Albane A. Bizet
Inserm(FR)Université Paris Cité(FR)Institut des Maladies Génétiques Imagine(FR)
Publications by Year
Research Areas
Genetic and Kidney Cyst Diseases, TGF-β signaling in diseases, Renal and related cancers, Fetal and Pediatric Neurological Disorders, NF-κB Signaling Pathways
Most-Cited Works
- → Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans(2013)226 cited
- → Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations(2012)214 cited
- → Identification of CD109 as part of the TGF‐β receptor system in human keratinocytes(2006)143 cited
- → Combined NGS Approaches Identify Mutations in the Intraflagellar Transport Gene IFT140 in Skeletal Ciliopathies with Early Progressive Kidney Disease(2013)138 cited
- → The TGF-β co-receptor, CD109, promotes internalization and degradation of TGF-β receptors(2011)135 cited
- → A Homozygous Missense Mutation in the Ciliary Gene TTC21B Causes Familial FSGS(2014)121 cited
- → Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization(2015)102 cited
- → CD109‐mediated degradation of TGF‐β receptors and inhibition of TGF‐β responses involve regulation of SMAD7 and Smurf2 localization and function(2011)84 cited
- → DCDC2Mutations Cause Neonatal Sclerosing Cholangitis(2016)74 cited
- → KIF13B establishes a CAV1-enriched microdomain at the ciliary transition zone to promote Sonic hedgehog signalling(2017)68 cited