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Plos One
|
July 5, 2013
An integrated diagnosis strategy for congenital myopathies
Johann Böhm, Nasim Vasli, Edoardo Malfatti, et al.
Cell Reports
|
October 21, 2016
Lsd1 Ablation Triggers Metabolic Reprogramming of Brown Adipose Tissue
Delphine 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 ataxia
Aurore 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 disorders
Marina 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 SCA2
Anna 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 neurodegeneration
Aline 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 sclerosis
Gina 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 dystrophy
Charlotte Fugier, Arnaud F Klein, Caroline Hammer, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 108) with videos related to
Sort By:
Page
of 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 myopathies
Johann Böhm, Nasim Vasli, Edoardo Malfatti, et al.
Cell Reports
|
October 21, 2016
Lsd1 Ablation Triggers Metabolic Reprogramming of Brown Adipose Tissue
Delphine 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 ataxia
Aurore 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 disorders
Marina 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 SCA2
Anna 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 neurodegeneration
Aline 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 sclerosis
Gina 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 dystrophy
Charlotte Fugier, Arnaud F Klein, Caroline Hammer, et al.
Page
of 11