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P Winn

Showing results (101-110 of 115) with videos related to

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Genomics|June 15, 1999
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneityM P Winn, P J Conlon, K L Lynn, et al.
Kidney International|August 26, 2011
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosisRasheed A Gbadegesin, Peter J Lavin, Gentzon Hall, et al.
American Journal of Hypertension|November 20, 2010
Modulation of the BP response to diet by genes in the renin-angiotensin system and the adrenergic nervous systemLaura P Svetkey, Emily L Harris, Eden Martin, et al.
Journal of the American Society of Nephrology : JASN|May 26, 2012
A hybrid CFHR3-1 gene causes familial C3 glomerulopathyTalat H Malik, Peter J Lavin, Elena Goicoechea de Jorge, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 9, 2005
Association of genetic polymorphisms with risk of renal injury after coronary bypass graft surgeryMark Stafford-Smith, Mihai Podgoreanu, Madhav Swaminathan, et al.
Kidney International|April 14, 1999
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental GlomerulosclerosisM P Winn, P J Conlon, K L Lynn, et al.
Journal of the American Society of Nephrology : JASN|January 25, 2011
TRPC6 enhances angiotensin II-induced albuminuriaJason Eckel, Peter J Lavin, Elizabeth A Finch, et al.
Science (New York, N.Y.)|May 10, 2005
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosisMichelle P Winn, Peter J Conlon, Kelvin L Lynn, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2011
Screening for NPHS2 mutations may help predict FSGS recurrence after transplantationTherese C Jungraithmayr, Katrin Hofer, Pierre Cochat, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2014
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGSGentzon Hall, Rasheed A Gbadegesin, Peter Lavin, et al.
Pageof 12

Showing results (101-110 of 115) with videos related to

Sort By:
Pageof 12
Genomics|June 15, 1999
Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneityM P Winn, P J Conlon, K L Lynn, et al.
Kidney International|August 26, 2011
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosisRasheed A Gbadegesin, Peter J Lavin, Gentzon Hall, et al.
American Journal of Hypertension|November 20, 2010
Modulation of the BP response to diet by genes in the renin-angiotensin system and the adrenergic nervous systemLaura P Svetkey, Emily L Harris, Eden Martin, et al.
Journal of the American Society of Nephrology : JASN|May 26, 2012
A hybrid CFHR3-1 gene causes familial C3 glomerulopathyTalat H Malik, Peter J Lavin, Elena Goicoechea de Jorge, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 9, 2005
Association of genetic polymorphisms with risk of renal injury after coronary bypass graft surgeryMark Stafford-Smith, Mihai Podgoreanu, Madhav Swaminathan, et al.
Kidney International|April 14, 1999
Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis. International Collaborative Group for the Study of Familial Focal Segmental GlomerulosclerosisM P Winn, P J Conlon, K L Lynn, et al.
Journal of the American Society of Nephrology : JASN|January 25, 2011
TRPC6 enhances angiotensin II-induced albuminuriaJason Eckel, Peter J Lavin, Elizabeth A Finch, et al.
Science (New York, N.Y.)|May 10, 2005
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosisMichelle P Winn, Peter J Conlon, Kelvin L Lynn, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2011
Screening for NPHS2 mutations may help predict FSGS recurrence after transplantationTherese C Jungraithmayr, Katrin Hofer, Pierre Cochat, et al.
Journal of the American Society of Nephrology : JASN|August 23, 2014
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGSGentzon Hall, Rasheed A Gbadegesin, Peter Lavin, et al.
Pageof 12