Showing results (2261-2270 of 3,275) with videos related to

Sort By:
Pageof 328
Cancer Research|November 13, 2003
Prolonged culture of telomerase-immortalized human fibroblasts leads to a premalignant phenotypeMichael Milyavsky, Igor Shats, Neta Erez, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 4, 2012
Differential expression of microRNAs during allograft rejectionL Wei, M Wang, X Qu, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality|January 1, 1996
Outpatient management of diabetes mellitus in five Arizona Medicare managed care plansC L Marshall, M Bluestein, C Chapin, et al.
The Anatomical Record. Part A, Discoveries in Molecular, Cellular, and Evolutionary Biology|March 31, 2004
Development of multiorgan pathology in the wpk rat model of polycystic kidney diseaseVincent H Gattone, Benjamin A Tourkow, Chad M Trambaugh, et al.
Nature|June 9, 1994
Crystal structure of human chorionic gonadotropinA J Lapthorn, D C Harris, A Littlejohn, et al.
Kidney International|January 8, 2015
p47(phox) contributes to albuminuria and kidney fibrosis in miceHongtao Wang, Xiwu Chen, Yan Su, et al.
Nicotine & Tobacco Research : Official Journal of the Society for Research on Nicotine and Tobacco|October 24, 2017
Consortium on Methods Evaluating Tobacco: Research Tools to Inform US Food and Drug Administration Regulation of SnusMicah L Berman, Warren K Bickel, Andrew C Harris, et al.
Kidney International|October 1, 2015
Proximal tubule-derived colony stimulating factor-1 mediates polarization of renal macrophages and dendritic cells, and recovery in acute kidney injuryYinqiu Wang, Jian Chang, Bing Yao, et al.
Anatomical Record (Hoboken, N.J. : 2007)|July 29, 2010
Disease stage characterization of hepatorenal fibrocystic pathology in the PCK rat model of ARPKDStephen B Mason, Yun Liang, Rachel M Sinders, et al.
Journal of the American Society of Nephrology : JASN|April 27, 2007
Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosisCarla G Monico, Sandro Rossetti, Heidi A Schwanz, et al.
Pageof 328