(Q24312139)

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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

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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)

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author name string

S M Bell

1

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M Shaw

2

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Y S Jou

3

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R M Myers

4

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M A Knowles

5

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language of work or name

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publication date

1 September 1997

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44

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2

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163-70

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The spectrum of TP53 mutations in bladder carcinoma

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

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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

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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

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

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CpG islands in vertebrate genomes

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

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

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

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

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The distribution of genes in the human genome

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

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SH2 and SH3 domains

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CpG-rich islands and the function of DNA methylation

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

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Protein modules and signalling networks

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

1 reference

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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

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

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

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Organization and expression of eucaryotic split genes coding for proteins

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Identifiers

10.1006/GENO.1997.4849

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