Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis - Test2 - elhamkhani - TriplyDB

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q28943310

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CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis GWAS of 126,559 individuals identifies genetic variants associated with educational attainment Effects of ALS-related SOD1 mutants on dynein- and KIF5-mediated retrograde and anterograde axonal transport Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study Molecular motor proteins and amyotrophic lateral sclerosis State of play in amyotrophic lateral sclerosis genetics A Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During Disease Emerging mechanisms of molecular pathology in ALS Candidate proteins, metabolites and transcripts in the Biomarkers for Spinal Muscular Atrophy (BforSMA) clinical study A high-density genome-wide association screen of sporadic ALS in US veterans Platelet serotonin level predicts survival in amyotrophic lateral sclerosis Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.Deficits in axonal transport precede ALS symptoms in vivo.Gene expression profiling for human iPS-derived motor neurons from sporadic ALS patients reveals a strong association between mitochondrial functions and neurodegeneration.The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.Simultaneous determination of multiple mRNA levels utilizing MALDI-TOF mass spectrometry and biotinylated dideoxynucleotides.The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis.Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.Genome-wide association study of smoking behaviours among Bangladeshi adults.Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice.Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles.Linking disease associations with regulatory information in the human genome.Genetic heterogeneity of amyotrophic lateral sclerosis: implications for clinical practice and research.Genome-wide association studies in neurology.Quantifying disease progression in amyotrophic lateral sclerosis.The association between ALS and population density: A population based study Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Controversies and priorities in amyotrophic lateral sclerosis.Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases Moving toward a predictive and personalized clinical approach in amyotrophic lateral sclerosis: novel developments and future directions in diagnosis, genetics, pathogenesis and therapies DISC1 genetics, biology and psychiatric illness Single-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese Cohort Use of biomarkers in ALS drug development and clinical trials Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci.PATHOLOGIES OF AXONAL TRANSPORT IN NEURODEGENERATIVE DISEASES

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Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q28943310

description

2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունիսին հրատարակված գիտական հոդված

@hy

article publié dans les Procee ...... f the United States of America

@fr

artículu científicu espublizáu en 2009

@ast

im Juni 2009 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

wetenschappelijk artikel (gepubliceerd op 2009/06/02)

@nl

наукова стаття, опублікована в червні 2009

@uk

مقالة علمية (نشرت في 2-6-2009)

@ar

name

Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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type

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Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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PNAS.0812937106

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Proceedings of the National Academy of Sciences of the United States of America

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Reduced expression of the Kine ...... amyotrophic lateral sclerosis

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Adrian J. Ivinson

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Alayna Barnes-Nessa

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Anne-Marie Wills

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Aslihan Ozoguz

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Betsy A. Hosler

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Christiaan G. J. Saris

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Christopher E. Shaw

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Diane M. McKenna-Yasek

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Franck Georges

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Frank P. Diekstra

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P2860

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis.

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Sp1- and Krüppel-like transcription factors

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

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9004–9009

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106

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H. Robert Horvitz

Vincent Meininger

Ammar Al-Chalabi

Ildefonso Rodriguez-Leyva

Vincenzo Silani

Claire L Simpson

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2009-06-02T00:00:00Z

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19451621

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amyotrophic lateral sclerosis

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2683883

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