Publications by authors named "Safa Saker"

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Amyotrophic lateral sclerosis transcriptomics reveals immunological effects of low-dose interleukin-2.
Ilaria Giovannelli, Nadhim Bayatti, Abigail Brown, Dennis Wang, Marius Mickunas, Safa Saker

Brain Commun· June 2021

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Repeated 5-day cycles of low dose aldesleukin in amyotrophic lateral sclerosis (IMODALS): A phase 2a randomised, double-blind, placebo-controlled trial.
William Camu, Marius Mickunas, Jean-Luc Veyrune, Christine Payan, Cecilia Garlanda, Safa Saker

EBioMedicine· September 2020

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Assessment of DNA encapsulation, a new room-temperature DNA storage method.
Dominique Clermont, Sylvain Santoni, Safa Saker, Maite Gomard, Eliane Gardais

Biopreserv Biobank· June 2014

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An autosomal-recessive form of cutis laxa is due to homozygous elastin mutations, and the phenotype may be modified by a heterozygous fibulin 5 polymorphism.
Hala Mégarbané, Jobard Florence, Jörn Oliver Sass, Susanne Schwonbeck, Mario Foglio, Safa Saker

J Invest Dermatol· July 2009

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A p.C217R mutation in fibulin-5 from cutis laxa patients is associated with incomplete extracellular matrix formation in a skin equivalent model.
Stephanie Claus, Judith Fischer, Hala Mégarbané, André Mégarbané, Florence Jobard, Safa Saker

J Invest Dermatol· June 2008

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Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.
Fabienne Lesueur, Bakar Bouadjar, Caroline Lefèvre, Florence Jobard, Stéphanie Audebert, Safa Saker

J Invest Dermatol· April 2007

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Postmortem diagnosis of Diamond-Blackfan anemia.
Anne Beauchamp-Nicoud, Lydie Da Costa, Alexis Proust, Patricia Rincé, Safa Saker

J Pediatr Hematol Oncol· December 2004

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Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis.
Caroline Lefèvre, Bakar Bouadjar, Aysen Karaduman, Florence Jobard, Safa Saker

Hum Mol Genet· October 2004

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Cell complementation using Genebridge 4 human:rodent hybrids for physical mapping of novel mitochondrial respiratory chain deficiency genes.
Pascale De Lonlay, Claude Mugnier, Damien Sanlaville, Karine Chantrel-Groussard, Paule Bénit, Safa Saker

Hum Mol Genet· December 2002

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