CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
about
Mitochondrial dysfunction in Parkinson's diseaseLoss of function CHCHD10 mutations in cytoplasmic TDP-43 accumulation and synaptic integrityLoss of Parkinson's disease-associated protein CHCHD2 affects mitochondrial crista structure and destabilizes cytochrome cLoss of α-Synuclein Does Not Affect Mitochondrial Bioenergetics in Rodent Neurons.Genome-Scale Networks Link Neurodegenerative Disease Genes to α-Synuclein through Specific Molecular Pathways.Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disordersUnderstanding the susceptibility of dopamine neurons to mitochondrial stressors in Parkinson's disease.The ubiquitin signal and autophagy: an orchestrated dance leading to mitochondrial degradationThe Evolution of Genetics: Alzheimer's and Parkinson's Diseases.Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.Gsk3β and Tomm20 are substrates of the SCFFbxo7/PARK15 ubiquitin ligase associated with Parkinson's disease.Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease.Parkinson's Disease: From Pathogenesis to PharmacogenomicsDecreased long-chain acylcarnitines from insufficient β-oxidation as potential early diagnostic markers for Parkinson's disease.Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.Genetics of movement disorders in the next-generation sequencing era.Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.MNRR1, a Biorganellar Regulator of Mitochondria.New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.[Epidemiology and causes of Parkinson's disease].Progress toward an integrated understanding of Parkinson's disease.A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's diseaseMutation analysis of CHCHD10 in different neurodegenerative diseasesMolecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome.Mitochondria: A Common Target for Genetic Mutations and Environmental Toxicants in Parkinson's Disease.Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature.The genetic architecture of mitochondrial dysfunction in Parkinson's disease.Precise Evaluation of Striatal Oxidative Stress Corrected for Severity of Dopaminergic Neuronal Degeneration in Patients with Parkinson's Disease: A Study with 62Cu-ATSM PET and 123I-FP-CIT SPECT.Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.Mitochondrial-Associated Membranes in Parkinson's Disease.Varied pathological and therapeutic response effects associated with CHCHD2 mutant and risk variants.Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.Mitochondrial Dysfunction in Parkinson's Disease: New Mechanistic Insights and Therapeutic Perspectives.Current perspective of mitochondrial biology in Parkinson's disease.Parkinson Disease from Mendelian Forms to Genetic Susceptibility: New Molecular Insights into the Neurodegeneration Process.Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.Mitochondrial Dysfunction in Parkinson's Disease.Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson's Disease Penetrance.Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction
P2860
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P2860
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
description
2015 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մարտին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2015
@ast
scientific journal article
@en
vedecký článok (publikovaný 2015/03/01)
@sk
vědecký článek publikovaný v roce 2015
@cs
wetenschappelijk artikel (gepubliceerd op 2015/03/01)
@nl
наукова стаття, опублікована в березні 2015
@uk
مقالة علمية (نشرت في مارس 2015)
@ar
name
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@ast
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@en
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@nl
type
label
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@ast
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@en
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@nl
prefLabel
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@ast
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@en
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@nl
P2093
P50
P3181
P1433
P1476
CHCHD2 mutations in autosomal ...... e linkage and sequencing study
@en
P2093
Hidemoto Saiki
Hiroyo Yoshino
Hiroyuki Tomiyama
Junji Yamaguchi
Kazuko Hasegawa
Kenya Nishioka
Kotaro Ogaki
Nobutaka Hattori
P304
P356
10.1016/S1474-4422(14)70266-2
P577
2015-02-04T00:00:00Z