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Junko Oshima

Showing results (81-90 of 90) with videos related to

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The Journal of Clinical Investigation|August 29, 2017
Dysfunction of the MDM2/p53 axis is linked to premature agingDavor Lessel, Danyi Wu, Carlos Trujillo, et al.
Aging|July 27, 2018
Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and <i>ex vivo</i> studiesSteve Horvath, Junko Oshima, George M Martin, et al.
Aging|May 2, 2023
Renal dysfunction, malignant neoplasms, atherosclerotic cardiovascular diseases, and sarcopenia as key outcomes observed in a three-year follow-up study using the Werner Syndrome RegistryYukari Maeda, Masaya Koshizaka, Mayumi Shoji, et al.
Aging|December 3, 2024
Less frequent skin ulcers among patients with Werner syndrome treated with pioglitazone: findings from the Japanese Werner Syndrome RegistryKazuto Aono, Masaya Koshizaka, Mayumi Shoji, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.
Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, et al.
Nature Genetics|September 29, 2014
Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid featuresDavor Lessel, Bruno Vaz, Swagata Halder, et al.
BMC Genetics|December 30, 2014
Genetic diversity is a predictor of mortality in humansNathan A Bihlmeyer, Jennifer A Brody, Albert Vernon Smith, et al.
Autophagy|January 23, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
The Journal of Clinical Investigation|August 29, 2017
Dysfunction of the MDM2/p53 axis is linked to premature agingDavor Lessel, Danyi Wu, Carlos Trujillo, et al.
Aging|July 27, 2018
Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and <i>ex vivo</i> studiesSteve Horvath, Junko Oshima, George M Martin, et al.
Aging|May 2, 2023
Renal dysfunction, malignant neoplasms, atherosclerotic cardiovascular diseases, and sarcopenia as key outcomes observed in a three-year follow-up study using the Werner Syndrome RegistryYukari Maeda, Masaya Koshizaka, Mayumi Shoji, et al.
Aging|December 3, 2024
Less frequent skin ulcers among patients with Werner syndrome treated with pioglitazone: findings from the Japanese Werner Syndrome RegistryKazuto Aono, Masaya Koshizaka, Mayumi Shoji, et al.
Human Genetics|May 6, 2010
WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterationsKatrin Friedrich, Lin Lee, Dru F Leistritz, et al.
Human Mutation|September 27, 2016
WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational ProspectsKoutaro Yokote, Sirisak Chanprasert, Lin Lee, et al.
Human Mutation|May 5, 2006
The spectrum of WRN mutations in Werner syndrome patientsShurong Huang, Lin Lee, Nancy B Hanson, et al.
Nature Genetics|September 29, 2014
Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid featuresDavor Lessel, Bruno Vaz, Swagata Halder, et al.
BMC Genetics|December 30, 2014
Genetic diversity is a predictor of mortality in humansNathan A Bihlmeyer, Jennifer A Brody, Albert Vernon Smith, et al.
Autophagy|January 23, 2016
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, et al.
Pageof 9