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Junko Oshima

Showing results (71-80 of 90) with videos related to

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Human Molecular Genetics|January 30, 2023
Accelerated epigenetic aging and DNA methylation alterations in Berardinelli-Seip congenital lipodystrophyAbeer Qannan, Yosra Bejaoui, Mahmoud Izadi, et al.
Human Genetics|May 19, 2009
Regional genomic instability predisposes to complex dystrophin gene rearrangementsJunko Oshima, Daniel B Magner, Jennifer A Lee, et al.
Genes & Development|July 5, 2003
Werner syndrome protein limits MYC-induced cellular senescenceCarla Grandori, Kou-Juey Wu, Paula Fernandez, et al.
Lancet (London, England)|August 21, 2003
LMNA mutations in atypical Werner's syndromeLishan Chen, Lin Lee, Brian A Kudlow, et al.
Journal of Medical Genetics|May 9, 2022
Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome casesDanny E Miller, Lin Lee, Miranda Galey, et al.
Human Mutation|November 7, 2017
ERCC4 variants identified in a cohort of patients with segmental progeroid syndromesTakayasu Mori, Matthew J Yousefzadeh, Maryam Faridounnia, et al.
European Journal of Human Genetics : EJHG|February 5, 2015
Truncated prelamin A expression in HGPS-like patients: a transcriptional studyFlorian Barthélémy, Claire Navarro, Racha Fayek, et al.
Journal of the Endocrine Society|September 17, 2020
Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an <i>LMNA</i> p.R349W VariantIram Hussain, Ruilin Raelene Jin, Howard B A Baum, et al.
Human Mutation|July 15, 2015
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeDavor Lessel, Fuki M Hisama, Katalin Szakszon, et al.
Geriatrics & Gerontology International|February 10, 2025
For early diagnosis of young patients with Werner syndrome: Indication for genetic testingTetta Sato, Yoshiro Maezawa, Hisaya Kato, et al.
Pageof 9

Showing results (71-80 of 90) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|January 30, 2023
Accelerated epigenetic aging and DNA methylation alterations in Berardinelli-Seip congenital lipodystrophyAbeer Qannan, Yosra Bejaoui, Mahmoud Izadi, et al.
Human Genetics|May 19, 2009
Regional genomic instability predisposes to complex dystrophin gene rearrangementsJunko Oshima, Daniel B Magner, Jennifer A Lee, et al.
Genes & Development|July 5, 2003
Werner syndrome protein limits MYC-induced cellular senescenceCarla Grandori, Kou-Juey Wu, Paula Fernandez, et al.
Lancet (London, England)|August 21, 2003
LMNA mutations in atypical Werner's syndromeLishan Chen, Lin Lee, Brian A Kudlow, et al.
Journal of Medical Genetics|May 9, 2022
Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome casesDanny E Miller, Lin Lee, Miranda Galey, et al.
Human Mutation|November 7, 2017
ERCC4 variants identified in a cohort of patients with segmental progeroid syndromesTakayasu Mori, Matthew J Yousefzadeh, Maryam Faridounnia, et al.
European Journal of Human Genetics : EJHG|February 5, 2015
Truncated prelamin A expression in HGPS-like patients: a transcriptional studyFlorian Barthélémy, Claire Navarro, Racha Fayek, et al.
Journal of the Endocrine Society|September 17, 2020
Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an <i>LMNA</i> p.R349W VariantIram Hussain, Ruilin Raelene Jin, Howard B A Baum, et al.
Human Mutation|July 15, 2015
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeDavor Lessel, Fuki M Hisama, Katalin Szakszon, et al.
Geriatrics & Gerontology International|February 10, 2025
For early diagnosis of young patients with Werner syndrome: Indication for genetic testingTetta Sato, Yoshiro Maezawa, Hisaya Kato, et al.
Pageof 9