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Articles: Basic Science/Genetics |
Kidney injury molecule-1 in renal disease
The Journal of Pathology, 11/20/09
NAD(P)H Oxidase Mediates TGF-[beta]1–Induced Activation of Kidney Myofibroblasts
Journal of the American Society of Nephrology, 11/20/09 Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia
Journal of the American Society of Nephrology, 11/20/09
Prior Articles
Molecular testing for adult type Alport syndrome
BMC Nephrology, 11/18/09 Tracing the Origin of Glomerular Extracapillary Lesions from Parietal Epithelial Cells
Journal of the American Society of Nephrology, 11/18/09 Exclusive Author Commentary Temporal and spatial expression of a growth-regulated network of imprinted genes in growth plate
Pediatric Nephrology, 11/18/09 Functional Significance of Wnt Inhibitory Factor-1 Gene in Kidney Cancer
Cancer Research, 11/17/09 A Plate Reader Based Method For Cell Water Permeability Measurement
American Journal of Physiology: Renal Physiology, 11/17/09 Stretch Reduces Nephrin Expression via an Angiotensin II-AT1-dependent Mechanism in Human Podocytes: Effect of Rosiglitazone
American Journal of Physiology: Renal Physiology, 11/17/09 Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene
BMC Nephrology, 11/16/09 Mercaptopyruvate Inhibits Tissue-Nonspecific Alkaline Phosphatase and Calcium Pyrophosphate Dihydrate Crystal Dissolution
Journal of Rheumatology, 11/13/09 Reductions in laminin beta2 mRNA translation are responsible for impaired IGFBP-5-mediated mesangial cell migration in the presence of high glucose
American Journal of Physiology: Renal Physiology, 11/13/09 Intrarenal expression of microRNAs in patients with IgA nephropathy
Laboratory Investigation, 11/12/09 CYP3A4 and CYP3A5 Polymorphisms and Blood Pressure Response to Amlodipine among African-American Men and Women with Early Hypertensive Renal Disease
American Journal of Nephrology, 11/12/09 The first Chinese Pierson syndrome with novel mutations in LAMB2
Nephrology Dialysis Transplantation, 11/12/09 Homozygous loss of BHD causes early embryonic lethality and kidney tumor development with activation of mTORC1 and mTORC2
Proceedings of the National Academy of Sciences of the United States of America, 11/11/09 Renal tumor suppressor function of the Birt-Hogg-Dube syndrome gene product folliculin
Journal of Medical Genetics, 11/10/09 Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes
Diabetic Medicine, 11/09/09 Multidrug Resistance-Associated Protein 2 Gene (ABCC2) Variant in Kidney Allograft Recipients
Transplantation Proceedings, 11/06/09 Regulation of adenosine system at the onset of peritonitis
Nephrology Dialysis Transplantation, 11/05/09
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Indexed Journals: Kidney International, Hemodialysis International, Nephrology Dialysis Transplantation
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250 Available Pages
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