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R Pollak

Showing results (241-250 of 326) with videos related to

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The Journal of Clinical Investigation|April 3, 2003
The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormoneClaudine H Kos, Andrew C Karaplis, Ji-Bin Peng, et al.
American Journal of Physiology. Endocrinology and Metabolism|October 3, 2009
The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretionLakshmi Kantham, Steven J Quinn, Ogo I Egbuna, et al.
Kidney International|July 30, 2010
A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9Giulio Genovese, Stephen J Tonna, Andrea U Knob, et al.
The Journal of Clinical Investigation|June 5, 2003
Mice deficient in alpha-actinin-4 have severe glomerular diseaseClaudine H Kos, Tu Cam Le, Sumita Sinha, et al.
European Journal of Haematology|March 27, 2013
Parathyroid hormone ablation alters erythrocyte parameters that are rescued by calcium-sensing receptor gene deletionJose R Romero, Rodeler Youte, Edward M Brown, et al.
Journal of the American Society of Nephrology : JASN|January 12, 2020
FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in PodocytesBalajikarthick Subramanian, Justin Chun, Chandra Perez-Gill, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2019
Recruitment of APOL1 kidney disease risk variants to lipid droplets attenuates cell toxicityJustin Chun, Jia-Yue Zhang, Maris S Wilkins, et al.
Kidney International|February 12, 2004
NPHS2 R229Q functional variant is associated with microalbuminuria in the general populationAlexandre C Pereira, Aparecido B Pereira, Glória F Mota, et al.
Nature Genetics|November 1, 1994
Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutationM R Pollak, E M Brown, H L Estep, et al.
Science Advances|November 13, 2024
INF2 mutations cause kidney disease through a gain-of-function mechanismBalajikarthick Subramanian, Sarah Williams, Sophie Karp, et al.
Pageof 33

Showing results (241-250 of 326) with videos related to

Sort By:
Pageof 33
The Journal of Clinical Investigation|April 3, 2003
The calcium-sensing receptor is required for normal calcium homeostasis independent of parathyroid hormoneClaudine H Kos, Andrew C Karaplis, Ji-Bin Peng, et al.
American Journal of Physiology. Endocrinology and Metabolism|October 3, 2009
The calcium-sensing receptor (CaSR) defends against hypercalcemia independently of its regulation of parathyroid hormone secretionLakshmi Kantham, Steven J Quinn, Ogo I Egbuna, et al.
Kidney International|July 30, 2010
A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9Giulio Genovese, Stephen J Tonna, Andrea U Knob, et al.
The Journal of Clinical Investigation|June 5, 2003
Mice deficient in alpha-actinin-4 have severe glomerular diseaseClaudine H Kos, Tu Cam Le, Sumita Sinha, et al.
European Journal of Haematology|March 27, 2013
Parathyroid hormone ablation alters erythrocyte parameters that are rescued by calcium-sensing receptor gene deletionJose R Romero, Rodeler Youte, Edward M Brown, et al.
Journal of the American Society of Nephrology : JASN|January 12, 2020
FSGS-Causing INF2 Mutation Impairs Cleaved INF2 N-Fragment Functions in PodocytesBalajikarthick Subramanian, Justin Chun, Chandra Perez-Gill, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 9, 2019
Recruitment of APOL1 kidney disease risk variants to lipid droplets attenuates cell toxicityJustin Chun, Jia-Yue Zhang, Maris S Wilkins, et al.
Kidney International|February 12, 2004
NPHS2 R229Q functional variant is associated with microalbuminuria in the general populationAlexandre C Pereira, Aparecido B Pereira, Glória F Mota, et al.
Nature Genetics|November 1, 1994
Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutationM R Pollak, E M Brown, H L Estep, et al.
Science Advances|November 13, 2024
INF2 mutations cause kidney disease through a gain-of-function mechanismBalajikarthick Subramanian, Sarah Williams, Sophie Karp, et al.
Pageof 33