Rchr
J-GLOBAL ID:201801001298986617
Update date: Jul. 16, 2024
Junko Oshima
オオシマ ジュンコ | Junko Oshima
Affiliation and department:
Job title:
Research Professor Emeritus
Other affiliations (1):
Homepage URL (2):
http://www.pathology.washington.edu/faculty/oshima
,
http://www.pathology.washington.edu/research/werner/registry/registry.html
Research field (1):
Internal medicine - General
Research keywords (5):
Progeria
, Internal medicine
, Aging
, Genome
, Genetics
Research theme for competitive and other funds (7):
- 2019 - 2025 Genetic and Non-Genetic Modulators of Morbidity/Disability Compression in aLarge Population-Based Study of Cognitive and Physical Impairment with Emphasis on Alzheimer's Disease and Related Dementias
- 2021 - 2024 脂肪や血管組織老化に伴う機能変容における老化関連長鎖非コードRNAの基盤的研究
- 2016 - 2022 International Registry of Werner Syndrome
- 2017 - 2020 早老症の遺伝原因同定と、正常加齢への寄与の検索
- 2016 - 2018 Genetic Modulations of Morbidity Compression:A Population-Based Study
- 2012 - 2018 International Registry of Werner Syndrome
- 2015 - 2017 Nathan Shock Center Storage of NLTCS Biospecimens
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Papers (131):
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Danny E Miller, Lin Lee, Miranda Galey, Renuka Kandhaya-Pillai, Marc Tischkowitz, Deepak Amalnath, Avadh Vithlani, Koutaro Yokote, Hisaya Kato, Yoshiro Maezawa, et al. Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases. Journal of medical genetics. 2022. 59. 11. 1087-94
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Renuka Kandhaya-Pillai, Deyin Hou, Jiaming Zhang, Xiaomeng Yang, Goli Compoginis, Takayasu Mori, Tamara Tchkonia, George M Martin, Fuki M Hisama, James L Kirkland, et al. 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. 2021. 43. 3. 1481-1496
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Junko Oshima, George M Martin, Fuki M Hisama. Werner Syndrome. 2021
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George M Martin, Fuki M Hisama, Junko Oshima. Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!. The journals of gerontology. Series A, Biological sciences and medical sciences. 2021. 76. 2. 253-259
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Iram Hussain, Ruilin Raelene Jin, Howard B A Baum, Jerry R Greenfield, Sophie Devery, Chao Xing, Robert A Hegele, Barbara G Carranza-Leon, Macrae F Linton, Frank Vuitch, et al. Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an LMNA p.R349W Variant. Journal of the Endocrine Society. 2020. 4. 10. bvaa104
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MISC (7):
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B. Saha, G. Zitnik, S. Johnson, Q. Nguyen, G. M. Martin, J. Oshima. TRF2 Degradation and DNA Damage Accumulation in LMNA Mutant Atypical Werner Syndrome Fibroblasts. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL. 2012. 48. 48-48
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J Oshima, A Garg, GM Martin, BK Kennedy. LMNA mutations in atypical Werner's syndrome - Reply. LANCET. 2003. 362. 9395. 1586-1586
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MJ Moser, J Oshima, RJ Monnat. WRN mutations in Werner syndrome (vol 13, pg 271, 1998). HUMAN MUTATION. 1999. 14. 1. 84-85
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L Ye, T Miki, J Nakura, J Oshima, A Morishima, H Rakugi, H Ikegami, J Higaki, D Edland, M Martin, et al. A polymorphic variant of Werner syndrome gene (WRN) association with myocardial infarction (MI) in Japanese population. AMERICAN JOURNAL OF HUMAN GENETICS. 1997. 61. 4. A301-A301
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L Ye, T Miki, J Nakura, J Oshima, K Kamino, H Rakugi, H Ikegami, J Higaki, SD Edland, GM Martin, et al. Rapid publication: Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population (vol 68, pg 494, 1997). AMERICAN JOURNAL OF MEDICAL GENETICS. 1997. 70. 1. 103-103
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Lectures and oral presentations (18):
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The Spectrum of WRN Mutations in Werner Syndrome Patients
(日本老年医学会 2021)
-
Genetics of Aging: Molecular Mechanisms of Progeroid Syndromes”
(Seminars in Medical Sciences Series 2019)
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Genetics of Aging: Molecular Mechanisms of Progeroid Syndromes
(Leading Seminar, Chiba University 2019)
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International Registry of Werner Syndrome: Search for progeroid syndrome mutations and mechanisms
(Cold Spring Harbor Laboratory Meeting “Mechanism of Aging”. 2018)
-
International Registry of Werner Syndrome: Search for progeroid syndrome mutations and mechanisms
(International Meeting on RECQ Helicases and Related Diseases 2018, 2018)
more...
Education (3):
- 1986 - 1992 Boston University School of Medicine Doctoral course of Garaduate School Department of Biochemistry
- 1978 - 1984 University of Tsukuba School School of Medicine
- 1975 - 1978 Nagano Prefectural Nagano Senior Hihg School
Professional career (2):
- MD, PhD, FACMG
- M. D. (筑波大学医学専門学群)
Work history (13):
- 2016/08/01 - University of Washington School of Medicine Pathology Research Professor Emeritus
- 2015/12/01 - Chiba University Graduate School of Medicine Innovation Medicine Professor
- 2013/07/01 - 2015/07/31 University of Washington School of Medicine Pathology Research Professor
- 2001/06/01 - 2013/06/30 University of Washington School of Medicine Pathology Research Associate Professor
- 1996/03/01 - 2001/05/31 University of Washington School of Medicine Pathology Research Assistant Professor
- 1992/05/01 - 1996/02/29 University of Washington School of Medicine Pathology Fellow
- 1990/11/01 - 1992/04/30 University of California at Berkeley Lawrence Berkeley Laboratory Research Associate
- 1986/09/01 - 1992/04/30 Boston University, School of Medicine Graduate School of Medicine, Biochemistry Doctoral student
- 1987/09/01 - 1990/10/31 Boston University, School of Medicine Biochemistry Research Associate
- 1985/06/01 - 1986/07/31 National Medical Center Medical Resident
- 1984/06/01 - 1985/05/31 Harvard University School of Medicine, Beth Israel Hospital Department of General Medicine Fellow
- 1984/04/01 - 1984/05/31 University of Tsukuba Hospital Medical Resident
- 1978/04/01 - 1984/03/01 University of Tsukuba School of Medicine Student
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Committee career (19):
- 2006/01 - 現在 American Federation for Aging Research, New York, NY National Scientific Advisory
- 2021/04 - NIH study section, NIH NIA ZAG1 LRP
- 2020/04 - NIH study section, NIH NIA ZAG1 LRP
- 2019/05 - NIH study section NIH NIA ZAG1 ZIJ-4 (M5) LRP
- 2018/10 - NIH study section NIH NIA ZAG1 ZIJ-G (J4) PPG
- 2018/06 - Reviewer
- 2018/05 - NIH study section NIH NIA ZAG1 ZIJ-G (O2) PPG
- 2018/05 - NIH study section NIH NIA ZAG1 ZIJ-4 (M2) LRP
- 2017/05 - NIH study section NIH NIA ZAG1 ZIJ-4 (M2) LRP
- 2016/04 - NIH study section NIH NIA ZAG1 ZAI1 AWA-M(S1) LRP
- 2007/02 - 2015/05 Mechanisms of Ageing and Development, Elsevier, London Editorial Board
- 2015/04 - NIH study section NIH NIA ZAG1 ZIJ-2 (M2) LRP
- 2013/10 - NIH study section NIA ZAG1 SRC(99) PPG
- 2013/04 - NIH study section NIH NIA ZAG1 ZIJ-2 (A1) LRP
- 2011/07 - Frontiers in Genetics of Aging, Switzerland Associate Editorial Board,
- 2001/01 - 2010/05 TheScienceWorldJournal, San Diego, CA Editorial Board
- 2009/07 - NIH study section ZRG1 BDA-B (10) SBIR/STTR
- 2004/07 - NIH study section NIA-B CMAD Cellular Mechanism of Aging and Development
- 1998/03 - NIH study section NIA-B CMAD Cellular Mechanism of Aging and Development
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Awards (1):
- 1999 - Gerontological Society of America Nathan Shock New Investigators Award
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