Literature DB >> 8594564

Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation.

M Hollstein1, B Shomer, M Greenblatt, T Soussi, E Hovig, R Montesano, C C Harris.   

Abstract

In 1994 we described a list of approximately 2500 point mutations in the p53 gene of human tumors and cell lines which we had compiled from the published literature and made available electronically through the file server at the EMBL Data Library. This database, updated twice a year, now contains records on 4496 published mutations (July 1995 release) and can be obtained from the EMBL Outstation-the European Bioinformatics Institute (EBI) through the network or on CD-ROM. This report describes the criteria for inclusion of data in this database, a description of the current format and a brief discussion of the current relevance of p53 mutation analysis to clinical and biological questions.

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Year:  1996        PMID: 8594564      PMCID: PMC145616          DOI: 10.1093/nar/24.1.141

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  22 in total

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Authors:  T A Kunkel
Journal:  Biochemistry       Date:  1990-09-04       Impact factor: 3.162

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3.  SRS--an indexing and retrieval tool for flat file data libraries.

Authors:  T Etzold; P Argos
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4.  Geographic variation of p53 mutational profile in nonmalignant human liver.

Authors:  F Aguilar; C C Harris; T Sun; M Hollstein; P Cerutti
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5.  Short direct repeats flanking deletions, and duplicating insertions in p53 gene in human cancers.

Authors:  N Jego; G Thomas; R Hamelin
Journal:  Oncogene       Date:  1993-01       Impact factor: 9.867

Review 6.  p53 mutations in human cancers.

Authors:  M Hollstein; D Sidransky; B Vogelstein; C C Harris
Journal:  Science       Date:  1991-07-05       Impact factor: 47.728

7.  A role for sunlight in skin cancer: UV-induced p53 mutations in squamous cell carcinoma.

Authors:  D E Brash; J A Rudolph; J A Simon; A Lin; G J McKenna; H P Baden; A J Halperin; J Pontén
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8.  Somatic spectrum of cancer-associated single basepair substitutions in the TP53 gene is determined mainly by endogenous mechanisms of mutation and by selection.

Authors:  M Krawczak; B Smith-Sorensen; J Schmidtke; V V Kakkar; D N Cooper; E Hovig
Journal:  Hum Mutat       Date:  1995       Impact factor: 4.878

9.  Excision repair at individual bases of the Escherichia coli lacI gene: relation to mutation hot spots and transcription coupling activity.

Authors:  S Kunala; D E Brash
Journal:  Proc Natl Acad Sci U S A       Date:  1992-11-15       Impact factor: 11.205

10.  Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas.

Authors:  S J Baker; E R Fearon; J M Nigro; S R Hamilton; A C Preisinger; J M Jessup; P vanTuinen; D H Ledbetter; D F Barker; Y Nakamura; R White; B Vogelstein
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  94 in total

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Authors:  B C McKay; F Chen; C R Perumalswami; F Zhang; M Ljungman
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2.  Benign clonal keratinocyte patches with p53 mutations show no genetic link to synchronous squamous cell precancer or cancer in human skin.

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Journal:  Am J Pathol       Date:  1997-05       Impact factor: 4.307

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Journal:  J Virol       Date:  2003-11       Impact factor: 5.103

Review 4.  The role of DNA exonucleases in protecting genome stability and their impact on ageing.

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Review 5.  Polycyclic aromatic hydrocarbon-DNA adduct formation in prostate carcinogenesis.

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6.  Cooperative fluctuations point to the dimerization interface of p53 core domain.

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Review 7.  8-Hydroxy-2'-deoxyguanosine as a marker of oxidative DNA damage related to occupational and environmental exposures.

Authors:  A Pilger; H W Rüdiger
Journal:  Int Arch Occup Environ Health       Date:  2006-05-10       Impact factor: 3.015

8.  Repair of hydantoins, one electron oxidation product of 8-oxoguanine, by DNA glycosylases of Escherichia coli.

Authors:  T K Hazra; J G Muller; R C Manuel; C J Burrows; R S Lloyd; S Mitra
Journal:  Nucleic Acids Res       Date:  2001-05-01       Impact factor: 16.971

9.  p53 alterations in oesophageal cancer: association with clinicopathological features, risk factors, and survival.

Authors:  A G Casson; M Tammemagi; S Eskandarian; M Redston; J McLaughlin; H Ozcelik
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10.  Elevated ornithine decarboxylase levels activate ataxia telangiectasia mutated-DNA damage signaling in normal keratinocytes.

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