A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.

A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.

Item
http://www.wikidata.org/entity/Q34511443
In silico gene prioritization by integrating multiple data sourcesAssociation between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implicationsTyrosine hydroxylase gene: another piece of the genetic puzzle of Parkinson's diseaseCopy number variability in Parkinson's disease: assembling the puzzle through a systems biology approachCommon genes for non-syndromic deafness are uncommon in sub-Saharan Africa: a report from Nigeria.Interactogeneous: disease gene prioritization using heterogeneous networks and full topology scores.Whole-genome sequencing for optimized patient managementRecurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeatsIncreased Rate of Sporadic and Recurrent Rare Genic Copy Number Variants in Parkinson's Disease Among Ashkenazi JewsThe beneficial role of thiamine in Parkinson disease.Validation of reference genes for quantitative gene expression analysis in experimental epilepsy.Functional studies of tyrosine hydroxylase missense variants reveal distinct patterns of molecular defects in Dopa-responsive dystonia.Novel EYA1 variants causing Branchio-oto-renal syndrome.Inhibition of protein kinase (PK) Cδ attenuates methamphetamine-induced dopaminergic toxicity via upregulation of phosphorylation of tyrosine hydroxylase at Ser40 by modulation of protein phosphatase 2A and PKA.
P2860

A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.

Item
http://www.wikidata.org/entity/Q34511443
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@ast
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@en
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@nl
type
label
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@ast
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@en
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@nl
prefLabel
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@ast
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@en
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@nl
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P5875
P698
P921
P932
P356
P1433
P1476
A rare novel deletion of the tyrosine hydroxylase gene in Parkinson disease.
@en
P2093
P2860
P304
P31
P356
P433
P478
P50
P577
P5875
P698
P921
P932