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The American Journal of Pathology
|
August 9, 2012
Generation of isogenic D4Z4 contracted and noncontracted immortal muscle cell clones from a mosaic patient: a cellular model for FSHD
Yvonne D Krom, Julie Dumonceaux, Kamel Mamchaoui, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 4, 2017
Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy
Yusuke Echigoya, Kenji Rowel Q Lim, Nhu Trieu, et al.
Nucleic Acids Research
|
August 11, 2016
Nuclear poly(A)-binding protein aggregates misplace a pre-mRNA outside of SC35 speckle causing its abnormal splicing
Pierre Klein, Martine Oloko, Fanny Roth, et al.
Annals of Neurology
|
May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy
Virginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Cell Death & Disease
|
January 29, 2026
Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy
Massimo Ganassi, Claudia Strafella, Marco Savarese, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 10, 2017
Skeletal Muscle Regenerative Potential of Human MuStem Cells following Transplantation into Injured Mice Muscle
Judith Lorant, Charlotte Saury, Cindy Schleder, et al.
Disease Models & Mechanisms
|
February 12, 2017
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds
Ludovic Arandel, Micaela Polay Espinoza, Magdalena Matloka, et al.
Disease Models & Mechanisms
|
December 13, 2019
Altered <i>in vitro</i> muscle differentiation in X-linked myopathy with excessive autophagy
Stephanie A Fernandes, Camila F Almeida, Lucas S Souza, et al.
EMBO Molecular Medicine
|
December 16, 2017
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy
Sara Benedetti, Narumi Uno, Hidetoshi Hoshiya, et al.
American Journal of Human Genetics
|
December 22, 2015
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders
Daria Wojtal, Dwi U Kemaladewi, Zeenat Malam, et al.
Page
of 19
Search research articles
Search
Showing results (161-170 of 187) with videos related to
Sort By:
Page
of 19
The American Journal of Pathology
|
August 9, 2012
Generation of isogenic D4Z4 contracted and noncontracted immortal muscle cell clones from a mosaic patient: a cellular model for FSHD
Yvonne D Krom, Julie Dumonceaux, Kamel Mamchaoui, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 4, 2017
Quantitative Antisense Screening and Optimization for Exon 51 Skipping in Duchenne Muscular Dystrophy
Yusuke Echigoya, Kenji Rowel Q Lim, Nhu Trieu, et al.
Nucleic Acids Research
|
August 11, 2016
Nuclear poly(A)-binding protein aggregates misplace a pre-mRNA outside of SC35 speckle causing its abnormal splicing
Pierre Klein, Martine Oloko, Fanny Roth, et al.
Annals of Neurology
|
May 29, 2015
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy
Virginie Mariot, Stephane Roche, Christophe Hourdé, et al.
Cell Death & Disease
|
January 29, 2026
Biallelic PAX7 variants cause a novel Satellite Cell-opathy with progressive muscle involvement resembling facioscapulohumeral muscular dystrophy
Massimo Ganassi, Claudia Strafella, Marco Savarese, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
December 10, 2017
Skeletal Muscle Regenerative Potential of Human MuStem Cells following Transplantation into Injured Mice Muscle
Judith Lorant, Charlotte Saury, Cindy Schleder, et al.
Disease Models & Mechanisms
|
February 12, 2017
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds
Ludovic Arandel, Micaela Polay Espinoza, Magdalena Matloka, et al.
Disease Models & Mechanisms
|
December 13, 2019
Altered <i>in vitro</i> muscle differentiation in X-linked myopathy with excessive autophagy
Stephanie A Fernandes, Camila F Almeida, Lucas S Souza, et al.
EMBO Molecular Medicine
|
December 16, 2017
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy
Sara Benedetti, Narumi Uno, Hidetoshi Hoshiya, et al.
American Journal of Human Genetics
|
December 22, 2015
Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders
Daria Wojtal, Dwi U Kemaladewi, Zeenat Malam, et al.
Page
of 19