(Q30976876)

27 June 2017

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

1 reference

27 June 2017

Wang J

1

1 reference

PubMed ID

11121410

27 June 2017

Dreyfuss G

series ordinal

2

1 reference

PubMed ID

11121410

27 June 2017

language of work or name

English

0 references

publication date

19 December 2000

1 reference

Journal of Biological Chemistry

27 June 2017

1 reference

27 June 2017

276

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27 June 2017

9599-9605

1 reference

27 June 2017

13

1 reference

The genetic component in child mortality

27 June 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

A frame-shift deletion in the survival motor neuron gene in Spanish spinal muscular atrophy patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Identification and characterization of a spinal muscular atrophy-determining gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Molecular analysis of the SMN and NAIP genes in Spanish spinal muscular atrophy (SMA) families and correlation between number of copies of cBCD541 and SMA phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Correlation between severity and SMN protein level in spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

The survival motor neuron protein in spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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.M009162200

Is the sphere organelle/coiled body a universal nuclear component?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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.M009162200

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.M009162200

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.M009162200

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.M009162200

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.M009162200

Identification of survival motor neuron as a transcriptional activator-binding protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

The survival motor neuron protein interacts with the transactivator FUSE binding protein from human fetal brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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.M009162200

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.M009162200

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.M009162200

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.M009162200

A mouse model for spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Increased ratio of targeted to random integration after transfection of chicken B cell lines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Targeted disruption of an essential vertebrate gene: ASF/SF2 is required for cell viability

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Tight control of gene expression in mammalian cells by tetracycline-responsive promoters

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Broad, but not universal, transcriptional requirement for yTAFII17, a histone H3-like TAFII present in TFIID and SAGA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

The histone H3-like TAF is broadly required for transcription in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

TAF25p, a non-histone-like subunit of TFIID and SAGA complexes, is essential for total mRNA gene transcription in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Classification of spinal muscular atrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

Histone-like TAFs are essential for transcription in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

yTAFII61 has a general role in RNA polymerase II transcription and is required by Gcn4p to recruit the SAGA coactivator complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M009162200

21 January 2018

Identifiers

DOI

10.1074/JBC.M009162200

1 reference

27 June 2017

1 reference

PubMed ID

11121410