Spinal muscular atrophy: recent advances and future prospects. - Wikidata - wikimedia - TriplyDB

Spinal muscular atrophy: recent advances and future prospects.

Spinal muscular atrophy: recent advances and future prospects.

http://www.wikidata.org/entity/Q34737033

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Drug treatment for spinal muscular atrophy types II and III Drug treatment for spinal muscular atrophy type I Drug treatment for spinal muscular atrophy types II and III Drug treatment for spinal muscular atrophy type I Drug treatment for spinal muscular atrophy type I Drug treatment for spinal muscular atrophy types II and III Skeletal muscle DNA damage precedes spinal motor neuron DNA damage in a mouse model of Spinal Muscular Atrophy (SMA)Positive regulation of ASK1-mediated c-Jun NH(2)-terminal kinase signaling pathway by the WD-repeat protein Gemin5 Effective heritable gene knockdown in zebrafish using synthetic microRNAs.Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy.AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy Expression of Muscle-Specific MiRNA 206 in the Progression of Disease in a Murine SMA Model A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle.Activin Receptor Type IIB Inhibition Improves Muscle Phenotype and Function in a Mouse Model of Spinal Muscular Atrophy Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes Targeting RNA-splicing for SMA treatment.Perceptions of equine-assisted activities and therapies by parents and children with spinal muscular atrophy.Mechanobiology of embryonic skeletal development: Insights from animal models Biophysical stimuli induced by passive movements compensate for lack of skeletal muscle during embryonic skeletogenesis.Survival motor neuron (SMN) protein interacts with transcription corepressor mSin3A.DNA Damage Response and DNA Repair in Skeletal Myocytes From a Mouse Model of Spinal Muscular Atrophy.Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons.Management of children with spinal muscular atrophy type 1 in Australia.Compensatory axon sprouting for very slow axonal die-back in a transgenic model of spinal muscular atrophy type III.Tissue-specific models of spinal muscular atrophy confirm a critical role of SMN in motor neurons from embryonic to adult stages.Aquatic therapy for a child with type III spinal muscular atrophy: a case report.Carrier testing in children: exploration of genetic health professionals' practices in Australia.

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Spinal muscular atrophy: recent advances and future prospects.

http://www.wikidata.org/entity/Q34737033

description

2002 nî lūn-bûn

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2002 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2002 թվականի հուլիսին հրատարակված գիտական հոդված

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2002年の論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年論文

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2002年论文

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name

Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Spinal muscular atrophy: recent advances and future prospects.

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Muscle and Nerve

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Spinal muscular atrophy: recent advances and future prospects

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Carmen Cifuentes Diaz

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Judith Melki

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P2860

A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein

Gemin5, a novel WD repeat protein component of the SMN complex that binds Sm proteins

The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

A functional interaction between the survival motor neuron complex and RNA polymerase II

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4-13

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scholarly article

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10.1002/MUS.10110

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1

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26

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2002-07-01T00:00:00Z

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12115944

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spinal muscular atrophy