Published in Stem Cells on December 20, 2007
Eset partners with Oct4 to restrict extraembryonic trophoblast lineage potential in embryonic stem cells. Genes Dev (2009) 2.18
Promoter DNA methylation couples genome-defence mechanisms to epigenetic reprogramming in the mouse germline. Development (2012) 1.55
Deletion of the pluripotency-associated Tex19.1 gene causes activation of endogenous retroviruses and defective spermatogenesis in mice. PLoS Genet (2008) 1.23
Defending the genome from the enemy within: mechanisms of retrotransposon suppression in the mouse germline. Cell Mol Life Sci (2013) 0.97
In vivo and in vitro aging is detrimental to mouse spermatogonial stem cell function. Biol Reprod (2010) 0.94
The ubiquitin ligase Ubr2, a recognition E3 component of the N-end rule pathway, stabilizes Tex19.1 during spermatogenesis. PLoS One (2010) 0.83
TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse. EMBO Mol Med (2015) 0.82
Restricting retrotransposons: a review. Mob DNA (2016) 0.79
Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes. BMC Evol Biol (2015) 0.75
Human germ/stem cell-specific gene TEX19 influences cancer cell proliferation and cancer prognosis. Mol Cancer (2017) 0.75
Tex19.1 promotes Spo11-dependent meiotic recombination in mouse spermatocytes. PLoS Genet (2017) 0.75
Derivation of oocytes from mouse embryonic stem cells. Science (2003) 4.03
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency. Am J Hum Genet (2008) 2.04
Highly dynamic and sex-specific expression of microRNAs during early ES cell differentiation. PLoS Genet (2009) 1.96
Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine. Haematologica (2010) 1.79
PipeAlign: A new toolkit for protein family analysis. Nucleic Acids Res (2003) 1.78
The place of 'social sexing' in medicine and science. Hum Reprod (2002) 1.44
A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation. Am J Hum Genet (2011) 1.33
TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells. Genome Res (2012) 1.29
Retinoids and spermatogenesis: lessons from mutant mice lacking the plasma retinol binding protein. Dev Dyn (2006) 1.20
DPY19L2 deletion as a major cause of globozoospermia. Am J Hum Genet (2011) 1.20
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population. Hum Mol Genet (2009) 1.17
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia. Dis Model Mech (2012) 1.13
UHRF1 recruits the histone acetyltransferase Tip60 and controls its expression and activity. Biochem Biophys Res Commun (2009) 1.10
The small alpha5beta1 integrin antagonist, SJ749, reduces proliferation and clonogenicity of human astrocytoma cells. Cancer Res (2006) 1.07
Down-regulation of UHRF1, associated with re-expression of tumor suppressor genes, is a common feature of natural compounds exhibiting anti-cancer properties. J Exp Clin Cancer Res (2011) 1.07
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots. Hum Mol Genet (2012) 1.05
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres. Eur J Hum Genet (2011) 1.03
Human induced pluripotent stem cells improve stroke outcome and reduce secondary degeneration in the recipient brain. Cell Transplant (2012) 0.98
Combinatorial signalling controls Neurogenin2 expression at the onset of spinal neurogenesis. Dev Biol (2008) 0.97
Search for mutations involved in human globozoospermia. Hum Reprod (2005) 0.97
The pluripotency-associated gene Dppa4 is dispensable for embryonic stem cell identity and germ cell development but essential for embryogenesis. Mol Cell Biol (2009) 0.97
Nuclear proteome analysis of undifferentiated mouse embryonic stem and germ cells. Electrophoresis (2008) 0.96
Fluorescence in situ hybridization sperm analysis of six translocation carriers provides evidence of an interchromosomal effect. Fertil Steril (2005) 0.95
TNF pretreatment interferes with mitochondrial apoptosis in the mouse liver by A20-mediated down-regulation of Bax. J Immunol (2007) 0.94
High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis. In Vitro Cell Dev Biol Anim (2010) 0.94
Induction of apoptosis by thymoquinone in lymphoblastic leukemia Jurkat cells is mediated by a p73-dependent pathway which targets the epigenetic integrator UHRF1. Biochem Pharmacol (2009) 0.92
Extended passaging increases the efficiency of neural differentiation from induced pluripotent stem cells. BMC Neurosci (2011) 0.90
Identification of integrin-alpha4, Rb1, and syncytin a as murine placental target genes of the transcription factor GCMa/Gcm1. J Biol Chem (2007) 0.89
Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology. Eur J Hum Genet (2013) 0.87
PromAn: an integrated knowledge-based web server dedicated to promoter analysis. Nucleic Acids Res (2006) 0.87
Red wine polyphenols cause growth inhibition and apoptosis in acute lymphoblastic leukaemia cells by inducing a redox-sensitive up-regulation of p73 and down-regulation of UHRF1. Eur J Cancer (2010) 0.86
New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications. Eur J Hum Genet (2004) 0.82
Aronia melanocarpa juice induces a redox-sensitive p73-related caspase 3-dependent apoptosis in human leukemia cells. PLoS One (2012) 0.82
Selective proapoptotic activity of polyphenols from red wine on teratocarcinoma cell, a model of cancer stem-like cell. Invest New Drugs (2009) 0.82
Down-regulation of cyclic nucleotide phosphodiesterase PDE1A is the key event of p73 and UHRF1 deregulation in thymoquinone-induced acute lymphoblastic leukemia cell apoptosis. Cell Signal (2010) 0.81
The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported development. Hum Reprod (2013) 0.81
[START domain-containing proteins: a review of their role in lipid transport and exchange]. Med Sci (Paris) (2009) 0.81
Multiplex PCR combining deltaF508 mutation and intragenic microsatellites of the CFTR gene for pre-implantation genetic diagnosis (PGD) of cystic fibrosis. Eur J Hum Genet (2002) 0.81
Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia. Hum Reprod (2012) 0.81
UHRF1 Links the Histone code and DNA Methylation to ensure Faithful Epigenetic Memory Inheritance. Genet Epigenet (2010) 0.80
Genetic diagnosis of embryos: clear explanation, not rhetoric, is needed. CMAJ (2009) 0.80
Proteome analysis of the culture environment supporting undifferentiated mouse embryonic stem and germ cell growth. Electrophoresis (2007) 0.80
Encouraging results despite complexity of multidisciplinary care of HIV-infected women using assisted reproduction techniques. Hum Reprod (2005) 0.79
CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders. J Med Genet (2013) 0.79
Preimplantation genetic diagnosis for achondroplasia: genetics and gynaecological limits and difficulties. Hum Reprod (2003) 0.77
Tex 19 paralogs exhibit a gonad and placenta-specific expression in the mouse. J Reprod Dev (2012) 0.77
Selective ROS-dependent p53-associated anticancer effects of the hypoxoside derivative rooperol on human teratocarcinomal cancer stem-like cells. Invest New Drugs (2014) 0.77
Duplex, triplex and quadruplex PCR for the preimplantation genetic diagnosis (PGD) of cystic fibrosis (CF), an exhaustive approach. Prenat Diagn (2004) 0.77
Case report: birth after preimplantation genetic diagnosis of a subtle mutation in SMN1 gene. Prenat Diagn (2006) 0.76
[TBP, a universal transcription factor?]. Med Sci (Paris) (2004) 0.76
Birth after pre-implantation genetic diagnosis (PGD) of spinocerebellar ataxia 2 (Sca2). Prenat Diagn (2008) 0.76
Autosomal mutations and human spermatogenic failure. Biochim Biophys Acta (2012) 0.76
Central data collection on PGD and screening. Reprod Biomed Online (2006) 0.75
[An overview of pluripotent stem cell lines]. Med Sci (Paris) (2010) 0.75
"OpenLAB": A 2-hour PCR-based practical for high school students. Biochem Mol Biol Educ (2010) 0.75
[Ontogenesis of primordial germ cells]. Med Sci (Paris) (2004) 0.75
[Follow-up of children born by ICSI]. Med Sci (Paris) (2004) 0.75
Duplex PCR for preimplantation genetic diagnosis (PGD) of spinal muscular atrophy. Prenat Diagn (2003) 0.75
[The acrosome: comparative morphology and development, contribution of a human familial globozoospermia case report]. J Soc Biol (2008) 0.75