Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sherry Kamiya"'
Autor:
Lauren Herl Martens, Jiasheng Zhang, Sami J. Barmada, Ping Zhou, Sherry Kamiya, Binggui Sun, Sang-Won Min, Li Gan, Steven Finkbeiner, Eric J. Huang, Robert V. Farese Jr
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/e1a9c0e0f6b14866a258fab75e500c8f
Autor:
Jiasheng Zhang, Binggui Sun, Steven Finkbeiner, Lauren Herl Martens, Sherry Kamiya, Ping Zhou, Sami J. Barmada, Robert V. Farese, Li Gan, Sang-Won Min, Eric J. Huang
Publikováno v:
The Journal of clinical investigation, vol 122, iss 11
Martens, LH; Zhang, J; Barmada, SJ; Zhou, P; Kamiya, S; Sun, B; et al.(2012). Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury. Journal of Clinical Investigation, 122(11), 3955-3959. doi: 10.1172/JCI63113. UCSF: Retrieved from: http://www.escholarship.org/uc/item/6gd8v9s5
The Journal of Clinical Investigation
Martens, LH; Zhang, J; Barmada, SJ; Zhou, P; Kamiya, S; Sun, B; et al.(2012). Progranulin deficiency promotes neuroinflammation and neuron loss following toxin-induced injury. Journal of Clinical Investigation, 122(11), 3955-3959. doi: 10.1172/JCI63113. UCSF: Retrieved from: http://www.escholarship.org/uc/item/6gd8v9s5
The Journal of Clinical Investigation
Progranulin (PGRN) is a widely expressed secreted protein that is linked to inflammation. In humans, PGRN haploinsufficiency is a major inherited cause of frontotemporal dementia (FTD), but how PGRN deficiency causes neurodegeneration is unknown. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86b36882373f91af0a696f85d22705b4
https://pubmed.ncbi.nlm.nih.gov/23041626
https://pubmed.ncbi.nlm.nih.gov/23041626
Publikováno v:
J Neurosci
The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 40, iss 3
The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 40, iss 3
Mitochondria are important sources of energy, but they are also the target of cellular stress, toxin exposure, and aging-related injury. Persistent accumulation of damaged mitochondria has been implicated in many neurodegenerative diseases. One highl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76088e4a6b40db7372f1dbdc4439df0f
https://pubmed.ncbi.nlm.nih.gov/31776210
https://pubmed.ncbi.nlm.nih.gov/31776210
Autor:
Sherry Kamiya, Haiyan Qiu, James Shorter, Michael C. Oldham, Erik D. Roberson, Hansen Lui, Hejia Wang, Eric J. Huang, Warren G. Tourtellotte, Steven Finkbeiner, Kin Fai Au, Li-Huei Tsai, Amy A. Tang, Bin Chen, Wen-Yuan Wang, Sebum Lee, Anthony J. Filiano, Yulei Shang, Sami J. Barmada, Caitlin E. Carlton
Publikováno v:
Qiu, H; Lee, S; Shang, Y; Wang, WY; Au, KF; Kamiya, S; et al.(2014). ALS-associated mutation FUS-R521C causes DNA damage and RNA splicing defects. Journal of Clinical Investigation, 124(3), 981-999. doi: 10.1172/JCI72723. UC Santa Cruz: Retrieved from: http://www.escholarship.org/uc/item/9qr3x2vf
The Journal of clinical investigation, vol 124, iss 3
J Clin Invest
The Journal of clinical investigation, vol 124, iss 3
J Clin Invest
Autosomal dominant mutations of the RNA/DNA binding protein FUS are linked to familial amyotrophic lateral sclerosis (FALS); however, it is not clear how FUS mutations cause neurodegeneration. Using transgenic mice expressing a common FALS-associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6b1dafbd6aa37059b6eb75a24d4b9e3
http://www.escholarship.org/uc/item/9qr3x2vf
http://www.escholarship.org/uc/item/9qr3x2vf
Autor:
Shu-Ting Lin, Ying-Hui Fu, Sherry Kamiya, Eric J. Huang, Quasar S Padiath, Yong Huang, Mary Y. Heng, Ying Tong, Laure Verret, Jorge J. Palop, Louis J. Ptáček
Publikováno v:
The Journal of clinical investigation, vol 123, iss 6
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2013, 123 (6), pp.2719-2729. ⟨10.1172/JCI66737⟩
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2013, 123 (6), pp.2719-2729. ⟨10.1172/JCI66737⟩
Adult-onset autosomal-dominant leukodystrophy (ADLD) is a progressive and fatal neurological disorder characterized by early autonomic dysfunction, cognitive impairment, pyramidal tract and cerebellar dysfunction, and white matter loss in the central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51a1f46de2fbfec67e1f2933f74e1958
https://escholarship.org/uc/item/7873f5f9
https://escholarship.org/uc/item/7873f5f9