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Results: 1-16 |
Results: 16
Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects
Authors: Lu, WN Shen, XH Pavlova, A Lakkis, M Ward, CJ Pritchard, L Harris, PC Genest, DR Perez-Atayde, AR Zhou, J
Citation: Wn. Lu et al., Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects, HUM MOL GEN, 10(21), 2001, pp. 2385-2396
Treatment prospects for autosomal-dominant polycystic kidney disease
Authors: Qian, Q Harris, PC Torres, VE
Citation: Q. Qian et al., Treatment prospects for autosomal-dominant polycystic kidney disease, KIDNEY INT, 59(6), 2001, pp. 2005-2022
Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel
Authors: Gonzalez-Perrett, S Kim, K Ibarra, C Damiano, AE Zotta, E Batelli, M Harris, PC Reisin, IL Arnaout, MA Cantiello, HF
Citation: S. Gonzalez-perrett et al., Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel, P NAS US, 98(3), 2001, pp. 1182-1187
Mutation analysis of the entire PKD1 gene: Genetic and diagnostic implications
Authors: Rossetti, S Strmecki, L Gamble, V Burton, S Sneddon, V Peral, B Roy, S Bakkaloglu, A Komel, R Winearls, CG Harris, PC
Citation: S. Rossetti et al., Mutation analysis of the entire PKD1 gene: Genetic and diagnostic implications, AM J HU GEN, 68(1), 2001, pp. 46-63
High-rate foam fracturing: Fluid friction and perforation erosion
Authors: Harris, PC Pippin, PM
Citation: Pc. Harris et Pm. Pippin, High-rate foam fracturing: Fluid friction and perforation erosion, SPE PROD FA, 15(1), 2000, pp. 27-32
Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL
Authors: Brown, J Horsley, SW Jung, C Saracoglu, K Janssen, B Brough, M Daschner, M Beedgen, B Kerkhoffs, G Eils, R Harris, PC Jauch, A Kearney, L
Citation: J. Brown et al., Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay,M-TEL, EUR J HUM G, 8(12), 2000, pp. 903-910
A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype
Authors: Pritchard, L Sloane-Stanley, JA Sharpe, JA Aspinwall, R Lu, WN Buckle, V Strmecki, L Walker, D Ward, CJ Alpers, CE Zhou, J William, WG Harris, PC
Citation: L. Pritchard et al., A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype, HUM MOL GEN, 9(18), 2000, pp. 2617-2627
Rhys-Davies exsanguinator: Pressure characteristics and technique for improving performance
Authors: Harris, PC Atkinson, D Evans, RA
Citation: Pc. Harris et al., Rhys-Davies exsanguinator: Pressure characteristics and technique for improving performance, J HAND S-BR, 25B(6), 2000, pp. 578-581
Late onset of renal and hepatic cysts in Pkd1-targeted heterozygotes
Authors: Lu, WN Fan, XH Basora, N Babakhanlou, H Law, T Rifai, N Harris, PC Perez-Atayde, AR Rennke, HG Zhou, J
Citation: Wn. Lu et al., Late onset of renal and hepatic cysts in Pkd1-targeted heterozygotes, NAT GENET, 21(2), 1999, pp. 160-161
Identification of a human homologue of the sea urchin receptor for egg jelly: a polycystic kidney disease-like protein
Authors: Hughes, J Ward, CJ Aspinwall, R Butler, R Harris, PC
Citation: J. Hughes et al., Identification of a human homologue of the sea urchin receptor for egg jelly: a polycystic kidney disease-like protein, HUM MOL GEN, 8(3), 1999, pp. 543-549
Autosomal dominant polycystic kidney disease: clues to pathogenesis
Authors: Harris, PC
Citation: Pc. Harris, Autosomal dominant polycystic kidney disease: clues to pathogenesis, HUM MOL GEN, 8(10), 1999, pp. 1861-1866
Genome duplications and other features in 12 Mb of DNA sequence from humanchromosome 16p and 16q
Authors: Loftus, BJ Kim, UJ Sneddon, VP Kalush, F Brandon, R Fuhrmann, J Mason, T Crosby, ML Barnstead, M Cronin, L Mays, AD Cao, YC Xu, RX Kang, HL Mitchell, S Eichler, EE Harris, PC Venter, JC Adams, MD
Citation: Bj. Loftus et al., Genome duplications and other features in 12 Mb of DNA sequence from humanchromosome 16p and 16q, GENOMICS, 60(3), 1999, pp. 295-308
Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue
Authors: Ong, ACM Harris, PC Davies, DR Pritchard, L Rossetti, S Biddolph, S Vaux, DJT Migone, N Ward, CJ
Citation: Acm. Ong et al., Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue, KIDNEY INT, 56(4), 1999, pp. 1324-1333
Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissue
Authors: Ong, ACM Ward, CJ Butler, RJ Biddolph, S Bowker, C Torra, P Pei, Y Harris, PC
Citation: Acm. Ong et al., Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissue, AM J PATH, 154(6), 1999, pp. 1721-1729
Rheological properties of low-gel-loading borate fracture gels
Authors: Harris, PC Heath, SJ
Citation: Pc. Harris et Sj. Heath, Rheological properties of low-gel-loading borate fracture gels, SPE PROD FA, 13(4), 1998, pp. 230-235
Physical mapping of the short arm of human chromosome 16
Authors: Mole, SE Breuning, MH Ceccherini, I Harris, PC Lushnikova, T
Citation: Se. Mole et al., Physical mapping of the short arm of human chromosome 16, BIOM HLTH R, 23, 1998, pp. 129-149
Risultati: 1-16 |