User profiles for Stéphane Viville

Stéphane Viville

Université de Strasbourg
Verified email at unistra.fr
Cited by 8674

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

L Lefebvre, S Viville, SC Barton, F Ishino, EB Keverne… - Nature …, 1998 - nature.com
Mest (also known as Peg1), an imprinted gene expressed only from the paternal allele during
development, was disrupted by gene targeting in embryonic stem (ES) cells. The targeted …

[PDF][PDF] Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia

…, C Lagier-Tourenne, H van Bokhoven, S Viville - The American Journal of …, 2007 - cell.com
Globozoospermia is a rare (incidence <0.1% in male infertile patients) form of teratozoospermia,
mainly characterized by round-headed spermatozoa that lack an acrosome. It originates …

[HTML][HTML] Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine

…, N Hebert, A Francina, G Andreu, S Viville… - …, 2010 - ncbi.nlm.nih.gov
Background Ex vivo manufacture of red blood cells from stem cells is a potential means to
ensure an adequate and safe supply of blood cell products. Advances in somatic cell …

Mice lacking the MHC class II-associated invariant chain

S Viville, J Neefjes, V Lotteau, A Dierich, M Lemeur… - Cell, 1993 - cell.com
The invariant chain (ii) has aroused much interest because of its close association with
major histocompatibiiity complex (MHC) class ii molecules. Various functions have been …

[PDF][PDF] A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation

…, B Sèle, S Hennebicq, V Satre, S Viville… - The American Journal of …, 2011 - cell.com
An increasing number of couples require medical assistance to achieve a pregnancy, and
more than 2% of the births in Western countries now result from assisted reproductive …

[PDF][PDF] DPY19L2 deletion as a major cause of globozoospermia

…, P Ray, Z Kilani, CLR Barratt, S Viville - The American Journal of …, 2011 - cell.com
Globozoospermia, characterized by round-headed spermatozoa, is a rare (< 0.1% in male
infertile patients) and severe teratozoospermia consisting primarily of spermatozoa lacking an …

TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells

…, L Fasching, TS Macfarlan, Y Tarabay, S Viville… - Genome …, 2013 - genome.cshlp.org
TRIM28 is critical for the silencing of endogenous retroviruses (ERVs) in embryonic stem (ES)
cells. Here, we reveal that an essential impact of this process is the protection of cellular …

Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia

…, SN Schiffmann, S Viville… - Disease models & …, 2013 - journals.biologists.com
Friedreich’s ataxia (FRDA) is a recessive neurodegenerative disorder commonly associated
with hypertrophic cardiomyopathy. FRDA is due to expanded GAA repeats within the first …

Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family

…, E Goossens, M Bahceci, S Viville - Human molecular …, 2015 - academic.oup.com
Infertility is a global healthcare problem, and despite long years of assisted reproductive
activities, a significant number of cases remain idiopathic. Our currently restricted understanding …

ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004

…, J Traeger-Synodinos, K Vesela, S Viville… - Human …, 2007 - academic.oup.com
The sixth report of the ESHRE PGD Consortium is presented, relating to cycles collected for
the calendar year 2003 and follow-up of the pregnancies and babies born up to October …