(Q38424000)

English

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software

scientific article published on March 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

relational database

1 reference

based on heuristic

inferred from title

George P Patrinos

8

object named as

George P Patrinos

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

author name string

Sophia Zaimidou

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Sjozef van Baal

2

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Timothy D Smith

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Konstantinos Mitropoulos

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Mila Ljujic

5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Dragica Radojkovic

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Richard G Cotton

7

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

1 March 2009

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

30

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

308-313

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

UMD (Universal mutation database): a generic software to build and analyze locus-specific databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Recommendations for locus-specific databases and their curation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

The long suffering of Frederic Chopin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

The Electrophoretic α;1-Globulin Pattern of Serum in α;1-Antitrypsin Deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Complete sequence of the cDNA for human .alpha.1-antitrypsin and the gene for the S variant

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Alpha1-antitrypsin deficiency. 1: epidemiology of alpha1-antitrypsin deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

DNA, diseases and databases: disastrously deficient

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Hellenic National Mutation database: a prototype database for mutations leading to inherited disorders in the Hellenic population.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

VariVis: a visualisation toolkit for variation databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Alpha1-antitrypsin deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

Alpha1-antitrypsin deficiency in childhood.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

National and ethnic mutation databases: recording populations' genography

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

21 January 2018

MuStaR and other software for locus-specific mutation databases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

A survey of locus-specific database curation. Human Genome Variation Society

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthesis of antithrombin III and alpha-1-antitrypsin by the perfused rat liver

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

Alpha1-antitrypsin polymerization and the serpinopathies: pathobiology and prospects for therapy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic predisposition to chronic obstructive pulmonary disease: advances in alpha1-antitrypsin deficiency and the serpinopathies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

Endothelial nitric oxide synthase as a potential susceptibility gene in the pathogenesis of emphysema in alpha1-antitrypsin deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20857

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.20857

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

ResearchGate publication ID

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