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Marius Teletin

Showing results (21-30 of 32) with videos related to

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Nature Genetics|November 21, 2007
Loss of Trim24 (Tif1alpha) gene function confers oncogenic activity to retinoic acid receptor alphaKonstantin Khetchoumian, Marius Teletin, Johan Tisserand, et al.
Human Reproduction (Oxford, England)|May 16, 2013
The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported developmentYara Tarabay, Emmanuelle Kieffer, Marius Teletin, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 3, 2011
Transcription cofactors TRIM24, TRIM28, and TRIM33 associate to form regulatory complexes that suppress murine hepatocellular carcinomaBenjamin Herquel, Khalid Ouararhni, Konstantin Khetchoumian, et al.
Human Molecular Genetics|July 23, 2015
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish familyOzlem Okutman, Jean Muller, Yoni Baert, et al.
Molecular Human Reproduction|February 7, 2014
ONSL and OSKM cocktails act synergistically in reprogramming human somatic cells into induced pluripotent stem cellsLaura Jung, Philippe Tropel, Yohann Moal, et al.
Cell Transplantation|August 15, 2012
Human induced pluripotent stem cells improve stroke outcome and reduce secondary degeneration in the recipient brainJérôme Polentes, Pavla Jendelova, Michel Cailleret, et al.
Frontiers in Endocrinology|September 18, 2023
A 16-year bicentric retrospective analysis of ovarian tissue cryopreservation in pediatric units: indications, results, and outcomeMarine Grellet-Grün, Béatrice Delepine, Pauline Le Van Quyen, et al.
Disease Models & Mechanisms|November 9, 2012
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxiaAurore Hick, Marie Wattenhofer-Donzé, Satyan Chintawar, et al.
Occupational and Environmental Medicine|May 25, 2023
Testicular germ cell tumour risk by occupation and industry: a French case-control study - TESTISMargot Guth, Astrid Coste, Marie Lefevre, et al.
Journal of Assisted Reproduction and Genetics|April 13, 2017
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish familyOzlem Okutman, Jean Muller, Valerie Skory, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Nature Genetics|November 21, 2007
Loss of Trim24 (Tif1alpha) gene function confers oncogenic activity to retinoic acid receptor alphaKonstantin Khetchoumian, Marius Teletin, Johan Tisserand, et al.
Human Reproduction (Oxford, England)|May 16, 2013
The mammalian-specific Tex19.1 gene plays an essential role in spermatogenesis and placenta-supported developmentYara Tarabay, Emmanuelle Kieffer, Marius Teletin, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 3, 2011
Transcription cofactors TRIM24, TRIM28, and TRIM33 associate to form regulatory complexes that suppress murine hepatocellular carcinomaBenjamin Herquel, Khalid Ouararhni, Konstantin Khetchoumian, et al.
Human Molecular Genetics|July 23, 2015
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish familyOzlem Okutman, Jean Muller, Yoni Baert, et al.
Molecular Human Reproduction|February 7, 2014
ONSL and OSKM cocktails act synergistically in reprogramming human somatic cells into induced pluripotent stem cellsLaura Jung, Philippe Tropel, Yohann Moal, et al.
Cell Transplantation|August 15, 2012
Human induced pluripotent stem cells improve stroke outcome and reduce secondary degeneration in the recipient brainJérôme Polentes, Pavla Jendelova, Michel Cailleret, et al.
Frontiers in Endocrinology|September 18, 2023
A 16-year bicentric retrospective analysis of ovarian tissue cryopreservation in pediatric units: indications, results, and outcomeMarine Grellet-Grün, Béatrice Delepine, Pauline Le Van Quyen, et al.
Disease Models & Mechanisms|November 9, 2012
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxiaAurore Hick, Marie Wattenhofer-Donzé, Satyan Chintawar, et al.
Occupational and Environmental Medicine|May 25, 2023
Testicular germ cell tumour risk by occupation and industry: a French case-control study - TESTISMargot Guth, Astrid Coste, Marie Lefevre, et al.
Journal of Assisted Reproduction and Genetics|April 13, 2017
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish familyOzlem Okutman, Jean Muller, Valerie Skory, et al.
Pageof 4