(Q33829131)

29 July 2017

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title

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

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29 July 2017

Miserez AR

1

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29 July 2017

Muller PY

series ordinal

2

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29 July 2017

publication date

1 February 2000

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29 July 2017

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29 July 2017

volume

148

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29 July 2017

issue

2

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29 July 2017

page(s)

433-436

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Differences in the Phenotypic Characteristics of Subjects With Familial Defective Apolipoprotein B-100 and Familial Hypercholesterolemia

29 July 2017

cites work

1 reference

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The A985G mutation in the medium-chain acyl-CoA dehydrogenase gene: high prevalence in the Swiss population resident in Geneva

7 January 2021

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In vivo evidence for reduced binding of low density lipoproteins to receptors as a cause of primary moderate hypercholesterolemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

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

7 January 2021

1 reference

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

7 January 2021

1 reference

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Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

Familial defective apolipoprotein B-100 and myocardial infarction. The ECTIM study

7 January 2021

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Familial defective apo B-100, characterization of an Italian family

7 January 2021

1 reference

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Differences in the phenotype between children with familial defective apolipoprotein B-100 and familial hypercholesterolemia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

Familial defective apolipoprotein B-100: mild hypercholesterolaemia without atherosclerosis in a homozygous patient

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

Familial defective apolipoprotein B100: clinical characteristics of 54 cases

7 January 2021

1 reference

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

7 January 2021

1 reference

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Knockout of the mouse apolipoprotein B gene results in embryonic lethality in homozygotes and protection against diet-induced hypercholesterolemia in heterozygotes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2899%2900470-0

10.1016/S0021-9150(99)00470-0

7 January 2021

Identifiers

DOI

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29 July 2017

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