Evidence for a fragile X messenger ribonucleoprotein 1 ( <i>FMR1</i> ) <scp>mRNA</scp> gain‐of‐function toxicity mechanism contributing to the pathogenesis of fragile X‐associated premature ovarian insufficiency-Reference-Cited by-同舟云学术

Evidence for a fragile X messenger ribonucleoprotein 1 ( FMR1 ) mRNA gain‐of‐function toxicity mechanism contributing to the pathogenesis of fragile X‐associated premature ovarian insufficiency

Published:2022-10-17 Issue:11 Volume:36 Page:
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:The FASEB Journal

Author:

Rosario Roseanne¹²,Stewart Hazel L.¹,Choudhury Nila Roy³,Michlewski Gracjan³⁴⁵^ORCID,Charlet‐Berguerand Nicholas⁶,Anderson Richard A.¹

Affiliation:

1. MRC Centre for Reproductive Health, Queen's Medical Research Institute University of Edinburgh Edinburgh UK

2. Biomedical Sciences University of Edinburgh Edinburgh UK

3. Infection Medicine University of Edinburgh Edinburgh UK

4. Zhejiang University‐University of Edinburgh Institute Zhejiang University Zhejiang P.R. China

5. Dioscuri Centre for RNA‐Protein Interactions in Human Health and Disease International Institute of Molecular and Cell Biology in Warsaw Warsaw Poland

6. Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) INSERM U 1258, CNRS UMR 7104, Université of Strasbourg Illkirch France

Funder

Wellbeing of Women

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.202200468RR

Reference64 articles.

1. Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles

2. Familial transmission of the FMR1 CGG repeat;Nolin SL;Am J Hum Genet,1996