Sequence and functional changes in a putative enhancer region upstream of the apolipoprotein(a) gene (Q78663526)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12482558%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

title

Sequence and functional changes in a putative enhancer region upstream of the apolipoprotein(a) gene (English)

1 reference

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15 December 2019

author name string

Loretto H Puckey

series ordinal

1

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15 December 2019

Brian L Knight

series ordinal

2

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15 December 2019

publication date

1 January 2003

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15 December 2019

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15 December 2019

volume

166

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15 December 2019

issue

1

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15 December 2019

page(s)

119-127

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Epidemiology of Lp(a) lipoprotein: its role in atherosclerotic/thrombotic disease.

15 December 2019

cites work

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cDNA sequence of human apolipoprotein(a) is homologous to plasminogen

7 January 2021

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Molecular definition of the extreme size polymorphism in apolipoprotein(a).

7 January 2021

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Apolipoprotein(a) gene accounts for greater than 90% of the variation in plasma lipoprotein(a) concentrations

7 January 2021

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The apolipoprotein (a) gene: a transcribed hypervariable locus controlling plasma lipoprotein (a) concentration

7 January 2021

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Intracellular metabolism of human apolipoprotein(a) in stably transfected Hep G2 cells

7 January 2021

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Variation in lipoprotein(a) concentration associated with different apolipoprotein(a) alleles

7 January 2021

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Detection and quantitation of apolipoprotein(a) mRNA in human liver and its relationship with plasma lipoprotein(a) concentration

7 January 2021

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5' control regions of the apolipoprotein(a) gene and members of the related plasminogen gene family

7 January 2021

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Sequence polymorphisms in the apolipoprotein (a) gene. Evidence for dissociation between apolipoprotein(a) size and plasma lipoprotein(a) levels.

7 January 2021

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C/T polymorphism in the 5' untranslated region of the apolipoprotein(a) gene introduces an upstream ATG and reduces in vitro translation

7 January 2021

1 reference

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Polymorphisms in the apolipoprotein(a) gene and their relationship to allele size and plasma lipoprotein(a) concentration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900315-5

Characterization of multiple enhancer regions upstream of the apolipoprotein(a) gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900315-5

Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664----leu mutation in the LDL receptor gene

7 January 2021

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

7 January 2021

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Estimation of linkage disequilibrium in randomly mating populations

7 January 2021

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Impact of apo(a) length polymorphism and the control of plasma Lp(a) concentrations: evidence for a threshold effect.

7 January 2021

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Lp(a) glycoprotein phenotypes. Inheritance and relation to Lp(a)-lipoprotein concentrations in plasma

7 January 2021

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Interaction of oestrogen and peroxisome proliferator-activated receptors with apolipoprotein(a) gene enhancers

7 January 2021

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LINE-1: a human transposable element

7 January 2021

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Gene structure of apolipoprotein(a) and the regulation of its expression

7 January 2021

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Sequence polymorphisms in the apo(a) gene associated with specific levels of Lp(a) in plasma

7 January 2021

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A pentanucleotide repeat polymorphism in the 5' control region of the apolipoprotein(a) gene is associated with lipoprotein(a) plasma concentrations in Caucasians

7 January 2021

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Genetic architecture and evolution of the lipoprotein(a) trait

7 January 2021

1 reference

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Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibrium

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900315-5

Molecular basis of congenital lp(a) deficiency: a frequent apo(a) 'null' mutation in caucasians

7 January 2021

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Single nucleotide polymorphisms in exons of the apo(a) kringles IV types 6 to 10 domain affect Lp(a) plasma concentrations and have different patterns in Africans and Caucasians

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900315-5

10.1016/S0021-9150(02)00315-5

7 January 2021

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12482558%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

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