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Mutation Research
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July 22, 2008
Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in mice
Mitsuko L Yamamoto, Ramune Reliene, Junko Oshima, et al.
European Journal of Human Genetics : EJHG
|
September 4, 2014
Clinical utility gene card for: Werner Syndrome--Update 2014
Fuki M Hisama, Christian Kubisch, George M Martin, et al.
Nature Communications
|
November 28, 2025
Maternal histone methyltransferases antagonistically regulate autosomal random monoallelic expression (aRMAE) in C. elegans
Bryan Sands, Soo R Yun, Junko Oshima, et al.
Biorxiv : the Preprint Server for Biology
|
February 8, 2024
Maternal histone methyltransferases antagonistically regulate monoallelic expression in <i>C. elegans</i>
Bryan Sands, Soo R Yun, Junko Oshima, et al.
Cancer Research
|
January 26, 2002
Lack of WRN results in extensive deletion at nonhomologous joining ends
Junko Oshima, Shurong Huang, Chong Pae, et al.
American Journal of Medical Genetics. Part A
|
September 14, 2023
Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant
S Deepak Amalnath, Jothivanan, Junko Oshima, et al.
Neurobiology of Aging
|
February 2, 2016
Aβ 1-40 enhances the proliferation of human diploid fibroblasts
Lindsey Theda, Michelle K Drews, Galynn Zitnik, et al.
Aging
|
April 6, 2017
Accelerated epigenetic aging in Werner syndrome
Anna Maierhofer, Julia Flunkert, Junko Oshima, et al.
Experimental Cell Research
|
September 18, 2007
Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A
Shurong Huang, Rosa Ana Risques, George M Martin, et al.
Aging
|
May 29, 2025
Investigating telomere length in progeroid syndromes: implications for aging disorders
Luma Srour, Abeer Qannan, Junko Oshima, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 90) with videos related to
Sort By:
Page
of 9
Mutation Research
|
July 22, 2008
Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in mice
Mitsuko L Yamamoto, Ramune Reliene, Junko Oshima, et al.
European Journal of Human Genetics : EJHG
|
September 4, 2014
Clinical utility gene card for: Werner Syndrome--Update 2014
Fuki M Hisama, Christian Kubisch, George M Martin, et al.
Nature Communications
|
November 28, 2025
Maternal histone methyltransferases antagonistically regulate autosomal random monoallelic expression (aRMAE) in C. elegans
Bryan Sands, Soo R Yun, Junko Oshima, et al.
Biorxiv : the Preprint Server for Biology
|
February 8, 2024
Maternal histone methyltransferases antagonistically regulate monoallelic expression in <i>C. elegans</i>
Bryan Sands, Soo R Yun, Junko Oshima, et al.
Cancer Research
|
January 26, 2002
Lack of WRN results in extensive deletion at nonhomologous joining ends
Junko Oshima, Shurong Huang, Chong Pae, et al.
American Journal of Medical Genetics. Part A
|
September 14, 2023
Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant
S Deepak Amalnath, Jothivanan, Junko Oshima, et al.
Neurobiology of Aging
|
February 2, 2016
Aβ 1-40 enhances the proliferation of human diploid fibroblasts
Lindsey Theda, Michelle K Drews, Galynn Zitnik, et al.
Aging
|
April 6, 2017
Accelerated epigenetic aging in Werner syndrome
Anna Maierhofer, Julia Flunkert, Junko Oshima, et al.
Experimental Cell Research
|
September 18, 2007
Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A
Shurong Huang, Rosa Ana Risques, George M Martin, et al.
Aging
|
May 29, 2025
Investigating telomere length in progeroid syndromes: implications for aging disorders
Luma Srour, Abeer Qannan, Junko Oshima, et al.
Page
of 9