Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Abnormalities and ADAMTS13[original query] |
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A novel quantitative hemolytic assay coupled with restriction fragment length polymorphisms analysis enabled early diagnosis of atypical hemolytic uremic syndrome and identified unique predisposing mutations in Japan. PloS one 2015 10 (5): e0124655. Yoshida Yoko, Miyata Toshiyuki, Matsumoto Masanori, Shirotani-Ikejima Hiroko, Uchida Yumiko, Ohyama Yoshifumi, Kokubo Tetsuro, Fujimura Yoshihi |
ADAMTS13 Gene Mutations Influence ADAMTS13 Conformation and Disease Age-Onset in the French Cohort of Upshaw-Schulman Syndrome. Thrombosis and haemostasis 2018 10 118 (11): 1902-1917. Joly Bérangère S, Boisseau Pierre, Roose Elien, Stepanian Alain, Biebuyck Nathalie, Hogan Julien, Provot François, Delmas Yahsou, Garrec Céline, Vanhoorelbeke Karen, Coppo Paul, Veyradier Agnès, |
The ADAMTS13-VWF axis is dysregulated in chronic thromboembolic pulmonary hypertension. The European respiratory journal 2019 1 53 (3): . Newnham Michael, South Kieron, Bleda Marta, Auger William R, Barberà Joan A, Bogaard Harm, Bunclark Katherine, Cannon John E, Delcroix Marion, Hadinnapola Charaka, Howard Luke S, Jenkins David, Mayer Eckhard, Ng Choo, Rhodes Christopher J, Screaton Nicholas, Sheares Karen, Simpson Michael A, Southwood Mark, Su Li, Taboada Dolores, Traylor Matthew, Trembath Richard C, Villar Sofia S, Wilkins Martin R, Wharton John, Gräf Stefan, Pepke-Zaba Joanna, Laffan Michael, Lane David A, Morrell Nicholas W, Toshner Ma |
The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse. International urogynecology journal 2022 1 33 (2): 267-274. Li Lei, Ma Yidi, Yang Hua, Sun Zhijing, Chen Juan, Zhu L |
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- Page last updated:Mar 25, 2024
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