(Q46866530)

English

CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool

scientific article published in March 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

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1 reference

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author name string

Rebecca E Saunders

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

Stephen J Perkins

2

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

publication date

1 March 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

29

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

333-344

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

Exon and domain evolution in the proenzymes of blood coagulation and fibrinolysis

1 reference

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Databases in peril

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Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency

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Automatic extraction of mutations from Medline and cross-validation with OMIM.

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Comparative protein modelling by satisfaction of spatial restraints

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Factor XI deficiency database: an interactive web database of mutations, phenotypes, and structural analysis tools

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An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations

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The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

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Locus-specific mutation databases: pitfalls and good practice based on the p53 experience

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The extended interactions and Gla domain of blood coagulation factor Xa

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Identifiers

10.1002/HUMU.20629

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/18058827

ResearchGate publication ID

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