Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nicholas S. Knowlton"'
Autor:
Joan M. Bathon, Michael Centola, Xiaoqian Liu, Zhicheng Jin, Weihua Ji, Nicholas S. Knowlton, Iván Ferraz-Amaro, Qin Fu, Jon T. Giles, Mary Chester Wasko, C. Michael Stein, Jennifer E. Van Eyk
Publikováno v:
Arthritis Research & Therapy, Vol 25, Iss 1, Pp 1-12 (2023)
Abstract Background Cardiovascular (CV) risk estimation calculators for the general population underperform in patients with rheumatoid arthritis (RA). The purpose of this study was to identify relevant protein biomarkers that could be added to tradi
Externí odkaz:
https://doaj.org/article/f49305ff219a466d96de08cfc25c96e6
Autor:
Stephen M.F. Jamieson, Peter Tsai, Maria K. Kondratyev, Pratha Budhani, Arthur Liu, Neil N. Senzer, E. Gabriela Chiorean, Shadia I. Jalal, John J. Nemunaitis, Dennis Kee, Avik Shome, Way W. Wong, Dan Li, Nooriyah Poonawala-Lohani, Purvi M. Kakadia, Nicholas S. Knowlton, Courtney R.H. Lynch, Cho R. Hong, Tet Woo Lee, Reidar A. Grénman, Laura Caporiccio, Trevor D. McKee, Mark Zaidi, Sehrish Butt, Andrew M.J. Macann, Nicholas P. McIvor, John M. Chaplin, Kevin O. Hicks, Stefan K. Bohlander, Bradly G. Wouters, Charles P. Hart, Cristin G. Print, William R. Wilson, Michael A. Curran, Francis W. Hunter
Publikováno v:
JCI Insight, Vol 8, Iss 4 (2023)
Externí odkaz:
https://doaj.org/article/b8265d5c0ed44e2583f6823d2b9a7cc0
Autor:
Annette Lasham, Peter Tsai, Sandra J. Fitzgerald, Sunali Y. Mehta, Nicholas S. Knowlton, Antony W. Braithwaite, Cristin G. Print
Publikováno v:
Cancers, Vol 12, Iss 3, p 769 (2020)
TP53, the most commonly-mutated gene in cancer, undergoes complex alternative splicing. Different TP53 transcripts play different biological roles, both in normal function and in the progression of diseases such as cancer. The study of TP53’s alter
Externí odkaz:
https://doaj.org/article/aee6eb5b9e634709b10848cb3a6c7cc8
Autor:
Daniele C. DeFreese, John K. Wiencke, Bobby A. Gramling, Eldon R. Jupe, Thomas W. Pugh, Rei Miike, Christopher C. Benz, Nicholas S. Knowlton, Sharmila Manjeshwar, Kathie M. Dalessandri, John J. Mulvihill, Lue Ping Zhao
Publikováno v:
BBA Clinical
Background We have combined functional gene polymorphisms with clinical factors to improve prediction and understanding of sporadic breast cancer risk, particularly within a high incidence Caucasian population. Methods A polyfactorial risk model (PFR
Publikováno v:
Journal of the Senologic International Society.
Breast cancer is a complex disease with risk determined by both genetic and clinical risk factors. Inherited germline mutations in genes such as BRCA1/2, TP53 and PTEN strongly contribute to breast cancer risk but are very rare and not relevant to cl
Autor:
Karl R. Hansen, Nicholas S. Knowlton, Angela C. Thyer, Jay S. Charleston, Michael R. Soules, Nancy A. Klein
Publikováno v:
Human Reproduction; Mar2008, Vol. 23 Issue 3, p699-699, 1p