Takamiya et al., 2002 - Google Patents
Human factor VII deficiency caused by S339C mutation located adjacent to the specificity pocket of the catalytic domainTakamiya et al., 2002
- Document ID
- 15319946554406991586
- Author
- Takamiya O
- Seta M
- Tanaka K
- Ishida F
- Publication year
- Publication venue
- Clinical & Laboratory Haematology
External Links
Snippet
This report documents our identification of a novel factor VII (FVII) gene mutation in a Japanese boy with FVII deficiency. The proband's FVII activity was 34% and his FVII antigen level was 40% of normal controls. DNA sequence analysis of the proband's FVII gene …
- 230000035772 mutation 0 title abstract description 39
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases Endopeptidases (3.4.21-3.4.25)
- C12N9/64—Proteinases Endopeptidases (3.4.21-3.4.25) derived from animal tissue
- C12N9/6421—Proteinases Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
- C12N9/6424—Serine endopeptidases (3.4.21)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/914—Hydrolases (3)
- G01N2333/948—Hydrolases (3) acting on peptide bonds (3.4)
- G01N2333/95—Proteinases, i.e. endopeptidases (3.4.21-3.4.99)
- G01N2333/964—Proteinases, i.e. endopeptidases (3.4.21-3.4.99) derived from animal tissue
- G01N2333/96425—Proteinases, i.e. endopeptidases (3.4.21-3.4.99) derived from animal tissue from mammals
- G01N2333/96427—Proteinases, i.e. endopeptidases (3.4.21-3.4.99) derived from animal tissue from mammals in general
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Green et al. | A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals. | |
Ljung et al. | Haemophilia B mutations in Sweden: a population‐based study of mutational heterogeneity | |
Matsumoto et al. | Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome | |
Roemisch et al. | The frequent Marburg I polymorphism impairs the pro-urokinase activating potency of the factor VII activating protease (FSAP) | |
Bernardi et al. | Biochemical, molecular and clinical aspects of coagulation factor VII and its role in hemostasis and thrombosis | |
Medina et al. | Contribution of polymorphisms in the endothelial protein C receptor gene to soluble endothelial protein C receptor and circulating activated protein C levels, and thrombotic risk | |
Millar et al. | Molecular analysis of the genotype-phenotype relationship in factor VII deficiency | |
Montagnana et al. | An overview of thrombophilia and associated laboratory testing | |
Peyvandi et al. | Gene mutations and three‐dimensional structural analysis in 13 families with severe factor X deficiency | |
Bereczky et al. | Protein C and protein S deficiencies: similarities and differences between two brothers playing in the same game | |
Henriksen et al. | Prothrombin Greenville, Arg517→ Gln, identified in an individual heterozygous for dysprothrombinemia | |
Martincic et al. | Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprinting | |
Takamiya et al. | Human factor VII deficiency caused by S339C mutation located adjacent to the specificity pocket of the catalytic domain | |
Christiansen et al. | The effect of a single nucleotide polymorphism on human α2-antiplasmin activity | |
Zhang et al. | Endogenous plasmin converts Glu-plasminogen to Lys-plasminogen on the monocytoid cell surface | |
Awidi et al. | Study of mutations in Jordanian patients with haemophilia A: identification of five novel mutations | |
Kemkes‐Matthes et al. | R255h amino acid substitution of protein Z identified in patients with factor V Leiden mutation | |
Corral et al. | Factor XIII Val 34 Leu polymorphism in primary intracerebral haemorrhage | |
EP0846185B1 (en) | T-pa polymorphism and use thereof in diagnosis of risk of thrombus associated disease | |
Shen et al. | Novel mutations in the Factor VII gene of Taiwanese Factor VII‐deficient patients | |
Hewitt et al. | Severe FVII deficiency caused by a new point mutation combined with a previously undetected gene deletion | |
Tamura et al. | In vitro exploration of latent prothrombin mutants conveying antithrombin resistance | |
Goel et al. | ADAMTS13 missense variants associated with defective activity and secretion of ADAMTS13 in a patient with non-cirrhotic portal hypertension | |
Nagaizumi et al. | Two double heterozygous mutations in the F7 gene show different manifestations | |
Lippi et al. | Genomics and proteomics in venous thromboembolism: building a bridge toward a rational personalized medicine framework |