Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis. (Q47073257)

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21 December 2019

title

Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis (English)

1 reference

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Survival of motor neuron 1, telomeric

21 December 2019

main subject

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ribonucleoprotein complex

GOA release 2020-03-11

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8

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21 December 2019

author name string

Tessa L Carrel

1

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21 December 2019

Michelle L McWhorter

2

1 reference

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21 December 2019

Eileen Workman

3

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21 December 2019

Honglai Zhang

4

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21 December 2019

Elizabeth C Wolstencroft

5

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21 December 2019

Christian Lorson

6

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21 December 2019

Gary J Bassell

7

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21 December 2019

Christine E Beattie

9

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language of work or name

English

0 references

publication date

1 October 2006

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21 December 2019

published in

Journal of Neuroscience

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volume

26

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issue

43

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page(s)

11014-11022

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describes a project that uses

21 December 2019

ImageQuant

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11 June 2022

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inferred from PubMed Central ID database lookup

cites work

A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

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12 December 2020

A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.

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

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Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy

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Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord

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An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN

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An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA).

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Nova-1 regulates neuron-specific alternative splicing and is essential for neuronal viability

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Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins

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12 December 2020

The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

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12 December 2020

Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy

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12 December 2020

Neurotrophin-induced transport of a beta-actin mRNP complex increases beta-actin levels and stimulates growth cone motility.

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12 December 2020

Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?

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12 December 2020

Survival motor neuron (SMN) protein: role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development.

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Essential role for the SMN complex in the specificity of snRNP assembly

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A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy.

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Neuromuscular defects in a Drosophila survival motor neuron gene mutant.

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Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization.

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Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding.

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12 December 2020

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

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12 December 2020

Why do cells need an assembly machine for RNA-protein complexes?

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12 December 2020

RNA translation in axons

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12 December 2020

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.

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12 December 2020

A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels

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12 December 2020

Tudor domains bind symmetrical dimethylated arginines

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12 December 2020

The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy

1 reference

12 December 2020

A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.

1 reference

12 December 2020

Is spinal muscular atrophy the result of defects in motor neuron processes?

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12 December 2020

Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy

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12 December 2020

Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins.

1 reference

12 December 2020

Spinal muscular atrophy: a deficiency in a ubiquitous protein; a motor neuron-specific disease

1 reference

12 December 2020

Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons

1 reference

12 December 2020

Classification of spinal muscular atrophies

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12 December 2020

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

12 December 2020

A novel nuclear structure containing the survival of motor neurons protein

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12 December 2020

The neurobiology of childhood spinal muscular atrophy.

1 reference

12 December 2020

Promoter analysis in living zebrafish embryos identifies a cis-acting motif required for neuronal expression of GATA-2.

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12 December 2020

Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number

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12 December 2020

Correlation between severity and SMN protein level in spinal muscular atrophy

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12 December 2020

The survival motor neuron protein in spinal muscular atrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

SMN oligomerization defect correlates with spinal muscular atrophy severity

1 reference

12 December 2020

10.1523/JNEUROSCI.1637-06.2006

Identifiers

DOI

1 reference

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21 December 2019

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21 December 2019

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