Assignment of the gene encoding the beta‐subunit of the human fibronectin receptor (β‐FNR) to chromosome 10p11.2
Explore this paper's citation graph
Summary
A cDNA corresponding to the β‐subunit of the human fibronectin receptor (β‐FNR) was used as a probe in Southern blot analysis of mouse/human somatic cell hybrid DNAs and in in situ hybridization to metaphase chrmosomes.
- Type
- article
- Published
- 1989-01-01
- Cited by
- 53
- References
- 23
- OpenAlex
- https://openalex.org/W2004963822
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:36485270
Keywords
Complementary DNA, Biology, Molecular biology, Southern blot, Somatic cell
References
- The VLA protein family. Characterization of five distinct cell surface heterodimers each with a common 130,000 molecular weight beta subunit.
- Biochemical characterization of VLA-1 and VLA-2. Cell surface heterodimers on activated T cells.
- Use of the monoclonal antibody 12F1 to characterize the differentiation antigen VLA-2.
- Monoclonal antibody DH12 reacts with a cell surface and a precursor form of the beta subunit of the human fibronectin receptor.
- Somatic cell genetic analysis of human cell surface antigens: chromosomal assignments and regulation of expression in rodent-human hybrid cells.
- Fibronectin receptor structures in the VLA family of heterodimers
- Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage
- Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization
- A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10
- A polymorphic locus, D10S5, at 10q21.1
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
- The very late antigen family of heterodimers is part of a superfamily of molecules involved in adhesion and embryogenesis.
- Monoclonal Antibodies to Three Widely Distributed Human Cell Surface Antigens
- Genetic Analysis with Human—Mouse Somatic Cell Hybrids
- Mapping of human fibronectin receptorβ subunit gene to chromosome 10
- Identification and isolation of a 140 kd cell surface glycoprotein with properties expected of a fibronectin receptor.
- High-resolution chromosomal localization of human genes for amylase, proopiomelanocortin, somatostatin, and a DNA fragment (D3S1) by in situ hybridization.
- The hypervariable gene locus PUM, which codes for the tumour associated epithelial mucins, is located on chromosome 1, within the region 1g21–24
- A human cell‐surface antigen defined by a monoclonal antibody and controlled by a gene on human chromosome 1
- Amino acid sequence of the human fibronectin receptor
Cited by
- Genetic analysis of 24 French families with multiple endocrine neoplasia type 2A.
- Search for the gene for multiple endocrine neoplasia type 2A.
- Histopathology of Blistering Diseases
- The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10.
- Parent-of-origin effects in multiple endocrine neoplasia type 2B.
- Evidence for increased prevalence of SRY mutations in XY females with complete rather than partial gonadal dysgenesis.
- Role of fibronectin-stimulated tumor cell migration in glioma invasion in vivo: clinical significance of fibronectin and fibronectin receptor expressed in human glioma tissues
- The linkage between β1 integrin and the actin cytoskeleton is differentially regulated by tyrosine and serine/threonine phosphorylation of β1 integrin in normal and cancerous human breast cells
- Human repeat element-mediated PCR: cloning and mapping of chromosome 10 DNA markers.
- A multiple interval physical map of the pericentromeric region of human chromosome 10
- Mapping of the α-subunit of the fox fibronectin receptor (FNRA) to Chromosome 8
- The involvement of the cell matrix receptors, or VLA integrins, in the morphogenetic behavior of normal and malignant cells is gradually being uncovered.
- Generation of a panel of somatic cell hybrids containing unselected fragments of human chromosome 10 by X-ray irradiation and cell fusion: Application to isolating theMEN2A region in hybrid cells
- Application of bioinformatics-coupled experimental analysis reveals a new transport-competent nuclear localization signal in the nucleoprotein of Influenza A virus strain
- Characterisation and mapping of the human SOX14 gene
- The fibronectin receptor, alpha subunit (Itga5) maps to murine Chromosome 15, distal to D15Mit16
- A human integrin beta 1 subunit with a unique cytoplasmic domain generated by alternative mRNA processing.
- Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal
- Assignment of three rat integrin genes to Chromosome 19 (ITGB1), Chromosome 3 (ITGA4), and Chromosome 7 (ITGA5)
- Restrictive dermopathy: a disorder of skin differentiation with abnormal integrin expression
Related papers
- Genomic analysis of transgenic animals: Southern blotting.
- Major karyotypic abnormalities in a near-tetraploid erythroleukemia.
- The densitometric study of G bands on human metaphase chromosomes
- Study on construction of cDNA library of the treated changliver cell and quality analysis
- Construction of cDNA Library of Hylarana latouchii Skin Tissue with Cloning and Sequence Analysis of the cDNA Encoding Antimicrobial Peptides Brevinin-2LTs
- Construction of cDNA library of the treated Changliver cell and quality analysis
- Construction of genomic library of rabbit
- Genetic mapping of the structural gene for antithrombin III to human chromosome 1