BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
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Genetic variation in an individual human exomeDefects in tongue papillae and taste sensation indicate a problem with neurotrophic support in various neurological diseases.Increased prevalence of val(66)met BDNF genotype among subjects with cervical dystoniaBDNF and the diseased nervous system: a delicate balance between adaptive and pathological processes of gene regulation.Treatment of Parkinson's disease with trophic factors.Pathways to neurodegeneration: mechanistic insights from GWAS in Alzheimer's disease, Parkinson's disease, and related disordersFTY720/Fingolimod Reduces Synucleinopathy and Improves Gut Motility in A53T Mice: CONTRIBUTIONS OF PRO-BRAIN-DERIVED NEUROTROPHIC FACTOR (PRO-BDNF) AND MATURE BDNF.Pharmacological therapy in Parkinson's disease: focus on neuroprotection.Association between the BDNF G196A and C270T polymorphisms and Parkinson's disease: a meta-analysis.Role of BDNF in central motor structures and motor diseases.BDNF 196 G/A and 270 C/T polymorphisms and susceptibility to Parkinson's disease: a meta-analysis.Challenges and promises in the development of neurotrophic factor-based therapies for Parkinson's disease.Molecular mechanisms of dopaminergic subset specification: fundamental aspects and clinical perspectives.Neurotrophic factors in Alzheimer's and Parkinson's diseases: implications for pathogenesis and therapy.Genetic polymorphisms and the adequacy of brain stimulation: state of the art.Brain-derived neurotrophic factor serum levels correlate with cognitive performance in Parkinson's disease patients with mild cognitive impairment.Huntington's disease: the case for genetic modifiers.Alpha-synuclein: one key opens many locks.Development of a new genotyping assay for detection of the BDNF Val66Met polymorphism using melting-curve analysis.Antidepressant-like effects of ginsenoside Rg3 in mice via activation of the hippocampal BDNF signaling cascade.Effect of the BDNF V166M polymorphism on working memory in healthy adolescents.SNCA: major genetic modifier of age at onset of Parkinson's disease.Brain-derived neurotrophic factor plasma levels in patients with Turner syndrome.BDNF Polymorphism: A Review of Its Diagnostic and Clinical Relevance in Neurodegenerative Disorders.
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BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
description
article
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im Dezember 2005 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2005
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name
BDNF genetic variants are asso ...... arkinson disease: GenePD Study
@en
BDNF genetic variants are asso ...... arkinson disease: GenePD Study
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type
label
BDNF genetic variants are asso ...... arkinson disease: GenePD Study
@en
BDNF genetic variants are asso ...... arkinson disease: GenePD Study
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prefLabel
BDNF genetic variants are asso ...... arkinson disease: GenePD Study
@en
BDNF genetic variants are asso ...... arkinson disease: GenePD Study
@nl
P2093
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BDNF genetic variants are asso ...... arkinson disease: GenePD Study
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A L DeStefano
B A Racette
B N J Growdon
G F Wooten
G Nicholson
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10.1212/01.WNL.0000187075.81589.FD
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P577
2005-12-01T00:00:00Z