Publications by authors named "Meriem Garfa Traore"

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Missense Variants in the Second Transmembrane Domain of TMEM17 Disrupt Its Stability and Function and Lead to a Wide Phenotypic Spectrum of Ciliopathies.
Lucile Boutaud, Chunmei Li, Candice Moncler, Laure Verlin, Meriem Garfa-Traoré

Clin Genet· August 2025

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The AMPK-Sirtuin 1-YAP axis is regulated by fluid flow intensity and controls autophagy flux in kidney epithelial cells.
Aurore Claude-Taupin, Pierre Isnard, Alessia Bagattin, Nicolas Kuperwasser, Federica Roccio

Nat Commun· December 2023

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Fluid shear stress triggers cholesterol biosynthesis and uptake in inner medullary collecting duct cells, independently of nephrocystin-1 and nephrocystin-4.
Meriem Garfa Traoré, Federica Roccio, Caterina Miceli, Giulia Ferri, Mélanie Parisot

Front Mol Biosci· October 2023

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Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla.
Aude Tessier, Nathalie Roux, Lucile Boutaud, Elodie Lunel, Leila Hakkakian

Acta Neuropathol Commun· February 2023

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Agonists of prostaglandin E receptors as potential first in class treatment for nephronophthisis and related ciliopathies.
Hugo Garcia, Alice S Serafin, Flora Silbermann, Esther Porée, Amandine Viau, Meriem Garfa-Traore

Proc Natl Acad Sci U S A· May 2022

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ATG9A protects the plasma membrane from programmed and incidental permeabilization.
Aurore Claude-Taupin, Jingyue Jia, Zambarlal Bhujabal, Meriem Garfa-Traoré, Suresh Kumar

Nat Cell Biol· August 2021

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Mobilized Multipotent Hematopoietic Progenitors Promote Expansion and Survival of Allogeneic Tregs and Protect Against Graft Versus Host Disease.
Maud D'Aveni, Anne-Béatrice Notarantonio, Viviane A Agbogan, Allan Bertrand, Guillemette Fouquet

Front Immunol· June 2021

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Three-dimensional architecture of nephrons in the normal and cystic kidney.
Thomas Blanc, Nicolas Goudin, Mohamad Zaidan, Meriem Garfa Traore, Frank Bienaime

Kidney Int· March 2021

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Comparison of different clearing and acquisition methods for 3D imaging of murine intestinal organoids.
Louison Lallemant, Corinne Lebreton, Meriem Garfa-Traoré

J Biol Methods· December 2020

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Light sheet fluorescence microscopy versus confocal microscopy: in quest of a suitable tool to assess drug and nanomedicine penetration into multicellular tumor spheroids.
Gianpiero Lazzari, Daniele Vinciguerra, Anna Balasso, Valerie Nicolas, Nicolas Goudin, Meriem Garfa-Traore

Eur J Pharm Biopharm· September 2019

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Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion.
Marie Alice Dupont, Camille Humbert, Céline Huber, Quentin Siour, Ida Chiara Guerrera

Hum Mol Genet· August 2019

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Ependymal cilia beating induces an actin network to protect centrioles against shear stress.
Alexia Mahuzier, Asm Shihavuddin, Clémence Fournier, Pauline Lansade, Marion Faucourt

Nat Commun· June 2018

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Impaired Transferrin Receptor Palmitoylation and Recycling in Neurodegeneration with Brain Iron Accumulation.
Anthony Drecourt, Joël Babdor, Michael Dussiot, Floriane Petit, Nicolas Goudin

Am J Hum Genet· February 2018

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Constitutively-active FGFR3 disrupts primary cilium length and IFT20 trafficking in various chondrocyte models of achondroplasia.
Ludovic Martin, Nabil Kaci, Valentin Estibals, Nicolas Goudin, Meriem Garfa-Traore

Hum Mol Genet· January 2018

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Functional characterization of tektin-1 in motile cilia and evidence for TEKT1 as a new candidate gene for motile ciliopathies.
Rebecca Ryan, Marion Failler, Madeline Louise Reilly, Meriem Garfa-Traore, Marion Delous

Hum Mol Genet· January 2018

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Mutations in TUBB4B Cause a Distinctive Sensorineural Disease.
Romain Luscan, Sabrina Mechaussier, Antoine Paul, Guoling Tian, Xavier Gérard

Am J Hum Genet· December 2017

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UNC93B1 interacts with the calcium sensor STIM1 for efficient antigen cross-presentation in dendritic cells.
Sophia Maschalidi, Paula Nunes-Hasler, Clarissa R Nascimento, Ignacio Sallent, Valérie Lannoy, Meriem Garfa-Traore

Nat Commun· November 2017

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WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells.
Mara Cavallin, Maria A Rujano, Nathalie Bednarek, Daniel Medina-Cano, Antoinette Bernabe Gelot, Meriem Garfa-Traore

Brain· October 2017

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IRAP endosomes restrict TLR9 activation and signaling.
Joel Babdor, Delphyne Descamps, Aimé Cézaire Adiko, Mira Tohmé, Sophia Maschalidi, Meriem Garfa-Traore

Nat Immunol· May 2017

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Polygenic mutations in the cytotoxicity pathway increase susceptibility to develop HLH immunopathology in mice.
Fernando E Sepulveda, Alexandrine Garrigue, Sophia Maschalidi, Meriem Garfa-Traore, Gaël Ménasché

Blood· April 2016

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IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.
Isabelle Perrault, Jan Halbritter, Jonathan D Porath, Xavier Gérard, Daniela A Braun, Meriem Garfa-Traore

J Med Genet· October 2015

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Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization.
Albane A Bizet, Anita Becker-Heck, Rebecca Ryan, Kristina Weber, Emilie Filhol, Meriem Garfa-Traore

Nat Commun· October 2015

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Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome.
Caroline Alby, Kevin Piquand, Céline Huber, André Megarbané, Amale Ichkou, Meriem Garfa-Traore

Am J Hum Genet· August 2015

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Human fucci pancreatic Beta cell lines: new tools to study Beta cell cycle and terminal differentiation.
Géraldine Carlier, Alicia Maugein, Corinne Cordier, Séverine Pechberty, Meriem Garfa-Traoré

PLoS One· June 2015

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G-CSF mobilizes CD34+ regulatory monocytes that inhibit graft-versus-host disease.
Maud D'Aveni, Julien Rossignol, Tereza Coman, Shivajanani Sivakumaran, Stephen Henderson

Sci Transl Med· April 2015

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