Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis. - Wikidata - wikimedia - TriplyDB

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q34989297

about

Matrix Metalloproteinases in Non-Neoplastic Disorders.Friends or Foes: Matrix Metalloproteinases and Their Multifaceted Roles in Neurodegenerative Diseases Microglia centered pathogenesis in ALS: insights in cell interconnectivity Protective Microglia and Their Regulation in Parkinson's Disease Multifaceted role of matrix metalloproteinases (MMPs)Neuronal matrix metalloproteinase-9 is a determinant of selective neurodegeneration Association of histamine N-methyltransferase Thr105Ile polymorphism with Parkinson's disease and schizophrenia in Han Chinese: a case-control study.Associations of Matrix Metalloproteinase-9 and Tissue Inhibitory Factor-1 Polymorphisms With Parkinson Disease in Taiwan.Whole-exome sequencing of 228 patients with sporadic Parkinson's disease Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in amyotrophic lateral sclerosis (ALS).MMP-9 in translation: from molecule to brain physiology, pathology, and therapy.Advances in understanding genomic markers and pharmacogenetics of Parkinson's disease.Repeated Social Defeat, Neuroinflammation, and Behavior: Monocytes Carry the Signal.Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese.Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population.Glycoursodeoxycholic acid reduces matrix metalloproteinase-9 and caspase-9 activation in a cellular model of superoxide dismutase-1 neurodegeneration.Altered Expression of Matrix Metalloproteinases and Their Endogenous Inhibitors in a Human Isogenic Stem Cell Model of Huntington's Disease.

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P2860

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q34989297

description

2013 nî lūn-bûn

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2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

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Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

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Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

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type

label

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

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Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

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Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

@nl

prefLabel

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

@ast

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

@en

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

@nl

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JOURNAL.PONE.0073777

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Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

@en

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Hua Jia

http://www.w3.org/2001/XMLSchema#string

Jing Hu

http://www.w3.org/2001/XMLSchema#string

Lifang Zhang

http://www.w3.org/2001/XMLSchema#string

Lihua Yu

http://www.w3.org/2001/XMLSchema#string

Ran An

http://www.w3.org/2001/XMLSchema#string

Xianghua He

http://www.w3.org/2001/XMLSchema#string

Xiaoli Yao

http://www.w3.org/2001/XMLSchema#string

Yanming Xu

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Zhuolin Liu

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P2860

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism

Beyond Parkinson disease: amyotrophic lateral sclerosis and the axon guidance pathway

DCTN1 mutations in Perry syndrome.

Roles of dioxins and heavy metals in cancer and neurological diseases using ROS-mediated mechanisms.

Ataxin-2 repeat-length variation and neurodegeneration

Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.

Transgenic mice with human mutant genes causing Parkinson's disease and amyotrophic lateral sclerosis provide common insight into mechanisms of motor neuron selective vulnerability to degeneration.

Signal transduction and cell-type specific regulation of matrix metalloproteinase gene expression: can MMPs be good for you?

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10.1371/JOURNAL.PONE.0073777

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