Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy (Q28137718)

3

object named as

R Lührmann

0 references

author name string

D Bühler

1

0 references

V Raker

2

0 references

U Fischer

Correlation between severity and SMN protein level in spinal muscular atrophy

4

0 references

language of work or name

English

0 references

publication date

December 1999

0 references

published in

Human Molecular Genetics

0 references

volume

8

0 references

issue

13

0 references

page(s)

2351-7

0 references

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

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/10.1093%2FHMG%2F8.13.2351

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Small nuclear ribonucleoprotein particle assembly in vivo: demonstration of a 6S RNA-free core precursor and posttranslational modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

The trimethylguanosine cap structure of U1 snRNA is a component of a bipartite nuclear targeting signal

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Cap trimethylation of U snRNA is cytoplasmic and dependent on U snRNP protein binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

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/10.1093%2FHMG%2F8.13.2351

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Tudor domains in proteins that interact with RNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Characterization of a gene encoding survival motor neuron (SMN)-related protein, a constituent of the spliceosome complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Analysis of mutations in the tudor domain of the survival motor neuron protein SMN

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Monoclonal antibodies to nucleic acid-containing cellular constituents: probes for molecular biology and autoimmune disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

Spliceosomal U snRNP core assembly: Sm proteins assemble onto an Sm site RNA nonanucleotide in a specific and thermodynamically stable manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351

pICln inhibits snRNP biogenesis by binding core spliceosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2351