Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chinyere Okunji"'
Autor:
Nathan C Edwards, Zachary A Hing, Avital Perry, Adam Blaisdell, David B Kopelman, Robert Fathke, William Plum, Jordan Newell, Courtni E Allen, Geetha S, Aaron Shapiro, Chinyere Okunji, Idit Kosti, Noam Shomron, Vahan Grigoryan, Teresa M Przytycka, Zuben E Sauna, Raheleh Salari, Yael Mandel-Gutfreund, Anton A Komar, Chava Kimchi-Sarfaty
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e38864 (2012)
Synonymous variations, which are defined as codon substitutions that do not change the encoded amino acid, were previously thought to have no effect on the properties of the synthesized protein(s). However, mounting evidence shows that these "silent"
Externí odkaz:
https://doaj.org/article/1425d58426564ce68f4b13d5944197e4
Autor:
Zuben E Sauna, Chinyere Okunji, Ryan C Hunt, Tanvi Gupta, Courtni E Allen, Elizabeth Plum, Adam Blaisdell, Vahan Grigoryan, S Geetha, Robert Fathke, Kenji Soejima, Chava Kimchi-Sarfaty
Publikováno v:
PLoS ONE, Vol 4, Iss 8, p e6506 (2009)
BACKGROUND:The zinc metalloprotease ADAMTS13 is a multidomain protein that cleaves von Willebrand Factor (VWF) and is implicated in Thrombotic Thrombocytopenic Purpura (TTP) pathogenesis. Understanding the mechanism of this protein is an important go
Externí odkaz:
https://doaj.org/article/b97e435ff0124e57aef88ea631d1b582
Autor:
Jordan Newell, Aaron Shapiro, Robert Fathke, Noam Shomron, Courtni E. Allen, Vahan Grigoryan, Adam Blaisdell, Zachary A. Hing, David B. Kopelman, Anton A. Komar, Zuben E. Sauna, Yael Mandel-Gutfreund, Chinyere Okunji, William Plum, Nathan C. Edwards, S Geetha, Avital Perry, Raheleh Salari, Chava Kimchi-Sarfaty, Teresa M. Przytycka, Idit Kosti
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 6, p e38864 (2012)
PLoS ONE, Vol 7, Iss 6, p e38864 (2012)
Synonymous variations, which are defined as codon substitutions that do not change the encoded amino acid, were previously thought to have no effect on the properties of the synthesized protein(s). However, mounting evidence shows that these "silent"
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c514c4795dfb9422a5f40fcfa6bbc2be
https://doi.org/10.1371/journal.pone.0038864
https://doi.org/10.1371/journal.pone.0038864
Autor:
Atiq Javaid, Adam Friedman, David Kopelman, Anton A. Komar, Nathan Edwards, Chinyere Okunji, Chava Kimchi-Sarfaty, Nobuko Katagiri, Zuben E. Sauna, Vijaya L. Simhadri
Publikováno v:
Blood. 116:2197-2197
Abstract 2197 Hemophilia B is characterized by structural and functional defects in coagulation factor IX (FIX) caused by mutations in the F9 gene. Various mutations (nonsense, missense, etc.) are known to be associated with the disease, including a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2ae25699939338360479a3640be35c3
https://doi.org/10.1182/blood.v116.21.2197.2197
https://doi.org/10.1182/blood.v116.21.2197.2197