Your search matched a total of 35 documents. Results 1 - 10.
Mus musculus
Gene: ... Disease relevance of Gabrb3 Among 20 p deletions tested, there was complete concordance between alterations at the Gabrb3 transcription unit and inability to complement the cleft- palate defect. Gabrb3 gene... coeruleus dendrites. High impact information on Gabrb3 To test the hypothesis that deletion of Gabrb3... / Synonyms: Gabrb-3
Homo sapiens
Gene: ... Disease relevance of GABRB3 Chromosomal rearrangement breakpoints -- in one Angelman syndrome( AS... -- are located within the large GABRB3 intron. In order to determine the genomic organization of the GABAA receptor beta 3 subunit gene( GABRB3) and alpha 5 subunit gene( GABRA5) in chromosome 15q11- q13, we have...
MeSH term: ... Family Domain organization of allele- specific replication within the GABRB3 gene cluster requires... spacer sequences; some or all of these spacer sequences are members of a predominantly centromeric.... melanogaster glutamate tRNA gene cluster. All members of the MHC multigene family respond to thyroid hormone...
MeSH term: ... information on Linkage Disequilibrium The convergence of GABRB3 as a positional and functional candidate along with the linkage- disequilibrium data suggests the need for further investigation of the role of GABRB3 or adjacent...
Chemical compound: ... receptor subunit beta 3( GABRB3) and alpha 5( GABRA5) genes. Studies in the nematode Caenorhabditis elegans... in individuals with Rett syndrome. In mice of all ages lacking an isoform of GABA( gamma- aminobutyric acid... patterns. As a consequence of the mutation, her1 plants accumulate high GABA levels in all their organs...
MeSH term: ... subunits of the type A gamma- aminobutyric acid receptor( Gabra5 and Gabrb3, respectively ), contains... formation in the presence of all- trans- retinoic acid( RA) and defined anomalous patterns within... -/- mice displayed a wide range of developmental anomalies encompassing almost all of the common DGS/ VCFS...
MeSH term: ... with class II( BP2/ 3) deletions. The loss of the single gene, gabrb3, in these mice is sufficient to cause... expression of the GABRB3 gene in humans probably contributes to the overall phenotype of Angelman syndrome...( PWS) and Angelman syndrome( AS) using probes for loci D15S11, SNRPN, D15S10, and GABRB3. We conclude...
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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







