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Junko Oshima

Showing results (41-50 of 90) with videos related to

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Human Genetics|September 24, 2008
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosisMeltem Muftuoglu, Junko Oshima, Cayetano von Kobbe, et al.
Frontiers in Genetics|July 13, 2013
DNA damage accumulation and TRF2 degradation in atypical Werner syndrome fibroblasts with LMNA mutationsBidisha Saha, Galynn Zitnik, Simon Johnson, et al.
Plos One|May 4, 2010
A flanking gene problem leads to the discovery of a Gprc5b splice variant predominantly expressed in C57Bl/6J mouse brain and in maturing neuronsBethany H Cool, Guy C-K Chan, Lin Lee, et al.
Geroscience|February 10, 2025
The role of protective genetic variants in modulating epigenetic agingYosra Bejaoui, Luma Srour, Abeer Qannan, et al.
DNA Repair|April 16, 2013
Functional deficit associated with a missense Werner syndrome mutationTakashi Tadokoro, Ivana Rybanska-Spaeder, Tomasz Kulikowicz, et al.
Geroscience|August 21, 2023
Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndromeFuki M Hisama, Renuka Kandhaya Pillai, Julia Sidorova, et al.
Aging Pathobiology and Therapeutics|September 21, 2020
Novel LMNA mutations in Greek and Myanmar Patients with Progeroid Features and Cardiac ManifestationsRenuka Kandhaya-Pillai, Fuki M Hisama, Stephanie A Bucks, et al.
BMC Medical Genetics|March 3, 2007
SOD2 polymorphisms: unmasking the effect of polymorphism on splicingJing Shao, Lishan Chen, Brian Marrs, et al.
Biochemical and Biophysical Research Communications|December 8, 2006
Collagen expression in fibroblasts with a novel LMNA mutationDesiree Nguyen, Dru F Leistritz, Lesley Turner, et al.
Aging|May 23, 2023
Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complexRenuka Kandhaya-Pillai, Francesc Miro-Mur, Jaume Alijotas-Reig, et al.
Pageof 9

Showing results (41-50 of 90) with videos related to

Sort By:
Pageof 9
Human Genetics|September 24, 2008
The clinical characteristics of Werner syndrome: molecular and biochemical diagnosisMeltem Muftuoglu, Junko Oshima, Cayetano von Kobbe, et al.
Frontiers in Genetics|July 13, 2013
DNA damage accumulation and TRF2 degradation in atypical Werner syndrome fibroblasts with LMNA mutationsBidisha Saha, Galynn Zitnik, Simon Johnson, et al.
Plos One|May 4, 2010
A flanking gene problem leads to the discovery of a Gprc5b splice variant predominantly expressed in C57Bl/6J mouse brain and in maturing neuronsBethany H Cool, Guy C-K Chan, Lin Lee, et al.
Geroscience|February 10, 2025
The role of protective genetic variants in modulating epigenetic agingYosra Bejaoui, Luma Srour, Abeer Qannan, et al.
DNA Repair|April 16, 2013
Functional deficit associated with a missense Werner syndrome mutationTakashi Tadokoro, Ivana Rybanska-Spaeder, Tomasz Kulikowicz, et al.
Geroscience|August 21, 2023
Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndromeFuki M Hisama, Renuka Kandhaya Pillai, Julia Sidorova, et al.
Aging Pathobiology and Therapeutics|September 21, 2020
Novel LMNA mutations in Greek and Myanmar Patients with Progeroid Features and Cardiac ManifestationsRenuka Kandhaya-Pillai, Fuki M Hisama, Stephanie A Bucks, et al.
BMC Medical Genetics|March 3, 2007
SOD2 polymorphisms: unmasking the effect of polymorphism on splicingJing Shao, Lishan Chen, Brian Marrs, et al.
Biochemical and Biophysical Research Communications|December 8, 2006
Collagen expression in fibroblasts with a novel LMNA mutationDesiree Nguyen, Dru F Leistritz, Lesley Turner, et al.
Aging|May 23, 2023
Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complexRenuka Kandhaya-Pillai, Francesc Miro-Mur, Jaume Alijotas-Reig, et al.
Pageof 9