Resultados de procura - Song‐Ro Yoon

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  1. 1
    Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B

    Positive Selection for New Disease Mutations in the Human Germline: Evidence from the Heritable Cancer Syndrome Multiple Endocrine Neoplasia Type 2B por Soo‐Kyung Choi, Song‐Ro Yoon, Peter Calabrese, Norman Arnheim

    Publicado 2012
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  2. 2
    A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations

    A germ-line-selective advantage rather than an increased mutation rate can explain some unexpectedly common human disease mutations por Soo‐Kyung Choi, Song‐Ro Yoon, Peter Calabrese, Norman Arnheim

    Publicado 2008
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  3. 3
    Huntington disease expansion mutations in humans can occur before meiosis is completed

    Huntington disease expansion mutations in humans can occur before meiosis is completed por Song‐Ro Yoon, Louis Dubeau, Margot de Young, Nancy S. Wexler, Norman Arnheim

    Publicado 2003
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  4. 4
    Age-Dependent Germline Mosaicism of the Most Common Noonan Syndrome Mutation Shows the Signature of Germline Selection

    Age-Dependent Germline Mosaicism of the Most Common Noonan Syndrome Mutation Shows the Signature of Germline Selection por Song‐Ro Yoon, Soo-Kung Choi, Jordan Eboreime, Bruce D. Gelb, Peter Calabrese, Norman Arnheim

    Publicado 2013
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  5. 5
    The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes

    The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes por Jian Qin, Peter Calabrese, Irene Tiemann‐Boege, Deepali N. Shinde, Song‐Ro Yoon, David H. Gelfand, Keith Bauer, Norman Arnheim

    Publicado 2007
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  6. 6
    The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect

    The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect por Song-Ro Yoon, Jian Qin, Rivka L. Glaser, Ethylin Wang Jabs, Nancy S. Wexler, Rebecca Z. Sokol, Norman Arnheim, Peter Calabrese

    Publicado 2009
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  7. 7
    Contributions by MutL Homologues <i>Mlh3</i> and <i>Pms2</i> to DNA Mismatch Repair and Tumor Suppression in the Mouse

    Contributions by MutL Homologues <i>Mlh3</i> and <i>Pms2</i> to DNA Mismatch Repair and Tumor Suppression in the Mouse por Peng‐Chieh Chen, Sandra Dudley, Wayne Hagen, Diana Dizon, Leslie Paxton, Denise Reichow, Song-Ro Yoon, Kan Yang, Norman Arnheim, R. Michael Liskay, Steven M. Lipkin

    Publicado 2005
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  8. 8
    Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain

    Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain por Peggy Shelbourne, Christine E. Keller-McGandy, Wenya Linda Bi, Song‐Ro Yoon, Louis Dubeau, Nicola Veitch, Jean Paul Vonsattel, Nancy S. Wexler, Norman Arnheim, Sarah J. Augood

    Publicado 2007
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