Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region. (Q38905795)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

main subject

Italy

0 references

factor VII deficiency

1 reference

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

author name string

F Bernardi

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

P Patracchini

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

M Ferrati

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

P Arcieri

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

M Papacchini

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

R Redaelli

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

F Baudo

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

G Mariani

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

G Marchetti

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

publication date

1 November 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

volume

92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

page(s)

446-450

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8244334%20AND%20SRC:MED&resulttype=core&format=json

Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male

27 October 2019

cites work

1 reference

12 December 2020

The human factor VII gene is polymorphic due to variation in repeat copy number in a minisatellite

1 reference

12 December 2020

Factor IX is activated in vivo by the tissue factor mechanism

1 reference

12 December 2020

A frequent factor XII gene mutation in Hageman trait

1 reference

12 December 2020

A de novo and heterozygous gene deletion causing a variant of von Willebrand disease

1 reference

12 December 2020

Activation of factor VII bound to tissue factor: a key early step in the tissue factor pathway of blood coagulation

1 reference

12 December 2020

Congenital SPCA deficiency: a hitherto unrecognized coagulation defect with hemorrhage rectified by serum and serum fractions

1 reference

12 December 2020

A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide

1 reference

12 December 2020

Factor VII congenital deficiency. Clinical picture and classification of the variants

1 reference

12 December 2020

Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7)

1 reference

12 December 2020

Expression of factor X and its significance for the determination of paramyxovirus tropism in the chick embryo

1 reference

12 December 2020

Carrier detection in factor VII congenital deficiency

1 reference

12 December 2020

Factor XI deficiency in Ashkenazi Jews in Israel

1 reference

12 December 2020

Mechanism of activation of bovine factor VII. Products of cleavage by factor Xa

1 reference

12 December 2020

PCR detection of a repeat polymorphism within the F7 gene

1 reference

12 December 2020

Factor VII Padua defect: the heterozygote population

1 reference

12 December 2020

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

12 December 2020

Purification and properties of human coagulation factor VII.

1 reference

12 December 2020

Cooperative activation of human factor IX by the human extrinsic pathway of blood coagulation

1 reference

12 December 2020

Dynamic mutations: a new class of mutations causing human disease

1 reference

12 December 2020

Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation

1 reference

12 December 2020

Characterization of a cDNA coding for human factor VII

1 reference

12 December 2020

Prenatal exclusion of severe factor VII deficiency by DNA sequencing

1 reference

12 December 2020

Structure and evolution of the human genes encoding protein C and coagulation factors VII, IX, and X

1 reference

12 December 2020