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Plos Biology
|
October 26, 2022
Global genome decompaction leads to stochastic activation of gene expression as a first step toward fate commitment in human hematopoietic cells
Romuald Parmentier, Laëtitia Racine, Alice Moussy, et al.
BMC Genetics
|
April 1, 2009
Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta
Peter Brooks, Charles Marcaillou, Maud Vanpeene, et al.
Annals of Clinical and Translational Neurology
|
April 16, 2016
Natural history of LGMD2A for delineating outcome measures in clinical trials
Isabelle Richard, Jean-Yves Hogrel, Daniel Stockholm, et al.
Acta Biomaterialia
|
October 12, 2017
Vectofusin-1, a potent peptidic enhancer of viral gene transfer forms pH-dependent α-helical nanofibrils, concentrating viral particles
Louic S Vermeer, Loic Hamon, Alicia Schirer, et al.
BMC Biology
|
March 12, 2024
Differentiation is accompanied by a progressive loss in transcriptional memory
Camille Fourneaux, Laëtitia Racine, Catherine Koering, et al.
Blood
|
October 24, 2002
Gene therapy of RAG-2-/- mice: sustained correction of the immunodeficiency
Frank Yates, Michèle Malassis-Séris, Daniel Stockholm, et al.
Plos One
|
June 6, 2012
Lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy
William Lostal, Marc Bartoli, Carinne Roudaut, et al.
Blood
|
September 22, 2005
Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicity
Chantal Lagresle-Peyrou, Frank Yates, Michèle Malassis-Séris, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 19, 2008
Stable and functional lymphoid reconstitution in artemis-deficient mice following lentiviral artemis gene transfer into hematopoietic stem cells
Fatine Benjelloun, Alexandrine Garrigue, Corinne Demerens-de Chappedelaine, et al.
Science Advances
|
October 22, 2025
Lysosomal damage is a therapeutic target in Duchenne muscular dystrophy
Abbass Jaber, Laura Palmieri, Rania Bakour, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Plos Biology
|
October 26, 2022
Global genome decompaction leads to stochastic activation of gene expression as a first step toward fate commitment in human hematopoietic cells
Romuald Parmentier, Laëtitia Racine, Alice Moussy, et al.
BMC Genetics
|
April 1, 2009
Robust physical methods that enrich genomic regions identical by descent for linkage studies: confirmation of a locus for osteogenesis imperfecta
Peter Brooks, Charles Marcaillou, Maud Vanpeene, et al.
Annals of Clinical and Translational Neurology
|
April 16, 2016
Natural history of LGMD2A for delineating outcome measures in clinical trials
Isabelle Richard, Jean-Yves Hogrel, Daniel Stockholm, et al.
Acta Biomaterialia
|
October 12, 2017
Vectofusin-1, a potent peptidic enhancer of viral gene transfer forms pH-dependent α-helical nanofibrils, concentrating viral particles
Louic S Vermeer, Loic Hamon, Alicia Schirer, et al.
BMC Biology
|
March 12, 2024
Differentiation is accompanied by a progressive loss in transcriptional memory
Camille Fourneaux, Laëtitia Racine, Catherine Koering, et al.
Blood
|
October 24, 2002
Gene therapy of RAG-2-/- mice: sustained correction of the immunodeficiency
Frank Yates, Michèle Malassis-Séris, Daniel Stockholm, et al.
Plos One
|
June 6, 2012
Lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy
William Lostal, Marc Bartoli, Carinne Roudaut, et al.
Blood
|
September 22, 2005
Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicity
Chantal Lagresle-Peyrou, Frank Yates, Michèle Malassis-Séris, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 19, 2008
Stable and functional lymphoid reconstitution in artemis-deficient mice following lentiviral artemis gene transfer into hematopoietic stem cells
Fatine Benjelloun, Alexandrine Garrigue, Corinne Demerens-de Chappedelaine, et al.
Science Advances
|
October 22, 2025
Lysosomal damage is a therapeutic target in Duchenne muscular dystrophy
Abbass Jaber, Laura Palmieri, Rania Bakour, et al.
Page
of 5