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Find link is a tool written by Edward Betts.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 217 found (3869 total)
alternate case: molecular genetics
Amgen
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Amgen Inc. (formerly Applied Molecular Genetics Inc.) is an American multinational biopharmaceutical company headquartered in Thousand Oaks, CaliforniaAnnual plant (1,424 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. GloballySelank (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 withUsha 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. UshaYangochiroptera (579 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 remainsEndothelin 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 mutationGenetic 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 genesFraser syndrome (1,526 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 16244325Jeffrey 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 BOutline 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,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 ofBattenin (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 KERajesh 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 SkeletalSMN1 (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. TalbotTSC1 (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 AKJanet Rossant (1,123 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 geneticYinpterochiroptera (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 megabatsTwist-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, LeeOncogenomics (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 cancerCharles 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–JakobPMM2 (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 10527672Tiger 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 recessiveDSC3 (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, occupyingFOXL2 (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. UhlenhautMethionine 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. BanerjeeWilliam 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 ProfessorKenneth 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 MedicinePMPCB (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 SSClear-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 InactivationCarsten 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 physicsAtaxin 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-PepeRPGRIP1 (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 10958647Spinal muscular atrophy (10,015 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 26931466Protoporphyrinogen oxidase (1,619 words) [view diff] case mismatch in snippet view article find links to article
protoporphyrinogen oxidase gene in patients with variegate porphyria". Human Molecular Genetics. 5 (3): 407–10. doi:10.1093/hmg/5.3.407. PMID 8852667. Lam H, DraganJoachim 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 interactionsYeast 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 et3-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: 198–209Grant 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)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 BiomolecularACADS (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 PDMLX (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 GPCDH15 (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 14028314Morula (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 orMichigan 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 ProbabilityGem-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. WangHuntingtin (3,381 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. EliasDistal 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:10ALG6 (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. "EntrezSIM1 (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. "EntrezGPR143 (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 18697795Ornithine 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 goalMethylmalonyl-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 (2,852 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, GoldsteinTatiana 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 IndianaFrataxin (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. ArchivedOligodendroglioma (3,020 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 occurPOMT1 (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 12925572Retinitis 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 8817343Diabetic 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 hypoglycemiaSMN2 (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 19329542Paolo 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.Guanidinoacetate methyltransferase deficiency (2,075 words) [view diff] case mismatch in snippet view article find links to article
individuals and recommendations for diagnosis, treatment and monitoring". Molecular Genetics and Metabolism. 111 (1): 16–25. doi:10.1016/j.ymgme.2013.10.018. ISSN 1096-7192Johnjoe 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 inThe Locust (2,587 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 allExpressivity (genetics) (1,763 words) [view diff] case mismatch in snippet view article
phenotype resemble those of human Saethre-Chotzen syndrome". Human Molecular Genetics. 7 (6): 945–957. doi:10.1093/hmg/7.6.945. ISSN 1460-2083. PMID 9580658CRX (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 DABernard 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 infectiousLinda 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 fromSurvival 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. MourelatosMYO7A (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, WeilShort-stature homeobox gene (1,255 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, CusinMYOT (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 16176213Herchel Smith Professor of Pure Mathematics (195 words) [view diff] case mismatch in snippet view article find links to article
of Pure Mathematics, Physics, Biochemistry, Molecular Biology, and Molecular Genetics." When the position was advertised in 2004, the first holder was expectedCladosporium 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 asChris 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 StateLethal arthrogryposis with anterior horn cell disease (284 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 foetusChris 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 StateJournal 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 DifferencesIduronate-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, SteglichLewis 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 SeniorSuzanne 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 antibioticPremee 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. MohamedMalcolm 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. CasadabanCentre for DNA Fingerprinting and Diagnostics (713 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 conceptualisedWolfgang 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 1993Carnitine 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 16996287Anne 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 seniorKCNB2 (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 18676988Institute For Medical Research, Israel-Canada (1,499 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 SciencesPhotoreceptor 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. MilamABCC11 (2,431 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 certainMyotonin-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. WansinkWilliam Pearson (262 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 PearsonPeter St George-Hyslop (756 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 UniversityAtrophin 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, YuanRalf 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 FreiburgJoanne 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 photosynthesisJames 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 ofKRIT1 (1,402 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 19088124UGT1A9 (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 19419973Fumarylacetoacetate 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,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 AATRX (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. GibbonsATP2C1 (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. "EntrezFANCF (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. GordonOPN1SW (634 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"Bananaquit (2,566 words) [view diff] exact match in snippet view article find links to article
bird in the tanager family Thraupidae. Before the development of molecular genetics in the 21st century, its relationship to other species was uncertainStephen 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 presidentFreckle (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:20.500Cav2.1 (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 22174220Louis 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 CellSMC1A (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: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 departmentGYPB (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 pseudoexonPRPF3 (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-KayAKTIP (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 hyperplasiaRBMX (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. AjuhEkkehard 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, inEXT2 (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,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 receivedEXT2 (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,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, inPachychilidae (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)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-ChancellorNeurospora crassa (2,700 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 AprilOne 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 developmentVincent 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 researchMarjorie 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 inMonica 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 GenomeDDX20 (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. AnderssonTyrosinemia (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 23036342SOS 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 WileyElissa Hallem (273 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. Her lab focuses on the ability for skin-penetrating nematodesACADSB (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 17945527Cold 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 haveCartilage 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 19846465AFF2 (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 JCComplement 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. 43Gastric-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 NewcastleThyrotropin-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 44982871William 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 genesPlant 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 morphologyGlycogen 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 ReportsAutoimmune regulator (3,097 words) [view diff] case mismatch in snippet view article find links to article
features of APECED phenotype and show altered immune response". Human Molecular Genetics. 11 (4): 397–409. doi:10.1093/hmg/11.4.397. PMID 11854172. Iioka TDAX1 (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. GoodfellowTina 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 PressGeneralist 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"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 9259278Manuel Buchwald (250 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. FromHAND1 (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 YMSue 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 MayN-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.2010.02Glycophorin 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 pseudoexonFBLN5 (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 12111551Myelin 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. VolParagus 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.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-xZNF217 (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. LittlepageSimpson–Golabi–Behmel syndrome (1,700 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 11286501Fanconi 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-HigueraIsoleucine (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.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 1096-7192Phil 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 ofJurgen Del-Favero (404 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 theLeslie 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 DiseasesKeratin 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:10SGSH (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, clinicalGLUT2 (1,334 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.Joseph Heitman (2,782 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 HeitmanHsien 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 methodSGCG (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. "EntrezOPA3 (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 YMuenke 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%). MuenkeKeratin 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,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 approachMariel 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 theX-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. JensenCollagen, 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 WRSGCA (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 DJFisheries 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 nutritionMucolipidosis 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;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. AscunceSLC22A5 (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. AscuncePaxillosida (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). InvertebrateHermine 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 theC1QTNF5 (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. ShapiroCongenital disorder of glycosylation (3,800 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,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 7757070RecA (1,426 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 9781555819750Andrew 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 GeneticsXRCC2 (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, SchildHypoxanthine-guanine phosphoribosyltransferase (1,614 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 TMNT (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. MeroniP. 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 MedicalFMR1 (3,455 words) [view diff] case mismatch in snippet view article find links to article
retardation protein is a negative regulator of translation". Human Molecular Genetics. 10 (4): 329–38. doi:10.1093/hmg/10.4.329. PMID 11157796. Hou L, AntionKDM5C (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, EllisonMarie 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 professorE3 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, NiederführJay 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 ofJohanna Rommens (1,350 words) [view diff] case mismatch in snippet view article find links to article
SickKids Research Institute and a professor in the Department of Molecular Genetics at the University of Toronto. Rommens grew up on a farm in easternMethylmalonyl-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.2017.10.002KHDRBS3 (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, BurrPendrin (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 BPrelamin-A/C (2,525 words) [view diff] case mismatch in snippet view article find links to article
sequence map to human chromosomes 1q12.1-q23 and 10". Somatic Cell and Molecular Genetics. 19 (2): 203–208. doi:10.1007/BF01233534. PMID 8511676. S2CID 32913788FANCE (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-HigueraAlpha-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. FaulknerEuroBioBank (293 words) [view diff] case mismatch in snippet view article find links to article
Collection), University of Munich DNA biobank of the Department of Molecular Genetics and Diagnostics, National Institute of Environmental Health (NIEH)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 hisAndrew W. Murray (140 words) [view diff] case mismatch in snippet view article find links to article
his research on budding yeast. He is the Herchel Smith Professor of Molecular Genetics and a Howard Hughes Medical Institute Professor at Harvard UniversityKeiko Ozato (714 words) [view diff] case mismatch in snippet view article find links to article
invoke epigenetic memory. She is Senior Investigator at the Section on Molecular Genetics of Immunity at the Eunice Kennedy Shriver National Institute of ChildRob Elles (197 words) [view diff] case mismatch in snippet view article find links to article
retiring in 2013. In the 1990s he served as Secretary of the Clinical Molecular Genetics Society, and as co-chair of the expert group developing the OrganisationList of Northwestern University faculty (1,886 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, computationalClair Francomano (828 words) [view diff] case mismatch in snippet view article find links to article
specializing in Ehlers–Danlos syndromes. She is Professor of Medical and Molecular Genetics at Indiana University. Clair Ann Francomano was born to Mrs. and CharlesVirginia Institute for Psychiatric and Behavioral Genetics (233 words) [view diff] case mismatch in snippet view article find links to article
subsidiaries of the Department of Psychiatry and the Department of Human and Molecular Genetics, respectively, at the VCU School of Medicine. The Institute's associatePAFAH1B1 (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:Sherif El-Khamisy (369 words) [view diff] case mismatch in snippet view article find links to article
Sherif El- Khamisy is an Egyptian Professor of Biochemistry and Molecular Genetics. He is the Director of Research and Innovation and co-founder of the