Torthaí cuardaigh - Raymond J. Monnat
- 1 - 20 toradh as 38 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Human RECQ helicases: Roles in DNA metabolism, mutagenesis and cancer biology de réir Raymond J. Monnat
Foilsithe / Cruthaithe 2010Revisão -
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Nucleotide sequence preservation of human mitochondrial DNA. de réir Raymond J. Monnat, Lawrence A. Loeb
Foilsithe / Cruthaithe 1985Artigo -
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WRN mutations in Werner syndrome de réir Michael Möser, Junko Oshima, Raymond J. Monnat
Foilsithe / Cruthaithe 1999Revisão -
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DNA Recognition and Cleavage by the LAGLIDADG Homing Endonuclease I-Cre I de réir Melissa S. Jurica, Raymond J. Monnat, Barry Stoddard
Foilsithe / Cruthaithe 1998Artigo -
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PARP-mediated repair, homologous recombination, and back-up non-homologous end joining-like repair of single-strand nicks de réir Michael J. Metzger, Barry Stoddard, Raymond J. Monnat
Foilsithe / Cruthaithe 2013Artigo -
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Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions de réir Junko Oshima, Julia M. Sidorova, Raymond J. Monnat
Foilsithe / Cruthaithe 2016Revisão -
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Mutator phenotype of Werner syndrome is characterized by extensive deletions. de réir Ken-ichiro Fukuchi, George M. Martin, Raymond J. Monnat
Foilsithe / Cruthaithe 1989Artigo -
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Loss of Werner syndrome protein function promotes aberrant mitotic recombination de réir P.R. Prince, Mary J. Emond, Raymond J. Monnat
Foilsithe / Cruthaithe 2001Artigo -
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Identification of a human centrosomal calmodulin-binding protein that shares homology with pericentrin de réir Mark R. Flory, Michael J. Moser, Raymond J. Monnat, Trisha N. Davis
Foilsithe / Cruthaithe 2000Artigo -
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Spectrum and Risk of Neoplasia in Werner Syndrome: A Systematic Review de réir Julia M. Lauper, Alison J. Krause, Thomas L. Vaughan, Raymond J. Monnat
Foilsithe / Cruthaithe 2013Revisão -
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Design, Activity, and Structure of a Highly Specific Artificial Endonuclease de réir B. Chevalier, Tanja Kortemme, Meggen S. Chadsey, David Baker, Raymond J. Monnat, Barry Stoddard
Foilsithe / Cruthaithe 2002Artigo -
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Homologous Recombination Resolution Defect in Werner Syndrome de réir Yannick Saintigny, Kate Makienko, Cristina L. Swanson, Mary J. Emond, Raymond J. Monnat
Foilsithe / Cruthaithe 2002Artigo -
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Generation of a nicking enzyme that stimulates site-specific gene conversion from the I-AniI LAGLIDADG homing endonuclease de réir Audrey McConnell Smith, Ryo Takeuchi, Stefan Pellenz, Luther Davis, Nancy Maizels, Raymond J. Monnat, Barry Stoddard
Foilsithe / Cruthaithe 2009Artigo -
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Computational redesign of endonuclease DNA binding and cleavage specificity de réir J. R. Ashworth, James J. Havranek, Carlos M. Duarte, Django Sussman, Raymond J. Monnat, Barry Stoddard, David Baker
Foilsithe / Cruthaithe 2006Artigo -
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Somatic Mutations Are Frequent and Increase with Age in Human Kidney Epithelial Cells de réir George M. Martin, Charles E. Ogburn, Lorel M. Colgin, Allen M. Gown, Steven D. Edland, Raymond J. Monnat
Foilsithe / Cruthaithe 1996Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
DNA
Helicase
RNA
Cell biology
DNA repair
DNA damage
Genome instability
Molecular biology
Werner syndrome
Chromosome
Computational biology
DNA replication
RecQ helicase
Cancer research
Homologous recombination
Mutation
Bloom syndrome
Cancer
Endonuclease
Homing endonuclease
Chromosome instability
Eukaryotic DNA replication
Medicine
Biochemistry
Cell
Cell cycle
Control of chromosome duplication