検索結果 - Junko Oshima

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  1. 1
    Homozygous and compound heterozygous mutations at the Werner syndrome locus

    Homozygous and compound heterozygous mutations at the Werner syndrome locus 著者: Junko Oshima

    出版事項 1996
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    Artigo
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  2. 2
    WRN mutations in Werner syndrome

    WRN mutations in Werner syndrome 著者: Michael Möser, Junko Oshima, Raymond J. Monnat

    出版事項 1999
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  3. 3
    Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions

    Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions 著者: Junko Oshima, Julia M. Sidorova, Raymond J. Monnat

    出版事項 2016
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  4. 4
    Rapamycin decreases <scp>DNA</scp> damage accumulation and enhances cell growth of <scp>WRN</scp>‐deficient human fibroblasts

    Rapamycin decreases <scp>DNA</scp> damage accumulation and enhances cell growth of <scp>WRN</scp>‐deficient human fibroblasts 著者: Bidisha Saha, A. Cypro, George M. Martin, Junko Oshima

    出版事項 2013
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    Artigo
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  5. 5
    Characterization of Werner syndrome protein DNA helicase activity: Directionality, substrate dependence and stimulation by replication protein A

    Characterization of Werner syndrome protein DNA helicase activity: Directionality, substrate dependence and stimulation by replication protein A 著者: Jiangchuan Shen, Matthew D. Gray, Junko Oshima, Lawrence A. Loeb

    出版事項 1998
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    Artigo
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  6. 6
    Werner protein recruits DNA polymerase δ to the nucleolus

    Werner protein recruits DNA polymerase δ to the nucleolus 著者: Anna Szekely, Yao-Hui Chen, Chunyu Zhang, Junko Oshima, Sherman M. Weissman

    出版事項 2000
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    Artigo
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  7. 7
    Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A

    Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A 著者: Shurong Huang, Rosa Ana Risques, George M. Martin, Peter S. Rabinovitch, Junko Oshima

    出版事項 2007
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  8. 8
    Characterization of the human and mouse WRN 3'-&gt;5' exonuclease

    Characterization of the human and mouse WRN 3'-&gt;5' exonuclease 著者: Shurong Huang, Sergey Beresten, Baomin Li, Junko Oshima, Nathan A. Ellis, Judith Campisi

    出版事項 2000
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  9. 9
    Accelerated epigenetic aging in Werner syndrome

    Accelerated epigenetic aging in Werner syndrome 著者: Anna Maierhofer, Julia Flunkert, Junko Oshima, George M. Martin, Thomas Haaf, Steve Horvath

    出版事項 2017
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  10. 10
    The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease

    The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease 著者: Shurong Huang, Baomin Li, Matthew D. Gray, Junko Oshima, Shahzad I. Mian, Judith Campisi

    出版事項 1998
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    Carta
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  11. 11
    <scp>rDNA</scp> Copy Number Variation and Methylation During Normal and Premature Aging

    <scp>rDNA</scp> Copy Number Variation and Methylation During Normal and Premature Aging 著者: Alva B. C. Geisen, Nathalie Acevedo, Junko Oshima, Marcus Dittrich, Ramya Potabattula, Thomas Haaf

    出版事項 2025
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    Artigo
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  12. 12
    <scp>TNF</scp>‐α/<scp>IFN</scp>‐γ synergy amplifies senescence‐associated inflammation and <scp>SARS‐CoV</scp>‐2 receptor expression via hyper‐activated <scp>JAK</scp>/<scp>STAT1</scp>

    <scp>TNF</scp>‐α/<scp>IFN</scp>‐γ synergy amplifies senescence‐associated inflammation and <scp>SARS‐CoV</scp>‐2 receptor expression via hyper‐activated <scp>JAK</scp>/<scp>STAT1</... 著者: Renuka Kandhaya‐Pillai, Xiaomeng Yang, Tamar Tchkonia, George M. Martin, James L. Kirkland, Junko Oshima

    出版事項 2022
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    Artigo
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  13. 13
    Werner Syndrome Protein

    Werner Syndrome Protein 著者: Jiang-Cheng Shen, Matthew D. Gray, Junko Oshima, Ashwini S. Kamath‐Loeb, Michael Fry, Lawrence A. Loeb

    出版事項 1998
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    Artigo
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  14. 14
    The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis

    The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis 著者: Meltem Müftüoğlu, Junko Oshima, Cayetano von Kobbe, Wen‐Hsing Cheng, Dru F. Leistritz, Vilhelm A. Bohr

    出版事項 2008
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    Revisão
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  15. 15
    The role of protective genetic variants in modulating epigenetic aging

    The role of protective genetic variants in modulating epigenetic aging 著者: Yosra Bejaoui, Luma Srour, Abeer Qannan, Junko Oshima, Chadi Saad, Steve Horvath, Hamdi Mbarek, Nady El Hajj

    出版事項 2025
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    Artigo
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  16. 16
    Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complex

    Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complex 著者: Renuka Kandhaya‐Pillai, Francesc Miró‐Mur, Jaume Alijotas‐Reig, Tamar Tchkonia, Simó Schwartz, James L. Kirkland, Junko Oshima

    出版事項 2023
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    Artigo
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  17. 17
    The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription

    The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcription 著者: Weiliang Tang, Ana I. Robles, Richard P. Beyer, Lucas T. Gray, Giang Huong Nguyen, Junko Oshima, Nancy Maizels, Curtis C. Harris, Raymond J. Monnat

    出版事項 2016
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    Artigo
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  18. 18
    The Werner Syndrome Protein Is Involved in RNA Polymerase II Transcription

    The Werner Syndrome Protein Is Involved in RNA Polymerase II Transcription 著者: Adayabalam S. Balajee, Amrita Machwe, Alfred May, Matthew D. Gray, Junko Oshima, George M. Martin, Jan O. Nehlin, Robert Brosh, David K. Orren, Vilhelm A. Bohr

    出版事項 1999
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    Artigo
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  19. 19
    <i><scp>CTC</scp>1</i> mutations in a Brazilian family with progeroid features and recurrent bone fractures

    <i><scp>CTC</scp>1</i> mutations in a Brazilian family with progeroid features and recurrent bone fractures 著者: Forough Sargolzaeiaval, Jiaming Zhang, Jennifer Schleit, Davor Lessel, Christian Kubisch, Débora Rossi Precioso, David Sillence, Fuki M. Hisama, Michael O. Dorschner, George M. Martin, Junko Oshima

    出版事項 2018
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  20. 20
    Coronary artery disease in a Werner syndrome‐like form of progeria characterized by low levels of progerin, a splice variant of lamin A

    Coronary artery disease in a Werner syndrome‐like form of progeria characterized by low levels of progerin, a splice variant of lamin A 著者: Fuki M. Hisama, Davor Lessel, Dru F. Leistritz, Katrin Friedrich, Kim L. McBride, Matthew Pastore, Gary S. Gottesman, Bidisha Saha, George M. Martin, Christian Kubisch, Junko Oshima

    出版事項 2011
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