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The missense Thr211 Pro mutation in the factor X activation peptide of a bleeding patient causes molecular defect in the clotting cascade

Author
QIULAN DING1 ; YIPING SHEN2 3 ; LIKUI YANG4 ; XUEFENG WANG1 ; REZAIE, Alireza R4
[1] Department of Laboratory Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China
[2] Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai, China
[3] Department of Laboratory Medicine and Pathology, Children's Hospital, Boston, Harvard Medical School, Massachusetts, United States
[4] Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, Missouri, United States
Source

Thrombosis and haemostasis. 2013, Vol 110, Num 1, pp 53-61, 9 p ; ref : 23 ref

CODEN
THHADQ
ISSN
0340-6245
Scientific domain
Cardiology, blood circulation, phlebology; Hematology
Publisher
Schattauer, Stuttgart
Publication country
Germany
Document type
Article
Language
English
Author keyword
Coagulation factors factor VIII protein function / activity thrombin tissue factor / factor VII
Keyword (fr)
Activité biologique Facteur Stuart Facteur antihémophilique A Facteur coagulation Facteur tissulaire Homme Hémorragie Mutation faux sens Peptide Proconvertine Protéine Thrombin Enzyme Hydrolases Peptidases Serine endopeptidases
Keyword (en)
Biological activity Factor X Factor VIII Coagulation factor Tissue factor Human Hemorrhage Missense mutation Peptides Factor VII Protein Thrombin Enzyme Hydrolases Peptidases Serine endopeptidases
Keyword (es)
Actividad biológica Factor Stuart Factor antihemofílico A Factor coagulación Factor tisular Hombre Hemorragia Mutación falso sentido Péptido Proconvertina Proteína Thrombin Enzima Hydrolases Peptidases Serine endopeptidases
Classification
Pascal
002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A04 Molecular and cellular biology / 002A04I Blood coagulation. Blood cells

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19C Platelet diseases and coagulopathies

Discipline
Blood diseases Molecular and cell biology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
27476907

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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