(Q68214111)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634227%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

title

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

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22 September 2019

3

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22 September 2019

author name string

G Marchetti

1

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22 September 2019

P Patracchini

2

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22 September 2019

V DeRosa

4

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22 September 2019

M Pinotti

5

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22 September 2019

G Rodorigo

6

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22 September 2019

A Casonato

7

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22 September 2019

A Girolami

8

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22 September 2019

F Bernardi

9

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22 September 2019

publication date

1 July 1992

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22 September 2019

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22 September 2019

volume

89

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22 September 2019

issue

5

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22 September 2019

page(s)

497-502

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https://scigraph.springernature.com/pub.10.1007/bf00219173

22 September 2019

exact match

0 references

cites work

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

1 reference

12 December 2020

Partial structure of the human alpha 2(IV) collagen chain and chromosomal localization of the gene (COL4A2)

1 reference

12 December 2020

Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8

1 reference

12 December 2020

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

1 reference

12 December 2020

Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene

1 reference

12 December 2020

Detection of single base substitutions in total genomic DNA

1 reference

12 December 2020

Molecular pathology of haemophilia B

1 reference

12 December 2020

Classical factor X deficiency. Report of a further case

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

DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory

1 reference

12 December 2020

Epidemiological investigation of the prevalence of von Willebrand's disease

1 reference

12 December 2020

Activation of human factor VII in plasma and in purified systems: roles of activated factor IX, kallikrein, and activated factor XII

1 reference

12 December 2020

Factor VIIa-catalyzed activation of factor X independent of tissue factor: its possible significance for control of hemophilic bleeding by infused factor VIIa

1 reference

12 December 2020

Factor VII Padua 2: another factor VII abnormality with defective ox brain thromboplastin activation and a complex hereditary pattern

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

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

1 reference

12 December 2020

Use of human factor VIIa in the treatment of two hemophilia A patients with high-titer inhibitors

1 reference

12 December 2020

Factor VII Padua defect: the heterozygote population

1 reference

12 December 2020

Concurrence of von Willebrand's disease and hemophilia A: implications for carrier detection and prevalence

1 reference

12 December 2020

DNA sequencing with Thermus aquaticus DNA polymerase and direct sequencing of polymerase chain reaction-amplified DNA

1 reference

12 December 2020

DNA sequencing with chain-terminating inhibitors

1 reference

12 December 2020

Factor VII verona coagulation disorder: double heterozygosis with an abnormal factor VII and heterozygous factor VII deficiency

1 reference

12 December 2020

Purification and properties of human coagulation factor VII.

1 reference

12 December 2020

Molecular defect in coagulation factor XFriuli results from a substitution of serine for proline at position 343

1 reference

12 December 2020

The single copy gene coding for human alpha 1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13.

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

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene

1 reference

12 December 2020

Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern

1 reference

12 December 2020

Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34)

1 reference

12 December 2020

Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysis.

1 reference

12 December 2020

Activation of bovine factor VII (proconvertin) by factor XIIa (activated Hageman factor)

1 reference

12 December 2020

Amino acid sequence and posttranslational modifications of human factor VIIa from plasma and transfected baby hamster kidney cells

1 reference

12 December 2020

Identification of molecular sites on factor VII which mediate its assembly and function in the extrinsic pathway activation complex

1 reference

12 December 2020

Gene for human factor X: a blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C.

1 reference

12 December 2020

Structural genes of coagulation factors VII and X located on 13q34.

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

Identifiers

DOI

10.1007/BF00219173

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1634227%20AND%20SRC:MED&resulttype=core&format=json

22 September 2019

1 reference