(Q34207867)

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Expression of the familial hypercholesterolemia gene in heterozygotes: mechanism for a dominant disorder in man.

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Europe PubMed Central

31 July 2017

Expression of the familial hypercholesterolemia gene in heterozygotes: mechanism for a dominant disorder in man. (English)

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31 July 2017

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familial hypercholesterolemia

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2

J L Goldstein

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31 July 2017

M S Brown

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4366052

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English

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1 July 1974

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31 July 2017

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185

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61-63

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31 July 2017

4145

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Regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in human fibroblasts by lipoproteins

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.185.4145.61

Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.185.4145.61

Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.185.4145.61

The metabolism of low density lipoprotein in familial type II hyperlipoproteinemia

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.185.4145.61

THE INHERITANCE OF ESSENTIAL FAMILIAL HYPERCHOLESTEROLEMIA

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1126/SCIENCE.185.4145.61

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10.1126/SCIENCE.185.4145.61

1 reference

stated in

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

PubMed ID

4366052

retrieved

31 July 2017

(Q34207867)

Expression of the familial hypercholesterolemia gene in heterozygotes: mechanism for a dominant disorder in man.

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