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Nadia Messaddeq

Showing results (101-110 of 108) with videos related to

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Plos One|July 5, 2013
An integrated diagnosis strategy for congenital myopathiesJohann Böhm, Nasim Vasli, Edoardo Malfatti, et al.
Cell Reports|October 21, 2016
Lsd1 Ablation Triggers Metabolic Reprogramming of Brown Adipose TissueDelphine Duteil, Milica Tosic, Franziska Lausecker, et al.
Disease Models & Mechanisms|November 9, 2012
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxiaAurore Hick, Marie Wattenhofer-Donzé, Satyan Chintawar, et al.
Brain, Behavior, and Immunity|June 15, 2026
Astrocytes exploit a neutrophil extracellular trap - like mechanism for myelin management: A new perspective on myelin-related disordersMarina G Yefimova, Anne Cantereau-Becq, Noémie Pénaud, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 23, 2021
SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2Anna Niewiadomska-Cimicka, Frédéric Doussau, Jean-Baptiste Perot, et al.
Human Molecular Genetics|September 18, 2015
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegenerationAline Dubos, Anna Castells-Nobau, Hamid Meziane, et al.
Nature Neuroscience|October 9, 2019
FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosisGina Picchiarelli, Maria Demestre, Amila Zuko, et al.
Nature Medicine|May 31, 2011
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophyCharlotte Fugier, Arnaud F Klein, Caroline Hammer, et al.
Pageof 11

Showing results (101-110 of 108) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 108 results.
Plos One|July 5, 2013
An integrated diagnosis strategy for congenital myopathiesJohann Böhm, Nasim Vasli, Edoardo Malfatti, et al.
Cell Reports|October 21, 2016
Lsd1 Ablation Triggers Metabolic Reprogramming of Brown Adipose TissueDelphine Duteil, Milica Tosic, Franziska Lausecker, et al.
Disease Models & Mechanisms|November 9, 2012
Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxiaAurore Hick, Marie Wattenhofer-Donzé, Satyan Chintawar, et al.
Brain, Behavior, and Immunity|June 15, 2026
Astrocytes exploit a neutrophil extracellular trap - like mechanism for myelin management: A new perspective on myelin-related disordersMarina G Yefimova, Anne Cantereau-Becq, Noémie Pénaud, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 23, 2021
SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2Anna Niewiadomska-Cimicka, Frédéric Doussau, Jean-Baptiste Perot, et al.
Human Molecular Genetics|September 18, 2015
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegenerationAline Dubos, Anna Castells-Nobau, Hamid Meziane, et al.
Nature Neuroscience|October 9, 2019
FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosisGina Picchiarelli, Maria Demestre, Amila Zuko, et al.
Nature Medicine|May 31, 2011
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophyCharlotte Fugier, Arnaud F Klein, Caroline Hammer, et al.
Pageof 11