Generation and mutational analysis of a transgenic mouse model of human SRY-Reference-Cited by-同舟云学术

Generation and mutational analysis of a transgenic mouse model of human SRY

Published:2021-12-28 Issue: Volume: Page:
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Thomson Ella¹²,Zhao Liang¹,Chen Yen‐Shan³,Longmuss Enya¹,Ng Ee Ting¹,Sreenivasan Rajini⁴,Croft Brittany⁴,Song Xin²,Sinclair Andrew⁴,Weiss Michael³,Koopman Peter¹,Pelosi Emanuele¹²^ORCID

Affiliation:

1. Institute for Molecular Bioscience The University of Queensland Brisbane Queensland Australia

2. Centre for Clinical Research The University of Queensland Brisbane Queensland Australia

3. Department of Biochemistry & Molecular Biology Indiana University School of Medicine Indianapolis Indiana USA

4. Murdoch Children's Research Institute and Department of Paediatrics University of Melbourne Melbourne Victoria Australia

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24318

Reference57 articles.

1. The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo

2. Two new point mutations of the SRY gene identified in two Italian 46,XY females with gonadal dysgenesis

3. Genetic evidence equating SRY and the testis-determining factor

4. A De Novo Mutation (Gln2Stop) at the 5′ End of the SRY Gene Leads to Sex Reversal with Partial Ovarian Function

5. Wt1 directs the lineage specification of sertoli and granulosa cells by repressing Sf1 expression

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2. Tenuous transcriptional threshold of human sex determination. II. SRY exploits water-mediated clamp at the edge of ambiguity;Frontiers in Endocrinology;2022-12-02

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