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CHCHD10
Whole Exome Should Be Preferred Over Sanger Sequencing in Suspected Mitochondrial Myopathy
Metabolic and Muscle-Derived Serum Biomarkers Define CHCHD10-Linked Late-Onset Spinal Muscular Atrophy
Mutation Analysis of CHCHD10 in Different Neurodegenerative Diseases
Regulation of COX Assembly and Function by Twin CX9C Proteins—Implications for Human Disease
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family
Chchd10, a Novel Bi-Organellar Regulator of Cellular Metabolism: Implications in Neurodegeneration
Nucleocytoplasmic Transport: Regulatory Mechanisms and the Implications in Neurodegeneration
Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degenerations: Similarities in Genetic Background
Novel Functions of Mitochondrial Proteins in Health and Disease
Loss of Function CHCHD10 Mutations in Cytoplasmic TDP-43 Accumulation and Synaptic Integrity
CHCHD10 Is Involved in the Development of Parkinson's
The ATP Synthase Deficiency in Human Diseases
ALS/FTD Mutant CHCHD10 Mice Reveal a Tissue-Specific Toxic Gain
The Role of White Matter Dysfunction and Leukoencephalopathy
Analysis of the CHCHD10 Gene in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis from Spain
Spinal Muscular Atrophies Precision Panel Overview
The Impact of Mitochondrial Deficiencies in Neuromuscular
Blueprint Genetics Spinal Muscular Atrophy Panel
Top View
Causes Axonal Charcot-Marie-Tooth Disease
Novel FUS and CHCHD10 Models to Investigate Pathogenic Mechanisms in Amyotrophic Lateral Sclerosis Annis-Rayan Bourefis
The Wide Genetic Landscape of Clinical Frontotemporal Dementia: Systematic Combined Sequencing of 121 Consecutive Subjects
Chchd2 Regulates Mitochondrial Morphology by Modulating the Levels of Opa1
A CHCHD10 Variant Causing ALS Elicits an Unfolded Protein Response
Genetics of Dementia
Gene Expression Profiling and Functional Studies of Astrocytes in SOD1-Related Amyotrophic Lateral Sclerosis
CHCHD10 Mutations and Motor Neuron Disease: the Distribution In
The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
TDP-43 Proteinopathies: a New Wave of Neurodegenerative Diseases
Twin CHCH Proteins, CHCHD2, and CHCHD10: Key Molecules of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Frontotempor
Molecular Mechanisms and Biomarkers of Familial FTD/ALS
Letter to the Editor
1 CHCHD10 OR CHCHD2 ARE NOT REQUIRED for HUMAN MOTOR NEURON DIFFERENTIATION in VITRO but MODIFY SYNAPTIC TRANSCRIPTOMES Sandra
CHCHD10 Variants in Amyotrophic Lateral Sclerosis: Where Is the Evidence?
Neuropathologic Description of CHCHD10 Mutated Amyotrophic Lateral Sclerosis
A Novel CHCHD10 Mutation Implicates a Mia40- Dependent Mitochondrial Import Deficit in ALS
A Novel CHCHD10 Mutation Implicates a Mia40‐Dependent