Search Results - "Kane, Michael F."
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Separated at birth? The functional and molecular divergence of OLIG1 and OLIG2
Published in Nature reviews. Neuroscience (01-12-2012)“…Despite their structural similarities and seemingly coordinated expression patterns, oligodendrocyte transcription factor 1 (OLIG1) and OLIG2 have largely…”
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The Central Nervous System-Restricted Transcription Factor Olig2 Opposes p53 Responses to Genotoxic Damage in Neural Progenitors and Malignant Glioma
Published in Cancer cell (08-03-2011)“…High-grade gliomas are notoriously insensitive to radiation and genotoxic drugs. Paradoxically, the p53 gene is structurally intact in the majority of these…”
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3
Phosphorylation State of Olig2 Regulates Proliferation of Neural Progenitors
Published in Neuron (Cambridge, Mass.) (10-03-2011)“…The bHLH transcription factors that regulate early development of the central nervous system can generally be classified as either antineural or proneural…”
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Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility
Published in Genes & development (01-03-2003)“…Exonuclease 1 (Exo1) is a 5'-3' exonuclease that interacts with MutS and MutL homologs and has been implicated in the excision step of DNA mismatch repair. To…”
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Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in mice
Published in Nature genetics (01-07-2005)“…Most cancers have multiple chromosomal rearrangements; the molecular mechanisms that generate them remain largely unknown. Mice carrying a heterozygous…”
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hMSH2 Forms Specific Mispair-Binding Complexes with hMSH3 and hMSH6
Published in Proceedings of the National Academy of Sciences - PNAS (26-11-1996)“…The genetic and biochemical properties of three human MutS homologues, hMSH2, hMSH3, and hMSH6, have been examined. The full-length hMSH6 cDNA and genomic…”
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Haploinsufficiency of Flap Endonuclease (Fen1) Leads to Rapid Tumor Progression
Published in Proceedings of the National Academy of Sciences - PNAS (23-07-2002)“…Flap endonuclease (Fen1) is required for DNA replication and repair, and defects in the gene encoding Fen1 cause increased accumulation of mutations and genome…”
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Approaching a complete repository of sequence-verified protein-encoding clones for Saccharomyces cerevisiae
Published in Genome Research (01-04-2007)“…The availability of an annotated genome sequence for the yeast Saccharomyces cerevisiae has made possible the proteome-scale study of protein function and…”
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Mutation in the mismatch repair gene Msh6 causes cancer susceptibility
Published in Cell (14-11-1997)“…Mice carrying a null mutation in the mismatch repair gene Msh6 were generated by gene targeting. Cells that were homozygous for the mutation did not produce…”
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An amino terminal phosphorylation motif regulates intranuclear compartmentalization of Olig2 in neural progenitor cells
Published in The Journal of neuroscience (18-06-2014)“…The bHLH transcription factor Olig2 is expressed in cycling neural progenitor cells but also in terminally differentiated, myelinating oligodendrocytes…”
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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
Published in Cancer research (Chicago, Ill.) (01-03-1997)“…Somatic mutations in DNA mismatch repair genes have been observed in sporadic tumors as well as cell lines and xenografts derived from such tumors implicating…”
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MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
Published in Genes & development (01-05-2000)“…Msh4 (MutS homolog 4) is a member of the mammalian mismatch repair gene family whose members are involved in postreplicative DNA mismatch repair as well as in…”
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Incidence and Functional Consequences of hMLH1 Promoter Hypermethylation in Colorectal Carcinoma
Published in Proceedings of the National Academy of Sciences - PNAS (09-06-1998)“…Inactivation of the genes involved in DNA mismatch repair is associated with microsatellite instability (MSI) in colorectal cancer. We report that…”
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Germ-line msh6 mutations in colorectal cancer families
Published in Cancer research (Chicago, Ill.) (15-10-1999)“…Hereditary nonpolyposis colorectal carcinoma (HNPCC) is due primarily to inherited mutations in two mismatch repair genes, MSH2 and MLH1, whereas germ-line…”
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Identification and Characterization of Saccharomyces cerevisiae EXO1, a Gene Encoding an Exonuclease that Interacts with MSH2
Published in Proceedings of the National Academy of Sciences - PNAS (08-07-1997)“…A two-hybrid screen was used to identify Saccharomyces cerevisiae genes encoding proteins that interact with MSH2. One gene was found to encode a homologue of…”
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Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations
Published in Genomics (San Diego, Calif.) (01-12-1994)“…Hereditary nonpolyposis colorectal carcinoma (HNPCC) is a major cancer susceptibility syndrome known to be caused by inheritance of mutations in genes such as…”
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Saccharomyces cerevisiae MSH2, a mispaired base recognition protein, also recognizes Holliday junctions in DNA
Published in Journal of molecular biology (01-01-1997)“…Genetic and biochemical studies have suggested that mismatch repair proteins interact with recombination intermediates to prevent recombina tion, or to limit…”
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A human compound heterozygote for two MLH1 missense mutations
Published in Nature genetics (01-10-1997)“…Hereditary nonpolyposis colorectal cancer (HNPCC) is associated with germline mutations in MLH1 and MSH2, which are active in DNA mismatch repair (MMR)…”
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An Exploratory Analysis of Stop the Demand – Waco Program
Published 01-01-2017“…Much research on prostitution focuses on the general morality of this phenomenon. Currently, many local entities are attempting to control, reduce or eliminate…”
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Dissertation -
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Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer
Published in Journal of medical genetics (01-09-1999)“…Germline mutations in the MSH2 and MLH1 mismatch repair genes account for most cases of hereditary non-polyposis colon cancer syndrome (HNPCC). In addition,…”
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