(Q36679415)

15 August 2017

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title

ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature (English)

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15 August 2017

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5

Ghazi S Zaatari

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15 August 2017

6

Rami A R Mahfouz

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15 August 2017

3

Zaher K Otrock

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15 August 2017

1

Amira S Sabbagh

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15 August 2017

4

Rabab N Abdel Khalek

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15 August 2017

Rose T Daher

2

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15 August 2017

8 December 2006

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Molecular Biology Reports

15 August 2017

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15 August 2017

34

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15 August 2017

4

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15 August 2017

267-270

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https://scigraph.springernature.com/pub.10.1007/s11033-006-9041-7

15 August 2017

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cites work

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

1 reference

12 December 2020

The molecular basis of familial hypercholesterolaemia in Turkish patients

1 reference

12 December 2020

Familial hypercholesterolemia in Morocco: first report of mutations in the LDL receptor gene.

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12 December 2020

Structure of the human apolipoprotein B gene.

1 reference

12 December 2020

[Familial defect of apo B-100 in subjects with clinically diagnosed primary hypercholesterolemia: identification of the first family with this disorder in Spain]

1 reference

12 December 2020

Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from southern Italy

1 reference

12 December 2020

Familial hypercholesterolemia in St-Petersburg: the known and novel mutations found in the low density lipoprotein receptor gene in Russia

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12 December 2020

Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patients

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12 December 2020

[Application of DNA analysis for differential diagnosis of familial hypercholesterolemia and familial defect of apolipoprotein b-100]

1 reference

12 December 2020

The molecular mechanism for the genetic disorder familial defective apolipoprotein B100.

1 reference

12 December 2020

[Absence of DNA polymorphisms on the region of the APOV gene coding the proposed low density lipoprotein-binding domain of the ApoB-100 protein]

1 reference

12 December 2020

A receptor-mediated pathway for cholesterol homeostasis

1 reference

12 December 2020

Estimation of the age of the ancestral arginine3500-->glutamine mutation in human apoB-100

1 reference

12 December 2020

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

1 reference

12 December 2020

LDL-R and Apo-B-100 gene mutations in Polish familial hypercholesterolemias

1 reference

12 December 2020

Molecular characterization of familial hypercholesterolemia in German and Greek patients.

1 reference

12 December 2020

Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding

1 reference

12 December 2020

The mutation APOB-100 R3500Q in Eastern Europe

1 reference

12 December 2020

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

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12 December 2020

High frequency of the ApoB-100 R3500Q mutation in Bulgarian hypercholesterolaemic subjects

1 reference

12 December 2020

Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics.

1 reference

12 December 2020

Turkish Heart Study: lipids, lipoproteins, and apolipoproteins

1 reference

12 December 2020

Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia.

1 reference

12 December 2020

Familial defective apolipoprotein B-100: a mutation emerged in the mesolithic ancestors of Celtic peoples?

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12 December 2020

[Incidence of familial defective apolipoprotein B-100 in cases of patients diagnosed with familial hypercholesterolemia]

1 reference

12 December 2020

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

1 reference

12 December 2020

A unique haplotype of the apolipoprotein B-100 allele associated with familial defective apolipoprotein B-100 in a Chinese man discovered during a study of the prevalence of this disorder.

1 reference

12 December 2020

Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich

1 reference

12 December 2020

Familial defective apolipoprotein B-100: detection and haplotype analysis of the Arg(3500)-->Gln mutation in hyperlipidemic Chinese

1 reference

12 December 2020

Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol

1 reference

12 December 2020

Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language

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12 December 2020

The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia

1 reference

12 December 2020

High prevalence of familial defective apolipoprotein B-100 in Switzerland.

1 reference

12 December 2020

10.1007/S11033-006-9041-7

Identifiers

DOI

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15 August 2017

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PubMed ID

17160438