RNA processing defects associated with diseases of the motor neuron - Test2 - elhamkhani - TriplyDB

RNA processing defects associated with diseases of the motor neuron

RNA processing defects associated with diseases of the motor neuron

http://www.wikidata.org/entity/Q36846566

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Classification, diagnosis and potential mechanisms in pontocerebellar hypoplasia The RNA helicase database Lack of effect of methylene blue in the SOD1 G93A mouse model of amyotrophic lateral sclerosis Candidate proteins, metabolites and transcripts in the Biomarkers for Spinal Muscular Atrophy (BforSMA) clinical study Microarray analysis of peripheral blood lymphocytes from ALS patients and the SAFE detection of the KEGG ALS pathway.Senataxin mutations and amyotrophic lateral sclerosis.The Gemin associates of survival motor neuron are required for motor function in Drosophila.Identification of cytoplasmic capping targets reveals a role for cap homeostasis in translation and mRNA stability Spinal muscular atrophy: a timely review.Dysregulation of axonal transport and motorneuron diseases.Common pathways of autoimmune inflammatory myopathies and genetic neuromuscular disorders.Spliceosomal small nuclear ribonucleoprotein biogenesis defects and motor neuron selectivity in spinal muscular atrophy.Spinal muscular atrophy and the antiapoptotic role of survival of motor neuron (SMN) protein.Genetic and epigenetic studies of amyotrophic lateral sclerosis.Gem depletion: amyotrophic lateral sclerosis and spinal muscular atrophy crossover.Altered RNA metabolism due to a homozygous RBM7 mutation in a patient with spinal motor neuropathy.EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement.

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P2860

RNA processing defects associated with diseases of the motor neuron

http://www.wikidata.org/entity/Q36846566

description

2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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2010年论文

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name

RNA processing defects associated with diseases of the motor neuron

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RNA processing defects associated with diseases of the motor neuron

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RNA processing defects associated with diseases of the motor neuron

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Muscle and Nerve

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RNA processing defects associated with diseases of the motor neuron

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Daniel R Schoenberg

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Scott Sutton

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Stephen J Kolb

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P2860

Two distinct cytokines released from a human aminoacyl-tRNA synthetase

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

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

Long-range structural effects of a Charcot-Marie-Tooth disease-causing mutation in human glycyl-tRNA synthetase

Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome

Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs

IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1)

Isolation of cDNA encoding a binding protein specific to 5'-phosphorylated single-stranded DNA with G-rich sequences

Lethal congenital contractural syndrome type 2 (LCCS2) is caused by a mutation in ERBB3 (Her3), a modulator of the phosphatidylinositol-3-kinase/Akt pathway

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10.1002/MUS.21428

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1

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41

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