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Phosphorylation State of Olig2 Regulates Proliferation of Neural Progenitors

Neuron (Cambridge, Mass.), 2011-03, Vol.69 (5), p.906-917

2011

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The Central Nervous System-Restricted Transcription Factor Olig2 Opposes p53 Responses to Genotoxic Damage in Neural Progenitors and Malignant Glioma

Cancer cell, 2011-03, Vol.19 (3), p.359-371

2011

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Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2

Nature reviews. Neuroscience, 2012-12, Vol.13 (12), p.819-831

2012

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

Genes & development, 2003-03, Vol.17 (5), p.603-614

2003

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hMSH2 Forms Specific Mispair-Binding Complexes with hMSH3 and hMSH6

Proceedings of the National Academy of Sciences - PNAS, 1996-11, Vol.93 (24), p.13629-13634

1996

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Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in mice

Nature genetics, 2005-07, Vol.37 (7), p.750-755

2005

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Haploinsufficiency of Flap Endonuclease (Fen1) Leads to Rapid Tumor Progression

Proceedings of the National Academy of Sciences - PNAS, 2002-07, Vol.99 (15), p.9924-9929

2002

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Approaching a complete repository of sequence-verified protein-encoding clones for Saccharomyces cerevisiae

Genome Research, 2007-04, Vol.17 (4), p.536-543

2007

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Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

Cell, 1997-11, Vol.91 (4), p.467-477

1997

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Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines

Cancer research (Chicago, Ill.), 1997-03, Vol.57 (5), p.808-811

1997

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An amino terminal phosphorylation motif regulates intranuclear compartmentalization of Olig2 in neural progenitor cells

The Journal of neuroscience, 2014-06, Vol.34 (25), p.8507-8518

2014

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MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice

Genes & development, 2000-05, Vol.14 (9), p.1085-1097

2000

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Incidence and Functional Consequences of hMLH1 Promoter Hypermethylation in Colorectal Carcinoma

Proceedings of the National Academy of Sciences - PNAS, 1998-06, Vol.95 (12), p.6870-6875

1998

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Germ-line msh6 mutations in colorectal cancer families

Cancer research (Chicago, Ill.), 1999-10, Vol.59 (20), p.5068-5074

1999

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Identification and Characterization of Saccharomyces cerevisiae EXO1, a Gene Encoding an Exonuclease that Interacts with MSH2

Proceedings of the National Academy of Sciences - PNAS, 1997-07, Vol.94 (14), p.7487-7492

1997

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Structure of the Human MSH2 Locus and Analysis of Two Muir-Torre Kindreds for msh2 Mutations

Genomics (San Diego, Calif.), 1994-12, Vol.24 (3), p.516-526

1994

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Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA

Journal of molecular biology, 1997-01, Vol.265 (3), p.289-301

1997

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A human compound heterozygote for two MLH1 missense mutations

Nature genetics, 1997-10, Vol.17 (2), p.135-136

1997

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An Exploratory Analysis of Stop the Demand – Waco Program

Kane, Michael F

2017

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Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations

Cancer research (Chicago, Ill.), 1995-01, Vol.55 (2), p.242-248

1995

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Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer

Journal of medical genetics, 1999-09, Vol.36 (9), p.678-682

1999

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Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas

Human molecular genetics, 1995-11, Vol.4 (11), p.2065-2072

1995

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Identification and characterization of the Escherichia coli RecT protein, a protein encoded by the recE region that promotes renaturation of homologous single-stranded DNA

Journal of Bacteriology, 1993-01, Vol.175 (1), p.277-287

1993

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Low frequency of hMSH2 mutations in Swedish HNPCC families

International journal of cancer, 1997-02, Vol.74 (1), p.134-137

1997

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Mononucleotide microsatellite instability and germlineMSH6 mutation analysis in early onset colorectal cancer

Journal of medical genetics, 1999-09, Vol.36 (9), p.678

1999

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Phosphorylation State of Olig2 Regulates Proliferation of Neural Progenitors

The Central Nervous System-Restricted Transcription Factor Olig2 Opposes p53 Responses to Genotoxic Damage in Neural Progenitors and Malignant Glioma

Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2

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

hMSH2 Forms Specific Mispair-Binding Complexes with hMSH3 and hMSH6

Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in mice

Haploinsufficiency of Flap Endonuclease (Fen1) Leads to Rapid Tumor Progression

Approaching a complete repository of sequence-verified protein-encoding clones for Saccharomyces cerevisiae

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines

An amino terminal phosphorylation motif regulates intranuclear compartmentalization of Olig2 in neural progenitor cells

MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice

Incidence and Functional Consequences of hMLH1 Promoter Hypermethylation in Colorectal Carcinoma

Germ-line msh6 mutations in colorectal cancer families

Identification and Characterization of Saccharomyces cerevisiae EXO1, a Gene Encoding an Exonuclease that Interacts with MSH2

Structure of the Human MSH2 Locus and Analysis of Two Muir-Torre Kindreds for msh2 Mutations

Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA

A human compound heterozygote for two MLH1 missense mutations

An Exploratory Analysis of Stop the Demand – Waco Program

Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations

Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer

Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas

Identification and characterization of the Escherichia coli RecT protein, a protein encoded by the recE region that promotes renaturation of homologous single-stranded DNA

Low frequency of hMSH2 mutations in Swedish HNPCC families

Mononucleotide microsatellite instability and germlineMSH6 mutation analysis in early onset colorectal cancer

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