Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders-Reference-Cited by-同舟云学术

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Mutsβ generates both expansions and contractions in a mouse model of the Fragile X-associated disorders

Published:2015-09-29 Issue: Volume: Page:ddv408
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Zhao Xiao-Nan,Kumari Daman,Gupta Shikha,Wu Di,Evanitsky Maya,Yang Wei,Usdin Karen

Funder

NIDDK

K

U

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/24/7087/17262945/ddv408.pdf

Reference58 articles.

1. Unstable mutations in the FMR1 gene and the phenotypes;Loesch;Adv. Exp. Med. Biol.,2012

2. Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model

3. Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles

4. Gender and Cell-Type-Specific Effects of the Transcription-Coupled Repair Protein, ERCC6/CSB, on Repeat Expansion in a Mouse Model of the Fragile X-Related Disorders

5. Mosaicism in a fragile X male including a de novo deletion in theFMR1 gene

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1. Somatic and intergenerational G4C2 hexanucleotide repeat instability in a human C9orf72 knock-in mouse model;Nucleic Acids Research;2024-04-10

2. Tandem MutSβ binding to long extruded DNA trinucleotide repeats underpins pathogenic expansions;2023-12-13

3. Massive contractions of myotonic dystrophy type 2-associated CCTG tetranucleotide repeats occur via double-strand break repair with distinct requirements for DNA helicases;G3: Genes, Genomes, Genetics;2023-11-10

4. Genetic modifiers of repeat expansion disorders;Emerging Topics in Life Sciences;2023-10-20

5. A small molecule binding to TGGAA pentanucleotide repeats that cause spinocerebellar ataxia type 31;Bioorganic & Medicinal Chemistry Letters;2023-01

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