(Q24304268)

identical protein binding

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Survival motor neuron Dmel_CG16725

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Rpp20 Dmel_CG33931

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Biochemical and Biophysical Research Communications

author name string

Yimin Hua

series ordinal

1

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Jianhua Zhou

series ordinal

2

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language of work or name

English

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publication date

30 January 2004

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published in

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volume

314

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issue

1

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page(s)

268-76

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cites work

A novel nuclear structure containing the survival of motor neurons protein

1 reference

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7 January 2021

Identification and characterization of a spinal muscular atrophy-determining gene

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Axonal protein synthesis provides a mechanism for localized regulation at an intermediate target

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Human ribonuclease P: subunits, function, and intranuclear localization

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

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7 January 2021

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

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Rpp2, an essential protein subunit of nuclear RNase P, is required for processing of precursor tRNAs and 35S precursor rRNA in Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Protein-protein interactions with subunits of human nuclear RNase P

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component

1 reference

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7 January 2021

Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Determinants of the interaction of the spinal muscular atrophy disease protein SMN with the dimethylarginine-modified box H/ACA small nucleolar ribonucleoprotein GAR1

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Inhibition of apoptosis by Z-VAD-fmk in SMN-depleted S2 cells

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Localization in the nucleolus and coiled bodies of protein subunits of the ribonucleoprotein ribonuclease P

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

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7 January 2021

RNA-binding proteins TIA-1 and TIAR link the phosphorylation of eIF-2 alpha to the assembly of mammalian stress granules

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

RNA binding in an Sm core domain: X-ray structure and functional analysis of an archaeal Sm protein complex

1 reference

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7 January 2021

The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy

1 reference

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7 January 2021

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

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Neuromuscular defects in a Drosophila survival motor neuron gene mutant.

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Unique Sm core structure of U7 snRNPs: assembly by a specialized SMN complex and the role of a new component, Lsm11, in histone RNA processing

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Lsm proteins are required for normal processing of pre-tRNAs and their efficient association with La-homologous protein Lhp1p

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Eukaryotic ribonuclease P: a plurality of ribonucleoprotein enzymes

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

Cajal body proteins SMN and Coilin show differential dynamic behaviour in vivo

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.BBRC.2003.12.084

7 January 2021

10.1016/J.BBRC.2003.12.084

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4732729

OpenCitations bibliographic resource ID

4732729

1 reference