V E Torres|S Rossetti|P C Harris - JoVE Visualize

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Molecular and Cellular Probes|December 1, 1996

A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1)E Bresin, S Rossetti, S Englisch, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 1, 1997

Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndromeA E Turco, E Bresin, S Rossetti, et al.

Journal of the American Society of Nephrology : JASN|October 1, 1992

Cyst fluid from human autosomal dominant polycystic kidneys promotes cyst formation and expansion by renal epithelial cells in vitroM Ye, M Grant, M Sharma, et al.

Mayo Clinic Proceedings|March 1, 1984

Meclofenamate treatment of recurrent idiopathic nephrotic syndrome with focal segmental glomerulosclerosis after renal transplantationV E Torres, J A Velosa, K E Holley, et al.

International Journal of Systematic and Evolutionary Microbiology|April 12, 2000

'Candidatus Nostocoida limicola', a filamentous bacterium from activated sludgeL L Blackall, E M Seviour, D Bradford, et al.

Letters in Applied Microbiology|July 1, 1997

The characterization and description of representatives of 'G' bacteria from activated sludge plantsL L Blackall, S Rossetti, C Christensson, et al.

Nature|August 30, 1990

A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)nA O Wilkie, J Lamb, P C Harris, et al.

Genomics|June 1, 1996

The mouse homologue of the polycystic kidney disease gene (Pkd1) is a single-copy geneP G Olsson, C Löhning, S Horsley, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993

Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomereM A Vickers, P Vyas, P C Harris, et al.

British Heart Journal|October 1, 1993

Pathogenesis of oedema in chronic severe anaemia: studies of body water and sodium, renal function, haemodynamic variables, and plasma hormonesI S Anand, Y Chandrashekhar, R Ferrari, et al.

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Showing results (111-120 of 224) with videos related to

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Pageof 23

Molecular and Cellular Probes|December 1, 1996

A common polymorphism in exon 46 of the human autosomal dominant polycystic kidney disease 1 gene (PKD1)E Bresin, S Rossetti, S Englisch, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 1, 1997

Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndromeA E Turco, E Bresin, S Rossetti, et al.

Journal of the American Society of Nephrology : JASN|October 1, 1992

Cyst fluid from human autosomal dominant polycystic kidneys promotes cyst formation and expansion by renal epithelial cells in vitroM Ye, M Grant, M Sharma, et al.

Mayo Clinic Proceedings|March 1, 1984

Meclofenamate treatment of recurrent idiopathic nephrotic syndrome with focal segmental glomerulosclerosis after renal transplantationV E Torres, J A Velosa, K E Holley, et al.

International Journal of Systematic and Evolutionary Microbiology|April 12, 2000

'Candidatus Nostocoida limicola', a filamentous bacterium from activated sludgeL L Blackall, E M Seviour, D Bradford, et al.

Letters in Applied Microbiology|July 1, 1997

The characterization and description of representatives of 'G' bacteria from activated sludge plantsL L Blackall, S Rossetti, C Christensson, et al.

Nature|August 30, 1990

A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)nA O Wilkie, J Lamb, P C Harris, et al.

Genomics|June 1, 1996

The mouse homologue of the polycystic kidney disease gene (Pkd1) is a single-copy geneP G Olsson, C Löhning, S Horsley, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 15, 1993

Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomereM A Vickers, P Vyas, P C Harris, et al.

British Heart Journal|October 1, 1993

Pathogenesis of oedema in chronic severe anaemia: studies of body water and sodium, renal function, haemodynamic variables, and plasma hormonesI S Anand, Y Chandrashekhar, R Ferrari, et al.

Pageof 23