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Longer titles found: Treatment of Rett syndrome (view)

searching for Rett syndrome 62 found (253 total)

KCNJ10 (1,324 words) [view diff] exact match in snippet view article find links to article

mechanosensitive stereocilia of the sensory hair cells that make hearing possible. Rett syndrome is a neurological disorder characterized by a mutation in the MeCP2

Forme fruste (943 words) [view diff] case mismatch in snippet view article find links to article

malignancy and symptomatic relief of symptoms. "Forme fruste Rett Syndrome", variant of Rett Syndrome which has a later age of onset compared with the classical

Michael E. Greenberg (1,529 words) [view diff] case mismatch in snippet view article find links to article

biology and genetics of autism spectrum disorders, specifically in Rett Syndrome, a disease that is caused by mutations in MeCP2, a methyl-DNA binding

Lactiplantibacillus plantarum PS128 (325 words) [view diff] exact match in snippet view article find links to article

presumption of safety" list of the European Food Safety Authority. A study on Rett syndrome patients found that probiotic Lactiplantibacillus plantarum PS128 supplementation

Netrin G1 (656 words) [view diff] exact match in snippet view article find links to article

of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome". European Journal of Human Genetics. 13 (8): 921–7. doi:10.1038/sj

Joanne Berger-Sweeney (1,707 words) [view diff] exact match in snippet view article find links to article

1093/ilar.53.3-4.322 (2011) Berger-Sweeney J. "Cognitive deficits in Rett syndrome: what we know and what we need to know to treat them". Neurobiology

PRPF40B (162 words) [view diff] exact match in snippet view article find links to article

domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome". Journal of Molecular Medicine. 82 (2): 135–43. doi:10.1007/s00109-003-0497-9

GABRB2 (5,576 words) [view diff] exact match in snippet view article find links to article

physiopathology of Rett syndrome. β2 subunit mRNA expression level was subjected to significant upregulation in a mouse model of Rett syndrome Deficits in the

Acadia Pharmaceuticals (1,013 words) [view diff] exact match in snippet view article find links to article

2023, the FDA approved trofinetide (marketed as Daybue) for use in Rett syndrome. Acadia started in 1993 as Receptor Technologies, based in Winooski

GLRA2 (492 words) [view diff] exact match in snippet view article find links to article

receptor alpha2 subunit gene and exclusion of this gene as a candidate for Rett syndrome". Am. J. Med. Genet. 78 (2): 176–8. doi:10.1002/(SICI)1096-8628(199

Mriganka Sur (1,572 words) [view diff] case mismatch in snippet view article find links to article

as autism. Stemming from this work, a pharmacological treatment for Rett Syndrome is in advanced clinical trials. By imaging calcium responses of single

Neurophysics (1,233 words) [view diff] exact match in snippet view article find links to article

epigenetic regulation of the brain and for identifying the gene that causes Rett syndrome". The other most relevant prizes that can be awarded to a neurophysicist

Goldendoodle (1,439 words) [view diff] exact match in snippet view article find links to article

Sniffing Out Peanuts". ABC News. Retrieved 16 May 2021. "Girl with Rett syndrome receives goldendoodle service dog from Make-A-Wish". KPTV.com. 27 September

DLX5 (1,108 words) [view diff] exact match in snippet view article find links to article

for MeCP2 provides a molecular link between genomic imprinting and Rett syndrome". BioEssays. 27 (7): 676–80. doi:10.1002/bies.20266. PMID 15954098.

Perl-UNC Prize (1,020 words) [view diff] case mismatch in snippet view article find links to article

Receptors in the Brain. 2007 Huda Zoghbi, Discovery of the Genetic Basis of Rett Syndrome. 2008 Michael E. Greenberg, Discovery of Signaling Pathways Underlying

Helen M. McLoraine (444 words) [view diff] case mismatch in snippet view article find links to article

atypical dementia research at the University of Chicago International Rett Syndrome Foundation ($1 million matching gift) Michael J. Fox Foundation for

GPM6B (627 words) [view diff] exact match in snippet view article find links to article

et al. (1998). "Mutation analysis of the M6b gene in patients with Rett syndrome". Am. J. Med. Genet. 78 (2): 165–8. doi:10.1002/(SICI)1096-8628(199

Gastrin-releasing peptide receptor (1,292 words) [view diff] exact match in snippet view article find links to article

gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome". Am. J. Med. Genet. 78 (2): 173–5. doi:10.1002/(SICI)1096-8628(199

Pat Frink (534 words) [view diff] exact match in snippet view article find links to article

ended, he focused on caring for his daughter, Kody, who was born with Rett syndrome and had a life expectancy of about seven years. She was 21 when she

GRIA3 (2,077 words) [view diff] exact match in snippet view article find links to article

Dahle EJ, Toriolo D, Zoghbi HY (2000). "Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in Xq". Am. J. Med. Genet. 90 (1):

List of awareness ribbons (1,486 words) [view diff] case mismatch in snippet view article find links to article

Lavender ribbon ? Craniosynostosis ? Epilepsy ? General cancer awareness ? Rett Syndrome Silver ribbon ? Parkinson's Disease 1993 Jean Singleton Schizophrenia

HCCS (gene) (1,014 words) [view diff] exact match in snippet view article

c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome". Am. J. Med. Genet. 78 (2): 179–81. doi:10.1002/(SICI)1096-8628(19

Breakthrough Prize in Life Sciences (354 words) [view diff] exact match in snippet view article find links to article

genetic causes and biochemical mechanisms of spinocerebellar ataxia and Rett syndrome, findings that have provided insight into the pathogenesis of neurodegenerative

Dirk Schübeler (758 words) [view diff] case mismatch in snippet view article find links to article

Deutsche Forschungsgemeinschaft 2000-2002: Postdoctoral Fellowship, Rett Syndrome Research Foundation 2006: EMBO Young Investigator Award 2006: Election

Peabody Picture Vocabulary Test (1,202 words) [view diff] case mismatch in snippet view article find links to article

(PPVT-R) Archived 2018-08-30 at the Wayback Machine," "Eye tracking gives Rett Syndrome patients a voice," Davis, John (2011). "Eye-Tracking Devices Help Disabled

GDI1 (1,241 words) [view diff] exact match in snippet view article find links to article

Francke U (1998). "Evaluation of two X chromosomal candidate genes for Rett syndrome: glutamate dehydrogenase-2 (GLUD2) and rab GDP-dissociation inhibitor

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

Raven Press. ISBN 978-0890048443. Haas RH, Rapin I, Moser HW (1988). Rett Syndrome and Autism. Year Book Medical Pub. ISBN 978-9990808179. Sandomir R (June

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

'Rusty' Gage appointed to 5-year term". San Diego Union-Tribune. Retrieved 2023-05-23. Salk Institute page Rett Syndrome Research Trust Gage Lab Website

Epilepsy-intellectual disability in females (4,409 words) [view diff] exact match in snippet view article find links to article

experiment, MECP2 protein was blocked; males died, and females developed Rett syndrome (seizures, cognitive and psychomotor problems, respiratory problems

Leriglitazone (349 words) [view diff] exact match in snippet view article find links to article

"Mitochondrial modulation with leriglitazone as a potential treatment for Rett syndrome". Journal of Translational Medicine. 21 (1): 756. doi:10.1186/s12967-023-04622-5

DLX6-AS1 (666 words) [view diff] exact match in snippet view article find links to article

in the balance between excitation and inhibition in a mouse model of Rett syndrome". Proc. Natl. Acad. Sci. U.S.A. 102 (35): 12560–12565. Bibcode:2005PNAS

GABRA3 (2,247 words) [view diff] exact match in snippet view article find links to article

EJ, Toriolo D, Zoghbi HY (January 2000). "Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in Xq". American Journal of Medical

Germline mosaicism (1,435 words) [view diff] exact match in snippet view article find links to article

Bruttini, M.; Meloni, I.; Pescucci, C. (2005). "Germline mosaicism in Rett syndrome identified by prenatal diagnosis". Clinical Genetics. 67 (3): 258–260

FXYD1 (776 words) [view diff] exact match in snippet view article find links to article

(2007). "FXYD1 is an MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice". Hum. Mol. Genet. 16 (6): 640–50. doi:10

Buchanan Medal (1,081 words) [view diff] case mismatch in snippet view article find links to article

silences transcription of methylated DNA and can reverse established Rett Syndrome in MeCP2 deficiency, the first demonstration that such neurodevelopmental

Ultraconserved element (4,445 words) [view diff] exact match in snippet view article find links to article

"Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms". Journal of Human Genetics. 52 (4):

Alexandru Darida (1,227 words) [view diff] case mismatch in snippet view article find links to article

2008 Sotheby's Legends of our Time Art Show and Auction benefiting The Rett Syndrome Research Foundation, 2001 [citation needed] Portrait of Mircea Eliade

The Eaton House Group of Schools (2,393 words) [view diff] case mismatch in snippet view article find links to article

2017. "Eight year old artist Rhea paints for Reverse Rett | Reverse Rett Syndrome". www.reverserett.org.uk. Retrieved 15 August 2017. Williams, Charles

William Dutton (speed skater) (1,752 words) [view diff] exact match in snippet view article

Dutton. He has three sisters Brandi, Abbey and Mila. Mila suffers from Rett syndrome a physically and mentally debilitating disease. Dutton has stated that

Hollis Cline (1,048 words) [view diff] exact match in snippet view article find links to article

of developmental neurological disorders such as fragile X syndrome, Rett syndrome, autism spectrum disorders, and schizophrenia - which are the result

Nuclear receptor co-repressor 2 (3,233 words) [view diff] exact match in snippet view article find links to article

de Lima Alves F, Rappsilber J, Greenberg ME, Bird A (July 2013). "Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor"

Shinya Yamanaka (3,481 words) [view diff] exact match in snippet view article find links to article

insights into the disease process. - Amyotrophic lateral sclerosis (ALS), Rett syndrome, spinal muscular atrophy (SMA), α1-antitrypsin deficiency, familial

Margarita Behrens (1,198 words) [view diff] exact match in snippet view article find links to article

inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome". eLife. 9. doi:10.7554/eLife.52981. PMC 7065908. PMID 32159514. Zhu

Julia Roberts filmography (3,034 words) [view diff] case mismatch in snippet view article find links to article

Law & Order Katrina Ludlow Episode: "Empire" 2000 Silent Angels: The Rett Syndrome Story Narrator Nature Herself Episode: "Wild Horses of Mongolia with

X-inactivation (5,683 words) [view diff] exact match in snippet view article find links to article

"Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins". BMC Biology. 2:

GABAA receptor (5,958 words) [view diff] exact match in snippet view article find links to article

numerous neurodevelopmental diseases, including fragile X syndrome, Rett syndrome, and Dravet syndrome, and that it is a crucial potential target for

Chromosome conformation capture (5,404 words) [view diff] exact match in snippet view article find links to article

"Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome". Nature Genetics. 37 (1): 31–40. doi:10.1038/ng1491. PMID 15608638

KIF1A (5,563 words) [view diff] exact match in snippet view article find links to article

researchers discovered novel de novo KIF1A variants in patients with Rett syndrome (RTT) and severe neurodevelopmental disorder that share clinical features

Charles A. Nelson III (1,958 words) [view diff] exact match in snippet view article find links to article

efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndrome". Proceedings of the National Academy of Sciences. 111 (12): 4596–4601

Neuroepigenetics (3,861 words) [view diff] case mismatch in snippet view article find links to article

has many ethical caveats. Some procedures, such as brain biopsies of Rett Syndrome patients, usually call for a fresh tissue sample that can only be extricated

Gyrification (4,561 words) [view diff] exact match in snippet view article find links to article

2012 found only one reported case of a mutation, in a patient with Rett syndrome (not ASD). The folds of autistic human brains are found to experience

The Apprentice (American TV series) season 8 (6,710 words) [view diff] case mismatch in snippet view article

$166,450 Clint Black Country singer KOTU 47 Katy, Texas International Rett Syndrome Foundation 12Fired in task 11 (2009–05–03) $20,000 Melissa Rivers Television

Epigenetics of depression (4,421 words) [view diff] exact match in snippet view article find links to article

trafficking in hippocampal neurons from Mecp2 knockout mice: implications for Rett syndrome". Frontiers in Cellular Neuroscience. 8: 68. doi:10.3389/fncel.2014

L'Oréal-UNESCO For Women in Science Awards (4,797 words) [view diff] exact match in snippet view article find links to article

proteins. Doctor Nam-Kyung Yu, Republic of Korea, Biological Sciences, Rett syndrome: neuronal cells come under fire Doctor Stephanie Fanucchi, South Africa

2003 Birthday Honours (14,994 words) [view diff] case mismatch in snippet view article find links to article

Nottingham. Dr. Alison Margaret Kerr. Paediatric Neurologist specialising in Rett Syndrome. For services to Medicine. Alan Edwin King. For services to the Church

1997 Birthday Honours (17,973 words) [view diff] case mismatch in snippet view article find links to article

Driving and to Road Safety. Yvonne Victoria, Mrs Milne, President, UK Rett Syndrome Association. For services to Health Care. Jeannette, Mrs Mitchell, Supervisor

2012 Queen's Birthday Honours (Australia) (39 words) [view diff] case mismatch in snippet view article

William Bernard Callaghan For service to community health through the Rett Syndrome Association of Australia. Kevin Joseph Callinan For service to the community

List of female nominees for the Nobel Prize (8,678 words) [view diff] case mismatch in snippet view article find links to article

October 2020). "Meet The Lebanese Geneticist Who Discovered Gene Behind Rett Syndrome". the961.com. Retrieved 31 January 2023. "Open letter to the Nobel Prize

List of women neuroscientists (9,050 words) [view diff] exact match in snippet view article find links to article

(born 1954), Lebanese-American geneticist known for research in the Rett syndrome and spinocerebellar ataxia type 1 Urtė Neniškytė (born 1983), researching

List of investigational hallucinogens and entactogens (7,759 words) [view diff] exact match in snippet view article find links to article

amyotrophic lateral sclerosis, anaesthesia, drug-induced dyskinesia, Rett syndrome – PharmaTher Ketamine intranasal – ionotropic glutamate NMDA receptor

List of Chopped episodes (season 41–present) (69 words) [view diff] case mismatch in snippet view article

Christmas tree Contestants: Chris Santos and Natalie McKenna (Charity: Rett Syndrome Research Trust) (eliminated after the appetizer) Marc Murphy and Pamela

List of Chopped episodes (seasons 21–40) (81 words) [view diff] case mismatch in snippet view article

(eliminated after the dessert) Chris and Mary Lou Santos (Charity: Rett Syndrome Research Trust) (winner) Notes: The contestants were Food Network chefs