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American Journal of Human Genetics|December 15, 2000
Mutation analysis of the entire PKD1 gene: genetic and diagnostic implicationsS Rossetti, L Strmecki, V Gamble, et al.Human Molecular Genetics|September 2, 1999
Autosomal dominant polycystic kidney disease: clues to pathogenesisP C HarrisKidney International|November 30, 2007
Genetic complexity in Joubert syndrome and related disordersP C HarrisJournal of Microbiological Methods|January 18, 2015
GeneCARD-FISH: detection of tceA and vcrA reductive dehalogenase genes in Dehalococcoides mccartyi by fluorescence in situ hybridizationB Matturro, S RossettiAmerican Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1986
Benefits and risks of nonsteroidal antiinflammatory drugs in steroid-resistant nephrotic syndromeJ A Velosa, V E TorresEuropean Journal of Clinical Investigation|February 9, 2008
Co-inheritance of a PKD1 mutation and homozygous PKD2 variant: a potential modifier in autosomal dominant polycystic kidney diseaseG V Z Dedoussis, Y Luo, P Starremans, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 4, 2000
Gender-dependent effect of L-NAME on polycystic kidney disease in Han:SPRD ratsI Yoshida, R Bengal, V E TorresThe Science of the Total Environment|January 10, 2016
Reductive dechlorination of tetrachloroethene in marine sediments: Biodiversity and dehalorespiring capabilities of the indigenous microbesB Matturro, E Presta, S RossettiCurrent Opinion in Nephrology and Hypertension|May 1, 1997
Cystic kidney diseasesM D Griffin, V E Torres, R KumarPageof 23