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Akademický článek
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Autor:
Joseph Emmerich, M. Gouault-Heilman, G Chadeuf, Martine Aiach, Martine Alhenc-Gelas, Jean-Noël Fiessinger, Pierre Toulon
Publikováno v:
Thrombosis and Haemostasis. 72:534-539
SummaryWe report three novel mutations accounting for cases of inherited type I antithrombin (AT) deficiency. Using the polymerase chain reaction (PCR) and direct sequencing of the coding sequences of the AT gene, we found one mutation in exon 4 and
Akademický článek
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Publikováno v:
Journal of Chromatography A. 539:493-500
Heparin cofactor II (HCII) is an inhibitor of thrombin in human plasma whose activity is enhanced by heparin and dermatan sulphate. HCII was purified to homogeneity from normal human plasma with an overall yield of 7.5%. After treatment with barium c
Publikováno v:
FEBS letters. 365(2-3)
We used an antithrombin autoantibody (IgG D), the epitope of which encompasses ABE1 and amino acids located within variable region 1, to study thrombin interactions with R358 alpha 1-AT and protein C. IgG D inhibited the thrombin interaction with R35
Autor:
Martine Alhenc-Gelas, Joseph Emmerich, G Chadeuf, Martine Aiach, D Vidaud, M. F. Aillaud, M Gouault-Heilmann
Publikováno v:
Arteriosclerosis and thrombosis : a journal of vascular biology. 14(12)
We have identified three novel mutations of the antithrombin (AT) gene in patients with thrombotic complications: a Cys 128 --> Tyr mutations, a G --> A mutation in the intervening sequence 4 (IVS4) 14 nucleotide 5' to exon 5, and a 9 bp deletion in
Autor:
M. J. Coetzee, Joseph Emmerich, Martine Alhenc-Gelas, Martine Aiach, G Chadeuf, Jean-Noël Fiessinger
Publikováno v:
Thrombosis research. 76(3)
In a South African family with antithrombin deficiency and unexplained thrombosis, genomic DNA analysis revealed a substitution of Phe 402 by Leu. This mutation involves an amino acid located in the carboxyterminal side of the antithrombin reactive l
Autor:
J, Emmerich, G, Chadeuf, M, Alhenc-Gelas, M, Gouault-Heilman, P, Toulon, J N, Fiessinger, M, Aiach
Publikováno v:
Thrombosis and haemostasis. 72(4)
We report three novel mutations accounting for cases of inherited type I antithrombin (AT) deficiency. Using the polymerase chain reaction (PCR) and direct sequencing of the coding sequences of the AT gene, we found one mutation in exon 4 and two in
Publikováno v:
Nephron. 60(2)
Heparin cofactor II (HCII) is a thrombin inhibitor in human plasma which displays similarities with antithrombin III (ATIII). Hereditary HCII deficiency was recently reported to be associated with thrombophilia. Since thromboembolism constitutes one
Publikováno v:
European journal of clinical investigation. 21(3)
Heparin cofactor II is a proteinase inhibitor which inhibits both chymotrypsin and thrombin, and displays great similarities with antithrombin III, the main inhibitor of thrombin in human plasma. Since acute pancreatitis is known to be associated wit