Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R Pollak

Showing results (281-290 of 326) with videos related to

Pageof 33
Sort By:
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|April 11, 2012
The APOL1 genotype of African American kidney transplant recipients does not impact 5-year allograft survivalB T Lee, V Kumar, T A Williams, et al.
Nature Genetics|March 4, 2000
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosisJ M Kaplan, S H Kim, K N North, et al.
The Journal of Clinical Investigation|December 5, 2002
NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated alleleHiroyasu Tsukaguchi, Akulapalli Sudhakar, Tu Cam Le, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2018
Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasiaYi Fan, Weiqing Liu, Ruiye Bi, et al.
Nature Genetics|February 26, 2013
Using population admixture to help complete maps of the human genomeGiulio Genovese, Robert E Handsaker, Heng Li, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 11, 2011
Genetic diagnosis in consanguineous families with kidney disease by homozygosity mapping coupled with whole-exome sequencingKhaldoun I Al-Romaih, Giulio Genovese, Hamad Al-Mojalli, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 21, 2024
Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working GroupNora Franceschini, David L Feldman, Jonathan S Berg, et al.
Journal of the American Society of Nephrology : JASN|September 22, 2022
Nephrotic Syndrome Gene <i>TBC1D8B</i> Is Required for Endosomal Maturation and Nephrin Endocytosis in <i>Drosophila</i>Julian Milosavljevic, Camille Lempicki, Konrad Lang, et al.
Journal of the American Society of Nephrology : JASN|May 8, 2026
Purine Metabolism Regulates the Severity of APOL1 NephropathyHuihui Huang, Calum Tattersfield, Sonako Jacas, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 25, 2022
ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuitCristian V Riella, Michelle McNulty, Guilherme T Ribas, et al.
Pageof 33

Showing results (281-290 of 326) with videos related to

Sort By:
Pageof 33
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|April 11, 2012
The APOL1 genotype of African American kidney transplant recipients does not impact 5-year allograft survivalB T Lee, V Kumar, T A Williams, et al.
Nature Genetics|March 4, 2000
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosisJ M Kaplan, S H Kim, K N North, et al.
The Journal of Clinical Investigation|December 5, 2002
NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated alleleHiroyasu Tsukaguchi, Akulapalli Sudhakar, Tu Cam Le, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 6, 2018
Interrelated role of Klotho and calcium-sensing receptor in parathyroid hormone synthesis and parathyroid hyperplasiaYi Fan, Weiqing Liu, Ruiye Bi, et al.
Nature Genetics|February 26, 2013
Using population admixture to help complete maps of the human genomeGiulio Genovese, Robert E Handsaker, Heng Li, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|June 11, 2011
Genetic diagnosis in consanguineous families with kidney disease by homozygosity mapping coupled with whole-exome sequencingKhaldoun I Al-Romaih, Giulio Genovese, Hamad Al-Mojalli, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 21, 2024
Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working GroupNora Franceschini, David L Feldman, Jonathan S Berg, et al.
Journal of the American Society of Nephrology : JASN|September 22, 2022
Nephrotic Syndrome Gene <i>TBC1D8B</i> Is Required for Endosomal Maturation and Nephrin Endocytosis in <i>Drosophila</i>Julian Milosavljevic, Camille Lempicki, Konrad Lang, et al.
Journal of the American Society of Nephrology : JASN|May 8, 2026
Purine Metabolism Regulates the Severity of APOL1 NephropathyHuihui Huang, Calum Tattersfield, Sonako Jacas, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 25, 2022
ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuitCristian V Riella, Michelle McNulty, Guilherme T Ribas, et al.
Pageof 33