Literature DB >> 9195162

Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation.

T Bienvenu1, H Der-Sarkissian, P Billuart, M Tissot, V Des Portes, T Brüls, J P Chabrolle, P Chauveau, M Cherry, A Kahn, D Cohen, C Beldjord, J Chelly, D Cherif.   

Abstract

Balanced chromosomal abnormalities such as translocations and inversions have been identified in many genetic diseases. Cloning of the breakpoints involved in these abnormalities has led to the identification of the disease-related genes. Recent reports suggest the presence of a mental retardation locus at Xq11-12. We have identified a female patient with a balanced translocation t (X;12) (q11;q15) associated with mild mental retardation. We identified a yeast artificial chromosome spanning the X-chromosome breakpoint by using fluorescent in situ hybridization techniques. A cosmid library of this YAC has been constructed and the search for candidate genes is in progress.

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Year:  1997        PMID: 9195162

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  12 in total

Review 1.  Rho-linked genes and neurological disorders.

Authors:  Nael Nadif Kasri; Linda Van Aelst
Journal:  Pflugers Arch       Date:  2007-11-15       Impact factor: 3.657

Review 2.  Balanced translocations in mental retardation.

Authors:  Geert Vandeweyer; R Frank Kooy
Journal:  Hum Genet       Date:  2009-04-05       Impact factor: 4.132

3.  Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.

Authors:  L Villard; S Briault; A M Lossi; C Paringaux; J Belougne; L Colleaux; D R Pincus; E Woollatt; J Lespinasse; A Munnich; C Moraine; M Fontès; J Gecz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

4.  A novel in-frame deletion affecting the BAR domain of OPHN1 in a family with intellectual disability and hippocampal alterations.

Authors:  Cíntia Barros Santos-Rebouças; Stefanie Belet; Luciana Guedes de Almeida; Márcia Gonçalves Ribeiro; Enrique Medina-Acosta; Paulo Roberto Valle Bahia; Antônio Francisco Alves da Silva; Flávia Lima dos Santos; Glenda Corrêa Borges de Lacerda; Márcia Mattos Gonçalves Pimentel; Guy Froyen
Journal:  Eur J Hum Genet       Date:  2013-10-09       Impact factor: 4.246

5.  The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors.

Authors:  Nael Nadif Kasri; Akiko Nakano-Kobayashi; Roberto Malinow; Bo Li; Linda Van Aelst
Journal:  Genes Dev       Date:  2009-06-01       Impact factor: 11.361

6.  Characterization of oligophrenin-1, a RhoGAP lost in patients affected with mental retardation: lentiviral injection in organotypic brain slice cultures.

Authors:  Nael Nadif Kasri; Eve-Ellen Govek; Linda Van Aelst
Journal:  Methods Enzymol       Date:  2008       Impact factor: 1.600

7.  The novel Rho-GTPase activating gene MEGAP/ srGAP3 has a putative role in severe mental retardation.

Authors:  Volker Endris; Birgit Wogatzky; Uwe Leimer; Dusan Bartsch; Malgorzata Zatyka; Farida Latif; Eamonn R Maher; Gholamali Tariverdian; Stefan Kirsch; Dieter Karch; Gudrun A Rappold
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-23       Impact factor: 11.205

8.  Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12.

Authors:  Björn Menten; Karen Buysse; Stefan Vermeulen; Valerie Meersschaut; Jo Vandesompele; Bee L Ng; Nigel P Carter; Geert R Mortier; Frank Speleman
Journal:  Eur J Med Genet       Date:  2007-08-06       Impact factor: 2.708

Review 9.  Regulation of the postsynaptic cytoskeleton: roles in development, plasticity, and disorders.

Authors:  Tatyana Svitkina; Wan-Hsin Lin; Donna J Webb; Ryohei Yasuda; Gary A Wayman; Linda Van Aelst; Scott H Soderling
Journal:  J Neurosci       Date:  2010-11-10       Impact factor: 6.167

Review 10.  X-linked disorders with cerebellar dysgenesis.

Authors:  Ginevra Zanni; Enrico S Bertini
Journal:  Orphanet J Rare Dis       Date:  2011-05-15       Impact factor: 4.123

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