Timing of Expansion of Fragile X Premutation Alleles During Intergenerational Transmission in a Mouse Model of the Fragile X-Related Disorders

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Timing of Expansion of Fragile X Premutation Alleles During Intergenerational Transmission in a Mouse Model of the Fragile X-Related Disorders

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im Januar 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

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Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

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Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

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Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

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Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

@en

Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

@nl

P1476

Timing of Expansion of Fragile ...... he Fragile X-Related Disorders

@en

P2093

Karen Usdin

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Xiao-Nan Zhao

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P2860

A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?

Continuous and periodic expansion of CAG repeats in Huntington's disease R6/1 mice

Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA).

Huntington disease expansion mutations in humans can occur before meiosis is completed.

Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis.

Flow cytometric characterization of viable meiotic and postmeiotic cells by Hoechst 33342 in mouse spermatogenesis.

Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.

Progressive GAA.TTC repeat expansion in human cell lines.

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314

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scholarly article

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10.3389/FGENE.2018.00314

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English

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2018-01-01T00:00:00Z

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30147707

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molecular medicine

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6096447

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