradation or impaired nuclear location". Human Molecular Genetics. 9 (5): 813–9. doi:10.1093/hmg/9.5.813. PMID 10749989. Seto ML, Lee

Oncogenomics (7,684 words) [view diff] no match in snippet view article find links to article

Oncogenomics is a sub-field of genomics that characterizes cancer-associated genes. It focuses on genomic, epigenomic and transcript alterations in cancer

PMM2 (1,071 words) [view diff] case mismatch in snippet view article find links to article

molecular basis of the classical Jaeken syndrome (CDGS type Ia)". Molecular Genetics and Metabolism. 68 (2): 220–6. doi:10.1006/mgme.1999.2914. PMID 10527672

Charles Weissmann (254 words) [view diff] exact match in snippet view article find links to article

expression of interferon and his contributions to the unraveling of the molecular genetics of neurogenerative prion diseases such as scrapie, Creutzfeldt–Jakob

FOXL2 (2,264 words) [view diff] case mismatch in snippet view article find links to article

FOXL2 provides insights into its physiopathological roles". Human Molecular Genetics. 21 (14): 3264–74. doi:10.1093/hmg/dds170. PMID 22544055. Uhlenhaut

DSC3 (1,471 words) [view diff] no match in snippet view article find links to article

Desmocollin-3 is a protein that in humans is encoded by the DSC3 gene. The desmosomal family members are arranged in two clusters on chromosome 18, occupying

Methionine synthase (3,437 words) [view diff] case mismatch in snippet view article find links to article

mapping and RNA analysis of the human methionine synthase gene". Human Molecular Genetics. 5 (12): 1851–1858. doi:10.1093/hmg/5.12.1851. PMID 8968735. Banerjee

Tiger eye (738 words) [view diff] no match in snippet view article find links to article

Tiger eye or goat eye is a gene causing diluted eye color in horses. There are two variants, Tiger-eye 1 (TE1) and Tiger-eye 2 (TE2), which are both recessive

PMPCB (983 words) [view diff] case mismatch in snippet view article find links to article

mutated frataxin by the mitochondrial processing peptidase". Human Molecular Genetics. 7 (9): 1485–9. doi:10.1093/hmg/7.9.1485. PMID 9700204. Branda SS

Kenneth Berns (244 words) [view diff] case mismatch in snippet view article find links to article

virologist who was a distinguished professor emeritus at the department of Molecular Genetics and Microbiology at the University of Florida College of Medicine

William D. Richardson (118 words) [view diff] case mismatch in snippet view article find links to article

1973) and King's College London (PhD, 1978). He was a Lecturer in Molecular Genetics at University College London from 1985 to 1990 and has been Professor

Ataxin 3 (1,245 words) [view diff] case mismatch in snippet view article find links to article

homologs of yeast DNA repair protein RAD23, HHR23A and HHR23B". Human Molecular Genetics. 9 (12): 1795–803. doi:10.1093/hmg/9.12.1795. PMID 10915768. Doss-Pepe

RPGRIP1 (1,188 words) [view diff] case mismatch in snippet view article find links to article

"Identification of a novel protein interacting with RPGR". Human Molecular Genetics. 9 (14): 2085–93. doi:10.1093/hmg/9.14.2085. hdl:1842/23251. PMID 10958647

Ataxin 3 (1,245 words) [view diff] case mismatch in snippet view article find links to article

homologs of yeast DNA repair protein RAD23, HHR23A and HHR23B". Human Molecular Genetics. 9 (12): 1795–803. doi:10.1093/hmg/9.12.1795. PMID 10915768. Doss-Pepe

Carsten Bresch (790 words) [view diff] case mismatch in snippet view article find links to article

of genetics of bacteriophages, writing the standard Classical and Molecular Genetics. Bresch was born on 5 September 1921 in Berlin. He studied physics

RPGRIP1 (1,188 words) [view diff] case mismatch in snippet view article find links to article

"Identification of a novel protein interacting with RPGR". Human Molecular Genetics. 9 (14): 2085–93. doi:10.1093/hmg/9.14.2085. hdl:1842/23251. PMID 10958647

Huntingtin (3,263 words) [view diff] case mismatch in snippet view article find links to article

alpha-adaptin-binding protein involved in receptor-mediated endocytosis". Human Molecular Genetics. 10 (17): 1807–17. doi:10.1093/hmg/10.17.1807. PMID 11532990. Elias

Yeast artificial chromosome (1,982 words) [view diff] exact match in snippet view article find links to article

the most important experimental organisms for studying eukaryotic molecular genetics. Beginning with the initial research of the Rankin et al., Strul et

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (1,860 words) [view diff] exact match in snippet view article find links to article

Gómez-Puertas, Paulino; Casals, Núria (2007). "Molecular genetics of HMG-CoA lyase deficiency". Molecular Genetics and Metabolism. 92 (3). Elsevier BV: 198–209

Joachim Messing (1,404 words) [view diff] exact match in snippet view article find links to article

activity on computational and structural biology and further emphasis on molecular genetics of the regulation of gene expression and biomolecular interactions

Clear-cell renal-cell carcinoma (270 words) [view diff] no match in snippet view article find links to article

Clear-cell renal-cell carcinoma (CCRCC) is a type of renal-cell carcinoma. Alterations of chromosome 3p segments occurs in 70–90% of CCRCCs Inactivation

Spinal muscular atrophy (10,010 words) [view diff] case mismatch in snippet view article find links to article

splicing modifier in mouse models of spinal muscular atrophy". Human Molecular Genetics. 25 (10): 1885–1899. doi:10.1093/hmg/ddw062. PMC 5062580. PMID 26931466

Grant Robert Sutherland (1,808 words) [view diff] case mismatch in snippet view article find links to article

cytogeneticist. He was the Director, Department of Cytogenetics and Molecular Genetics, Adelaide Women's and Children's Hospital for 27 years (1975-2002)

MLX (gene) (974 words) [view diff] case mismatch in snippet view article

is a new member of the Mlx transcription factor network". Human Molecular Genetics. 10 (6): 617–27. doi:10.1093/hmg/10.6.617. PMID 11230181. Meroni G

Benjamin Blencowe (976 words) [view diff] case mismatch in snippet view article find links to article

Toronto’s Donnelly Sequencing Centre. He teaches in the Department of Molecular Genetics and his lab is part of the Donnelly Centre for Cellular and Biomolecular

Morula (gastropod) (1,713 words) [view diff] no match in snippet view article

Morula is a genus of small, predatory sea snails, marine gastropod mollusks in the subfalily Ergalataxinae of the family Muricidae, the murex snails or

ACADS (1,232 words) [view diff] case mismatch in snippet view article find links to article

candidate founder mutation in individuals of Ashkenazi Jewish origin". Molecular Genetics and Metabolism. 93 (2): 179–189. doi:10.1016/j.ymgme.2007.09.021.

Microcephalin (1,808 words) [view diff] case mismatch in snippet view article find links to article

evolution of microcephalin, a gene determining human brain size". Human Molecular Genetics. 13 (11): 1131–7. doi:10.1093/hmg/ddh127. PMID 15056608. Evans PD

Michigan State University College of Natural Science (1,492 words) [view diff] case mismatch in snippet view article find links to article

Engineering Earth and Environmental Sciences Mathematics Microbiology and Molecular Genetics Physics and Astronomy Physiology Plant Biology Statistics and Probability

PCDH15 (798 words) [view diff] case mismatch in snippet view article find links to article

mutant alleles are responsible for both USH1F and DFNB23". Human Molecular Genetics. 12 (24): 3215–23. doi:10.1093/hmg/ddg358. PMID 14570705. S2CID 14028314

Oligodendroglioma (2,938 words) [view diff] no match in snippet view article find links to article

Oligodendrogliomas are a type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell. They occur

Morula (gastropod) (1,713 words) [view diff] no match in snippet view article

Morula is a genus of small, predatory sea snails, marine gastropod mollusks in the subfalily Ergalataxinae of the family Muricidae, the murex snails or

ALG6 (904 words) [view diff] case mismatch in snippet view article find links to article

glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency". Human Molecular Genetics. 11 (5): 599–604. doi:10.1093/hmg/11.5.599. PMID 11875054. "Entrez

Distal hereditary motor neuronopathies (226 words) [view diff] exact match in snippet view article find links to article

Jonghe, P; Timmerman, V (2004). "Molecular genetics of distal hereditary motor neuropathies". Human Molecular Genetics. 13 (suppl 2): R195–R202. doi:10

SIM1 (1,379 words) [view diff] case mismatch in snippet view article find links to article

reduction of the paraventricular nucleus of the hypothalamus". Human Molecular Genetics. 10 (14): 1465–73. doi:10.1093/hmg/10.14.1465. PMID 11448938. "Entrez

Gem-associated protein 2 (1,126 words) [view diff] case mismatch in snippet view article find links to article

protein and a specific subset of spliceosomal Sm proteins". Human Molecular Genetics. 9 (13): 1977–1986. doi:10.1093/hmg/9.13.1977. PMID 10942426. Wang

Ornithine transcarbamylase deficiency (1,702 words) [view diff] exact match in snippet view article find links to article

findings and biochemical testing, while confirmation is often done using molecular genetics techniques. Once an individual has been diagnosed, the treatment goal

GPR143 (1,194 words) [view diff] case mismatch in snippet view article find links to article

receptor, regulates melanosome transport in pigment cells". Human Molecular Genetics. 17 (22): 3487–3501. doi:10.1093/hmg/ddn241. PMC 2572695. PMID 18697795

Methylmalonyl-CoA mutase (2,921 words) [view diff] case mismatch in snippet view article find links to article

(2016-10-01). "Genetic and genomic systems to study methylmalonic acidemia". Molecular Genetics and Metabolism. 86 (1–2): 34–43. doi:10.1016/j.ymgme.2005.07.020.

Joseph L. Goldstein (2,840 words) [view diff] case mismatch in snippet view article find links to article

face of varying environmental circumstances. Goldstein is chair, Molecular Genetics at University of Texas Southwestern Medical Center. Together, Goldstein

Frataxin (2,715 words) [view diff] case mismatch in snippet view article find links to article

leads to early embryonic lethality without iron accumulation". Human Molecular Genetics. 9 (8): 1219–1226. doi:10.1093/hmg/9.8.1219. PMID 10767347. Archived

Joanne Chory (1,617 words) [view diff] exact match in snippet view article find links to article

the Salk Institute, which she joined in 1988, pioneered the use of molecular genetics to study how plants change their shape and size to optimize photosynthesis

POMT1 (1,019 words) [view diff] case mismatch in snippet view article find links to article

"Glycosylation defects: a new mechanism for muscular dystrophy?". Human Molecular Genetics. 12 Spec No 2 (90002): R259–64. doi:10.1093/hmg/ddg272. PMID 12925572

Retinitis pigmentosa GTPase regulator (2,273 words) [view diff] case mismatch in snippet view article find links to article

homology with the guanine-nucleotide-exchange factor RCC1". Human Molecular Genetics. 5 (7): 1035–41. doi:10.1093/hmg/5.7.1035. hdl:2066/22748. PMID 8817343

CRX (gene) (1,411 words) [view diff] case mismatch in snippet view article

involvement of CRX in the development of photoreceptor function". Human Molecular Genetics. 8 (2): 299–305. doi:10.1093/hmg/8.2.299. PMID 9931337. Bessant DA

The Locust (2,510 words) [view diff] case mismatch in snippet view article find links to article

together. On July 31, 2012, The Locust released a compilation album, Molecular Genetics from the Gold Standard Labs, through ANTI-. The album contains all

OPN1SW (503 words) [view diff] exact match in snippet view article find links to article

Library of Medicine. Nathans J, Thomas D, Hogness DS (Apr 1986). "Molecular genetics of human color vision: the genes encoding blue, green, and red pigments"

SMN2 (1,354 words) [view diff] case mismatch in snippet view article find links to article

mutation complements SMN2 restoring snRNPs and rescuing SMA mice". Human Molecular Genetics. 18 (12): 2215–29. doi:10.1093/hmg/ddp157. PMC 2685758. PMID 19329542

MYO7A (1,718 words) [view diff] case mismatch in snippet view article find links to article

presence/absence of myosin VIIA in the photoreceptor cells". Human Molecular Genetics. 5 (8): 1171–8. doi:10.1093/hmg/5.8.1171. PMID 8842737. Adato A, Weil

Diabetic Hypoglycemia (journal) (186 words) [view diff] exact match in snippet view article

all aspects of hypoglycemia in diabetes including: basic science, molecular genetics, pathophysiology, epidemiology, and clinical aspects of hypoglycemia

Survival of motor neuron (1,384 words) [view diff] case mismatch in snippet view article find links to article

protein and a specific subset of spliceosomal Sm proteins". Human Molecular Genetics. 9 (13): 1977–86. doi:10.1093/hmg/9.13.1977. PMID 10942426. Mourelatos

MYO7A (1,718 words) [view diff] case mismatch in snippet view article find links to article

presence/absence of myosin VIIA in the photoreceptor cells". Human Molecular Genetics. 5 (8): 1171–8. doi:10.1093/hmg/5.8.1171. PMID 8842737. Adato A, Weil

ABCC11 (2,217 words) [view diff] no match in snippet view article find links to article

ATP-binding cassette transporter sub-family C member 11, also MRP8 (Multidrug Resistance-Related Protein 8), is a membrane transporter that exports certain

Tatiana Foroud (266 words) [view diff] case mismatch in snippet view article find links to article

researcher and currently the Joe C. Christian Professor Medical and Molecular Genetics, Distinguished Professor and Chancellor's Professor at the Indiana

Short-stature homeobox gene (1,240 words) [view diff] case mismatch in snippet view article find links to article

gene for involvement in the short stature of Turner syndrome". Human Molecular Genetics. 6 (8): 1341–7. doi:10.1093/hmg/6.8.1341. PMID 9259282. Belin V, Cusin

Johnjoe McFadden (729 words) [view diff] case mismatch in snippet view article find links to article

an Anglo-Irish scientist, academic and writer. He is Professor of Molecular Genetics at the University of Surrey, United Kingdom. McFadden was born in

Institute For Medical Research, Israel-Canada (1,371 words) [view diff] case mismatch in snippet view article find links to article

Immunology and Cancer Research; Medical Neurobiology; and Microbiology and Molecular Genetics. IMRIC also offers a bachelor's degree course in Biomedical Sciences

MYOT (2,143 words) [view diff] case mismatch in snippet view article find links to article

encoded by a candidate gene for limb-girdle muscular dystrophy". Human Molecular Genetics. 8 (7): 1329–36. doi:10.1093/hmg/8.7.1329. PMID 10369880. S2CID 16176213

Iduronate-2-sulfatase (1,051 words) [view diff] case mismatch in snippet view article find links to article

type II) confirmed by in vitro mutagenesis and expression". Human Molecular Genetics. 1 (9): 755–7. doi:10.1093/hmg/1.9.755. PMID 1284597. Bunge S, Steglich

SYT11 (512 words) [view diff] case mismatch in snippet view article find links to article

parkin, interacts with and ubiquitinates synaptotagmin XI". Human Molecular Genetics. 12 (20): 2587–97. doi:10.1093/hmg/ddg269. PMID 12925569. Nomura N

Paolo Casali (125 words) [view diff] exact match in snippet view article find links to article

Antonio, and chairman of its department of microbiology, immunology and molecular genetics. He is editor-in-chief of Autoimmunity. "Paolo Casali, M.D." U.T.

Cladosporium herbarum (1,433 words) [view diff] no match in snippet view article find links to article

Cladosporium herbarum is a common fungus found worldwide in organic and inorganic matter. It is efficiently distributed in the air, where it exists as

Bernard N. Fields (671 words) [view diff] exact match in snippet view article find links to article

Lehman Professor and chairman of the department of microbiology and molecular genetics of Harvard Medical School, and he was the head of division of infectious

Photoreceptor cell-specific nuclear receptor (1,399 words) [view diff] case mismatch in snippet view article find links to article

causes retinal dysplasia and degeneration in rd7/rd7 mice". Human Molecular Genetics. 10 (16): 1619–26. doi:10.1093/hmg/10.16.1619. PMID 11487564. Milam

Chris Adami (490 words) [view diff] exact match in snippet view article find links to article

"Chris" Adami (born August 30, 1962) is a professor of microbiology and molecular genetics, as well as professor of physics and astronomy, at Michigan State

KCNB2 (536 words) [view diff] case mismatch in snippet view article find links to article

ion transport genes for involvement with common migraine". Human Molecular Genetics. 17 (21): 3318–3331. doi:10.1093/hmg/ddn227. PMC 2566523. PMID 18676988

Carnitine palmitoyltransferase II deficiency (3,163 words) [view diff] case mismatch in snippet view article find links to article

gene resulting in carnitine palmitoyltransferase II deficiency". Molecular Genetics and Metabolism. 89 (4): 323–31. doi:10.1016/j.ymgme.2006.08.004. PMID 16996287

Lewis E. Kay (331 words) [view diff] exact match in snippet view article find links to article

of the structure and behaviour of proteins. He is a professor of molecular genetics, biochemistry and chemistry at the University of Toronto and Senior

Centre for DNA Fingerprinting and Diagnostics (720 words) [view diff] exact match in snippet view article find links to article

molecular epidemiology of bacterial pathogens, structural genetics, molecular genetics, bioinformatics and computational biology. CDFD was conceptualised

Myotonin-protein kinase (2,426 words) [view diff] case mismatch in snippet view article find links to article

DMPK, is expressed almost exclusively in muscle and heart". Human Molecular Genetics. 9 (14): 2167–73. doi:10.1093/hmg/9.14.2167. PMID 10958655. Wansink

Linda Tyfield (164 words) [view diff] exact match in snippet view article find links to article

and head of molecular genetics and then head of the department of molecular genetics. She served as chair of the Clinical Molecular Genetics Society from

Journal of Individual Differences (94 words) [view diff] exact match in snippet view article find links to article

developmental aspects. It endeavors to integrate fields - for instance molecular genetics and theories of complex behavior. The Journal of Individual Differences

CLCN5 (4,939 words) [view diff] case mismatch in snippet view article find links to article

for Dent's disease (an X-linked hereditary nephrolithiasis)". Human Molecular Genetics. 3 (11): 2053–9. PMID 7874126. Fisher SE, van Bakel I, Lloyd SE, Pearce

Peter St George-Hyslop (613 words) [view diff] exact match in snippet view article find links to article

appointment at Harvard's Massachusetts General Hospital, where he taught molecular genetics and neurology from 1987 to 1991. He was appointed to the University

Anne Simon (331 words) [view diff] case mismatch in snippet view article find links to article

University of Maryland, College Park in the Department of Cell Biology and Molecular Genetics. Dr. Simon also heads the Virology Program at UMd, and is a senior

Lethal arthrogryposis with anterior horn cell disease (282 words) [view diff] no match in snippet view article find links to article

Lethal arthrogryposis with anterior horn cell disease (LAAHD) is an autosomal recessive genetic disorder characterized by reduced mobility of the foetus

Suzanne Walker (205 words) [view diff] case mismatch in snippet view article find links to article

Suzanne Walker is a professor of Microbiology and Molecular Genetics at Harvard University. Her research focuses on mechanisms of antibiotics and antibiotic

Malcolm Casadaban (429 words) [view diff] exact match in snippet view article find links to article

Casadaban (12 August 1949 – 13 September 2009) was associate professor of molecular genetics, cell biology and microbiology at the University of Chicago. Casadaban

UGT1A9 (1,338 words) [view diff] case mismatch in snippet view article find links to article

with bilirubin levels and unconjugated hyperbilirubinemia". Human Molecular Genetics. 18 (14): 2711–2718. doi:10.1093/hmg/ddp203. PMC 2701337. PMID 19419973

Premee Mohamed (462 words) [view diff] exact match in snippet view article find links to article

Editor for Escape Pod. Mohamed received her undergraduate degree in molecular genetics in 2002, and also holds a degree in environmental science. Mohamed

Fumarylacetoacetate hydrolase (2,536 words) [view diff] case mismatch in snippet view article find links to article

identification of a missense mutation abolishing enzymatic activity". Human Molecular Genetics. 2 (7): 941–6. doi:10.1093/hmg/2.7.941. PMID 8364576. Rootwelt H,

Wolfgang Joklik (1,033 words) [view diff] case mismatch in snippet view article find links to article

7, 2019) was a virologist and James B. Duke Professor Emeritus of Molecular Genetics and Microbiology at Duke University, from which he retired in 1993

Atrophin 1 (1,923 words) [view diff] case mismatch in snippet view article find links to article

SH3 domain of an insulin receptor tyrosine kinase substrate". Human Molecular Genetics. 8 (6): 947–57. doi:10.1093/hmg/8.6.947. PMID 10332026. Wood JD, Yuan

William Pearson (252 words) [view diff] exact match in snippet view article find links to article

Nottingham William Pearson (scientist), professor of biochemistry and molecular genetics in the School of Medicine at the University of Virginia William Pearson

Freckle (1,293 words) [view diff] case mismatch in snippet view article find links to article

melanocortin 1 receptor (MC1R) gene on human pigmentation". Human Molecular Genetics. 9 (17): 2531–2537. doi:10.1093/hmg/9.17.2531. hdl:20.500

ATP2C1 (1,013 words) [view diff] case mismatch in snippet view article find links to article

caused by mutations in ATP2C1 encoding a novel Ca(2+) pump". Human Molecular Genetics. 9 (7): 1131–1140. doi:10.1093/hmg/9.7.1131. PMID 10767338. "Entrez

GYPB (3,580 words) [view diff] exact match in snippet view article find links to article

1016/0005-2736(93)90170-5. PMID 8499461. Huang CH, Blumenfeld OO (April 1991). "Molecular genetics of human erythrocyte MiIII and MiVI glycophorins. Use of a pseudoexon

KRIT1 (1,398 words) [view diff] case mismatch in snippet view article find links to article

inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells". Human Molecular Genetics. 18 (5): 911–8. doi:10.1093/hmg/ddn420. PMC 2640205. PMID 19088124

James R. Lupski (249 words) [view diff] case mismatch in snippet view article find links to article

R. Lupski (born February 22, 1957) is the Cullen Endowed Chair in Molecular Genetics and Professor in the Department of Pediatrics at Baylor College of

Cav2.1 (1,826 words) [view diff] case mismatch in snippet view article find links to article

trinucleotide repeats derived from human brain". Somatic Cell and Molecular Genetics. 21 (4): 279–84. doi:10.1007/BF02255782. PMID 8525433. S2CID 22174220

FANCF (2,441 words) [view diff] case mismatch in snippet view article find links to article

FANCF forms a nuclear complex with FANCA, FANCC and FANCG". Human Molecular Genetics. 9 (18): 2665–74. doi:10.1093/hmg/9.18.2665. PMID 11063725. Gordon

Louis Siminovitch (730 words) [view diff] case mismatch in snippet view article find links to article

(Toronto). He was the founder and the first Chair of the Department of Molecular Genetics at the University of Toronto, then called Department of Medical Cell

ATRX (1,758 words) [view diff] case mismatch in snippet view article find links to article

characterization of a new human Xq13 gene, encoding a putative helicase". Human Molecular Genetics. 3 (11): 1957–64. doi:10.1093/hmg/3.11.1957. PMID 7874112. Gibbons

Ralf Baumeister (74 words) [view diff] case mismatch in snippet view article find links to article

September 1, 1961 in Schwabach) is a German professor (Bioinformatics and Molecular Genetics). He is currently co-director of the School of Life Sciences at Freiburg

Cold Spring Harbor Laboratory (3,981 words) [view diff] exact match in snippet view article find links to article

of institutions that played a central role in the development of molecular genetics and molecular biology. It has been home to eight scientists who have

One gene–one enzyme hypothesis (2,152 words) [view diff] exact match in snippet view article find links to article

genetics.' In actuality they proved to be the opening gun in what became molecular genetics and all the developments that have followed from that." The development

Amelogenesis imperfecta (2,439 words) [view diff] case mismatch in snippet view article find links to article

amelotin exons 3-6 is associated with amelogenesis imperfecta". Human Molecular Genetics. 25 (16): 3578–3587. doi:10.1093/hmg/ddw203. PMC 5179951. PMID 27412008

ZDHHC17 (558 words) [view diff] case mismatch in snippet view article find links to article

"Huntingtin interacts with a family of WW domain proteins". Human Molecular Genetics. 7 (9): 1463–74. doi:10.1093/hmg/7.9.1463. PMID 9700202. Goytain A

SMC1A (2,088 words) [view diff] case mismatch in snippet view article find links to article

segregation protein conserved in lower eukaryotes and prokaryotes". Human Molecular Genetics. 4 (2): 243–9. doi:10.1093/hmg/4.2.243. PMID 7757074. "Entrez Gene:

Neurospora crassa (2,698 words) [view diff] exact match in snippet view article find links to article

genetics'. In actuality, they proved to be the opening gun in what became molecular genetics and all developments that have followed from that." In the 24 April

ACADSB (1,142 words) [view diff] case mismatch in snippet view article find links to article

functional and molecular studies on a defect in isoleucine catabolism". Molecular Genetics and Metabolism. 93 (1): 30–5. doi:10.1016/j.ymgme.2007.09.002. PMID 17945527

Plakoglobin (4,698 words) [view diff] exact match in snippet view article find links to article

ARVD/ARVC is a disease of the cardiac muscle desmosome; advances in molecular genetics have illuminated this notion. Studies investigating the role of plakoglobin

PRPF3 (1,048 words) [view diff] case mismatch in snippet view article find links to article

pigmentosa maps in the pericentromeric region of chromosome 1". Human Molecular Genetics. 5 (8): 1193–7. doi:10.1093/hmg/5.8.1193. PMID 8842740. Wang A, Forman-Kay

EXT2 (gene) (2,057 words) [view diff] case mismatch in snippet view article

exostoses to the pericentromeric region of chromosome 11". Human Molecular Genetics. 3 (1): 167–71. doi:10.1093/hmg/3.1.167. PMID 8162019. Bridge JA,

Glycogen phosphorylase (2,918 words) [view diff] exact match in snippet view article find links to article

1021/ci9900332. Nogales-Gadea G, Arenas J, Andreu AL (January 2007). "Molecular genetics of McArdle's disease". Current Neurology and Neuroscience Reports

Stephen Harvey (biologist) (464 words) [view diff] case mismatch in snippet view article

2003, Harvey was professor in the Department of Biochemistry and Molecular Genetics at the University of Alabama at Birmingham (UAB). He is past president

Pachychilidae (1,033 words) [view diff] exact match in snippet view article find links to article

F. & Glaubrecht M. (2003). "Morphology, reproductive biology and molecular genetics of ovoviviparous freshwater gastropods (Cerithioidea: Pachychilidae)

EXT2 (gene) (2,057 words) [view diff] case mismatch in snippet view article

exostoses to the pericentromeric region of chromosome 11". Human Molecular Genetics. 3 (1): 167–71. doi:10.1093/hmg/3.1.167. PMID 8162019. Bridge JA,

Tyrosinemia (685 words) [view diff] case mismatch in snippet view article find links to article

Type III detected via neonatal screening: management and outcome". Molecular Genetics and Metabolism. 107 (3): 605–7. doi:10.1016/j.ymgme.2012.09.002. PMID 23036342

Thyrotropin-releasing hormone receptor (1,094 words) [view diff] case mismatch in snippet view article find links to article

thyrotropin-releasing hormone (TRH) receptor gene to chromosome 8". Somatic Cell and Molecular Genetics. 19 (6): 577–80. doi:10.1007/BF01233384. PMID 8128317. S2CID 44982871

DDX20 (1,639 words) [view diff] case mismatch in snippet view article find links to article

protein and a specific subset of spliceosomal Sm proteins". Human Molecular Genetics. 9 (13): 1977–1986. doi:10.1093/hmg/9.13.1977. PMID 10942426. Andersson

DAX1 (1,842 words) [view diff] case mismatch in snippet view article find links to article

hypoplasia congenita and glycerol kinase deficiency genes" (PDF). Human Molecular Genetics. 1 (8): 579–85. doi:10.1093/hmg/1.8.579. PMID 1301166. Goodfellow

Stephen Harvey (biologist) (464 words) [view diff] case mismatch in snippet view article

2003, Harvey was professor in the Department of Biochemistry and Molecular Genetics at the University of Alabama at Birmingham (UAB). He is past president

RBMX (1,026 words) [view diff] case mismatch in snippet view article find links to article

motor neuron (SMN) via direct interaction with Htra2-beta1". Human Molecular Genetics. 11 (17): 2037–49. doi:10.1093/hmg/11.17.2037. PMID 12165565. Ajuh

AKTIP (850 words) [view diff] no match in snippet view article find links to article

AKT-interacting protein is a protein that in humans is encoded by the AKTIP gene. The mouse homolog of this gene produces fused toes and thymic hyperplasia

Isoleucine (1,404 words) [view diff] case mismatch in snippet view article find links to article

(December 2006). "Inborn errors of isoleucine degradation: a review". Molecular Genetics and Metabolism. 89 (4): 289–299. doi:10.1016/j.ymgme.2006.07.010.

Plant morphology (4,684 words) [view diff] exact match in snippet view article find links to article

morphological data but also by evidence from molecular genetics. More recent evidence from molecular genetics provides further support for continuum morphology

Complement factor B (1,095 words) [view diff] exact match in snippet view article find links to article

37. PMC 3178140. PMID 21394116. Campbell RD (January 1987). "The molecular genetics and polymorphism of C2 and factor B". British Medical Bulletin. 43

Cartilage associated protein (829 words) [view diff] case mismatch in snippet view article find links to article

endoplasmic reticulum collagen prolyl 3-hydroxylation complex". Human Molecular Genetics. 19 (2): 223–234. doi:10.1093/hmg/ddp481. PMC 2796888. PMID 19846465

Anthony Mahowald (1,434 words) [view diff] exact match in snippet view article find links to article

November 24, 1932) is a molecular genetics and cellular biologist who served as the department chair of the molecular genetics and cellular biology department

SOS box (512 words) [view diff] exact match in snippet view article find links to article

response Henkin, Tina M.; Peters, Joseph E. (2020). Snyder and Champness molecular genetics of bacteria (Fifth ed.). Hoboken, NJ : Washington, D.C: John Wiley

Ekkehard Bautz (642 words) [view diff] case mismatch in snippet view article find links to article

Friedrich Bautz is a molecular biologist and chair of the Institute of Molecular Genetics at the University of Heidelberg. He was born September 24, 1933, in

Marjorie Hoy (456 words) [view diff] case mismatch in snippet view article find links to article

where pesticides are applied. Her books include the textbook Insect Molecular Genetics, the third edition of which was published in 2013. Hoy was born in

AFF2 (1,210 words) [view diff] case mismatch in snippet view article find links to article

the molecular pathology of FRAXE intellectual disability". Human Molecular Genetics. 20 (10): 1873–85. doi:10.1093/hmg/ddr069. PMID 21330300. Mulley JC

Gastric-brooding frog (2,191 words) [view diff] exact match in snippet view article find links to article

Rheobatrachinae, but others place them in their own family, Rheobatrachidae. Molecular genetics finds it sister to Mixophyes. Scientists at the University of Newcastle

HAND1 (2,187 words) [view diff] case mismatch in snippet view article find links to article

identifies HAND1 mutations in septation defects of the human heart". Human Molecular Genetics. 18 (19): 3567–78. doi:10.1093/hmg/ddp305. PMID 19586923. Zhou YM

Glycophorin A (4,101 words) [view diff] exact match in snippet view article find links to article

PMID 6172902. S2CID 27162982. Huang CH, Blumenfeld OO (April 1991). "Molecular genetics of human erythrocyte MiIII and MiVI glycophorins. Use of a pseudoexon

ZNF217 (967 words) [view diff] case mismatch in snippet view article find links to article

death associated with chemotherapy and telomere dysfunction". Human Molecular Genetics. 14 (21): 3219–25. doi:10.1093/hmg/ddi352. PMID 16203743. Littlepage

Elissa Hallem (246 words) [view diff] case mismatch in snippet view article find links to article

Graduate Studies in the Department of Microbiology, Immunology, and Molecular Genetics at UCLA. Elissa Hallem was born in Santa Monica, California, in 1977

Monica Justice (481 words) [view diff] case mismatch in snippet view article find links to article

developmental geneticist. She is the Canada Research Chair in Mammalian Molecular Genetics at the University of Toronto and Program Head of Genetics and Genome

John Beringer (143 words) [view diff] case mismatch in snippet view article find links to article

and the University of East Anglia (PhD, 1973). He was Professor of Molecular Genetics at the University of Bristol from 1984 to 2005, and Pro-Vice-Chancellor

Myelin protein zero (2,227 words) [view diff] case mismatch in snippet view article find links to article

1016/0168-9525(94)90214-3. PMID 7518101. Roa BB, Lupski JR (1994). "Molecular Genetics of Charcot-Marie-Tooth Neuropathy". Advances in Human Genetics. Vol

N-Acetylglutamate synthase (1,223 words) [view diff] case mismatch in snippet view article find links to article

(2010). "N-Acetylglutamate synthase: structure, function and defects". Molecular Genetics and Metabolism. 100 (Suppl 1): S13–9. doi:10.1016/j.ymgme.2010.02

Vincent Timmerman (245 words) [view diff] case mismatch in snippet view article find links to article

Timmerman is a Belgian scientist working at the VIB Department of Molecular Genetics at the University of Antwerp of Christine Van Broeckhoven. His research

Pyruvate dehydrogenase deficiency (2,217 words) [view diff] case mismatch in snippet view article find links to article

Deficiency: Clinical, Biochemical and Genetic Features in 371 Patients". Molecular Genetics and Metabolism. 105 (1): 34–43. doi:10.1016/j.ymgme.2011.09.032. ISSN 1096-7192

GLUT2 (1,330 words) [view diff] case mismatch in snippet view article find links to article

implications for understanding genetic association signals at this locus". Molecular Genetics and Metabolism. 104 (4): 648–53. doi:10.1016/j.ymgme.2011.08.026.

William R. Jacobs Jr. (315 words) [view diff] exact match in snippet view article find links to article

Hughes Medical Institute Investigator. Jacobs is a specialist in the molecular genetics of Mycobacteria. His research efforts are aimed at discovering genes

FBLN5 (1,401 words) [view diff] case mismatch in snippet view article find links to article

with apolipoprotein(a) mediated by the kringle IV-type 2 domain". Molecular Genetics and Genomics. 267 (4): 440–6. doi:10.1007/s00438-002-0673-6. PMID 12111551

Norma Andrews (368 words) [view diff] case mismatch in snippet view article find links to article

professor at the University of Maryland Department of Cell Biology and Molecular Genetics. She chaired the department from 2009 to 2014. Norma Andrews received

Emmanuel Mignot (1,118 words) [view diff] exact match in snippet view article find links to article

Yanagisawa, M. (1999-08-20). "Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation". Cell. 98 (4): 437–451. doi:10.1016/s0092-8674(00)81973-x

Emmanuel Mignot (1,118 words) [view diff] exact match in snippet view article find links to article

Yanagisawa, M. (1999-08-20). "Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation". Cell. 98 (4): 437–451. doi:10.1016/s0092-8674(00)81973-x

GLUT2 (1,330 words) [view diff] case mismatch in snippet view article find links to article

implications for understanding genetic association signals at this locus". Molecular Genetics and Metabolism. 104 (4): 648–53. doi:10.1016/j.ymgme.2011.08.026.

FXR2 (1,344 words) [view diff] case mismatch in snippet view article find links to article

of FMR1, FXR1 and FXR2 proteins in human brain and testis". Human Molecular Genetics. 6 (8): 1315–22. doi:10.1093/hmg/6.8.1315. hdl:1765/8709. PMID 9259278

Fanconi anemia, complementation group C (2,397 words) [view diff] case mismatch in snippet view article find links to article

FANCF forms a nuclear complex with FANCA, FANCC and FANCG". Human Molecular Genetics. 9 (18): 2665–74. doi:10.1093/hmg/9.18.2665. PMID 11063725. Garcia-Higuera

Simpson–Golabi–Behmel syndrome (1,690 words) [view diff] case mismatch in snippet view article find links to article

Molecular Basis for Overgrowth, Malformation, and Cancer Predisposition". Molecular Genetics and Metabolism. 72 (4): 279–86. doi:10.1006/mgme.2001.3150. PMID 11286501

Keratin 14 (1,175 words) [view diff] case mismatch in snippet view article find links to article

of keratin 14 in epidermolysis bullosa simplex: delta E375". Human Molecular Genetics. 2 (11): 1971–2. doi:10.1093/hmg/2.11.1971. PMID 7506606. Chan Y,

X-linked intellectual disability (2,017 words) [view diff] case mismatch in snippet view article find links to article

telencephalon, is mutated in X-linked mental retardation". Human Molecular Genetics. 11 (8): 981–991. doi:10.1093/hmg/11.8.981. PMID 11971879. Jensen

Paragus haemorrhous (682 words) [view diff] no match in snippet view article find links to article

Paragus haemorrhous, the Black-backed Grass Skimmer is a common widespread species of hoverfly found in many parts of Europe, Africa and the Nearctic.

Collagen, type VII, alpha 1 (2,218 words) [view diff] case mismatch in snippet view article find links to article

of fibronectin and the A domains of von Willebrand factor". Human Molecular Genetics. 1 (7): 475–481. doi:10.1093/hmg/1.7.475. PMID 1307247. Gammon WR

Manuel Buchwald (251 words) [view diff] exact match in snippet view article find links to article

Insurance Chair in Pediatric Research. His research interests are human molecular genetics, Fanconi anemia, cystic fibrosis and gene cloning and function. From

Joseph Heitman (2,758 words) [view diff] case mismatch in snippet view article find links to article

He is the James B. Duke Professor and Chair of the Department of Molecular Genetics and Microbiology at Duke University School of Medicine. Joseph Heitman

Generalist Genes hypothesis (286 words) [view diff] exact match in snippet view article find links to article

has important implications for education, cognitive sciences and molecular genetics. Plomin, R.; Kovas, Y. (2005). "Generalist genes and learning disabilities"

Keratin disease (141 words) [view diff] exact match in snippet view article find links to article

1111/j.1600-0625.1996.tb00133.x. PMID 9028791. Smith F (2003). "The molecular genetics of keratin disorders". Am J Clin Dermatol. 4 (5): 347–64. doi:10

SGCG (1,820 words) [view diff] case mismatch in snippet view article find links to article

of gypsies possibly predating their migration out of India". Human Molecular Genetics. 5 (12): 2019–22. doi:10.1093/hmg/5.12.2019. PMID 8968757. "Entrez

Tina Henkin (187 words) [view diff] case mismatch in snippet view article find links to article

is coauthor of the bacterial genetics textbook Snyder & Champness Molecular Genetics of Bacteria, published by the American Society of Microbiology Press

SLC22A5 (2,294 words) [view diff] case mismatch in snippet view article find links to article

Japanese pedigrees with primary systemic carnitine deficiency". Human Molecular Genetics. 8 (12): 2247–54. doi:10.1093/hmg/8.12.2247. PMID 10545605. Ascunce

Ataxin 7 (500 words) [view diff] case mismatch in snippet view article find links to article

ataxin-3 and ataxin-7 function by integrative bioinformatics". Human Molecular Genetics. 12 (21): 2845–2852. doi:10.1093/hmg/ddg297. PMID 12944423. Wolfe

Acetaldehyde dehydrogenase (1,523 words) [view diff] case mismatch in snippet view article find links to article

reactions, consumption and dependence: an integrated analysis", Human Molecular Genetics, 18(3):580-93. Crabb D, Xiao Q (Jun 1998). "Studies on the enzymology

KDM5C (855 words) [view diff] case mismatch in snippet view article find links to article

Y-linked homologue escapes X-inactivation in mouse and human". Human Molecular Genetics. 3 (6): 879–84. doi:10.1093/hmg/3.6.879. PMID 7951230. Wu J, Ellison

SGSH (1,168 words) [view diff] exact match in snippet view article find links to article

PMID 6796310. S2CID 24826103. Yogalingam G, Hopwood JJ (Oct 2001). "Molecular genetics of mucopolysaccharidosis type IIIA and IIIB: Diagnostic, clinical

List of Northwestern University faculty (1,855 words) [view diff] exact match in snippet view article find links to article

biomedical engineering, medicine (hematology/oncology), biochemistry and molecular genetics Ted Belytschko, professor of mechanical engineering, computational

Congenital disorder of glycosylation (3,798 words) [view diff] case mismatch in snippet view article find links to article

reflection of the mutations found in the functional gene". Human Molecular Genetics. 7 (2): 157–164. doi:10.1093/hmg/7.2.157. PMID 9425221. Paprocka,

Sue Jinks-Robertson (381 words) [view diff] case mismatch in snippet view article find links to article

and microbiology. She is currently a professor in the Department of Molecular Genetics and Microbiology at the Duke University School of Medicine. In May

SGCA (1,204 words) [view diff] case mismatch in snippet view article find links to article

form of autosomal recessive limb-girdle muscular dystrophy". Human Molecular Genetics. 4 (7): 1163–7. doi:10.1093/hmg/4.7.1163. PMID 8528203. Duggan DJ

Hsien Wu (516 words) [view diff] case mismatch in snippet view article find links to article

Wu's son, Ray J. Wu, became the Liberty Hyde Bailey Professor of Molecular Genetics and Biology at Cornell University, and developed the first method

Ray Wu (784 words) [view diff] case mismatch in snippet view article find links to article

American geneticist and served as Liberty Hyde Bailey Professor of Molecular Genetics and Biology at Cornell University. In 1970, Wu created the first approach

OPA3 (696 words) [view diff] case mismatch in snippet view article find links to article

untranslated region of the myotonic dystrophy protein kinase gene". Human Molecular Genetics. 6 (4): 563–569. doi:10.1093/hmg/6.4.563. PMID 9097959. Anikster Y

HNRNPR (1,425 words) [view diff] case mismatch in snippet view article find links to article

axonal beta-actin mRNA translocation in spinal motor neurons". Human Molecular Genetics. 19 (10): 1951–66. doi:10.1093/hmg/ddq073. ISSN 1460-2083. PMID 20167579

MNT (gene) (1,057 words) [view diff] case mismatch in snippet view article

is a new member of the Mlx transcription factor network". Human Molecular Genetics. 10 (6): 617–627. doi:10.1093/hmg/10.6.617. PMID 11230181. Meroni

Mucolipidosis type IV (946 words) [view diff] case mismatch in snippet view article find links to article

gene encoding a novel transient receptor potential channel". Human Molecular Genetics. 9 (17): 2471–8. doi:10.1093/hmg/9.17.2471. PMID 11030752. Dong, Xian-Ping;

Hypoxanthine-guanine phosphoribosyltransferase (1,610 words) [view diff] case mismatch in snippet view article find links to article

variants of hypoxanthine phosphoribosyltransferase deficiency". Human Molecular Genetics. 1 (6): 427–32. doi:10.1093/hmg/1.6.427. PMID 1301916. Lightfoot T

Phil Gilmartin (115 words) [view diff] case mismatch in snippet view article find links to article

specialises in plant genetics. Since 2011, he has been Professor of Plant Molecular Genetics and Executive Dean of the Faculty of Science at the University of

Acute intermittent porphyria (2,766 words) [view diff] case mismatch in snippet view article find links to article

Finland: 19 mutations in the porphobilinogen deaminase gene". Human Molecular Genetics. 4 (2): 215–222. doi:10.1093/hmg/4.2.215. ISSN 0964-6906. PMID 7757070

Leslie Joan Baier (211 words) [view diff] exact match in snippet view article find links to article

is an American scientist. She is a senior investigator in diabetes molecular genetics at the National Institute of Diabetes and Digestive and Kidney Diseases

Jurgen Del-Favero (396 words) [view diff] case mismatch in snippet view article find links to article

Del-Favero is a Belgian scientist working at the VIB Department of Molecular Genetics at the University of Antwerp. His research is directed towards the

Mariel Vázquez (500 words) [view diff] exact match in snippet view article find links to article

affiliated with the departments of mathematics and of microbiology and molecular genetics. Vázquez received her Bachelor of Science in Mathematics from the

RecA (1,428 words) [view diff] exact match in snippet view article find links to article

Joseph E.; Snyder, Larry; Champness, Wendy (2020). Snyder & Champness molecular genetics of bacteria (Fifth ed.). Hoboken, NJ: Wiley. pp. 368–371. ISBN 9781555819750

E3 binding protein (2,584 words) [view diff] case mismatch in snippet view article find links to article

gene in a case of pyruvate dehydrogenase complex deficiency". Human Molecular Genetics. 7 (3): 501–5. doi:10.1093/hmg/7.3.501. PMID 9467010. Gawin B, Niederführ

Alpha-actinin-2 (2,601 words) [view diff] case mismatch in snippet view article find links to article

and NUDEL: regulation and loss of interaction with mutation". Human Molecular Genetics. 12 (13): 1591–608. doi:10.1093/hmg/ddg162. PMID 12812986. Faulkner

XRCC2 (1,849 words) [view diff] case mismatch in snippet view article find links to article

interaction of FANCD2 with BRCA2 in DNA damage response pathways". Human Molecular Genetics. 13 (12): 1241–8. doi:10.1093/hmg/ddh135. PMID 15115758. Liu N, Schild

Fisheries and Illinois Aquaculture Center (236 words) [view diff] exact match in snippet view article find links to article

Research faculty in the Center have diverse capabilities including molecular genetics, aquatic toxicology, aquatic ecology, bioenergetics, fish nutrition

Paxillosida (184 words) [view diff] case mismatch in snippet view article find links to article

Paxillosida (Asteroidea) based on complete mitochondrial DNA sequences. Molecular Genetics and Evolution, 36, 598–605 Barnes, Robert D. (1982). Invertebrate

Muenke syndrome (1,041 words) [view diff] case mismatch in snippet view article find links to article

(Agochukwu et.al. 2006). According to the article Craniosynostosis: Molecular Genetics, penetrance is higher in females (87%) than in males (76%). Muenke

Pendrin (2,317 words) [view diff] case mismatch in snippet view article find links to article

genetic heterogeneity in the Middle Eastern Druze population". Human Molecular Genetics. 4 (9): 1637–1642. doi:10.1093/hmg/4.9.1637. PMID 8541853. Coyle B

Methylmalonyl-CoA (603 words) [view diff] case mismatch in snippet view article find links to article

Chapman KA (December 2017). "Propionyl-CoA carboxylase - A review". Molecular Genetics and Metabolism. 122 (4): 145–152. doi:10.1016/j.ymgme.2017.10.002

FANCE (2,255 words) [view diff] case mismatch in snippet view article find links to article

Fanconi anaemia proteins suggest a common functional pathway". Human Molecular Genetics. 10 (4): 423–9. doi:10.1093/hmg/10.4.423. PMID 11157805. Garcia-Higuera

C1QTNF5 (1,759 words) [view diff] case mismatch in snippet view article find links to article

degeneration: a genetic model for age-related macular degeneration". Human Molecular Genetics. 12 (20): 2657–67. doi:10.1093/hmg/ddg289. PMID 12944416. Shapiro

PAX6 (2,710 words) [view diff] case mismatch in snippet view article find links to article

factor genes and the developing eye: a genetic perspective". Human Molecular Genetics. 5 Spec No: 1471–88. doi:10.1093/hmg/5.Supplement_1.1471. PMID 8875254

Late onset congenital adrenal hyperplasia (4,673 words) [view diff] no match in snippet view article find links to article

Late onset congenital adrenal hyperplasia (LOCAH), also known as nonclassic congenital adrenal hyperplasia (NCCAH or NCAH), is a milder form of congenital

POU3F2 (1,170 words) [view diff] case mismatch in snippet view article find links to article

transcription activation by Brn-2 and affects cell survival". Human Molecular Genetics. 8 (6): 977–87. doi:10.1093/hmg/8.6.977. PMID 10332029. Hara Y, Rovescalli

Jay Tischfield (1,612 words) [view diff] case mismatch in snippet view article find links to article

of Medical Genetics in PhD Medical Genetics (1987 - ) and Clinical Molecular Genetics (1993 - 2019). He is a Founding Fellow of the American College of

Marie Celeste Simon (303 words) [view diff] case mismatch in snippet view article find links to article

School. In 1992, Simon became an Assistant Professor of Medicine and Molecular Genetics and Cell Biology at the University of Chicago. She became a professor

Hermine Maes (133 words) [view diff] case mismatch in snippet view article find links to article

geneticist and Associate Professor in both the Department of Human and Molecular Genetics at the Virginia Commonwealth University School of Medicine and the

KHDRBS3 (1,258 words) [view diff] case mismatch in snippet view article find links to article

with an RNA-binding protein implicated in spermatogenesis". Human Molecular Genetics. 8 (6): 959–69. doi:10.1093/hmg/8.6.959. PMID 10332027. Lee J, Burr

Andrew Read (213 words) [view diff] case mismatch in snippet view article find links to article

Emeritus upon formal retirement. He served as chair of the Clinical Molecular Genetics Society and was founder chair of the British Society for Human Genetics

SALL1 (1,309 words) [view diff] case mismatch in snippet view article find links to article

TRF1/PIN2 and localizes to pericentromeric heterochromatin". Human Molecular Genetics. 10 (26): 3017–24. doi:10.1093/hmg/10.26.3017. PMID 11751684. Netzer

P. Michael Conneally (591 words) [view diff] case mismatch in snippet view article find links to article

Indiana University School of Medicine in the Department of Medical and Molecular Genetics. He was certified in medical genetics by the American Board of Medical

Carbohydrate-responsive element-binding protein (891 words) [view diff] case mismatch in snippet view article find links to article

is a new member of the Mlx transcription factor network". Human Molecular Genetics. 10 (6): 617–627. doi:10.1093/hmg/10.6.617. PMID 11230181. de Luis

Eckard Wimmer (2,491 words) [view diff] exact match in snippet view article find links to article

American virologist, organic chemist and distinguished professor of molecular genetics and microbiology at Stony Brook University. He is best known for his

PAFAH1B1 (1,513 words) [view diff] case mismatch in snippet view article find links to article

isolated lissencephaly sequence and Miller-Dieker syndrome". Human Molecular Genetics. 6 (2): 157–64. doi:10.1093/hmg/6.2.157. PMID 9063735. "Entrez Gene:

Enamelin (1,622 words) [view diff] case mismatch in snippet view article find links to article

hypoplastic autosomal dominant amelogenesis imperfecta (AIH2)". Human Molecular Genetics. 11 (9): 1069–74. doi:10.1093/hmg/11.9.1069. PMID 11978766. "Entrez

CLCN2 (1,216 words) [view diff] case mismatch in snippet view article find links to article

chloride channel (CIC-2) cDNA widely expressed in human tissues". Human Molecular Genetics. 4 (3): 407–13. doi:10.1093/hmg/4.3.407. PMID 7795595. "Entrez Gene:

COX10 (1,374 words) [view diff] case mismatch in snippet view article find links to article

A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency". Human Molecular Genetics. 9 (8): 1245–9. doi:10.1093/hmg/9.8.1245. PMID 10767350. Online Mendelian

Columbian ground squirrel (3,531 words) [view diff] exact match in snippet view article find links to article

through writings produced by Lewis and Clark, while 21st century molecular genetics has more finely illuminated its ties with other close relatives. The