A polymorphism in thrombospondin-1 associated with familial premature coronary artery disease alters Ca2+ binding (Q45084832)

9 December 2017

title

A polymorphism in thrombospondin-1 associated with familial premature coronary artery disease alters Ca2+ binding (English)

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9 December 2017

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coronary artery disease

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Blue-leaf A Hannah

1

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9 December 2017

Tina M Misenheimer

series ordinal

2

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9 December 2017

Michelle M Pranghofer

series ordinal

3

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9 December 2017

Deane F Mosher

series ordinal

4

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9 December 2017

language of work or name

English

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publication date

28 September 2004

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Journal of Biological Chemistry

9 December 2017

published in

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9 December 2017

volume

279

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9 December 2017

issue

50

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9 December 2017

page(s)

51915-51922

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Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

9 December 2017

cites work

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21 January 2018

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21 January 2018

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21 January 2018

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Disulfide connectivity of recombinant C-terminal region of human thrombospondin 2

21 January 2018

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Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene

21 January 2018

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Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia

21 January 2018

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Mutations in cartilage oligomeric matrix protein causing pseudoachondroplasia and multiple epiphyseal dysplasia affect binding of calcium and collagen I, II, and IX

21 January 2018

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Cartilage oligomeric matrix protein is a calcium-binding protein, and a mutation in its type 3 repeats causes conformational changes

21 January 2018

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A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats

21 January 2018

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The structure of human thrombospondin, an adhesive glycoprotein with multiple calcium-binding sites and homologies with several different proteins

21 January 2018

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Pseudoachondroplasia and multiple epiphyseal dysplasia: mutation review, molecular interactions, and genotype to phenotype correlations

21 January 2018

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Interactions among the Three Structural Motifs of the C-Terminal Region of Human Thrombospondin-2

21 January 2018

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Measurements of the free luminal ER Ca(2+) concentration with targeted "cameleon" fluorescent proteins

21 January 2018

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Selective intracellular retention of extracellular matrix proteins and chaperones associated with pseudoachondroplasia

21 January 2018

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Molecular and functional differences induced in thrombospondin-1 by the single nucleotide polymorphism associated with the risk of premature, familial myocardial infarction

21 January 2018

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Control of von Willebrand factor multimer size by thrombospondin-1.

21 January 2018

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The von Willebrand factor-reducing activity of thrombospondin-1 is located in the calcium-binding/C-terminal sequence and requires a free thiol at position 974.

21 January 2018

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Thrombospondin-2 polymorphism is associated with a reduced risk of premature myocardial infarction

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M409632200

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9 December 2017

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