Literature DB >> 3652907

DNA sequence of the human apolipoprotein B gene.

E H Ludwig1, B D Blackhart, V R Pierotti, L Caiati, C Fortier, T Knott, J Scott, R W Mahley, B Levy-Wilson, B J McCarthy.   

Abstract

The sequence of the human apolipoprotein B gene comprises 43 kb divided into 29 exons, one of which is unusually long and contains 7572 bp. Comparison of the gene sequence with four complete and three partial cDNA sequences published elsewhere reveals a total of 60 nucleotide substitutions and 39 amino acid substitutions and one small deletion in the signal peptide.

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Year:  1987        PMID： 3652907     DOI： 10.1089/dna.1987.6.363

Source DB:  PubMed          Journal:  DNA        ISSN： 0198-0238


  23 in total

1.  Gene assignment in Ateles paniscus chamek (Platyrrhini, Primates). Allocation of 18 markers of human syntenic groups 1, 2, 7, 14, 15, 17 and 22.

Authors:  H N Seuánez; C R Lima; B Lemos; C R Bonvicino; M A Moreira; F C Canavez
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

2.  Low density lipoprotein heterogeneity in spontaneously hypercholesterolemic pigs.

Authors:  S T Cooper; R J Aiello; W J Checovich; A D Attie
Journal:  Mol Cell Biochem       Date:  1992-08-18       Impact factor: 3.396

3.  The elimination of primer-dimer accumulation in PCR.

Authors:  J Brownie; S Shawcross; J Theaker; D Whitcombe; R Ferrie; C Newton; S Little
Journal:  Nucleic Acids Res       Date:  1997-08-15       Impact factor: 16.971

4.  Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region.

Authors:  E Boerwinkle; W J Xiong; E Fourest; L Chan
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

5.  DNase I- and micrococcal nuclease-hypersensitive sites in the human apolipoprotein B gene are tissue specific.

Authors:  B Levy-Wilson; C Fortier; B D Blackhart; B J McCarthy
Journal:  Mol Cell Biol       Date:  1988-01       Impact factor: 4.272

6.  Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B (B-31). A unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins.

Authors:  S G Young; S T Hubl; R S Smith; S M Snyder; J F Terdiman
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

7.  Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

Authors:  C R Newton; A Graham; L E Heptinstall; S J Powell; C Summers; N Kalsheker; J C Smith; A F Markham
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

8.  The polymorphism ApoB/4311 in patients with myocardial infarction and controls: the ECTIM Study.

Authors:  J F Moreel; G Roizes; A E Evans; D Arveiler; J P Cambou; C Souriau; H J Parra; E Desmarais; J C Fruchart; P Ducimetière
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

9.  High-resolution analysis of a hypervariable region in the human apolipoprotein B gene.

Authors:  E H Ludwig; W Friedl; B J McCarthy
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

Review 10.  Recent advances in lipoprotein and atherosclerosis research at Baylor College of Medicine. Apolipoprotein B, lipoprotein[a], and transplantation arteriopathy.

Authors:  C M Ballantyne; L Chan; J Guevara; J D Morrisett; M P Mims; A M Gotto
Journal:  Tex Heart Inst J       Date:  1994
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