Page last updated: 2024-10-17

cytosine and Hemophilia A

cytosine has been researched along with Hemophilia A in 3 studies

Hemophilia A: The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.

Research Excerpts

ExcerptRelevanceReference
"DNA of 70 unrelated hemophilia B patients, including three inhibitor patients, was analyzed by using various restriction enzymes and was hybridized with both a factor IX cDNA and 3'- and 5'-flanking probes."1.28Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B. ( Brackmann, HH; Egli, H; Eigel, A; Horst, J; Ludwig, M; Olek, K; Schwaab, R, 1989)
"Hemophilia A is an X-linked disease of coagulation caused by deficiency of factor VIII."1.27Nonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides. ( Antonarakis, SE; Bell, W; Griffin, AM; Kazazian, HH; Youssoufian, H, 1988)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Liu, Q1
Sommer, SS1
Ludwig, M1
Schwaab, R1
Eigel, A1
Horst, J1
Egli, H1
Brackmann, HH1
Olek, K1
Youssoufian, H1
Antonarakis, SE1
Bell, W1
Griffin, AM1
Kazazian, HH1

Other Studies

3 other studies available for cytosine and Hemophilia A

ArticleYear
Subcycling-PCR for multiplex long-distance amplification of regions with high and low GC content: application to the inversion hotspot in the factor VIII gene.
    BioTechniques, 1998, Volume: 25, Issue:6

    Topics: Chromosome Inversion; Cytosine; Dimethyl Sulfoxide; DNA Mutational Analysis; DNA Primers; Factor VII

1998
Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B.
    American journal of human genetics, 1989, Volume: 45, Issue:1

    Topics: Chromosome Deletion; Cytosine; DNA; Factor IX; Female; Genes; Hemophilia A; Humans; Male; Mutation;

1989
Nonsense and missense mutations in hemophilia A: estimate of the relative mutation rate at CG dinucleotides.
    American journal of human genetics, 1988, Volume: 42, Issue:5

    Topics: Adolescent; Adult; Antigens; Base Sequence; Cytosine; Dinucleoside Phosphates; DNA; DNA Restriction

1988