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Anne Helbling-Leclerc

Showing results (1-10 of 8) with videos related to

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European Journal of Human Genetics : EJHG|April 26, 2002
Emery-Dreifuss muscular dystrophyAnne Helbling-Leclerc, Gisèle Bonne, Ketty Schwartz
Cell Death and Differentiation|March 16, 2021
Beyond DNA repair and chromosome instability-Fanconi anaemia as a cellular senescence-associated syndromeAnne Helbling-Leclerc, Cécile Garcin, Filippo Rosselli
Scientific Reports|November 21, 2019
Fanconi anemia proteins counteract the implementation of the oncogene-induced senescence programAnne Helbling-Leclerc, Françoise Dessarps-Freichey, Caroline Evrard, et al.
EMBO Reports|December 24, 2019
SMC5/6 acts jointly with Fanconi anemia factors to support DNA repair and genome stabilityFrancesco Rossi, Anne Helbling-Leclerc, Ryotaro Kawasumi, et al.
International Journal of Molecular Sciences|November 27, 2024
Biallelic Germline <i>BRCA1</i> Frameshift Mutations Associated with Isolated Diminished Ovarian ReserveAnne Helbling-Leclerc, Marie Falampin, Abdelkader Heddar, et al.
Human Molecular Genetics|November 19, 2004
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathiesTakuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.
American Journal of Human Genetics|June 21, 2002
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/CGiuseppe Novelli, Antoine Muchir, Federica Sangiuolo, et al.
Science Translational Medicine|December 16, 2016
The protein phosphatase 2A regulatory subunit PR70 is a gonosomal melanoma tumor suppressor geneLéon C L van Kempen, Margaret Redpath, Mounib Elchebly, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|April 26, 2002
Emery-Dreifuss muscular dystrophyAnne Helbling-Leclerc, Gisèle Bonne, Ketty Schwartz
Cell Death and Differentiation|March 16, 2021
Beyond DNA repair and chromosome instability-Fanconi anaemia as a cellular senescence-associated syndromeAnne Helbling-Leclerc, Cécile Garcin, Filippo Rosselli
Scientific Reports|November 21, 2019
Fanconi anemia proteins counteract the implementation of the oncogene-induced senescence programAnne Helbling-Leclerc, Françoise Dessarps-Freichey, Caroline Evrard, et al.
EMBO Reports|December 24, 2019
SMC5/6 acts jointly with Fanconi anemia factors to support DNA repair and genome stabilityFrancesco Rossi, Anne Helbling-Leclerc, Ryotaro Kawasumi, et al.
International Journal of Molecular Sciences|November 27, 2024
Biallelic Germline <i>BRCA1</i> Frameshift Mutations Associated with Isolated Diminished Ovarian ReserveAnne Helbling-Leclerc, Marie Falampin, Abdelkader Heddar, et al.
Human Molecular Genetics|November 19, 2004
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathiesTakuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.
American Journal of Human Genetics|June 21, 2002
Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/CGiuseppe Novelli, Antoine Muchir, Federica Sangiuolo, et al.
Science Translational Medicine|December 16, 2016
The protein phosphatase 2A regulatory subunit PR70 is a gonosomal melanoma tumor suppressor geneLéon C L van Kempen, Margaret Redpath, Mounib Elchebly, et al.
Pageof 1