Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jehangir S Wadia"'
Autor:
Harrison G Jones, Tina Ritschel, Gabriel Pascual, Just P J Brakenhoff, Elissa Keogh, Polina Furmanova-Hollenstein, Ellen Lanckacker, Jehangir S Wadia, Morgan S A Gilman, R Anthony Williamson, Dirk Roymans, Angélique B van 't Wout, Johannes P Langedijk, Jason S McLellan
Publikováno v:
PLoS Pathogens, Vol 14, Iss 3, p e1006935 (2018)
Respiratory syncytial virus (RSV) is a major cause of severe lower respiratory tract infections in infants and the elderly, and yet there remains no effective treatment or vaccine. The surface of the virion is decorated with the fusion glycoprotein (
Externí odkaz:
https://doaj.org/article/934d8568511a4a31a4fe4f3f7569d4dc
Publikováno v:
PLoS ONE, Vol 3, Iss 10, p e3314 (2008)
Transmissible spongiform encephalopathies, including variant-Creutzfeldt-Jakob disease (vCJD) in humans and bovine spongiform encephalopathies in cattle, are fatal neurodegenerative disorders characterized by protein misfolding of the host cellular p
Externí odkaz:
https://doaj.org/article/eae95a23e6e443c9a3161a5ec9850fb2
Autor:
Irina V. Lebedeva, Michelle V. Wagner, Sunil Sahdeo, Yi-Fan Lu, Anuli Anyanwu-Ofili, Matthew B. Harms, Jehangir S. Wadia, Gunaretnam Rajagopal, Michael J. Boland, David B. Goldstein
Publikováno v:
Cell Death and Disease, Vol 12, Iss 8, Pp 1-11 (2021)
Abstract Rare monogenic disorders often share molecular etiologies involved in the pathogenesis of common diseases. Congenital disorders of glycosylation (CDG) and deglycosylation (CDDG) are rare pediatric disorders with symptoms that range from mild
Externí odkaz:
https://doaj.org/article/6051833dfc5a4270995c32972ab427c8
Publikováno v:
Nature Medicine. Mar2004, Vol. 10 Issue 3, p310-315. 6p.
Publikováno v:
Cytometry; Nov2003, Vol. 56 Issue 1, p15, 8p