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Stéphanie Le Gras

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Genetics|July 9, 2010
A strategy for direct mapping and identification of mutations by whole-genome sequencingSteven Zuryn, Stéphanie Le Gras, Karine Jamet, et al.
Plos One|November 12, 2020
Ikaros antagonizes DNA binding by STAT5 in pre-B cellsBeate Heizmann, Stéphanie Le Gras, Célestine Simand, et al.
Plos One|January 29, 2021
Correction: Ikaros antagonizes DNA binding by STAT5 in pre-B cellsBeate Heizmann, Stéphanie Le Gras, Célestine Simand, et al.
Plos Genetics|February 9, 2017
TEAD transcription factors are required for normal primary myoblast differentiation in vitro and muscle regeneration in vivoShilpy Joshi, Guillaume Davidson, Stéphanie Le Gras, et al.
Journal of Cell Science|May 21, 2015
A Brn2-Zic1 axis specifies the neuronal fate of retinoic-acid-treated embryonic stem cellsSylvia Urban, Dominique Kobi, Marie Ennen, et al.
Nature Communications|November 10, 2015
Ikaros mediates gene silencing in T cells through Polycomb repressive complex 2Attila Oravecz, Apostol Apostolov, Katarzyna Polak, et al.
Plos One|July 24, 2015
Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription Regulatory NetworksMathilde de Taffin, Yannick Carrier, Laurence Dubois, et al.
Nature Structural & Molecular Biology|January 29, 2013
Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNAAnas Fadloun, Stéphanie Le Gras, Bernard Jost, et al.
Human Molecular Genetics|March 19, 2015
Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease miceMayada Achour, Stéphanie Le Gras, Céline Keime, et al.
Acta Neuropathologica|July 4, 2012
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutationJohann Böhm, Esther Leshinsky-Silver, Stéphane Vassilopoulos, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Genetics|July 9, 2010
A strategy for direct mapping and identification of mutations by whole-genome sequencingSteven Zuryn, Stéphanie Le Gras, Karine Jamet, et al.
Plos One|November 12, 2020
Ikaros antagonizes DNA binding by STAT5 in pre-B cellsBeate Heizmann, Stéphanie Le Gras, Célestine Simand, et al.
Plos One|January 29, 2021
Correction: Ikaros antagonizes DNA binding by STAT5 in pre-B cellsBeate Heizmann, Stéphanie Le Gras, Célestine Simand, et al.
Plos Genetics|February 9, 2017
TEAD transcription factors are required for normal primary myoblast differentiation in vitro and muscle regeneration in vivoShilpy Joshi, Guillaume Davidson, Stéphanie Le Gras, et al.
Journal of Cell Science|May 21, 2015
A Brn2-Zic1 axis specifies the neuronal fate of retinoic-acid-treated embryonic stem cellsSylvia Urban, Dominique Kobi, Marie Ennen, et al.
Nature Communications|November 10, 2015
Ikaros mediates gene silencing in T cells through Polycomb repressive complex 2Attila Oravecz, Apostol Apostolov, Katarzyna Polak, et al.
Plos One|July 24, 2015
Genome-Wide Mapping of Collier In Vivo Binding Sites Highlights Its Hierarchical Position in Different Transcription Regulatory NetworksMathilde de Taffin, Yannick Carrier, Laurence Dubois, et al.
Nature Structural & Molecular Biology|January 29, 2013
Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNAAnas Fadloun, Stéphanie Le Gras, Bernard Jost, et al.
Human Molecular Genetics|March 19, 2015
Neuronal identity genes regulated by super-enhancers are preferentially down-regulated in the striatum of Huntington's disease miceMayada Achour, Stéphanie Le Gras, Céline Keime, et al.
Acta Neuropathologica|July 4, 2012
Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutationJohann Böhm, Esther Leshinsky-Silver, Stéphane Vassilopoulos, et al.
Pageof 5