(Q45883457)

English

Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD).

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scholarly article

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

Two factor IX mutations in the family of an isolated haemophilia B patient: direct carrier diagnosis by amplification mismatch detection (AMD). (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

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coagulation factor IX

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1 reference

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inferred from title

author name string

A J Montandon

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

P M Green

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

D R Bentley

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

R Ljung

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

I M Nilsson

5

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

F Giannelli

6

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

publication date

1 July 1990

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Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

85

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

200-204

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

https://scigraph.springernature.com/pub.10.1007/bf00193196

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Structure of crystalline -chymotrypsin. V. The atomic structure of tosyl- -chymotrypsin at 2 A resolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel trypsin-like serine protease (hepsin) with a putative transmembrane domain expressed by human liver and hepatoma cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathology of haemophilia B

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of sickle cell anaemia and thalassaemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of an almost full-length cDNA coding for human blood coagulation factor X

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct detection of point mutations by mismatch analysis: application to haemophilia B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide sequence of the gene for human factor IX (antihemophilic factor B)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of normal factor IX detected by mouse monoclonal antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computer-generated models of blood coagulation factor Xa, factor IXa, and thrombin based upon structural homology with other serine proteases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The first EGF-like domain from human factor IX contains a high-affinity calcium binding site

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of beta-hydroxyaspartate and adjacent carboxylate residues in the first EGF domain of human factor IX

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a cDNA coding for human factor VII

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene structure of human anti-haemophilic factor IX.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the complementary deoxyribonucleic acid and gene coding for human prothrombin

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional localization of the human factor IX gene by molecular hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of a cDNA coding for human protein C

1 reference

https://pubmed.ncbi.nlm.nih.gov/2370049

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00193196

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/2370049

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