Flora Silbermann
Paris, 75015, France
Last Updated: 09/26/2026
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Found 10 publications
Agonists of prostaglandin E2 receptors as potential first in class treatment for nephronophthisis and related ciliopathies.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 28, 2022
The renal inflammatory network of nephronophthisis.
Journal: Human molecular genetics
Published: December 08, 2021
Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 28, 2019
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
Journal: American journal of human genetics
Published: July 10, 2017
Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis.
Journal: American journal of human genetics
Published: February 04, 2017
Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis.
Journal: American journal of human genetics
Published: May 13, 2016
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
Journal: PLoS genetics
Published: August 04, 2015
A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS.
Journal: Journal of the American Society of Nephrology : JASN
Published: May 31, 2014
Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans.
Journal: American journal of human genetics
Published: November 21, 2013
Dishevelled stabilization by the ciliopathy protein Rpgrip1l is essential for planar cell polarity.
Journal: The Journal of cell biology
Published: August 29, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026