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Junko Oshima

Showing results (51-60 of 90) with videos related to

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Aging Cell|July 2, 2019
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processesAnna Maierhofer, Julia Flunkert, Junko Oshima, et al.
Molecular Imaging and Biology|August 5, 2005
Transfection of neuroprogenitor cells with iron nanoparticles for magnetic resonance imaging tracking: cell viability, differentiation, and intracellular localizationSosuke Miyoshi, Jennifer A Flexman, Donna J Cross, et al.
Age and Ageing|February 6, 2008
Association between APOE epsilon 2/epsilon 3/epsilon 4 polymorphism and disability severity in a national long-term care survey sampleAlexander Kulminski, Svetlana V Ukraintseva, Konstantin G Arbeev, et al.
DNA and Cell Biology|November 22, 2019
Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP SynthesisJiaming Zhang, Deyin Hou, James Annis, et al.
Journal of the American Geriatrics Society|June 29, 2010
Leukocyte telomere length is associated with disability in older u.s. PopulationRosa Ana Risques, Konstantin G Arbeev, Anatoli I Yashin, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|January 21, 2020
Cell-to-Cell Variation in Gene Expression for Cultured Human Cells Is Controlled in Trans by Diverse Genes: Implications for the Pathobiology of AgingJiaming Zhang, Nikolay Burnaevskiy, James Annis, et al.
The American Journal of Medicine|December 14, 2004
The genetics of human longevityWarren S Browner, Arnold J Kahn, Elad Ziv, et al.
Journal of the American Geriatrics Society|January 9, 2008
Health-protective and adverse effects of the apolipoprotein E epsilon2 allele in older menAlexander M Kulminski, Svetlana V Ukraintseva, Konstantin G Arbeev, et al.
Human Molecular Genetics|March 18, 2016
The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcriptionWeiliang Tang, Ana I Robles, Richard P Beyer, et al.
Molecular Syndromology|August 25, 2018
Biallelic <i>WRN</i> Mutations in Newly Identified Japanese Werner Syndrome PatientsYoshiro Maezawa, Hisaya Kato, Minoru Takemoto, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
Aging Cell|July 2, 2019
Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processesAnna Maierhofer, Julia Flunkert, Junko Oshima, et al.
Molecular Imaging and Biology|August 5, 2005
Transfection of neuroprogenitor cells with iron nanoparticles for magnetic resonance imaging tracking: cell viability, differentiation, and intracellular localizationSosuke Miyoshi, Jennifer A Flexman, Donna J Cross, et al.
Age and Ageing|February 6, 2008
Association between APOE epsilon 2/epsilon 3/epsilon 4 polymorphism and disability severity in a national long-term care survey sampleAlexander Kulminski, Svetlana V Ukraintseva, Konstantin G Arbeev, et al.
DNA and Cell Biology|November 22, 2019
Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP SynthesisJiaming Zhang, Deyin Hou, James Annis, et al.
Journal of the American Geriatrics Society|June 29, 2010
Leukocyte telomere length is associated with disability in older u.s. PopulationRosa Ana Risques, Konstantin G Arbeev, Anatoli I Yashin, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|January 21, 2020
Cell-to-Cell Variation in Gene Expression for Cultured Human Cells Is Controlled in Trans by Diverse Genes: Implications for the Pathobiology of AgingJiaming Zhang, Nikolay Burnaevskiy, James Annis, et al.
The American Journal of Medicine|December 14, 2004
The genetics of human longevityWarren S Browner, Arnold J Kahn, Elad Ziv, et al.
Journal of the American Geriatrics Society|January 9, 2008
Health-protective and adverse effects of the apolipoprotein E epsilon2 allele in older menAlexander M Kulminski, Svetlana V Ukraintseva, Konstantin G Arbeev, et al.
Human Molecular Genetics|March 18, 2016
The Werner syndrome RECQ helicase targets G4 DNA in human cells to modulate transcriptionWeiliang Tang, Ana I Robles, Richard P Beyer, et al.
Molecular Syndromology|August 25, 2018
Biallelic <i>WRN</i> Mutations in Newly Identified Japanese Werner Syndrome PatientsYoshiro Maezawa, Hisaya Kato, Minoru Takemoto, et al.
Pageof 9