Literature DB >> 1360285

First International Workshop on Familial Defective apo B-100, Munich, November 1991.

H Schuster1, S Humphries, G Rauh, C Keller.   

Abstract

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Year:  1992        PMID： 1360285     DOI： 10.1007/bf00180448

Source DB:  PubMed          Journal:  Clin Investig        ISSN： 0941-0198


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  21 in total

1.  Poor response to simvastatin in familial defective apo-B-100.

Authors:  A Corsini; M Mazzotti; R Fumagalli; A L Catapano; L Romano; C Romano
Journal:  Lancet       Date:  1991-02-02       Impact factor: 79.321

2.  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

3.  Low density lipoprotein-induced growth of U937 cells: a novel method to determine the receptor binding of low density lipoprotein.

Authors:  J Frostegård; A Hamsten; M Gidlund; J Nilsson
Journal:  J Lipid Res       Date:  1990-01       Impact factor: 5.922

4.  Familial defective apolipoprotein B-100: enhanced binding of monoclonal antibody MB47 to abnormal low density lipoproteins.

Authors:  K H Weisgraber; T L Innerarity; Y M Newhouse; S G Young; K S Arnold; R M Krauss; G L Vega; S M Grundy; R W Mahley
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

5.  Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100.

Authors:  G Rauh; H Schuster; J Fischer; C Keller; G Wolfram; N Zöllner
Journal:  Klin Wochenschr       Date:  1991-05-03

6.  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

7.  Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemia.

Authors:  P Talmud; A Tybjaerg-Hansen; D Bhatnagar; A Mbewu; J P Miller; P Durrington; S Humphries
Journal:  Atherosclerosis       Date:  1991-08       Impact factor: 5.162

Review 8.  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

9.  Allele-specific and asymmetric polymerase chain reaction amplification in combination: a one step polymerase chain reaction protocol for rapid diagnosis of familial defective apolipoprotein B-100.

Authors:  H Schuster; G Rauh; S Müller; C Keller; G Wolfram; N Zöllner
Journal:  Anal Biochem       Date:  1992-07       Impact factor: 3.365

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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