Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia. - sprookjes - yvandenbroek - TriplyDB

Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia.

Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia.

http://www.wikidata.org/entity/Q34264724

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Dysregulation and functional roles of miR-183-96-182 cluster in cancer cell proliferation, invasion and metastasis Tau missorting and spastin-induced microtubule disruption in neurodegeneration: Alzheimer Disease and Hereditary Spastic Paraplegia The genetics of hair cell development and regeneration Gait Patterns in Patients with Hereditary Spastic Paraparesis.Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis.New perspectives on the development of muscle contractures following central motor lesions.Katanin-p80 gene promoter characterization and regulation via Elk1.

P2860

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P2860

Transcriptional and post-transcriptional regulation of SPAST, the gene most frequently mutated in hereditary spastic paraplegia.

http://www.wikidata.org/entity/Q34264724

description

2012 nî lūn-bûn

@nan

2012 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի մայիսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Transcriptional and post-trans ...... hereditary spastic paraplegia.

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Brian J Henson

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Jaime L Wetzel

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Kelsey Hardaway

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Mihaela Stefan

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Robert D Nicholls

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Wan Zhu

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Signaling mechanisms in cortical axon growth, guidance, and branching

A high-resolution map of human evolutionary constraint using 29 mammals

Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing

Recognition of C-terminal amino acids in tubulin by pore loops in Spastin is important for microtubule severing

Mammalian Ryk is a Wnt coreceptor required for stimulation of neurite outgrowth

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

Genome-wide promoter analysis of the SOX4 transcriptional network in prostate cancer cells

NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).

Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

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Kathryn M Albers

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