Disruption of SMN function by ectopic expression of the human SMN gene in Drosophila. (Q47808364)

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2 November 2019

title

Disruption of SMN function by ectopic expression of the human SMN gene in Drosophila (English)

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2 November 2019

1

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2 November 2019

author name string

Y B Chan

series ordinal

2

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2 November 2019

K E Davies

series ordinal

3

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2 November 2019

M van den Heuvel

series ordinal

4

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2 November 2019

language of work or name

English

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publication date

1 December 2000

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2 November 2019

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2 November 2019

volume

486

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2 November 2019

issue

2

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2 November 2019

page(s)

99-102

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The neurobiology of childhood spinal muscular atrophy.

2 November 2019

cites work

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Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

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Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.

21 January 2018

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Genomic variation and gene conversion in spinal muscular atrophy: implications for disease process and clinical phenotype

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Modeling human neurodegenerative diseases in Drosophila: on a wing and a prayer.

21 January 2018

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A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback

21 January 2018

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Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

21 January 2018

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Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?

21 January 2018

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Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos

21 January 2018

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The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability.

21 January 2018

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The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding.

21 January 2018

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SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

21 January 2018

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Tudor domains in proteins that interact with RNA.

21 January 2018

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Synergistic anti-apoptotic activity between Bcl-2 and SMN implicated in spinal muscular atrophy

21 January 2018

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

21 January 2018

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The survival motor neuron protein interacts with the transactivator FUSE binding protein from human fetal brain

21 January 2018

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

21 January 2018

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Analysis of compositionally biased regions in sequence databases

21 January 2018

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SMN oligomerization defect correlates with spinal muscular atrophy severity

21 January 2018

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The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms

21 January 2018

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A role for polyproline motifs in the spinal muscular atrophy protein SMN. Profilins bind to and colocalize with smn in nuclear gems

21 January 2018

1 reference

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10.1016/S0014-5793(00)02243-2

21 January 2018

Identifiers

DOI

1 reference

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2 November 2019

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