(Q46489328)

English

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation

scientific article published in July 2005

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

molecular genetics

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author name string

Jayandharan G

1

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Viswabandya A

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Baidya S

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Nair SC

4

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Shaji RV

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Chandy M

6

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Srivastava A

7

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

publication date

1 July 2005

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

Journal of Thrombosis and Haemostasis

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

3

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

7

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

1446-1453

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

The coagulation cascade: initiation, maintenance, and regulation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Nucleotide sequence of the gene for human prothrombin

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Human genes encoding prothrombin and ceruloplasmin map to 11p11-q12 and 3q21-24, respectively

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Rare coagulation deficiencies.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Recessively inherited coagulation disorders.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

A common mutation, Arg457-->Gln, links prothrombin deficiencies in the Puerto Rican population

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Phenotypic and genetic analysis of a compound heterozygote for dys- and hypoprothrombinaemia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Prothrombin Shanghai: hypoprothrombinaemia caused by substitution of Gla29 by Gly.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Prothrombin deficiency results in embryonic and neonatal lethality in mice

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

A critical role for Gly25 in the B chain of human thrombin.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

A natural prothrombin mutant reveals an unexpected influence of A-chain structure on the activity of human alpha-thrombin

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

The prothrombin Denver patient has two different prothrombin point mutations resulting in Glu-300-->Lys and Glu-309-->Lys substitutions

1 reference

https://api.crossref.org/works/10.1111%2FJ.1538-7836.2005.01402.X

21 January 2018

Identifiers

10.1111/J.1538-7836.2005.01402.X

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/15892853

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