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The Journal of Clinical Endocrinology and Metabolism|January 7, 2005
Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemiaNaoki Wakida, Do Gia Tuyen, Masataka Adachi, et al.
Kidney International Reports|May 20, 2024
Genetic Diagnosis of Adult Hemodialysis Patients With Unknown EtiologyTakuya Fujimaru, Takayasu Mori, Motoko Chiga, et al.
The Journal of Biological Chemistry|September 3, 2010
Human sodium phosphate transporter 4 (hNPT4/SLC17A3) as a common renal secretory pathway for drugs and uratePromsuk Jutabha, Naohiko Anzai, Kenichiro Kitamura, et al.
Scientific Reports|December 17, 2016
Pharmacological and genetic reappraisals of protease and oxidative stress pathways in a mouse model of obstructive lung diseasesTsuyoshi Shuto, Shunsuke Kamei, Hirofumi Nohara, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 17, 2019
Circulating angiopoietin-like protein 2 levels and mortality risk in patients receiving maintenance hemodialysis: a prospective cohort studyJun Morinaga, Tatsuyuki Kakuma, Hirotaka Fukami, et al.
Heliyon|September 9, 2020
Elevated levels of autoantibodies against DNAJC2 in sera of patients with atherosclerotic diseasesYoichi Yoshida, Xiao-Meng Zhang, Hao Wang, et al.
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