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Junko Oshima

Showing results (21-30 of 90) with videos related to

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Mutation Research|July 22, 2008
Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in miceMitsuko 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 2014Fuki 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. elegansBryan 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 endsJunko 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 variantS Deepak Amalnath, Jothivanan, Junko Oshima, et al.
Neurobiology of Aging|February 2, 2016
Aβ 1-40 enhances the proliferation of human diploid fibroblastsLindsey Theda, Michelle K Drews, Galynn Zitnik, et al.
Aging|April 6, 2017
Accelerated epigenetic aging in Werner syndromeAnna 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 AShurong Huang, Rosa Ana Risques, George M Martin, et al.
Aging|May 29, 2025
Investigating telomere length in progeroid syndromes: implications for aging disordersLuma Srour, Abeer Qannan, Junko Oshima, et al.
Pageof 9

Showing results (21-30 of 90) with videos related to

Sort By:
Pageof 9
Mutation Research|July 22, 2008
Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in miceMitsuko 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 2014Fuki 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. elegansBryan 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 endsJunko 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 variantS Deepak Amalnath, Jothivanan, Junko Oshima, et al.
Neurobiology of Aging|February 2, 2016
Aβ 1-40 enhances the proliferation of human diploid fibroblastsLindsey Theda, Michelle K Drews, Galynn Zitnik, et al.
Aging|April 6, 2017
Accelerated epigenetic aging in Werner syndromeAnna 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 AShurong Huang, Rosa Ana Risques, George M Martin, et al.
Aging|May 29, 2025
Investigating telomere length in progeroid syndromes: implications for aging disordersLuma Srour, Abeer Qannan, Junko Oshima, et al.
Pageof 9