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P C Harris

Showing results (51-60 of 89) with videos related to

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Circulation|August 1, 1989
Edema of cardiac origin. Studies of body water and sodium, renal function, hemodynamic indexes, and plasma hormones in untreated congestive cardiac failureI S Anand, R Ferrari, G S Kalra, et al.
Human Molecular Genetics|April 1, 1995
Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletionB Peral, V Gamble, J L San Millán, et al.
American Journal of Human Genetics|May 1, 1994
Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I populationB Peral, C J Ward, J L San Millán, et al.
American Journal of Human Genetics|January 1, 1996
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene reveals six novel mutationsB Peral, J L San Millán, A C Ong, et al.
Human Molecular Genetics|September 25, 1997
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosisM M Maheshwar, J P Cheadle, A C Jones, et al.
The American Journal of Pathology|June 11, 1999
Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissueA C Ong, C J Ward, R J Butler, et al.
American Journal of Human Genetics|June 1, 1997
Identification of mutations in the duplicated region of the polycystic kidney disease 1 gene (PKD1) by a novel approachB Peral, V Gamble, C Strong, et al.
Human Mutation|February 6, 1998
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British familiesR Torra, C Badenas, B Peral, et al.
Nature Genetics|June 1, 1995
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domainsJ Hughes, C J Ward, B Peral, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 1996
Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidneyC J Ward, H Turley, A C Ong, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Circulation|August 1, 1989
Edema of cardiac origin. Studies of body water and sodium, renal function, hemodynamic indexes, and plasma hormones in untreated congestive cardiac failureI S Anand, R Ferrari, G S Kalra, et al.
Human Molecular Genetics|April 1, 1995
Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletionB Peral, V Gamble, J L San Millán, et al.
American Journal of Human Genetics|May 1, 1994
Evidence of linkage disequilibrium in the Spanish polycystic kidney disease I populationB Peral, C J Ward, J L San Millán, et al.
American Journal of Human Genetics|January 1, 1996
Screening the 3' region of the polycystic kidney disease 1 (PKD1) gene reveals six novel mutationsB Peral, J L San Millán, A C Ong, et al.
Human Molecular Genetics|September 25, 1997
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosisM M Maheshwar, J P Cheadle, A C Jones, et al.
The American Journal of Pathology|June 11, 1999
Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissueA C Ong, C J Ward, R J Butler, et al.
American Journal of Human Genetics|June 1, 1997
Identification of mutations in the duplicated region of the polycystic kidney disease 1 gene (PKD1) by a novel approachB Peral, V Gamble, C Strong, et al.
Human Mutation|February 6, 1998
Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British familiesR Torra, C Badenas, B Peral, et al.
Nature Genetics|June 1, 1995
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domainsJ Hughes, C J Ward, B Peral, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 1996
Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidneyC J Ward, H Turley, A C Ong, et al.
Pageof 9