Localisation of the human gene encoding the cytoskeletal protein talin to chromosome 9p

No abstract is available for this paper.

• Publication year

  1995

• Venue

  Human Genetics

• Publication date

  1995-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF00207384PMID 7635475
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Cytological mapping of human chromosomes: results obtained with Quinacrine fluorescence and the Acetic-Saline-Giemsa techniques

  2004cited by this paper
• Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping

  1995cited by this paper
• A cell cycle regulator potentially involved in genesis of many tumour types

  1994cited by this paper
• Homozygous deletions within chromosomal bands 9p21-22 in bladder cancer.

  1994cited by this paper
• Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers

  1994cited by this paper
• A cell cycle regulator potentially involved in genesis of many tumor types.

  1994cited by this paper
• Molecular deletion of 9p sequences in non‐small cell lung cancer and malignant mesothelioma

  1993cited by this paper
• The cytoskeletal protein talin contains at least two distinct vinculin binding domains

  1993cited by this paper
• A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.

  1993cited by this paper
• Homozygous deletions within 9p21-p22 identify a small critical region of chromosomal loss in human malignant mesotheliomas.

  1993cited by this paper
• Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

  1993cited by this paper
• Wizardry at the cell cortex.

  1993cited by this paper
• Suppression of tumorigenicity in simian virus 40-transformed 3T3 cells transfected with alpha-actinin cDNA.

  1993cited by this paper
• Association of the APC gene product with beta-catenin.

  1993cited by this paper
• Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia.

  1992cited by this paper
• Cytoskeleton--plasma membrane interactions.

  1992cited by this paper
• Homozygous deletions within human chromosome band 9p21 in melanoma.

  1992cited by this paper
• Suppression of tumorigenicity in transformed cells after transfection with vinculin cDNA

  1992cited by this paper
• Augmentation of alpha-actinin-induced gelation of actin by talin.

  1992cited by this paper
• Sequence and domain structure of talin

  1990cited by this paper
• Functional studies of the domains of talin

  1990cited by this paper
• The gene for human complement component C9 mapped to chromosome 5 by polymerase chain reaction.

  1989cited by this paper
• Cytogenetic analysis of melanocytes from premalignant nevi and melanomas.

  1988cited by this paper
• Interaction of plasma membrane fibronectin receptor with talin—a transmembrane linkage

  1986cited by this paper
• Chromosomal localization of human cellular homologues of two viral oncogenes

  1982cited by this paper
• Assignment of the human acid alpha-glucosidase gene (alphaGLU) to chromosome 17 using somatic cell hybrids.

  1979cited by this paper
• Regional asssignments of the loci AK3, ACONS, and ASS on human chromosome 9.

  1979cited by this paper
• Assignment of the human acid α‐glucosidase gene (αGLU) to chromosome 17 using somatic cell hybrids

  1979cited by this paper
• Human gene mapping using an X/autosome translocation

  1976cited by this paper
• Differential staining of human and mouse chromosomes in interspecific cell hybrids

  1974cited by this paper

• Talin: a mechanosensitive molecule in health and disease

  2016cites this paper
• The sensors and regulators of cell–matrix surveillance in anoikis resistance of tumors

  2011cites this paper
• Short Arm of Chromosome 9 in Small Cell Lung Cancer Identification of Three Distinct Tumor Suppressor Loci on the Updated

  2006cites this paper
• Advances in Brief Identification of Three Distinct Tumor Suppressor Loci on the Short Arm of Chromosome 9 in Small Cell Lung Cancer '

  2006cites this paper
• URP1: a member of a novel family of PH and FERM domain-containing membrane-associated proteins is significantly over-expressed in lung and colon carcinomas.

  2003cites this paper
• Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes.

  2003cites this paper
• Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia.

  2001cites this paper
• Mapping of a gene for May-Hegglin anomaly to chromosome 22q

  1999cites this paper
• Characterization of the human talin (TLN) gene: genomic structure, chromosomal localization, and expression pattern.

  1999cites this paper
• Alterations of the p16-pRb pathway and the chromosome locus 9p21-22 in non-small-cell lung carcinomas: relationship with p53 and MDM2 protein expression.

  1998cites this paper
• Paracrine regulation of talin mRNA expression by androgen in human prostate

  1998cites this paper
• Identification of three distinct tumor suppressor loci on the short arm of chromosome 9 in small cell lung cancer.

  1997cites this paper
• Integrated Radiation Hybrid and Yeast Artificial Chromosome Map of Chromosome 9p

  1997cites this paper
• Talin contains three actin-binding sites each of which is adjacent to a vinculin-binding site.

  1996cites this paper
• Alterations of pl 6-pRb Pathway and Chromosome Locus 9 p 21-22 in Sporadic Invasive Breast Carcinomas

  year unknowncites this paper