Literature DB >> 9396817

Nested genetic bit analysis (N-GBA) for mutation detection in the p53 tumor suppressor gene.

S R Head1, Y H Rogers, K Parikh, G Lan, S Anderson, P Goelet, M T Boyce-Jacino.   

Abstract

There is a growing and significant demand for reliable, simple and sensitive methods for repeated scanning of a given gene or gene fragment for detection and characterization of mutations. Solid-phase sequencing by single base primer extension of nested GBATM primers on miniaturized DNA arrays can be used to effectively scan targeted sequences for missense, insertion and deletion mutations. This paper describes the use of N-GBA arrays designed to scan the sequence of a 33 base region of exon 8 of the p53 gene (codons 272-282) encompassing a hot spot for mutations associated with the development of cancer. Synthetic DNA templates containing various missense, insertion and deletion mutations, as well as DNA prepared from pancreatic and biliary tumor cells, were genotyped using the exon 8 arrays.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9396817      PMCID: PMC147127          DOI: 10.1093/nar/25.24.5065

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


  9 in total

Review 1.  The p53 tumour suppressor gene and product.

Authors:  A J Levine
Journal:  Cancer Surv       Date:  1992

2.  Accessing genetic information with high-density DNA arrays.

Authors:  M Chee; R Yang; E Hubbell; A Berno; X C Huang; D Stern; J Winkler; D J Lockhart; M S Morris; S P Fodor
Journal:  Science       Date:  1996-10-25       Impact factor: 47.728

Review 3.  The molecular epidemiology of p53 gene mutations in human breast cancer.

Authors:  A Hartmann; H Blaszyk; J S Kovach; S S Sommer
Journal:  Trends Genet       Date:  1997-01       Impact factor: 11.639

4.  Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis.

Authors:  J G Hacia; L C Brody; M S Chee; S P Fodor; F S Collins
Journal:  Nat Genet       Date:  1996-12       Impact factor: 38.330

5.  p53 mutations in pancreatic carcinoma and evidence of common involvement of homocopolymer tracts in DNA microdeletions.

Authors:  M S Redston; C Caldas; A B Seymour; R H Hruban; L da Costa; C J Yeo; S E Kern
Journal:  Cancer Res       Date:  1994-06-01       Impact factor: 12.701

6.  Allelotype of pancreatic adenocarcinoma using xenograft enrichment.

Authors:  S A Hahn; A B Seymour; A T Hoque; M Schutte; L T da Costa; M S Redston; C Caldas; C L Weinstein; A Fischer; C J Yeo
Journal:  Cancer Res       Date:  1995-10-15       Impact factor: 12.701

7.  Allelotype of pancreatic adenocarcinoma.

Authors:  A B Seymour; R H Hruban; M Redston; C Caldas; S M Powell; K W Kinzler; C J Yeo; S E Kern
Journal:  Cancer Res       Date:  1994-05-15       Impact factor: 12.701

8.  Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms.

Authors:  T T Nikiforov; R B Rendle; P Goelet; Y H Rogers; M L Kotewicz; S Anderson; G L Trainor; M R Knapp
Journal:  Nucleic Acids Res       Date:  1994-10-11       Impact factor: 16.971

9.  Mutation detection by highly sensitive methods indicates that p53 gene mutations in breast cancer can have important prognostic value.

Authors:  J S Kovach; A Hartmann; H Blaszyk; J Cunningham; D Schaid; S S Sommer
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-06       Impact factor: 11.205

  9 in total
  10 in total

Review 1.  Mutational analysis using oligonucleotide microarrays.

Authors:  J G Hacia; F S Collins
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

2.  Mining SNPs from EST databases.

Authors:  L Picoult-Newberg; T E Ideker; M G Pohl; S L Taylor; M A Donaldson; D A Nickerson; M Boyce-Jacino
Journal:  Genome Res       Date:  1999-02       Impact factor: 9.043

3.  A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays.

Authors:  T Pastinen; M Raitio; K Lindroos; P Tainola; L Peltonen; A C Syvänen
Journal:  Genome Res       Date:  2000-07       Impact factor: 9.043

4.  Predicting the success of primer extension genotyping assays using statistical modeling.

Authors:  Anton Yuryev; JianPing Huang; Mark Pohl; Robert Patch; Felicia Watson; Peter Bell; Miriam Donaldson; Michael S Phillips; Michael T Boyce-Jacino
Journal:  Nucleic Acids Res       Date:  2002-12-01       Impact factor: 16.971

5.  Sensitive detection of p53 gene mutations by a 'mutant enriched' PCR-SSCP technique.

Authors:  M Behn; M Schuermann
Journal:  Nucleic Acids Res       Date:  1998-03-01       Impact factor: 16.971

6.  Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays.

Authors:  J B Fan; X Chen; M K Halushka; A Berno; X Huang; T Ryder; R J Lipshutz; D J Lockhart; A Chakravarti
Journal:  Genome Res       Date:  2000-06       Impact factor: 9.043

7.  Evaluating the arrayed primer extension resequencing assay of TP53 tumor suppressor gene.

Authors:  Neeme Tõnisson; Jana Zernant; Ants Kurg; Hendrik Pavel; Georg Slavin; Hanno Roomere; Aune Meiel; Pierre Hainaut; Andres Metspalu
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-16       Impact factor: 11.205

8.  Advanced computational techniques for re-sequencing DNA with polymerase signaling assay arrays.

Authors:  Itsik Pe'er; Naama Arbili; Yi Liu; Colby Enck; Craig A Gelfand; Ron Shamir
Journal:  Nucleic Acids Res       Date:  2003-10-01       Impact factor: 16.971

9.  Multiplex detection and genotyping of point mutations involved in charcot-marie-tooth disease using a hairpin microarray-based assay.

Authors:  Yasser Baaj; Corinne Magdelaine; Virginie Ubertelli; Christophe Valat; Yoanne Mousseau; Hao Qiu; Benoît Funalot; Jean-Michel Vallat; Franck G Sturtz
Journal:  Res Lett Biochem       Date:  2009-06-11

10.  Towards Automation for Molecular Diagnosis of Cancer.

Authors:  Maurizio Ferrari; Paola Carrera
Journal:  EJIFCC       Date:  2005-05-17
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.