(Q28293026)

English

Association of PAP-1 and Prp3p, the products of causative genes of dominant retinitis pigmentosa, in the tri-snRNP complex

scientific article

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Association of PAP-1 and Prp3p, the products of causative genes of dominant retinitis pigmentosa, in the tri-snRNP complex (English)

0 references

1 reference

Hiroshi Maita

1

0 references

Hirotake Kitaura

series ordinal

2

0 references

Hiroyoshi Ariga

series ordinal

3

0 references

Sanae M M Iguchi-Ariga

series ordinal

4

0 references

language of work or name

English

0 references

publication date

1 January 2005

0 references

published in

Experimental Cell Research

0 references

volume

302

0 references

page(s)

61-8

0 references

issue

1

0 references

cites work

PAP-1, a novel target protein of phosphorylation by pim-1 kinase

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Retinitis pigmentosa: defined from a molecular point of view

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

TOK-1, a novel p21Cip1-binding protein that cooperatively enhances p21-dependent inhibitory activity toward CDK2 kinase

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

ORC1 interacts with c-Myc to inhibit E-box-dependent transcription by abrogating c-Myc-SNF5/INI1 interaction

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

SMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Central region of the human splicing factor Hprp3p interacts with Hprp4p

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Prp31p promotes the association of the U4/U6 x U5 tri-snRNP with prespliceosomes to form spliceosomes in Saccharomyces cerevisiae

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Disease mechanism for retinitis pigmentosa (RP11) caused by mutations in the splicing factor gene PRPF31

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Protein 61K, encoded by a gene (PRPF31) linked to autosomal dominant retinitis pigmentosa, is required for U4/U6*U5 tri-snRNP formation and pre-mRNA splicing

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factor

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2004.08.022

retrieved

7 January 2021

Identifiers

DOI

10.1016/J.YEXCR.2004.08.022

0 references

PubMed ID

15541726

0 references

(Q28293026)

Association of PAP-1 and Prp3p, the products of causative genes of dominant retinitis pigmentosa, in the tri-snRNP complex

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)