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Nature Reviews. Nephrology
|
February 27, 2013
APOL1 variants and kidney disease in people of recent African ancestry
Giulio Genovese, David J Friedman, Martin R Pollak
Current Opinion in Nephrology and Hypertension
|
January 20, 2012
APOL1 and kidney disease
Martin R Pollak, Giulio Genovese, David J Friedman
Physiology (Bethesda, Md.)
|
July 3, 2015
Calcium Sensing in the Renal Tubule
Hakan R Toka, Martin R Pollak, Pascal Houillier
Statistical Applications in Genetics and Molecular Biology
|
June 4, 2008
A SNP streak model for the identification of genetic regions identical-by-descent
Gregory Leibon, Daniel N Rockmore, Martin R Pollak
Advances in Chronic Kidney Disease
|
April 4, 2006
The genetic basis of human glomerular disease
Clemens C Möller, Martin R Pollak, Jochen Reiser
Kidney International
|
March 7, 2014
Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing
Elizabeth J Brown, Martin R Pollak, Moumita Barua
Journal of the American Society of Nephrology : JASN
|
April 10, 2009
Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury
Joel M Henderson, Mariam P Alexander, Martin R Pollak
Journal of the American Society of Nephrology : JASN
|
April 22, 2005
Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction formation
Jennifer L Hunt, Martin R Pollak, Bradley M Denker
Clinical Journal of the American Society of Nephrology : CJASN
|
October 19, 2007
A case of familial kidney disease
Martin R Pollak, Mariam Priya Alexander, Joel M Henderson
Pediatric Nephrology (Berlin, Germany)
|
May 29, 2007
Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS
Lawrence Copelovitch, Marta Guttenberg, Martin R Pollak, et al.
Page
of 17
Search research articles
Search
Showing results (31-40 of 167) with videos related to
Sort By:
Page
of 17
Nature Reviews. Nephrology
|
February 27, 2013
APOL1 variants and kidney disease in people of recent African ancestry
Giulio Genovese, David J Friedman, Martin R Pollak
Current Opinion in Nephrology and Hypertension
|
January 20, 2012
APOL1 and kidney disease
Martin R Pollak, Giulio Genovese, David J Friedman
Physiology (Bethesda, Md.)
|
July 3, 2015
Calcium Sensing in the Renal Tubule
Hakan R Toka, Martin R Pollak, Pascal Houillier
Statistical Applications in Genetics and Molecular Biology
|
June 4, 2008
A SNP streak model for the identification of genetic regions identical-by-descent
Gregory Leibon, Daniel N Rockmore, Martin R Pollak
Advances in Chronic Kidney Disease
|
April 4, 2006
The genetic basis of human glomerular disease
Clemens C Möller, Martin R Pollak, Jochen Reiser
Kidney International
|
March 7, 2014
Genetic testing for nephrotic syndrome and FSGS in the era of next-generation sequencing
Elizabeth J Brown, Martin R Pollak, Moumita Barua
Journal of the American Society of Nephrology : JASN
|
April 10, 2009
Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury
Joel M Henderson, Mariam P Alexander, Martin R Pollak
Journal of the American Society of Nephrology : JASN
|
April 22, 2005
Cultured podocytes establish a size-selective barrier regulated by specific signaling pathways and demonstrate synchronized barrier assembly in a calcium switch model of junction formation
Jennifer L Hunt, Martin R Pollak, Bradley M Denker
Clinical Journal of the American Society of Nephrology : CJASN
|
October 19, 2007
A case of familial kidney disease
Martin R Pollak, Mariam Priya Alexander, Joel M Henderson
Pediatric Nephrology (Berlin, Germany)
|
May 29, 2007
Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS
Lawrence Copelovitch, Marta Guttenberg, Martin R Pollak, et al.
Page
of 17