Literature DB >> 10727993

Sex determination and the Y chromosome.

K McElreavey1, M Fellous.   

Abstract

Although SRY was first identified 10 years ago, we still know remarkably little about its mode of action or downstream target genes. Recently, potential protein partners have been identified and there has been considerable activity to understand the roles of WT1, SF-1, DAX-1 and SOX9 in gonadogenesis. The emerging picture is one of complex interactions, involving both positive and negative regulatory signals that, depending on the cellular and promoter context, drive the expression of male-specific genes. Despite recent advances, however, we are still unable to explain the genetic cause of most cases of 46,XY gonadal dysgenesis or even a single case of Y-chromosome-negative 46,XX maleness. Copyright 2000 Wiley-Liss, Inc.

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Year:  1999        PMID: 10727993     DOI: 10.1002/(sici)1096-8628(19991229)89:4<176::aid-ajmg2>3.0.co;2-b

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  A novel sex determination system in a close relative of the house mouse.

Authors:  Frederic Veyrunes; Pascale Chevret; Josette Catalan; Riccardo Castiglia; Johan Watson; Gauthier Dobigny; Terence J Robinson; Janice Britton-Davidian
Journal:  Proc Biol Sci       Date:  2009-12-09       Impact factor: 5.349

2.  A SRY-HMG box frame shift mutation inherited from a mosaic father with a mild form of testicular dysgenesis syndrome in Turner syndrome patient.

Authors:  Mohammad Shahid; Varinderpal S Dhillon; Hesham Saleh Khalil; Shameemul Haque; Swaraj Batra; Syed Akhtar Husain; L H J Looijenga
Journal:  BMC Med Genet       Date:  2010-09-19       Impact factor: 2.103

3.  Correct dosage of Fog2 and Gata4 transcription factors is critical for fetal testis development in mice.

Authors:  Gerrit J Bouma; Linda L Washburn; Kenneth H Albrecht; Eva M Eicher
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-11       Impact factor: 11.205

Review 4.  New technologies for the identification of novel genetic markers of disorders of sex development (DSD).

Authors:  A Bashamboo; S Ledig; P Wieacker; J C Achermann; J Achermann; K McElreavey
Journal:  Sex Dev       Date:  2010-07-03       Impact factor: 1.824

5.  Failure of SOX9 regulation in 46XY disorders of sex development with SRY, SOX9 and SF1 mutations.

Authors:  Kevin C Knower; Sabine Kelly; Louisa M Ludbrook; Stefan Bagheri-Fam; Helena Sim; Pascal Bernard; Ryohei Sekido; Robin Lovell-Badge; Vincent R Harley
Journal:  PLoS One       Date:  2011-03-11       Impact factor: 3.240

6.  Integrating clinical and genetic approaches in the diagnosis of 46,XY disorders of sex development.

Authors:  Zofia Kolesinska; James Acierno; S Faisal Ahmed; Cheng Xu; Karina Kapczuk; Anna Skorczyk-Werner; Hanna Mikos; Aleksandra Rojek; Andreas Massouras; Maciej R Krawczynski; Nelly Pitteloud; Marek Niedziela
Journal:  Endocr Connect       Date:  2018-12       Impact factor: 3.335

7.  Transcriptional control of human gametogenesis.

Authors:  Fang Fang; Phillip J Iaquinta; Ninuo Xia; Lei Liu; Lei Diao; Renee A Reijo Pera
Journal:  Hum Reprod Update       Date:  2022-05-02       Impact factor: 17.179

8.  Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

Authors:  Hyewon Hahn; Young Mi Cho; Young Seo Park; Han Wook You; Hae Il Cheong
Journal:  J Korean Med Sci       Date:  2006-02       Impact factor: 2.153

  8 in total

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