(Q24312139)

English

Identification and characterization of the human homologue of SH3BP2, an SH3 binding domain protein within a common region of deletion at 4p16.3 involved in bladder cancer

scientific article

In more languages

Statements

scholarly article

0 references

Identification and characterization of the human homologue of SH3BP2, an SH3 binding domain protein within a common region of deletion at 4p16.3 involved in bladder cancer (English)

0 references

0 references

1 reference

based on heuristic

inferred from title

author name string

S M Bell

1

0 references

M Shaw

2

0 references

Y S Jou

3

0 references

R M Myers

4

0 references

M A Knowles

5

0 references

language of work or name

0 references

publication date

1 September 1997

0 references

0 references

44

0 references

163-70

0 references

2

0 references

The spectrum of TP53 mutations in bladder carcinoma

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Hormone-conditional transformation by fusion proteins of c-Abl and its transforming variants

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

The murine homologues of the Huntington disease gene (Hdh) and the alpha-adducin gene (Add1) map to mouse chromosome 5 within a region of conserved synteny with human chromosome 4p16.3

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of the alpha 2-macroglobulin receptor-associated protein 1 gene (LRPAP1) and other gene fragments to human chromosome 4p16.3 by direct cDNA selection

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

CpG islands in vertebrate genomes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetic follow-up of patients with nonlymphocytic leukemia. II. Acute nonlymphocytic leukemia

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Supernumerary isochromosome 4p in ANLL-M4 myelomonocytic type is associated with favorable prognosis

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

The distribution of genes in the human genome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

SH2 and SH3 domains

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

CpG-rich islands and the function of DNA methylation

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Protein modules and signalling networks

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a ten-amino acid proline-rich SH3 binding site

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Organization and expression of eucaryotic split genes coding for proteins

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.4849

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1006/GENO.1997.4849

0 references

0 references

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24312139&oldid=1523464250"