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Reversal of Female Infertility by Chk2 Ablation Reveals the Oocyte DNA Damage Checkpoint Pathway

Science (American Association for the Advancement of Science), 2014-01, Vol.343 (6170), p.533-536

2014

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Oocyte Elimination Through DNA Damage Signaling from CHK1/CHK2 to p53 and p63

Genetics (Austin), 2020-06, Vol.215 (2), p.373-378

2020

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Genome Maintenance in Mammalian Stem Cells

Annual review of genetics, 2022-11, Vol.56 (1), p.145-164

2022

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The Mouse Genomic Instability Mutation chaos1 Is an Allele of Polq That Exhibits Genetic Interaction with Atm

Molecular and Cellular Biology, 2004-12, Vol.24 (23), p.10381-10389

2004

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Sexually dimorphic DNA damage responses and mutation avoidance in the mouse germline

Genes & development, 2020-12, Vol.34 (23-24), p.1637-1649

2020

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Relevance, strategies, and added value of mouse models in androgenetics

Andrology (Oxford), 2024-09

2024

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Deficiency of Suppressor Enhancer Lin12 1 Like (SEL1L) in Mice Leads to Systemic Endoplasmic Reticulum Stress and Embryonic Lethality

The Journal of biological chemistry, 2010-04, Vol.285 (18), p.13694-13703

2010

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Phenotype-Based Identification of Mouse Chromosome Instability Mutants

Genetics (Austin), 2003-03, Vol.163 (3), p.1031-1040

2003

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Positional cloning and characterization of mouse mei8, a disrupted allele of the meiotic cohesin Rec8

Genesis (New York, N.Y. : 2000), 2004-11, Vol.40 (3), p.184-194

2004

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A segregating human allele of SPO11 modeled in mice disrupts timing and amounts of meiotic recombination, causing oligospermia and a decreased ovarian reserve

Biology of reproduction, 2019-08, Vol.101 (2), p.347-359

2019

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Meiotic epigenetic factor PRDM9 impacts sperm quality of hybrid mice

Reproduction (Cambridge, England), 2020-07, Vol.160 (1), p.53-64

2020

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L. C. Dunn and Donald Charles on Quantitative Traits in the Mouse

Genetics (Austin), 2016-03, Vol.202 (3), p.867-868

Schimenti, John C

2016

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Positional Cloning and Characterization of Mei1, a Vertebrate-Specific Gene Required for Normal Meiotic Chromosome Synapsis in Mice

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (26), p.15706-15711

2003

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In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes

Proceedings of the National Academy of Sciences - PNAS, 2023-07, Vol.120 (30), p.e2219925120-e2219925120

2023

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MCM9 deficiency delays primordial germ cell proliferation independent of the ATM pathway

Genesis (New York, N.Y. : 2000), 2015-11, Vol.53 (11), p.678-684

2015

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Testis formation in XX individuals resulting from novel pathogenic variants in Wilms’ tumor 1 (WT1) gene

Proceedings of the National Academy of Sciences - PNAS, 2020-06, Vol.117 (24), p.13680-13688

2020

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CDK2 kinase activity is a regulator of male germ cell fate

Development (Cambridge), 2019-11, Vol.146 (21)

2019

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MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans

The Journal of clinical investigation, 2012-03, Vol.122 (3), p.814-820

2012

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A reporter mouse for in vivo detection of DNA damage in embryonic germ cells

Genesis (New York, N.Y. : 2000), 2020-08, Vol.58 (8), p.e23368-n/a

2020

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Practical strategies for robust and inexpensive imaging of aqueous‐cleared tissues

Journal of microscopy (Oxford), 2023-09, Vol.291 (3), p.237-247

2023

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Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells

Biology of reproduction, 2012-02, Vol.86 (2), p.45-45

2012

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The Chromatin Remodeling Component Arid1a Is a Suppressor of Spontaneous Mammary Tumors in Mice

Genetics (Austin), 2016-08, Vol.203 (4), p.1601-1611

2016

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An Allelic Series Uncovers Novel Roles of the BRCT Domain-Containing Protein PTIP in Mouse Embryonic Vascular Development

Molecular and Cellular Biology, 2008-10, Vol.28 (20), p.6439-6451

2008

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Genetic evidence that synaptonemal complex axial elements govern recombination pathway choice in mice

Genetics (Austin), 2011-09, Vol.189 (1), p.71-82

2011

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Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells1

Biology of reproduction, 2012-02, Vol.86 (2)

2012

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Reversal of Female Infertility by Chk2 Ablation Reveals the Oocyte DNA Damage Checkpoint Pathway

Oocyte Elimination Through DNA Damage Signaling from CHK1/CHK2 to p53 and p63

Genome Maintenance in Mammalian Stem Cells

The Mouse Genomic Instability Mutation chaos1 Is an Allele of Polq That Exhibits Genetic Interaction with Atm

Sexually dimorphic DNA damage responses and mutation avoidance in the mouse germline

Relevance, strategies, and added value of mouse models in androgenetics

Deficiency of Suppressor Enhancer Lin12 1 Like (SEL1L) in Mice Leads to Systemic Endoplasmic Reticulum Stress and Embryonic Lethality

Phenotype-Based Identification of Mouse Chromosome Instability Mutants

Positional cloning and characterization of mouse mei8, a disrupted allele of the meiotic cohesin Rec8

A segregating human allele of SPO11 modeled in mice disrupts timing and amounts of meiotic recombination, causing oligospermia and a decreased ovarian reserve

Meiotic epigenetic factor PRDM9 impacts sperm quality of hybrid mice

L. C. Dunn and Donald Charles on Quantitative Traits in the Mouse

Positional Cloning and Characterization of Mei1, a Vertebrate-Specific Gene Required for Normal Meiotic Chromosome Synapsis in Mice

In vivo versus in silico assessment of potentially pathogenic missense variants in human reproductive genes

MCM9 deficiency delays primordial germ cell proliferation independent of the ATM pathway

Testis formation in XX individuals resulting from novel pathogenic variants in Wilms’ tumor 1 (WT1) gene

CDK2 kinase activity is a regulator of male germ cell fate

MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans

A reporter mouse for in vivo detection of DNA damage in embryonic germ cells

Practical strategies for robust and inexpensive imaging of aqueous‐cleared tissues

Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells

The Chromatin Remodeling Component Arid1a Is a Suppressor of Spontaneous Mammary Tumors in Mice

An Allelic Series Uncovers Novel Roles of the BRCT Domain-Containing Protein PTIP in Mouse Embryonic Vascular Development

Genetic evidence that synaptonemal complex axial elements govern recombination pathway choice in mice

Spata22, a Novel Vertebrate-Specific Gene, Is Required for Meiotic Progress in Mouse Germ Cells1

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