(Q34184346)

English

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

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

31 July 2017

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

1 reference

Europe PubMed Central

31 July 2017

1 reference

based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

author name string

Blue-leaf A Hannah

1

1 reference

Europe PubMed Central

31 July 2017

Tina M Misenheimer

2

1 reference

Europe PubMed Central

31 July 2017

Douglas S Annis

3

1 reference

Europe PubMed Central

31 July 2017

Deane F Mosher

4

1 reference

Europe PubMed Central

31 July 2017

language of work or name

0 references

publication date

1 March 2003

1 reference

Europe PubMed Central

31 July 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

31 July 2017

278

1 reference

Europe PubMed Central

31 July 2017

8929-8934

1 reference

Europe PubMed Central

31 July 2017

11

1 reference

Europe PubMed Central

31 July 2017

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Thrombospondins: multifunctional regulators of cell interactions

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Platelet-derived growth factor and heparin-like glycosaminoglycans regulate thrombospondin synthesis and deposition in the matrix by smooth muscle cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Mapping of epitopes for monoclonal antibodies against human platelet thrombospondin with electron microscopy and high sensitivity amino acid sequencing

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Identification of nine novel mutations in cartilage oligomeric matrix protein in patients with pseudoachondroplasia and multiple epiphyseal dysplasia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Trinucleotide expansion mutations in the cartilage oligomeric matrix protein (COMP) gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Mutations in the cartilage oligomeric matrix protein (COMP) gene in pseudoachondroplasia and multiple epiphyseal dysplasia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

A thrombospondin homologue in Drosophila melanogaster: cDNA and protein structure.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Functional measurements of [Ca2+] in the endoplasmic reticulum using a herpes virus to deliver targeted aequorin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Dynamics of [Ca2+] in the endoplasmic reticulum and cytoplasm of intact HeLa cells. A comparative study

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Theoretical estimation of the capacity of intracellular calcium stores in the Bergmann glial cell.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Smooth muscle cell immediate-early gene and growth factor activation follows vascular injury. A putative in vivo mechanism for autocrine growth.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Thrombospondin mediates migration and potentiates platelet-derived growth factor-dependent migration of calf pulmonary artery smooth muscle cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Thiol-disulfide exchange by thrombospondin: evidence for a thiol and a disulfide bond protected by calcium

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Multiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African family

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

A cartilage oligomeric matrix protein mutation associated with pseudoachondroplasia changes the structural and functional properties of the type 3 domain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Disease-causing mutations in cartilage oligomeric matrix protein cause an unstructured Ca2+ binding domain

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

The fate of cartilage oligomeric matrix protein is determined by the cell type in the case of a novel mutation in pseudoachondroplasia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Calreticulin, PDI, Grp94 and BiP chaperone proteins are associated with retained COMP in pseudoachondroplasia chondrocytes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Expression of recombinant matrix components using baculoviruses

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M211185200

21 January 2018

Identifiers

10.1074/JBC.M211185200

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34184346&oldid=1972049524"