About: A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

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About: A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome Goto Sponge NotDistinct Permalink

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description	articolo scientifico (it) 2001 թվականի մարտին հրատարակված գիտական հոդված (hy) مقالة علمية (نشرت في مارس 2001) (ar) наукова стаття, опублікована в березні 2001 (uk) 2001 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) artículu científicu espublizáu en 2001 (ast) vědecký článek publikovaný v roce 2001 (cs) vedecký článok (publikovaný 2001/03/01) (sk) wetenschappelijk artikel (gepubliceerd op 2001/03/01) (nl) article scientifique publié en 2001 (fr) scientific journal article (en) im März 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28504458-2EA5417D-4FD1-4DAD-8BDD-7C2F96276042
publication date	2001-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28504458-B2EF8B57-D5E0-4B43-9BFD-FC60D30CEC14
language of work or name	English
cites work	wds:Q28504458-17FDDDC9-CD55-403A-83A9-3F20AF34A0D2 wds:Q28504458-1E85E114-AFF4-4B7B-8445-73AAA7474770 wds:Q28504458-25397DF1-FE6A-4998-BC81-CEDF23DA8459 wds:Q28504458-25E762CE-2C5D-4B03-BD11-CAAED6FA4492 wds:Q28504458-2A4875A2-32F2-4312-8216-1772A3F0682A wds:Q28504458-2D5BD0C1-5676-48FD-8187-3B0D67E011BD wds:Q28504458-351E356E-D264-44D4-8885-9551E2B22DA3 wds:Q28504458-3BDE7E1F-45A3-45DB-BCA7-2D31F476F9A5 wds:Q28504458-45B7F9B8-A0B2-47F7-808C-E4D0C8E17545 wds:Q28504458-4FB549B9-A7E8-4886-969C-A0CC1954066A wds:Q28504458-56911F3C-44E2-452E-8027-3EBE19E47070 wds:Q28504458-64E20B0E-EB5C-4CE0-A2AA-D0EBC8DD1D66 wds:Q28504458-730F33F1-C106-4743-9699-89A42548FF27 wds:Q28504458-74F535F9-69AD-45D8-BB40-90DEBC72D50A wds:Q28504458-7631BF74-11B2-4309-876E-73FA115B6498 wds:Q28504458-7BD0A2CC-40A1-45A3-826D-C904051CF48B wds:Q28504458-8BC5CF56-B91B-450E-9285-AB073B83206A wds:Q28504458-9F78BFC3-8443-4601-8E76-E3B94A996A8B wds:Q28504458-A0EF5F43-9BA5-40E5-87C1-BB831836EFB4 wds:Q28504458-A7279BDE-42CF-4061-91D1-814ACC3F7172 wds:Q28504458-AA5D26D4-A6B2-46AD-B186-E2C5B5A17FAE wds:Q28504458-AD5B0412-D0E7-419F-962B-91C70E6DF35C wds:Q28504458-B8DD4588-8716-4D43-9ADC-357DF064A9F3 wds:Q28504458-BC3E00D0-8E1C-41CD-9785-C2D88F5CD6E8 wds:Q28504458-C0FF3601-6268-47EA-82CE-3D2CFE2E1069 wds:Q28504458-CF65405C-9932-4401-B81F-E485E5A6108E wds:Q28504458-DD00CF76-1253-43F7-8053-12F16E89FED9 wds:Q28504458-E25845C4-8723-4025-84E4-39E9EA3D91BB wds:Q28504458-E5E4F989-FD3A-4194-84C3-A6C174D32453 wds:Q28504458-FE3628C0-9D36-44E7-B965-BE47F84C795A
cites work	Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms Mutation screening in Rett syndrome patients. Mutations in the MECP2 gene in a cohort of girls with Rett syndrome Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice Active repression of methylated genes by the chromosomal protein MBD1 Site-specific DNA recombination in mammalian cells by the Cre recombinase of bacteriophage P1 Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription DNA methylation specifies chromosomal localization of MeCP2. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA Identification of a mammalian protein that binds specifically to DNA containing methylated CpGs. Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients. MECP2 mutations account for most cases of typical forms of Rett syndrome. Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse. MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells Methylation-mediated transcriptional silencing in euchromatin by methyl-CpG binding protein MBD1 isoforms Functional consequences of Rett syndrome mutations on human MeCP2. DNA recognition by the methyl-CpG binding domain of MeCP2. Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome
author name string	wds:Q28504458-C35E6550-E5B3-40DC-9205-F943E930FC0D wds:Q28504458-E4338205-F56B-4AF1-AE4D-F38EECF32D83 wds:Q28504458-F05C9BB2-09D2-4191-83E9-68DD91385588
OpenCitations bibliographic resource ID	wds:Q28504458-85C78958-986E-4410-A605-010E6669A5F1
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/636175
author name string	J. E. Martin J. Guy M. Holmes
OpenCitations bibliographic resource ID	636175
rdfs:label	A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (en) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (nl) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (ast)
skos:prefLabel	A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (en) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (nl) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (ast)
name	A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (en) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (nl) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome (ast)
author	wds:Q28504458-68B0147E-9946-4F2A-A1F2-16E85320F19D wds:Q28504458-B29E75DD-3841-4CA3-B06B-86465FC31DCC
author	Adrian Peter Bird Brian Hendrich
title	wds:Q28504458-40ACE143-8D96-4701-84FF-328D2671BF0A

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