Zobrazeno 1 - 10
of 1 168
pro vyhledávání: '"E J, Carlson"'
Autor:
Clark, Khaya1,2,3 Khaya.Clark@va.gov, Lovelace, Suheily4,5, Moring, John C.6, Thielman, Emily J.1, Thompson, Kassander A.7, Henry, James A.1,8, Zaugg, Tara9
Publikováno v:
American Journal of Audiology. Dec2024, Vol. 33 Issue 4, p1077-1091. 15p.
Publikováno v:
Handchirurgie Scan. :188-189
Autor:
Dougarem, Djouhayna1 (AUTHOR), Chen, Yi‐Xiao1 (AUTHOR), Sun, Yi‐Na1 (AUTHOR), Huang, He‐Feng2,3,4,5 (AUTHOR) huanghefg@hotmail.com, Luo, Qiong6 (AUTHOR) luoq@zju.edu.cn
Publikováno v:
Molecular Genetics & Genomic Medicine. Sep2024, Vol. 12 Issue 9, p1-7. 7p.
Autor:
Xu, Xiaona1 (AUTHOR), Gao, Chunyan1 (AUTHOR), Emusani, Ramya1 (AUTHOR), Jia, Chuancheng1 (AUTHOR) jiacc@nankai.edu.cn, Xiang, Dong1 (AUTHOR) xiangdongde@126.com
Publikováno v:
Advanced Science. 8/7/2024, Vol. 11 Issue 29, p1-38. 38p.
The results of sensitivity and Monte Carlo analyses on PEM fuel cell components and the overall system are presented including the most important cost factors and the effects of selected scenarios.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af1cc69da17918c8ac5eb08bf20865ed
https://doi.org/10.2172/862302
https://doi.org/10.2172/862302
Autor:
J R, Gum, J W, Hicks, A M, Gillespie, J L, Rius, P A, Treseler, S C, Kogan, E J, Carlson, C J, Epstein, Y S, Kim
Publikováno v:
Cancer research. 61(8)
Mucinous colorectal cancers exhibit a characteristic set of molecular genetic alterations and may be derived from progenitor cells committed to the goblet cell lineage. Previously, we demonstrated that the MUC2 mucin gene promoter drives transgene re
Autor:
Mishra, Srikanta K.1 srikanta.mishra@austin.utexas.edu, Rodrigo, Hansapani2, Balan, Jithin R.1
Publikováno v:
Journal of Speech, Language & Hearing Research. Jul2024, Vol. 67 Issue 7, p2473-2482. 10p.
Autor:
Van Vliet-Lanoë, Brigitte1 brigitte.vanvlietlanoë@univ-brest.fr, Andrieu, Valérie2, Cliquet, Dominique3, Authemayou, Christine1, Le Roy, Pascal1, Renouf, John C.4
Publikováno v:
Journal of Coastal Research. 2024, Vol. 40 Issue 3, p445-473. 29p.
Publikováno v:
Molecular and cellular biochemistry. 168(1-2)
All mutations in the human gene for CuZn superoxide dismutase (CuZnSOD) reported to date are associated with the disease amyotrophic lateral sclerosis (ALS). These mutations, mostly of a familial nature (ALS 1, MIM 105400), span all of the coding reg
BACKGROUND: To determine whether a higher level of copper zinc superoxide dismutase (CuZnSOD) can reduce the severity of oxygen induced retinopathy (OIR) in a mouse model. METHODS: CuZnSOD transgenic mice with a threefold increase in CuZnSOD activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8f76c90448dbbb94dfe3aa2e3d207d
https://europepmc.org/articles/PMC505495/
https://europepmc.org/articles/PMC505495/