Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Annals of Neurology|March 30, 2011
Neurologic features and genotype-phenotype correlation in Wolfram syndromeAnnabelle Chaussenot, Sylvie Bannwarth, Cecile Rouzier, et al.
Mitochondrion|February 19, 2011
Fatal heart failure associated with CoQ10 and multiple OXPHOS deficiency in a child with propionic acidemiaKonstantina Fragaki, Aline Cano, Jean-François Benoist, et al.
AIDS Research and Human Retroviruses|October 31, 2003
Additive activity between the trans-activation response RNA-binding protein, TRBP2, and cyclin T1 on HIV type 1 expression and viral production in murine cellsPier-Luigi Battisti, Aïcha Daher, Sylvie Bannwarth, et al.
Nature Communications|March 27, 2021
TDP-43 and PINK1 mediate CHCHD10S59L mutation-induced defects in Drosophila and in vitroMinwoo Baek, Yun-Jeong Choe, Sylvie Bannwarth, et al.
Mitochondrion|July 1, 2009
A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b geneKonstantina Fragaki, Vincent Procaccio, Sylvie Bannwarth, et al.
European Journal of Medical Genetics|October 17, 2022
Splicing variants in NARS2 are associated with milder phenotypes and intra-familial variabilitySamira Ait-El-Mkadem Saadi, Elsa Kaphan, Amaya Morales Jaurrieta, et al.
Bioinformatics (Oxford, England)|September 5, 2022
ABEILLE: a novel method for ABerrant Expression Identification empLoying machine LEarning from RNA-sequencing dataJustine Labory, Gwendal Le Bideau, David Pratella, et al.
Neuromuscular Disorders : NMD|November 7, 2016
A new mutation in the mitochondrial tRNAPro gene associated with early-onset neuromuscular phenotype and ragged-red fibersGodelieve Morel, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|June 3, 2022
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viabilityEmmanuelle C Genin, Sylvie Bannwarth, Baptiste Ropert, et al.
Pageof 6