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Tumour suppressor genes in disease and therapy
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instance of
scholarly article
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review article
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stated in
Europe PubMed Central
title
Tumour suppressor genes in disease and therapy
(English)
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author name string
G R Skuse
series ordinal
1
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J W Ludlow
series ordinal
2
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language of work or name
English
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publication date
8 April 1995
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published in
The Lancet
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volume
345
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page(s)
902-6
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issue
8954
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cites work
Mutation and cancer: statistical study of retinoblastoma
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A general theory of carcinogenesis
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Chromosomal deletion and retinoblastoma
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Crossref
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Suppression of the neoplastic phenotype by replacement of the RB gene in human cancer cells
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The gene responsible for the development of retinoblastoma and osteosarcoma
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The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity
1 reference
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Role of the retinoblastoma gene in the initiation and progression of human cancer
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Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism
1 reference
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Mapping of human chromosome 11: organization of genes within the Wilms' tumor region of the chromosome
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Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour
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Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
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Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1
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DNA recognition by splicing variants of the Wilms' tumor suppressor, WT1
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RNA editing in the Wilms' tumor susceptibility gene, WT1
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Introduction of a normal human chromosome 11 into a Wilms' tumor cell line controls its tumorigenic expression
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Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17
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Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17.
1 reference
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The neurofibromatosis type 1 gene encodes a protein related to GAP
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Brain tumors predominantly express the neurofibromatosis type 1 gene transcripts containing the 63 base insert in the region coding for GTPase activating protein-related domain.
1 reference
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Expression of two types of neurofibromatosis type 1 gene transcripts in gastric cancers and comparison of GAP activities
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Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred
1 reference
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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.
1 reference
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Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.
1 reference
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The DCC gene product in cellular differentiation and colorectal tumorigenesis
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Antisense RNA to the putative tumor suppressor gene "deleted in colorectal cancer" transforms fibroblasts
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Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers
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Association of the APC tumor suppressor protein with catenins
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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
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Microsatellite instability in cancer of the proximal colon
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Mutation of a mutL homolog in hereditary colon cancer
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Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas
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Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
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Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.
1 reference
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Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer
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1 reference
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7 January 2021
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Identifiers
DOI
10.1016/S0140-6736(95)90015-2
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PubMed ID
7707816
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