Molecular and genetic mechanisms of factor XIII a subunit deficiency

Seminars in Thrombosis and Hemostasis

Volumn 26, Issue 1, 2000, Pages 5-10

  Ichinose, Akitada ^a   Souri, Masayoshi ^a   Izumi, Tomonori ^a   Takahashi, Nobumasa ^a  

^a YAMAGATA UNIVERSITY   (Japan)

Author keywords

Bleeding disorder; Cross linking; Molecular abnormality; Transglutaminase; Wound healing

Indexed keywords

BLOOD CLOTTING FACTOR 13A; DNA; MESSENGER RNA; PROTEIN; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; TETRAMER;

ARTICLE; BLEEDING; BLOOD CLOTTING FACTOR DEFICIENCY; EXON; GENE; HUMAN; MISSENSE MUTATION; MOLECULAR MODEL; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; X RAY CRYSTALLOGRAPHY;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ANTIPLASMIN; BINDING SITES; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 6; DNA MUTATIONAL ANALYSIS; ENZYME ACTIVATION; FACTOR XIII DEFICIENCY; FIBRIN; HUMANS; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; POINT MUTATION; PROTEIN CONFORMATION; RNA, MESSENGER; SEQUENCE DELETION; STRUCTURE-ACTIVITY RELATIONSHIP; THROMBIN; TRANSGLUTAMINASES;

EID: 0034087597     PISSN: 00946176     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (39)

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