Your search matched a total of 102 documents. Results 1 - 10.
Homo sapiens
Gene: ... relationships of MECP2 The results of this study demonstrate that MBD2 gene is expressed in all samples and Me... was employed to sequence the entire MECP2 gene coding region in all cases. Long- read sequence analysis...Disease relevance of MECP2 MECP2 is highly mutated in X- linked mental retardation. Rett syndrome...
Mus musculus
Gene: ... days by HPLC methods. All four ID proteins were significantly increased in Mecp2- deficient mouse...Disease relevance of Mecp2 Our findings raise the possibility that mitochondrial dysfunction contributes to pathology of the Mecp2- null mouse and may contribute to the long- known resemblance between...
Rattus norvegicus
Gene: ... Disease relevance of Mecp2 Reduction of MeCP2 protein expression may influence the initiation and... related information on Mecp2 Rett syndrome( RS) is caused by mutations in the gene encoding methyl- Cp... information on Mecp2 In extracts from rodent tissues, cultured cells, and Xenopus laevis oocytes, we find...
Xenopus laevis
Gene: ... Psychiatry related information on MECP2 Although it is evident that phenotypes of MECP2 mutant mice that resemble those of Rett syndrome are attributable to lack of the MECP2 gene in the central nervous system( CNS ), there is little understanding of the neuropathological abnormalities in the CNS of MECP2- null...
MeSH term: ... Disease relevance of Rett Syndrome A mutation in the rett syndrome gene, MECP2, causes X- linked... of Rett Syndrome is seen in with ubiquitous deficiency in Mecp2 but not when it is confined to neurons... information on Rett Syndrome Consistent with this notion is the recent demonstration that MECP2 mutations...
MeSH term: No matches in the visible text, but in the meta information (e.g. in official synonyms of referenced entities).
MeSH term: ... for MECP2 mutations by direct sequencing and determined the pattern of X chromosome inactivation( XCI... steps is affected in all patients so far characterized. This consists of repeats of the tetranucleotide...
MeSH term: ... alcohol abuse. Perhaps MECP2 mutations in Rett syndrome not only influence brain development but also...
Chemical compound: ... seizure phenotype compared with other mouse absence models with Ca2 +- channel defects. All other...
MeSH term: ... receptor loci using PCR based X- inactivation analysis demonstrated that in all families analyzed...
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Steven Johnsen and Donald R. Forsdyke and Kehinde Ross and Andrew Perry and Jonathan Eisen and A. Shimabukuro-Vornhagen and Giuseppe Rotondo and Gordon Laurie and Berkley Lynch and Kung-Hao Liang and Matthias Gstaiger and Thomas Pfeiffer and Marta Ramirez and Grant MacGregor and Jingyu Li and Fedik Rahimov and M El Gizouli and Marta Ramirez Gaite and Oswaldo Ribeiro-filho and Ralf Weigel and Bjoern Hamberger and Alexander Kanitz and Andreas Zankl and Chunming Ding and Maruf Yunus and Jonathan S. Berg and Michael Cariaso and Zakir Thomas and Monique Timberlake-Brady and LC Dore and Nan Shen and R. Eric Collins and Kuang-Mao Chiang and Brendan McMahon and John Chew and Wen-Ming Yang and Robert Hoffmann and J.B. Stewart and Manuela Cucerea and Ignacio García and William James and Thomas Kelder and Gregory Melahn and YINGDE ZHU and Andres Muro and Gabriel Santpere and Jeff Freilich and Junbin Qian and Steffen Poulsen and Eric Villard and Rafael Sidi and Grant Cramer and Chris Sander and Alexandre Chigaev and Florian Uhle and Carl Fulp and Andrew Brown and Xiaozhu Zhou and Corina Dutu and Hilary Spencer and david germano and Abbas Dehghan and Eung-ju PARK and Chris Sander and Albert Vilella and Miao Tian and Anjali Bheda and Michael Nevels and Jun Liu and D Delano and Chitose Taya and Soomi Cheong and David Kavanagh and Maha Karnoub and Hilmar Lapp and Christian Pallasch and Daniel Mietchen and Biju Balakrishnan and Keith Ashman and Juan Carlos Sobrino and Anshu Bhardwaj and Grzegorz Wickiel and Matthew Day and Anthony Sebastian and Vedran Katavic and Liang Long and Barry Wanner and Sarah Snelling and Fernando Montanes and Omobosede Fashedemi and Gustavo Cervantes and Manoj Kumar and Edward D Great and Paul Paukstelis and Roy Soetikno and Ana I Caño-Delgado and Minsoo Choi and Lei Wang and Brenda Riley and A Michelle Moon and Jon Moulton and Mahmoud Elshahawy and Meagan Gillespie and Banundari Rachmawati and Qian Han and Eric Danner and Xavier Fouillet and Madhusudhan Acharya and Brian Young and Chandra Sekhar Mukhopadhyay and shrawan bhattacharjee and Marieke van der Linden and cj hoban and Sandi Pniauskas and jackie gao and Metin Bilgin and Gillian L. Dalgliesh and Karl Wotton and Iveta Herichova and Yuji Morita and Marta Hernandez and Gregor Krings and Marco Briones and Tim D. Smith and Yiumo Michael Chan and Zhenyu Guo and Barry Barclay and Hong Wang and tarali chowdhury and Tilman Brummer and Nuno Faria and Tamir Ben David and Myles Axton and Yannick Fonseca and Francis Castets and Modesto Redrejo-Rodríguez and Bruce Herron and Toshio Fujita and Elena Puccetti and Zhang Zhang and John Osborne and Illes J Farkas and Fernando Andres and Phyllis Pugh and Jonathan Court and Tim Vickers and Nir Friedman and Holger Dick and Ya-Chen Liang and Jonathan Froehlich and Haitham Sobhy and David Abraham and Stephane Krief and Yaroslav Nikolaev and Qiping Feng and d gupta and R Thapar and Susan Wee and Michael Rehman and SOUMITRA GHOSH and Mohamed Eweida and Cedric Uytingco and Nie hongchuan and David Steenblock and Mark A. Kukucka and Zoli Fekete and Sergei Kozlov and Javier Jara and Osama Naguib and Felix Benninger and jean-marc lo-guidice and VASUDEVA BHAT and Anne O. Summers and Bjoern Titz and Anna Levine and Klas Udekwu and Robert Hoffmann
