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Louis Mandel

Showing results (111-120 of 221) with videos related to

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Biochemical and Biophysical Research Communications|February 16, 2002
Functional redundancy in the myotubularin familyJocelyn Laporte, Laurence Liaubet, François Blondeau, et al.
Neuron|June 24, 2003
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X proteinAnnette Schenck, Barbara Bardoni, Caillin Langmann, et al.
Molecular Biology and Evolution|February 3, 2006
The evolutionary origin of peroxisomes: an ER-peroxisome connectionAgatha Schlüter, Stéphane Fourcade, Raymond Ripp, et al.
EMBO Reports|May 14, 2011
G-quadruplex RNA structure as a signal for neurite mRNA targetingMurugan Subramanian, Florence Rage, Ricardos Tabet, et al.
Human Molecular Genetics|March 5, 2002
Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathyAurora Pujol, Colette Hindelang, Noëlle Callizot, et al.
Journal of Neurodevelopmental Disorders|May 19, 2025
Contribution of families using the GenIDA database to the description of MED13L syndrome and literature reviewRoseline Caumes, Pauline Burger, Jean-Louis Mandel, et al.
Journal of Cell Science|July 16, 2002
The PtdIns3P phosphatase myotubularin is a cytoplasmic protein that also localizes to Rac1-inducible plasma membrane rufflesJocelyn Laporte, Francois Blondeau, Anne Gansmuller, et al.
American Journal of Medical Genetics. Part A|April 11, 2016
Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidismFrancesca Mattioli, Amelie Piton, Bénédicte Gérard, et al.
Nucleic Acids Research|July 26, 2008
The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancerMarie-Cécile Didiot, Zhaoxia Tian, Céline Schaeffer, et al.
Human Molecular Genetics|December 10, 2002
Progressive retinal degeneration and dysfunction in R6 Huntington's disease miceDominique Helmlinger, Gaël Yvert, Serge Picaud, et al.
Pageof 23

Showing results (111-120 of 221) with videos related to

Sort By:
Pageof 23
Biochemical and Biophysical Research Communications|February 16, 2002
Functional redundancy in the myotubularin familyJocelyn Laporte, Laurence Liaubet, François Blondeau, et al.
Neuron|June 24, 2003
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X proteinAnnette Schenck, Barbara Bardoni, Caillin Langmann, et al.
Molecular Biology and Evolution|February 3, 2006
The evolutionary origin of peroxisomes: an ER-peroxisome connectionAgatha Schlüter, Stéphane Fourcade, Raymond Ripp, et al.
EMBO Reports|May 14, 2011
G-quadruplex RNA structure as a signal for neurite mRNA targetingMurugan Subramanian, Florence Rage, Ricardos Tabet, et al.
Human Molecular Genetics|March 5, 2002
Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathyAurora Pujol, Colette Hindelang, Noëlle Callizot, et al.
Journal of Neurodevelopmental Disorders|May 19, 2025
Contribution of families using the GenIDA database to the description of MED13L syndrome and literature reviewRoseline Caumes, Pauline Burger, Jean-Louis Mandel, et al.
Journal of Cell Science|July 16, 2002
The PtdIns3P phosphatase myotubularin is a cytoplasmic protein that also localizes to Rac1-inducible plasma membrane rufflesJocelyn Laporte, Francois Blondeau, Anne Gansmuller, et al.
American Journal of Medical Genetics. Part A|April 11, 2016
Novel de novo mutations in ZBTB20 in Primrose syndrome with congenital hypothyroidismFrancesca Mattioli, Amelie Piton, Bénédicte Gérard, et al.
Nucleic Acids Research|July 26, 2008
The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancerMarie-Cécile Didiot, Zhaoxia Tian, Céline Schaeffer, et al.
Human Molecular Genetics|December 10, 2002
Progressive retinal degeneration and dysfunction in R6 Huntington's disease miceDominique Helmlinger, Gaël Yvert, Serge Picaud, et al.
Pageof 23