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Journal of Cell Science
|
May 9, 2014
Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors
Anne T Bertrand, Simindokht Ziaei, Camille Ehret, et al.
Human Molecular Genetics
|
November 18, 2011
DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death
Anne T Bertrand, Laure Renou, Aurélie Papadopoulos, et al.
Circulation Research
|
June 4, 2005
Downregulation of apoptosis-inducing factor in harlequin mutant mice sensitizes the myocardium to oxidative stress-related cell death and pressure overload-induced decompensation
Vanessa P M van Empel, Anne T Bertrand, Roel van der Nagel, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2011
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation
Rabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, et al.
Cells
|
May 28, 2020
Consequences of <i>Lmna</i> Exon 4 Mutations in Myoblast Function
Déborah Gómez-Domínguez, Carolina Epifano, Fernando de Miguel, et al.
Journal of the American College of Cardiology
|
August 15, 2006
EUK-8, a superoxide dismutase and catalase mimetic, reduces cardiac oxidative stress and ameliorates pressure overload-induced heart failure in the harlequin mouse mutant
Vanessa P M van Empel, Anne T Bertrand, Ralph J van Oort, et al.
Human Molecular Genetics
|
April 12, 2013
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity
Marie-Elodie Cattin, Anne T Bertrand, Saskia Schlossarek, et al.
Cardiovascular Research
|
May 2, 2013
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations
Takuro Arimura, Kenji Onoue, Yumiko Takahashi-Tanaka, et al.
The Journal of Experimental Medicine
|
May 9, 2007
Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy
Blanche Schroen, Joost J Leenders, Arie van Erk, et al.
American Journal of Human Genetics
|
September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy
Lucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
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Search research articles
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Showing results (21-30 of 30) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 30 results.
Journal of Cell Science
|
May 9, 2014
Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors
Anne T Bertrand, Simindokht Ziaei, Camille Ehret, et al.
Human Molecular Genetics
|
November 18, 2011
DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death
Anne T Bertrand, Laure Renou, Aurélie Papadopoulos, et al.
Circulation Research
|
June 4, 2005
Downregulation of apoptosis-inducing factor in harlequin mutant mice sensitizes the myocardium to oxidative stress-related cell death and pressure overload-induced decompensation
Vanessa P M van Empel, Anne T Bertrand, Roel van der Nagel, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2011
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation
Rabah Ben Yaou, Claire Navarro, Susana Quijano-Roy, et al.
Cells
|
May 28, 2020
Consequences of <i>Lmna</i> Exon 4 Mutations in Myoblast Function
Déborah Gómez-Domínguez, Carolina Epifano, Fernando de Miguel, et al.
Journal of the American College of Cardiology
|
August 15, 2006
EUK-8, a superoxide dismutase and catalase mimetic, reduces cardiac oxidative stress and ameliorates pressure overload-induced heart failure in the harlequin mouse mutant
Vanessa P M van Empel, Anne T Bertrand, Ralph J van Oort, et al.
Human Molecular Genetics
|
April 12, 2013
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity
Marie-Elodie Cattin, Anne T Bertrand, Saskia Schlossarek, et al.
Cardiovascular Research
|
May 2, 2013
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations
Takuro Arimura, Kenji Onoue, Yumiko Takahashi-Tanaka, et al.
The Journal of Experimental Medicine
|
May 9, 2007
Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy
Blanche Schroen, Joost J Leenders, Arie van Erk, et al.
American Journal of Human Genetics
|
September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy
Lucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
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of 3