Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Daniel E. Wong"'
Publikováno v:
Plastic & Reconstructive Surgery.
Publikováno v:
Burns.
Autor:
Gregory R. D. Evans, Alan D. Widgerow, Pauline Joy F Santos, Lohrasb R Sayadi, Daniel E. Wong, Derek A. Banyard
Publikováno v:
Journal of Plastic, Reconstructive & Aesthetic Surgery. 72:1207-1218
Summary Introduction Extracellular vesicles (EVs) are cell-secreted packages that deliver cargo to target cells to effect functional and phenotypic changes. They are secreted by many different cell types, including adipose-derived stem cells (ADSCs),
Autor:
Shan Li, Lin Gui, Henry J. Lin, Derek R. Moen, Tsui-Fen Chou, Rod Carlo A Columbres, Purbasha Nandi, Po-Lin Chiu, Daniel E. Wong, Xiaoyi Zhang
Publikováno v:
Biochem J
p97 protein is a highly conserved, abundant, functionally diverse, structurally dynamic homohexameric AAA enzyme-containing N, D1, and D2 domains. A truncated p97 protein containing the N and D1 domains and the D1–D2 linker (ND1L) exhibits 79% of w
Publikováno v:
Rhode Island medical journal (2013). 101(6)
Dermatomyositis is an idiopathic inflammatory myopathy known to occur as a paraneoplastic syndrome. The course of dermatomyositis is commonly reported to mirror the course of the malignancy. Here, we report a case of dermatomyositis that developed in
Autor:
Frank J. Schoenen, Tsui-Fen Chou, Kelin Li, Henry J. Lin, Daniel E. Wong, Lin Gui, Patrick Porubsky, Shan Li, Kevin J. Frankowski, Xiaoyi Zhang, Derek R. Moen
Publikováno v:
ChemMedChem
We previously found that the p97 cofactor, p47, significantly decreased the potency of some ATP-competitive p97 inhibitors such as ML240 [2-(2-amino-1H-benzo[d]imidazol-1-yl)-N-benzyl-8-methoxyquinazolin-4-amine] and ML241 [2-(2H-benzo[b][1,4]oxazin-
Autor:
Conrad C. Weihl, You Jin Lee, Pei Yin Shih, Valentina Sanghez, Henry J. Lin, Michelle R. Arkin, Lin Gui, Daniel E. Wong, Michelina Iacovino, Tsui-Fen Chou, Stacie L. Bulfer, Xiaoyi Zhang, Xiaoyan Zhang, Yanzhuang Wang, James Siho Lee, Lynn W. Lehmann
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, vol 112, iss 14
Dominant mutations in p97/VCP (valosin-containing protein) cause a rare multisystem degenerative disease with varied phenotypes that include inclusion body myopathy, Paget’s disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosi
Autor:
Tsui-Fen Chou, Xiaoyi Zhang, Daniel E. Wong, Derek R. Moen, Lin Gui, Kevin J. Frankowski, Patrick Porubsky, Shan Li, Henry J. Lin, Kelin Li, Frank J. Schoenen
Publikováno v:
ChemMedChem. 11:948-948