(Q24292040)

GOA release 2020-03-11

author

Juri Rappsilber

3

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Livio Pellizzoni

object named as

Livio Pellizzoni

1

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author name string

Jennifer Baccon

2

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Matthias Mann

4

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Gideon Dreyfuss

Journal of Biological Chemistry

5

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language of work or name

English

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publication date

1 March 2002

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published in

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volume

277

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page(s)

7540-5

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issue

9

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cites work

Spinal muscular atrophy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Identification and characterization of a spinal muscular atrophy-determining gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

A cell system with targeted disruption of the SMN gene: functional conservation of the SMN protein and dependence of Gemin2 on SMN.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Gemin5, a novel WD repeat protein component of the SMN complex that binds Sm proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Specific sequences of the Sm and Sm-like (Lsm) proteins mediate their interaction with the spinal muscular atrophy disease gene product (SMN).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Direct interaction of the spinal muscular atrophy disease protein SMN with the small nucleolar RNA-associated protein fibrillarin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

A functional interaction between the survival motor neuron complex and RNA polymerase II

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

SMN interacts with a novel family of hnRNP and spliceosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Mass Spectrometric Sequencing of Proteins from Silver-Stained Polyacrylamide Gels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Femtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Immunopurification of heterogeneous nuclear ribonucleoprotein particles reveals an assortment of RNA-binding proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Immunocytochemical analysis of the coiled body in the cell cycle and during cell proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Coiled bodies and gems: Janus or gemini?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

The spinal muscular atrophy disease gene product, SMN: A link between snRNP biogenesis and the Cajal (coiled) body

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Nuclear gems and Cajal (coiled) bodies in fetal tissues: nucleolar distribution of the spinal muscular atrophy protein, SMN

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Nuclear bodies: multifaceted subdomains of the interchromatin space.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

Spliceosomal UsnRNP biogenesis, structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

A novel nuclear structure containing the survival of motor neurons protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M110141200