Junko Oshima

ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 6

Top Venues

GeroScience

Aging cell

Molecular genetics & genomic medicine

Human mutation

This page only lists publications with an associated author ORCID identifier.

Publications

Fuki M Hisama, Renuka Kandhaya Pillai, Julia Sidorova, Karynne Patterson, Carolina Gokingco, Michal Yacobi-Bach, Junko Oshima
Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome. GeroScience (2023)
Renuka Kandhaya-Pillai, Xiaomeng Yang, Tamar Tchkonia, George M Martin, James L Kirkland, Junko Oshima
TNF-α/IFN-γ synergy amplifies senescence-associated inflammation and SARS-CoV-2 receptor expression via hyper-activated JAK/STAT1. Aging cell 21 (6) (2022)
Yosra Bejaoui, Aleem Razzaq, Noha A Yousri, Junko Oshima, Andre Megarbane, Abeer Qannan, Ramya Potabattula, Tanvir Alam, George M Martin, Henning F Horn, Thomas Haaf, Steve Horvath, Nady El Hajj
DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome. Aging cell 21 (2) (2022)
Renuka Kandhaya-Pillai, Deyin Hou, Jiaming Zhang, Xiaomeng Yang, Goli Compoginis, Takayasu Mori, Tamara Tchkonia, George M Martin, Fuki M Hisama, James L Kirkland, Junko Oshima
SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome. GeroScience 43 (3) (2021)
Forough Sargolzaeiaval, Jiaming Zhang, Jennifer Schleit, Davor Lessel, Christian Kubisch, Debora R Precioso, David Sillence, Fuki M Hisama, Michael Dorschner, George M Martin, Junko Oshima
CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures. Molecular genetics & genomic medicine 6 (6) (2018)
Takayasu Mori, Matthew J Yousefzadeh, Maryam Faridounnia, Jessica X Chong, Fuki M Hisama, Louanne Hudgins, Gabriela Mercado, Erin A Wade, Amira S Barghouthy, Lin Lee, George M Martin, Deborah A Nickerson, Michael J Bamshad, null null, Laura J Niedernhofer, Junko Oshima
ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes. Human mutation 39 (2) (2017)

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Publication Activity (10 Years)

Top Topics

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Junko Oshima