(Q45875043)

English

Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling

scientific article published in April 1993

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

Nucleotide substitutions at the -6 position in the promoter region of the factor IX gene result in different severity of hemophilia B Leyden: consequences for genetic counseling (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

0 references

coagulation factor IX

0 references

0 references

author name string

D Vidaud

1

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

M Tartary

2

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

J M Costa

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

B R Bahnak

4

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

S Gispert-Sanchez

5

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

E Fressinaud

6

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

C Gazengel

7

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

D Meyer

8

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

M Goossens

9

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

J M Lavergne

10

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

publication date

1 April 1993

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

91

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

3

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

241-244

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

https://scigraph.springernature.com/pub.10.1007/bf00218264

0 references

Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single base pair deletion in the promoter region of the factor IX gene is associated with haemophilia B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Why does the human factor IX gene have a G + C content of 40%?

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of antihemophilic factor on one-stage clotting tests; a presumptive test for hemophilia and a simple one-stage antihemophilic factor assy procedure

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and functional basis of the developmental regulation of human coagulation factor IX gene: factor IX Leyden

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that descendants of three founders constitute about 25% of hemophilia B in the United States

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zinc finger-DNA recognition: crystal structure of a Zif268-DNA complex at 2.1 A

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

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/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemophilia B: database of point mutations and short additions and deletions--second edition

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

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/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Another Genetic Variant of Haemophilia B: Haemophilia B Leyden

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A less severe form of Haemophilia B Leyden

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An A to T transversion at position −5 of the Factor IX promoter results in hemophilia B

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hemophilia B Leyden: a sex-linked hereditary disorder that improves after puberty

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification and properties of an abnormal blood coagulation factor IX (factor IXBm)/kinetics of its inhibition of factor X activation by factor VII and bovine tissue factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative sequence analysis of mammalian factor IX promoters.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of a C/EBP binding site in the factor IX promoter is associated with haemophilia B.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The putative factor IX gene promoter in hemophilia B Leyden

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection in severe (type III) von Willebrand disease using two intragenic restriction fragment length polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8478007

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00218264

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 December 2017

http://europepmc.org/abstract/MED/8478007

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