Literature DB >> 1612597

Strand-separating conformational polymorphism analysis: efficacy of detection of point mutations in the human ornithine delta-aminotransferase gene.

J Michaud1, L C Brody, G Steel, G Fontaine, L S Martin, D Valle, G Mitchell.   

Abstract

We tested the use of a modified method of single-strand conformational polymorphism (SSCP) analysis for the detection of point mutations in the human ornithine-delta-aminotransferase gene. Using a combination of three different electrophoretic conditions, we detected 20/20 known mutations. In a prospective study of 24 previously uncharacterized mutant OAT genes, we found 13 different mutations accounting for 19 (79%) of the 24. We conclude that SSCP is an efficient technique with high sensitivity and specificity.

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Year:  1992        PMID: 1612597     DOI: 10.1016/0888-7543(92)90258-t

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  27 in total

1.  Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection.

Authors:  P Kozlowski; W J Krzyzosiak
Journal:  Nucleic Acids Res       Date:  2001-07-15       Impact factor: 16.971

2.  High resolution SSCP by optimization of the temperature by transverse TGGE.

Authors:  X Chen; T Baumstark; G Steger; D Riesner
Journal:  Nucleic Acids Res       Date:  1995-11-11       Impact factor: 16.971

3.  Transverse formamide gradients as a simple and easy way to optimise DNA single-strand conformation polymorphism analysis.

Authors:  B Paccoud; J Bourguignon; M Diarra-Mehrpour; J P Martin; R Sesboüé
Journal:  Nucleic Acids Res       Date:  1998-05-01       Impact factor: 16.971

4.  HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q.

Authors:  G A Mitchell; P T Ozand; M F Robert; L Ashmarina; J Roberts; K M Gibson; R J Wanders; S Wang; I Chevalier; E Plöchl; H Miziorko
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

5.  Ornithine-δ-Aminotransferase Inhibits Neurogenesis During Xenopus Embryonic Development.

Authors:  Ying Peng; Sandra K Cooper; Yi Li; Jay M Mei; Shuwei Qiu; Gregory L Borchert; Steven P Donald; Hsiang-Fu Kung; James M Phang
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-04       Impact factor: 4.799

6.  Acute intermittent porphyria: identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal expression of the erythroid-specific enzyme.

Authors:  C H Chen; K H Astrin; G Lee; K E Anderson; R J Desnick
Journal:  J Clin Invest       Date:  1994-11       Impact factor: 14.808

7.  Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers.

Authors:  Paul J Goodfellow; Barbara M Buttin; Thomas J Herzog; Janet S Rader; Randall K Gibb; Elizabeth Swisher; Katherine Look; Ken C Walls; Ming-Yu Fan; David G Mutch
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-05       Impact factor: 11.205

8.  Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.

Authors:  C C Chang; S J Gould
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

9.  Single-strand conformational polymorphism and direct sequencing applied to carrier testing in families with ornithine transcarbamylase deficiency.

Authors:  M Y Tsai; R A Holzknecht; M Tuchman
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

10.  Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

Authors:  D S Warren; J C Morrell; H W Moser; D Valle; S J Gould
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

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