Literature DB >> 2690813

Detection of single base changes in nucleic acids.

R G Cotton1.   

Abstract

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Year:  1989        PMID： 2690813      PMCID： PMC1133383          DOI： 10.1042/bj2630001

Source DB:  PubMed          Journal:  Biochem J        ISSN： 0264-6021            Impact factor:   3.857


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  104 in total

1.  Detection of sickle-cell mutation by electrophoresis of partial RNA:DNA hybrids following solution hybridization.

Authors:  F S Jones; J I Grimberg; S G Fischer; J P Ford
Journal:  Gene       Date:  1985       Impact factor: 3.688

2.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Authors:  R K Saiki; S Scharf; F Faloona; K B Mullis; G T Horn; H A Erlich; N Arnheim
Journal:  Science       Date:  1985-12-20       Impact factor: 47.728

3.  A rapid method of gene detection using DNA bound to Sephacryl.

Authors:  J A Langdale; A D Malcolm
Journal:  Gene       Date:  1985       Impact factor: 3.688

4.  Mismatches in DNA double strands: thermodynamic parameters and their correlation to repair efficiencies.

Authors:  H Werntges; G Steger; D Riesner; H J Fritz
Journal:  Nucleic Acids Res       Date:  1986-05-12       Impact factor: 16.971

5.  Fluorescence detection in automated DNA sequence analysis.

Authors:  L M Smith; J Z Sanders; R J Kaiser; P Hughes; C Dodd; C R Connell; C Heiner; S B Kent; L E Hood
Journal:  Nature       Date:  1986 Jun 12-18       Impact factor: 49.962

6.  Detection of single base substitutions in influenza virus RNA molecules by denaturing gradient gel electrophoresis of RNA-RNA or DNA-RNA heteroduplexes.

Authors:  F I Smith; J D Parvin; P Palese
Journal:  Virology       Date:  1986-04-15       Impact factor: 3.616

7.  Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes.

Authors:  R M Myers; Z Larin; T Maniatis
Journal:  Science       Date:  1985-12-13       Impact factor: 47.728

8.  Detection of single base-pair mismatches in DNA by chemical modification followed by electrophoresis in 15% polyacrylamide gel.

Authors:  D F Novack; N J Casna; S G Fischer; J P Ford
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

9.  Detection of Coxsackie-B-virus-specific RNA sequences in myocardial biopsy samples from patients with myocarditis and dilated cardiomyopathy.

Authors:  N E Bowles; P J Richardson; E G Olsen; L C Archard
Journal:  Lancet       Date:  1986-05-17       Impact factor: 79.321

10.  Structure of an adenine-cytosine base pair in DNA and its implications for mismatch repair.

Authors:  W N Hunter; T Brown; N N Anand; O Kennard
Journal:  Nature       Date:  1986 Apr 10-16       Impact factor: 49.962
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  18 in total

1.  Multiplex allele-specific target amplification based on PCR suppression.

Authors:  N E Broude; L Zhang; K Woodward; D Englert; C R Cantor
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-02       Impact factor: 11.205

2.  Detection of multiallele polymorphisms within gene sequences by GC-clamped denaturing gradient gel electrophoresis.

Authors:  V C Sheffield; J S Beck; B Nichols; A Cousineau; A C Lidral; E M Stone
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

3.  Polymorphisms in the human X-linked pyruvate dehydrogenase E1 alpha gene.

Authors:  H H Dahl; W M Hutchison; Z Guo; S M Forrest; L L Hansen
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

Review 4.  Genetic causes of aortic aneurysms. Unlearning at least part of what the textbooks say.

Authors:  H Kuivaniemi; G Tromp; D J Prockop
Journal:  J Clin Invest       Date:  1991-11       Impact factor: 14.808

5.  Detection of single-base mutations by reaction of DNA heteroduplexes with a water-soluble carbodiimide followed by primer extension: application to products from the polymerase chain reaction.

Authors:  A Ganguly; D J Prockop
Journal:  Nucleic Acids Res       Date:  1990-07-11       Impact factor: 16.971

6.  Detection of DNA sequence polymorphisms among wheat varieties.

Authors:  S He; H Ohm; S Mackenzie
Journal:  Theor Appl Genet       Date:  1992-08       Impact factor: 5.699

7.  Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samples.

Authors:  S M Forrest; H H Dahl; D W Howells; I Dianzani; R G Cotton
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

8.  Inheritance of an RNA splicing mutation (G+ 1 IVS20) in the type III procollagen gene (COL3A1) in a family having aortic aneurysms and easy bruisability: phenotypic overlap between familial arterial aneurysms and Ehlers-Danlos syndrome type IV.

Authors:  S Kontusaari; G Tromp; H Kuivaniemi; R L Ladda; D J Prockop
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

Review 9.  Diagnosis of human genetic disease using recombinant DNA. Fourth edition.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

10.  Characterization of the mutations in three patients with pyruvate dehydrogenase E1 alpha deficiency.

Authors:  L L Hansen; G K Brown; D M Kirby; H H Dahl
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982
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