4.6 Article

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

Related references

Note: Only part of the references are listed.
Article Pathology

A Set of Assays for the Comprehensive Analysis of FMR1 Alleles in the Fragile X-Related Disorders

Bruce E. Hayward et al.

JOURNAL OF MOLECULAR DIAGNOSTICS (2016)

Article Biochemistry & Molecular Biology

Practical Selection Methods for Rat and Mouse Round Spermatids Without DNA Staining by Flow Cytometric Cell Sorting

Tomonari Hayama et al.

MOLECULAR REPRODUCTION AND DEVELOPMENT (2016)

Article Genetics & Heredity

High Functioning Male with Fragile X Syndrome and Fragile X-Associated Tremor/Ataxia Syndrome

Kirin Basuta et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)

Review Endocrinology & Metabolism

Stem Cells, Progenitor Cells, and Lineage Decisions in the Ovary

Katja Hummitzsch et al.

ENDOCRINE REVIEWS (2015)

Article Biochemistry & Molecular Biology

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

Xiao-Nan Zhao et al.

HUMAN MOLECULAR GENETICS (2015)

Letter Genetics & Heredity

A novel deletion to normal size in the sperm of a fragile X full mutation male

S. Luo et al.

CLINICAL GENETICS (2014)

Article Biochemistry & Molecular Biology

Two classes of ovarian primordial follicles exhibit distinct developmental dynamics and physiological functions

Wenjing Zheng et al.

HUMAN MOLECULAR GENETICS (2014)

Article Biochemistry & Molecular Biology

Chromosome fragility and the abnormal replication of the FMR1 locus in fragile X syndrome

Dmitry Yudkin et al.

HUMAN MOLECULAR GENETICS (2014)

Article Clinical Neurology

AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission

Carolyn M. Yrigollen et al.

JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2014)

Article Biochemistry & Molecular Biology

The DNA Replication Program Is Altered at the FMR1 Locus in Fragile X Embryonic Stem Cells

Jeannine Gerhardt et al.

MOLECULAR CELL (2014)

Article Biochemistry & Molecular Biology

Length-dependent CTG.CAG triplet-repeat expansion in myotonic dystrophy patient-derived induced pluripotent stem cells

Jintang Du et al.

HUMAN MOLECULAR GENETICS (2013)

Article Genetics & Heredity

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

Rachel Adihe Lokanga et al.

HUMAN MUTATION (2013)

Article Biochemistry & Molecular Biology

Role of Mismatch Repair Enzymes in GAA.TTC Triplet-repeat Expansion in Friedreich Ataxia Induced Pluripotent Stem Cells

Jintang Du et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2012)

Article Genetics & Heredity

Mismatch and base excision repair proficiency in murine embryonic stem cells

Elisia D. Tichy et al.

DNA REPAIR (2011)

Article Multidisciplinary Sciences

DNA Damage Responses in Human Induced Pluripotent Stem Cells and Embryonic Stem Cells

Olga Momcilovic et al.

PLOS ONE (2010)

Article Genetics & Heredity

Continuous and Periodic Expansion of CAG Repeats in Huntington's Disease R6/1 Mice

Linda Mollersen et al.

PLOS GENETICS (2010)

Article Biochemical Research Methods

Isolation and cultivation of stem cells from adult mouse testes

Kaomei Guan et al.

NATURE PROTOCOLS (2009)

Article Biochemistry & Molecular Biology

Replisome stalling and stabilization at CGG repeats, which are responsible for chromosomal fragility

Irina Voineagu et al.

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2009)

Article Genetics & Heredity

Progressive GAA.TTC Repeat Expansion in Human Cell Lines

Scott Ditch et al.

PLOS GENETICS (2009)

Article Multidisciplinary Sciences

DNA instability in postmitotic neurons

Roman Gonitel et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Biochemistry & Molecular Biology

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

Peggy F. Shelbourne et al.

HUMAN MOLECULAR GENETICS (2007)

Article Biochemistry & Molecular Biology

MSH2-dependent germinal CTG repeat expansions are produced continuously in spermatogonia from DM1 transgenic mice

C Savouret et al.

MOLECULAR AND CELLULAR BIOLOGY (2004)

Article Biochemistry & Molecular Biology

Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis

L Kennedy et al.

HUMAN MOLECULAR GENETICS (2003)

Article Multidisciplinary Sciences

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

SR Yoon et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)

Article Biochemistry & Molecular Biology

Mismatch repair gene Msh2 modifies the timing of early disease in HdhQ111 striatum

VC Wheeler et al.

HUMAN MOLECULAR GENETICS (2003)

Article Clinical Neurology

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

H Hashida et al.

JOURNAL OF THE NEUROLOGICAL SCIENCES (2001)

Article Genetics & Heredity

Trinucleotide expansion in haploid germ cells by gap repair

IV Kovtun et al.

NATURE GENETICS (2001)