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Results: 1-9 |
Results: 9
Autosomal dominant polycystic kidney disease: modification of disease progression
Authors: Peters, DJM Breuning, MH
Citation: Djm. Peters et Mh. Breuning, Autosomal dominant polycystic kidney disease: modification of disease progression, LANCET, 358(9291), 2001, pp. 1439-1444
Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells
Authors: Scheffers, MS van der Bent, P Prins, F Spruit, L Breuning, MH Litvinov, SV de Heer, E Peters, DJM
Citation: Ms. Scheffers et al., Polycystin-1, the product of the polycystic kidney disease 1 gene, co-localizes with desmosomes in MDCK cells, HUM MOL GEN, 9(18), 2000, pp. 2743-2750
The ACE insertion/deletion polymorphism has no influence on progression ofrenal function loss in autosomal dominant polycystic kidney disease
Authors: van Dijk, MA Breuning, MH Peters, DJM Chang, PC
Citation: Ma. Van Dijk et al., The ACE insertion/deletion polymorphism has no influence on progression ofrenal function loss in autosomal dominant polycystic kidney disease, NEPH DIAL T, 15(6), 2000, pp. 836-839
Rubinstein-Taybi syndrome caused by a de novo reciprocal translocation t(2;16)(q38.3;p13.3)
Authors: Petrij, F Dorsman, JC Dauwerse, HG Giles, RH Peeters, T Hennekam, RCM Breuning, MH Peters, DJM
Citation: F. Petrij et al., Rubinstein-Taybi syndrome caused by a de novo reciprocal translocation t(2;16)(q38.3;p13.3), AM J MED G, 92(1), 2000, pp. 47-52
Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations
Authors: Petrij, F Dauwerse, HG Blough, RI Giles, RH van der Smagt, JJ Wallerstein, R Maaswinkel-Mooy, PD van Karnebeek, CD van Ommen, GJB van Haeringen, A Rubinstein, JH Saal, HM Hennekam, RCM Peters, DJM Breuning, MH
Citation: F. Petrij et al., Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutations, J MED GENET, 37(3), 2000, pp. 168-176
The angiotensin-converting enzyme genotype and microalbuminuria in autosomal dominant polycystic kidney disease
Authors: van Dijk, MA Peters, DJM Breuning, MH Chang, PC
Citation: Ma. Van Dijk et al., The angiotensin-converting enzyme genotype and microalbuminuria in autosomal dominant polycystic kidney disease, J AM S NEPH, 10(9), 1999, pp. 1916-1920
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease
Authors: Reynolds, DM Hayashi, T Cai, YQ Veldhuisen, B Watnick, TJ Lens, XM Mochizuki, T Qian, F Maeda, Y Li, L Fossdal, R Coto, E Wu, GQ Breuning, MH Germino, GG Peters, DJM Somlo, S
Citation: Dm. Reynolds et al., Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease, J AM S NEPH, 10(11), 1999, pp. 2342-2351
Genes homologous to the autosomal dominant polycystic kidney disease genes(PKD1 and PKD2)
Authors: Veldhuisen, B Spruit, L Dauwerse, HG Breuning, MH Peters, DJM
Citation: B. Veldhuisen et al., Genes homologous to the autosomal dominant polycystic kidney disease genes(PKD1 and PKD2), EUR J HUM G, 7(8), 1999, pp. 860-872
Cellular localization and tissue distribution of polycystin-1
Authors: Peters, DJM Van de Wal, A Spruit, L Saris, JJ Breuning, MH Bruijn, JA De Heer, E
Citation: Djm. Peters et al., Cellular localization and tissue distribution of polycystin-1, J PATHOLOGY, 188(4), 1999, pp. 439-446
Risultati: 1-9 |