(Q45973869)

18 December 2017

title

Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy. (English)

1 reference

18 December 2017

Nicolas Pollet

8

0 references

author name string

Qods Ymlahi-Ouazzani

1

1 reference

18 December 2017

Odile J Bronchain

2

1 reference

18 December 2017

Elodie Paillard

3

1 reference

18 December 2017

Chantal Ballagny

4

1 reference

18 December 2017

Albert Chesneau

5

1 reference

18 December 2017

Aurélie Jadaud

6

1 reference

18 December 2017

André Mazabraud

7

1 reference

18 December 2017

publication date

11 June 2009

1 reference

18 December 2017

published in

Neurogenetics

1 reference

18 December 2017

volume

11

1 reference

18 December 2017

issue

1

1 reference

18 December 2017

page(s)

27-40

1 reference

18 December 2017

https://scigraph.springernature.com/pub.10.1007/s10048-009-0200-6

exact match

0 references

cites work

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

1 reference

12 December 2020

Functional motor neurons differentiating from mouse multipotent spinal cord precursor cells in culture and after transplantation into transected sciatic nerve.

1 reference

12 December 2020

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

1 reference

12 December 2020

Embryonic development of four different subsets of cholinergic neurons in rat cervical spinal cord

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel nuclear structure containing the survival of motor neurons protein

1 reference

12 December 2020

The olig family: phylogenetic analysis and early gene expression in Xenopus tropicalis.

1 reference

12 December 2020

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

1 reference

12 December 2020

Spinal muscular atrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

The neurobiology of childhood spinal muscular atrophy.

1 reference

12 December 2020

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

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

Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death

1 reference

12 December 2020

A mouse model for spinal muscular atrophy

1 reference

12 December 2020

Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis

1 reference

12 December 2020

Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy

1 reference

12 December 2020

Embryonic motor axon development in the severe SMA mouse

1 reference

12 December 2020

Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice

1 reference

12 December 2020

Correlation between severity and SMN protein level in spinal muscular atrophy

1 reference

12 December 2020

The Schizosaccharomyces pombe protein Yab8p and a novel factor, Yip1p, share structural and functional similarity with the spinal muscular atrophy-associated proteins SMN and SIP1.

1 reference

12 December 2020

Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous system

1 reference

12 December 2020

Spinal muscular atrophy

1 reference

12 December 2020

A single site on the epsilon subunit is responsible for the change in ACh receptor channel conductance during skeletal muscle development.

1 reference

12 December 2020

Spinal muscular atrophy: the RNP connection

1 reference

12 December 2020

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

1 reference

12 December 2020

Zfh1, a somatic motor neuron transcription factor, regulates axon exit from the CNS.

1 reference

12 December 2020

Regulation of SMN protein stability

1 reference

12 December 2020

The molecular bases of spinal muscular atrophy

1 reference

12 December 2020

Notch1 signaling influences v2 interneuron and motor neuron development in the spinal cord.

1 reference

12 December 2020

The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

1 reference

12 December 2020

Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy

1 reference

12 December 2020

Molecular diversity of myofibrillar proteins: gene regulation and functional significance

1 reference

12 December 2020

MyoD expression in the forming somites is an early response to mesoderm induction in Xenopus embryos

1 reference

12 December 2020

The SMN complex, an assemblyosome of ribonucleoproteins

1 reference

12 December 2020

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

1 reference

12 December 2020

A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs

1 reference

12 December 2020

Survival motor neuron (SMN) protein in rat is expressed as different molecular forms and is developmentally regulated.

1 reference

12 December 2020

Assisted RNP assembly: SMN and PRMT5 complexes cooperate in the formation of spliceosomal UsnRNPs

1 reference

12 December 2020

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy: new insights into molecular mechanisms responsible for the disease.

1 reference

12 December 2020

Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

1 reference

12 December 2020

10.1007/S10048-009-0200-6

Identifiers

DOI

1 reference

18 December 2017

Dimensions Publication ID

1004294230

0 references

Fatcat ID

release_fh3ehjqcirctxpk2auibeyvuey

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/fh3ehjqcirctxpk2auibeyvuey

24 November 2022

mapped directly with Wikidata item

PubMed ID

19517146

1 reference

18 December 2017