Impaired minor tri-snRNP assembly generates differential splicing defects of U12-type introns in lymphoblasts derived from a type I SMA patient. (Q52605306)

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scientific article published on 23 November 2010

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English	Impaired minor tri-snRNP assembly generates differential splicing defects of U12-type introns in lymphoblasts derived from a type I SMA patient.	scientific article published on 23 November 2010

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scholarly article

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Impaired minor tri-snRNP assembly generates differential splicing defects of U12-type introns in lymphoblasts derived from a type I SMA patient. (English)

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

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Nawal Boulisfane

1

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Maria Choleza

2

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Florence Rage

3

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Henry Neel

4

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Johann Soret

5

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Rémy Bordonné

6

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Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

publication date

23 November 2010

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Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

Human Molecular Genetics

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Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

20

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Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

4

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Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

641-648

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Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

The neurobiology of childhood spinal muscular atrophy.

1 reference

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Identification and characterization of a spinal muscular atrophy-determining gene

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The survival motor neuron protein in spinal muscular atrophy

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The SMN complex, an assemblyosome of ribonucleoproteins

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Deciphering the assembly pathway of Sm-class U snRNPs

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SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing

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Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene

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

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1 reference

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1 reference

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1 reference

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1 reference

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The Cajal body: a meeting place for spliceosomal snRNPs in the nuclear maze

1 reference

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Enhancement of U4/U6 small nuclear ribonucleoprotein particle association in Cajal bodies predicted by mathematical modeling

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Spliceosomal small nuclear ribonucleoprotein particles repeatedly cycle through Cajal bodies

1 reference

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Human autoantibody to a novel protein of the nuclear coiled body: immunological characterization and cDNA cloning of p80-coilin

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Immunological and ultrastructural studies of the nuclear coiled body with autoimmune antibodies.

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Coilin is essential for Cajal body organization in Drosophila melanogaster.

1 reference

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Reduced viability, fertility and fecundity in mice lacking the cajal body marker protein, coilin.

1 reference

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Coilin-dependent snRNP assembly is essential for zebrafish embryogenesis

1 reference

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Nuclear bodies: random aggregates of sticky proteins or crucibles of macromolecular assembly?

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21 January 2018

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

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

A novel spliceosome containing U11, U12, and U5 snRNPs excises a minor class (AT-AC) intron in vitro

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

Splicing of a rare class of introns by the U12-dependent spliceosome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

A revised model for U4atac/U6atac snRNA base pairing

1 reference

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21 January 2018

U6 snRNA maturation and stability

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

RNAi knockdown of hPrp31 leads to an accumulation of U4/U6 di-snRNPs in Cajal bodies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

The abundance of the spliceosomal snRNPs is not limiting the splicing of U12-type introns

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

The splicing of U12-type introns can be a rate-limiting step in gene expression

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ508

21 January 2018

Ataxin-10, the spinocerebellar ataxia type 10 neurodegenerative disorder protein, is essential for survival of cerebellar neurons

1 reference

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21 January 2018

Ataxin 10 induces neuritogenesis via interaction with G-protein beta2 subunit

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SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis.

1 reference

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21 January 2018

Evolutionary fates and origins of U12-type introns.

1 reference

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21 January 2018

A computational scan for U12-dependent introns in the human genome sequence

1 reference

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21 January 2018

Domains of yeast U4 spliceosomal RNA required for PRP4 protein binding, snRNP-snRNP interactions, and pre-mRNA splicing in vivo

1 reference

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21 January 2018

Identifiers

10.1093/HMG/DDQ508

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

1 reference

Europe PubMed Central

4 May 2018

http://europepmc.org/abstract/MED/21098506

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