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Human Molecular Genetics|March 1, 1996
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisisM Konrad, S Saunier, L Heidet, et al.Acta Paediatrica Scandinavica. Supplement|January 1, 1990
Recombinant human growth hormone treatment in short children with chronic renal disease, before transplantation or with functioning renal transplants: an interim report on five European studiesG Johansson, A Sietnieks, F Janssens, et al.Pediatric Nephrology (Berlin, Germany)|July 1, 1987
Alport's syndrome as a cause of renal failure in EuropeN Gretz, M Broyer, F P Brunner, et al.Nephrologie|January 1, 1996
[Value of cyclosporine in the treatment of the recurrence of nephrosis after renal transplantation]B Ranchin, M F Gagnadoux, M Broyer, et al.Journal of the American Chemical Society|June 26, 2009
Nanoscale growth factor patterns by immobilization on a heparin-mimicking polymerKaren L Christman, Vimary Vázquez-Dorbatt, Eric Schopf, et al.Kidney International|February 13, 2001
PAX2 mutations in oligomeganephroniaR Salomon, A L Tellier, T Attie-Bitach, et al.The Journal of Clinical Investigation|March 1, 1994
Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expressionC Antignac, B Knebelmann, L Drouot, et al.The EMBO Journal|September 22, 2001
Subtilisin-like autotransporter serves as maturation protease in a bacterial secretion pathwayL Coutte, R Antoine, H Drobecq, et al.Nature Genetics|April 1, 1993
A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2pC Antignac, C H Arduy, J S Beckmann, et al.Human Molecular Genetics|March 21, 1998
A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisisS Saunier, J Calado, R Heilig, et al.Pageof 29