Nature of the fibrinogen Aα gene Taql polymorphism

Thrombosis and Haemostasis

Volumn 86, Issue 3, 2001, Pages 935-936

  Remijn, J A ^a   Van Wijk, R ^a   De Groot, P G ^a   Van Solinge, W W ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FIBRINOGEN; MESSENGER RNA; POLYCLONAL ANTIBODY; TAQ POLYMERASE; TAQI POLYMERASE; UNCLASSIFIED DRUG; ENDODEOXYRIBONUCLEASE TAQI; PEPTIDE FRAGMENT; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

3' UNTRANSLATED REGION; AFIBRINOGENEMIA; AUTOSOMAL RECESSIVE INHERITANCE; BASE PAIRING; BLEEDING; BLOOD CLOTTING DISORDER; CLINICAL FEATURE; DISEASE SEVERITY; DNA SEQUENCE; EXON; FIBRINOGEN BLOOD LEVEL; GENE DUPLICATION; GENE FREQUENCY; GENE INSERTION; GENETIC CODE; GENETIC POLYMORPHISM; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INTRON; LETTER; MOLECULAR DYNAMICS; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; RESTRICTION MAPPING; RNA STABILITY; SEQUENCE ANALYSIS; CHEMISTRY; GENE EXPRESSION REGULATION; GENETICS; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION;

BASE SEQUENCE; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA MUTATIONAL ANALYSIS; EXONS; FIBRINOGEN; GENOTYPE; HUMANS; MOLECULAR SEQUENCE DATA; MUTAGENESIS, INSERTIONAL; PEPTIDE FRAGMENTS; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; SEQUENCE ANALYSIS, DNA;

EID: 0034741712     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1616160     Document Type: Letter

References (10)

1. Congenital afibrinogenemia
2. Absence of fibrinogen in afibrinogenemia results in large but loosely packed thrombi under flow conditions
3. The identification of a DNA polymorphism of the α fibrinogen gene and the regional assignment of the human fibrinogen genes to 4q26-qter
4. +1689 (AvaII), and BclI (β-fibrinogen) and TaqI (α-fibrinogen) and their detection by PCR
5. 420, the novel fibrinogen subclass: Newborn levels are higher than adult
6. Role of genetic variation at the fibrinogen locus in determination of plasma fibrinogen concentrations
7. Genetic variation at fibrinogen loci and plasma fibrinogen levels
8. Physical activity, fibrinogen plasma level and gene polymorphisms in postmenopausal women
9. Fibrinogen polymorphisms are not associated with the risk of myocardial infarction
10. A common pentanucleotide polymorphism of the 3′-untranslated part of the leptin receptor gene generates a putative stem-loop motif in the mRNA and is associated with serum insulin levels in obese individuals