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Junko Oshima

Showing results (31-40 of 90) with videos related to

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Pathology International|October 31, 2002
Alterations of chaperone protein expression in presenilin mutant neurons in response to glutamate excitotoxicityIzumi Maezawa, Baiping Wang, Qubai Hu, et al.
Journal of Cell Science|September 6, 2005
Accumulation of Werner protein at DNA double-strand breaks in human cellsLi Lan, Satoshi Nakajima, Kenshi Komatsu, et al.
Aging Cell|June 1, 2022
TNF-α/IFN-γ synergy amplifies senescence-associated inflammation and SARS-CoV-2 receptor expression via hyper-activated JAK/STAT1Renuka Kandhaya-Pillai, Xiaomeng Yang, Tamar Tchkonia, et al.
Human Genetics|October 7, 2005
Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interferenceShurong Huang, Lishan Chen, Nataliya Libina, et al.
Aging Cell|August 26, 2003
WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repairLishan Chen, Shurong Huang, Lin Lee, et al.
Aging Cell|January 24, 2025
rDNA Copy Number Variation and Methylation During Normal and Premature AgingAlva B C Geisen, Natalia Santana Acevedo, Junko Oshima, et al.
Cancer Research|January 26, 2002
Functional evidence for a metastasis suppressor gene for rat prostate cancer within a 60-kilobase region on human chromosome 8p21-p12Naoki Nihei, Natalya Kouprina, Vladimir Larionov, et al.
American Journal of Medical Genetics. Part A|November 22, 2016
High incidence of BSCL2 intragenic recombinational mutation in Peruvian type 2 Berardinelli-Seip syndromeNelson Purizaca-Rosillo, Takayasu Mori, Yamali Benites-Cóndor, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2005
Phenotypic heterogeneity in body fat distribution in patients with atypical Werner's syndrome due to heterozygous Arg133Leu lamin A/C mutationKatherine N Jacob, Fernando Baptista, Heloísa G dos Santos, et al.
Aging|October 18, 2024
Werner syndrome RECQ helicase participates in and directs maintenance of the protein complexes of constitutive heterochromatin in proliferating human cellsPavlo Lazarchuk, Matthew Manh Nguyen, Crina M Curca, et al.
Pageof 9

Showing results (31-40 of 90) with videos related to

Sort By:
Pageof 9
Pathology International|October 31, 2002
Alterations of chaperone protein expression in presenilin mutant neurons in response to glutamate excitotoxicityIzumi Maezawa, Baiping Wang, Qubai Hu, et al.
Journal of Cell Science|September 6, 2005
Accumulation of Werner protein at DNA double-strand breaks in human cellsLi Lan, Satoshi Nakajima, Kenshi Komatsu, et al.
Aging Cell|June 1, 2022
TNF-α/IFN-γ synergy amplifies senescence-associated inflammation and SARS-CoV-2 receptor expression via hyper-activated JAK/STAT1Renuka Kandhaya-Pillai, Xiaomeng Yang, Tamar Tchkonia, et al.
Human Genetics|October 7, 2005
Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interferenceShurong Huang, Lishan Chen, Nataliya Libina, et al.
Aging Cell|August 26, 2003
WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repairLishan Chen, Shurong Huang, Lin Lee, et al.
Aging Cell|January 24, 2025
rDNA Copy Number Variation and Methylation During Normal and Premature AgingAlva B C Geisen, Natalia Santana Acevedo, Junko Oshima, et al.
Cancer Research|January 26, 2002
Functional evidence for a metastasis suppressor gene for rat prostate cancer within a 60-kilobase region on human chromosome 8p21-p12Naoki Nihei, Natalya Kouprina, Vladimir Larionov, et al.
American Journal of Medical Genetics. Part A|November 22, 2016
High incidence of BSCL2 intragenic recombinational mutation in Peruvian type 2 Berardinelli-Seip syndromeNelson Purizaca-Rosillo, Takayasu Mori, Yamali Benites-Cóndor, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2005
Phenotypic heterogeneity in body fat distribution in patients with atypical Werner's syndrome due to heterozygous Arg133Leu lamin A/C mutationKatherine N Jacob, Fernando Baptista, Heloísa G dos Santos, et al.
Aging|October 18, 2024
Werner syndrome RECQ helicase participates in and directs maintenance of the protein complexes of constitutive heterochromatin in proliferating human cellsPavlo Lazarchuk, Matthew Manh Nguyen, Crina M Curca, et al.
Pageof 9