Zobrazeno 1 - 10 of 215 pro vyhledávání: '"S, Gandrille"'
1
[Clinical and biological features of patients with essential thrombocythaemia according to their mutational status JAK2 or CALR: Single-center study of 40 patients and review of the literature]
Autor: M, Ben Said, S, Gandrille, A M, Fischer, L, Darnige
Publikováno v: Pathologie-biologie. 63(3)
Somatic mutations in the calreticulin gene (CALR) were recently described in essential thrombocythemia (ET) and primary myelofibrosis with non-mutated JAK2 or MPL. The aim of this single-center study was to compare the clinical and biological feature
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::af504dbc034a628c524c899533f108f5
https://pubmed.ncbi.nlm.nih.gov/25840625
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2
Akademický článek
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3
Molecular basis for protein S hereditary deficiency: Genetic defects observed in 118 patients with type I and type IIa deficiencies1
Autor: D BORGEL, J DUCHEMIN, M ALHENCGELAS, C MATHERON, M AIACH, S GANDRILLE, null THE, null PROTEINSDEFICIENCIES
Publikováno v: Journal of Laboratory and Clinical Medicine. 128:218-227
Circulating protein S (PS) is partly bound to C4b-binding protein, and only free PS can act as a cofactor for protein C (PC), a natural anticoagulant. Two types of PS deficiencies are commonly observed in patients with unexplained thrombosis, and the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9c63411c788a7f3301cef3fe4784d28a
https://doi.org/10.1016/s0022-2143(96)90015-3
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5
Platelet dysfunction associated with the novel Trp29Cys thromboxane A₂ receptor variant
Autor: A D, Mumford, S, Nisar, L, Darnige, M L, Jones, C, Bachelot-Loza, S, Gandrille, F, Zinzindohoue, A-M, Fischer, S J, Mundell, P, Gaussem
Publikováno v: Journal of thrombosis and haemostasis : JTH. 11(3)
Genetic variations that affect the structure of the thromboxane A2 receptor (TP receptor) provide insights into the function of this key platelet and vascular receptor, but are very rare in unselected populations.To determine the functional consequen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a3de2d5101d00cae20daf7511e095b99
https://pubmed.ncbi.nlm.nih.gov/23279270
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6
Albumin concentration influences fibrinolytic activity in plasma and purified systems
Autor: M. Aiach, S. Gandrille
Publikováno v: Fibrinolysis. 4:225-232
Delayed clot lysis was observed in 9 patients with nephrotic syndrome. This delay, assessed by fibrin degradation product release, was corrected by supplementing patients' plasma with purified human albumin to reach the normal albumin concentration o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c4984ce8f958a1c38f9fca33ef12898
https://doi.org/10.1016/0268-9499(90)90019-g
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7
[Validation of a diagnostic kit for factor V Leiden mutation]
Autor: S, Gandrille, V, Remones, M, Aiach
Publikováno v: Annales de biologie clinique. 61(6)
The Stagen factor V Leiden mutation is a new kit allowing to perform all steps necessary to identify the Leiden mutation of Factor V, from DNA extraction from patient's blood sample to electrophoresis of amplification products. The method is based on
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cae76fa9e9a06abb1d0e03e13b4140d4
https://pubmed.ncbi.nlm.nih.gov/14711617
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8
Implication of protein S thrombin-sensitive region with membrane binding via conformational changes in the gamma-carboxyglutamic acid-rich domain
Autor: D, Borgel, P, Gaussem, C, Garbay, C, Bachelot-Loza, T, Kaabache, W Q, Liu, B, Brohard-Bohn, B, Le Bonniec, M, Aiach, S, Gandrille
Publikováno v: The Biochemical journal. 360(Pt 2)
In the vitamin K-dependent protein family, only protein S (PS) contains a thrombin-sensitive region (TSR), located between the domain containing the gamma-carboxyglutamic acid and the first epidermal growth factor-like domain. To better define the ro
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bd8fbd31c9465fae7fd5857f80826a00
https://pubmed.ncbi.nlm.nih.gov/11716779
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9
Thirty-three novel mutations in the protein C gene. French INSERM network on molecular abnormalities responsible for protein C and protein S
Autor: M, Alhenc-Gelas, S, Gandrille, M L, Aubry, M, Aiach
Publikováno v: Thrombosis and haemostasis. 83(1)
We analyzed the protein C gene (PROC) with the denaturing gradient gel electrophoresis (DGGE) scanning strategy in a series of 129 patients with suspected protein C (PC) deficiency (93 with low plasma PC levels and 36 with borderline level). At least
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f671495b125c56d3abeeb430540be7bd
https://pubmed.ncbi.nlm.nih.gov/10669160
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10
Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutation
Autor: V, Le Cam-Duchez, S, Gandrille, D, Trégouët, M, Alhenc-Gelas, J, Emmerich, J N, Fiessinger, J Y, Borg, M, Aiach
Publikováno v: British journal of haematology. 106(4)
The factor V (FV) Arg 506 to Gln mutation is the most common abnormality observed in familial thrombophilia. Many studies have shown that its clinical expression differs among families and among carriers. Some thrombotic patients carry an additional
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc6a7451d2f2e41aa330080548ceb465
https://pubmed.ncbi.nlm.nih.gov/10519989
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