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The Journal of Biological Chemistry
|
December 15, 2015
Wilms Tumor Suppressor, WT1, Cooperates with MicroRNA-26a and MicroRNA-101 to Suppress Translation of the Polycomb Protein, EZH2, in Mesenchymal Stem Cells
Murielle M Akpa, Diana Iglesias, LeeLee Chu, et al.
Journal of the American Society of Nephrology : JASN
|
August 23, 2014
Deficiency of the planar cell polarity protein Vangl2 in podocytes affects glomerular morphogenesis and increases susceptibility to injury
Brittany L Rocque, Sima Babayeva, Jane Li, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 26, 2008
Genetic interaction between members of the Vangl family causes neural tube defects in mice
Elena Torban, Anne-Marie Patenaude, Severine Leclerc, et al.
Development (Cambridge, England)
|
March 28, 2024
The CPLANE protein Fuzzy regulates ciliogenesis by suppressing actin polymerization at the base of the primary cilium via p190A RhoGAP
Rhythm Sharma, Rita Kalot, Yossef Levin, et al.
Scientific Reports
|
November 22, 2025
Translational readthrough therapy for ADPKD induces polycystin1 expression and partially rescues functional deficits in PKD1 mutant cells
Elena Torban, Lucie Canaff, Sima Babayeva, et al.
The Journal of Biological Chemistry
|
December 22, 2005
PAX2 activates WNT4 expression during mammalian kidney development
Elena Torban, Alison Dziarmaga, Diana Iglesias, et al.
Kidney International
|
August 18, 2019
From podocyte biology to novel cures for glomerular disease
Elena Torban, Fabian Braun, Nicola Wanner, et al.
Human Molecular Genetics
|
August 16, 2011
Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans
Jung Hwa Seo, Yulia Zilber, Sima Babayeva, et al.
European Journal of Human Genetics : EJHG
|
July 10, 2024
Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis
Zachary T Sentell, Zachary W Nurcombe, Lina Mougharbel, et al.
American Journal of Physiology. Renal Physiology
|
January 1, 2016
Novel unbiased assay for circulating podocyte-toxic factors associated with recurrent focal segmental glomerulosclerosis
Nadezda Kachurina, Chen-Fang Chung, Erin Benderoff, et al.
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Search research articles
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Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
The Journal of Biological Chemistry
|
December 15, 2015
Wilms Tumor Suppressor, WT1, Cooperates with MicroRNA-26a and MicroRNA-101 to Suppress Translation of the Polycomb Protein, EZH2, in Mesenchymal Stem Cells
Murielle M Akpa, Diana Iglesias, LeeLee Chu, et al.
Journal of the American Society of Nephrology : JASN
|
August 23, 2014
Deficiency of the planar cell polarity protein Vangl2 in podocytes affects glomerular morphogenesis and increases susceptibility to injury
Brittany L Rocque, Sima Babayeva, Jane Li, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 26, 2008
Genetic interaction between members of the Vangl family causes neural tube defects in mice
Elena Torban, Anne-Marie Patenaude, Severine Leclerc, et al.
Development (Cambridge, England)
|
March 28, 2024
The CPLANE protein Fuzzy regulates ciliogenesis by suppressing actin polymerization at the base of the primary cilium via p190A RhoGAP
Rhythm Sharma, Rita Kalot, Yossef Levin, et al.
Scientific Reports
|
November 22, 2025
Translational readthrough therapy for ADPKD induces polycystin1 expression and partially rescues functional deficits in PKD1 mutant cells
Elena Torban, Lucie Canaff, Sima Babayeva, et al.
The Journal of Biological Chemistry
|
December 22, 2005
PAX2 activates WNT4 expression during mammalian kidney development
Elena Torban, Alison Dziarmaga, Diana Iglesias, et al.
Kidney International
|
August 18, 2019
From podocyte biology to novel cures for glomerular disease
Elena Torban, Fabian Braun, Nicola Wanner, et al.
Human Molecular Genetics
|
August 16, 2011
Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans
Jung Hwa Seo, Yulia Zilber, Sima Babayeva, et al.
European Journal of Human Genetics : EJHG
|
July 10, 2024
Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis
Zachary T Sentell, Zachary W Nurcombe, Lina Mougharbel, et al.
American Journal of Physiology. Renal Physiology
|
January 1, 2016
Novel unbiased assay for circulating podocyte-toxic factors associated with recurrent focal segmental glomerulosclerosis
Nadezda Kachurina, Chen-Fang Chung, Erin Benderoff, et al.
Page
of 4