Literature DB >> 8478017

Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction.

Y Friedlander, E J Dann, E Leitersdorf.   

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Year:  1993        PMID： 8478017     DOI： 10.1007/bf00218280

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


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  14 in total

1.  Using mutagenic polymerase chain reaction primers to detect carriers of familial defective apolipoprotein B-100.

Authors:  C Motti; H Funke; S Rust; A Dergunov; G Assmann
Journal:  Clin Chem       Date:  1991-10       Impact factor: 8.327

2.  Apolipoprotein B gene mutations in Austrian subjects with heart disease and their kindred.

Authors:  W Friedl; E H Ludwig; M E Balestra; K S Arnold; B Paulweber; F Sandhofer; B J McCarthy; T L Innerarity
Journal:  Arterioscler Thromb       Date:  1991 Mar-Apr

3.  Hypercholesterolaemia due to familial defective apolipoprotein B-100 in two Australian families.

Authors:  J L Hosking; R Bais; P D Roach; D W Thomas
Journal:  Med J Aust       Date:  1991-10-21       Impact factor: 7.738

4.  Allele frequency estimation from data on relatives.

Authors:  M Boehnke
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

5.  Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten cases.

Authors:  A Tybjaerg-Hansen; J Gallagher; J Vincent; R Houlston; P Talmud; A M Dunning; M Seed; A Hamsten; S E Humphries; N B Myant
Journal:  Atherosclerosis       Date:  1990-01       Impact factor: 5.162

6.  Analysis of biochemical genetic data on Jewish populations: II. Results and interpretations of heterogeneity indices and distance measures with respect to standards.

Authors:  S Karlin; R Kenett; B Bonné-Tamir
Journal:  Am J Hum Genet       Date:  1979-05       Impact factor: 11.025

7.  The role of XbaI polymorphism of the apolipoprotein B gene in determining levels and covariability of lipid and lipoprotein variables in a sample of Israeli offspring with family history of myocardial infarction.

Authors:  Y Friedlander; N A Kaufmann; H Cedar; N Weinberg; J D Kark
Journal:  Atherosclerosis       Date:  1993-01-25       Impact factor: 5.162

8.  Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.

Authors:  L F Soria; E H Ludwig; H R Clarke; G L Vega; S M Grundy; B J McCarthy
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

Review 9.  Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.

Authors:  T L Innerarity; R W Mahley; K H Weisgraber; T P Bersot; R M Krauss; G L Vega; S M Grundy; W Friedl; J Davignon; B J McCarthy
Journal:  J Lipid Res       Date:  1990-08       Impact factor: 5.922

10.  Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100.

Authors:  E H Ludwig; B J McCarthy
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025
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  1 in total

Review 1.  ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature.

Authors:  Amira S Sabbagh; Rose T Daher; Zaher K Otrock; Rabab N Abdel Khalek; Ghazi S Zaatari; Rami A R Mahfouz
Journal:  Mol Biol Rep       Date:  2006-12-08       Impact factor: 2.316
  1 in total

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