Literature DB >> 1673116

Localisation of RFLPs of the medium chain acyl-CoA dehydrogenase gene.

A I Blakemore1, S Kolvraa, N Gregersen, P C Engel, D Curtis.   

Abstract

Six restriction fragment length polymorphisms (RFLPs) of the gene are described. Three of these are in linkage disequilibrium. Hybridisation with sub-probes allowed localisation of the RFLPs to different regions of the gene.

Entities:  

Mesh：

Substances：

Year:  1991        PMID： 1673116     DOI： 10.1007/bf00194652

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  5 in total

1.  BamHI and MspI RFLP's in strong linkage disequilibrium at the medium chain acyl-coenzyme A dehydrogenase locus (ACADM chromosome 1).

Authors:  A I Blakemore; P C Engel; D Curtis
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

2.  PstI RFLP at the medium chain acyl-coenzyme A dehydrogenase locus (ACADM chromosome 1).

Authors:  A I Blakemore; P C Engel; D Curtis
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

3.  Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci.

Authors:  J C Murray; R Shiang; L R Carlock; M Smith; K H Buetow
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

4.  Nucleotide sequence of medium-chain acyl-CoA dehydrogenase mRNA and its expression in enzyme-deficient human tissue.

Authors:  D P Kelly; J J Kim; J J Billadello; B E Hainline; T W Chu; A W Strauss
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

5.  Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli.

Authors:  N Gregersen; B S Andresen; P Bross; V Winter; N Rüdiger; S Engst; E Christensen; D Kelly; A W Strauss; S Kølvraa
Journal:  Hum Genet       Date:  1991-04       Impact factor: 4.132
  5 in total
  4 in total

1.  Most cases of medium-chain acyl-CoA dehydrogenase deficiency escape detection in France.

Authors:  B Fromenty; A Mansouri; J P Bonnefont; F Courtois; A Munnich; D Rabier
Journal:  Hum Genet       Date:  1996-03       Impact factor: 4.132

2.  The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene.

Authors:  S Kølvraa; N Gregersen; A I Blakemore; A K Schneidermann; V Winter; B S Andresen; D Curtis; P C Engel; D Pricille; W Rhead
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

3.  Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death.

Authors:  D P Kelly; D E Hale; S L Rutledge; M L Ogden; A J Whelan; Z Zhang; A W Strauss
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

4.  Three RFLPs defining a haplotype associated with the common mutation in human medium-chain acyl-CoA dehydrogenase (MCAD) deficiency occur in Alu repeats.

Authors:  Z Zhang; S Kolvraa; Y Zhou; D P Kelly; N Gregersen; A W Strauss
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.