BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 25102815)

  • 21. Decreased generation of procoagulant platelets detected by flow cytometric analysis in patients with bleeding diathesis.
    Daskalakis M; Colucci G; Keller P; Rochat S; Silzle T; Biasiutti FD; Barizzi G; Alberio L
    Cytometry B Clin Cytom; 2014 Nov; 86(6):397-409. PubMed ID: 24677789
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Platelet aggregation, platelet cAMP levels and thromboxane B2 synthesis in patients with diabetes mellitus.
    Chen SY; Yu BJ; Liang YQ; Lin WD
    Chin Med J (Engl); 1990 Apr; 103(4):312-8. PubMed ID: 2167823
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Current status and future prospects for platelet function testing in the diagnosis of inherited bleeding disorders.
    Dovlatova N
    Br J Haematol; 2015 Jul; 170(2):150-61. PubMed ID: 25920378
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Defective signal transduction through the thromboxane A2 receptor in a patient with a mild bleeding disorder: deficiency of the inositol 1,4,5-triphosphate formation despite normal G-protein activation.
    Mitsui T; Yokoyama S; Shimizu Y; Katsuura M; Akiba K; Hayasaka K
    Thromb Haemost; 1997 May; 77(5):991-5. PubMed ID: 9184416
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Role of phosphoinositide 3-kinase beta in platelet aggregation and thromboxane A2 generation mediated by Gi signalling pathways.
    Garcia A; Kim S; Bhavaraju K; Schoenwaelder SM; Kunapuli SP
    Biochem J; 2010 Jul; 429(2):369-77. PubMed ID: 20441566
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Human CalDAG-GEFI gene (RASGRP2) mutation affects platelet function and causes severe bleeding.
    Canault M; Ghalloussi D; Grosdidier C; Guinier M; Perret C; Chelghoum N; Germain M; Raslova H; Peiretti F; Morange PE; Saut N; Pillois X; Nurden AT; Cambien F; Pierres A; van den Berg TK; Kuijpers TW; Alessi MC; Tregouet DA
    J Exp Med; 2014 Jun; 211(7):1349-62. PubMed ID: 24958846
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The rare inherited coagulation disorders.
    Bolton-Maggs PH
    Pediatr Blood Cancer; 2013; 60 Suppl 1():S37-40. PubMed ID: 23109366
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Inherited defects in platelet signaling mechanisms.
    Rao AK; Jalagadugula G; Sun L
    Semin Thromb Hemost; 2004 Oct; 30(5):525-35. PubMed ID: 15497095
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deficiency of the human complement regulatory protein factor H associated with low levels of component C9.
    Falcão DA; Reis ES; Paixão-Cavalcante D; Amano MT; Delcolli MI; Florido MP; Albuquerque JA; Moraes-Vasconcelos D; Duarte AJ; Grumach AS; Isaac L
    Scand J Immunol; 2008 Oct; 68(4):445-55. PubMed ID: 18782275
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Molecular genetics and clinical features of nine patients with inherited coagulation factor VII deficiency].
    Jin YH; Wang MS; Zheng FX; Xie YS; Xie HX; Xu PF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):404-7. PubMed ID: 22875495
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Levobupivacaine differentially suppresses platelet aggregation by modulating calcium release in a dose-dependent manner.
    Liou JT; Mao CC; Liu FC; Lin HT; Hung LM; Liao CH; Day YJ
    Acta Anaesthesiol Taiwan; 2012 Sep; 50(3):112-21. PubMed ID: 23026170
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Adult-onset arterial thrombosis in a pedigree of homozygous and heterozygous protein C deficiency.
    Tajima K; Yamamoto H; Yamamoto M; Kato Y; Kato T
    Thromb Res; 2013 Jan; 131(1):102-4. PubMed ID: 23174622
    [No Abstract]   [Full Text] [Related]  

  • 33. Identification of a homozygous recessive variant in
    Chan MV; Hayman MA; Sivapalaratnam S; Crescente M; Allan HE; Edin ML; Zeldin DC; Milne GL; Stephens J; Greene D; Hanif M; O'Donnell VB; Dong L; Malkowski MG; Lentaigne C; Wedderburn K; Stubbs M; Downes K; Ouwehand WH; Turro E; BioResource N; Hart DP; Freson K; Laffan MA; Warner TD
    Haematologica; 2021 May; 106(5):1423-1432. PubMed ID: 32299908
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Perioperative monitoring of primary and secondary hemostasis in coronary artery bypass grafting.
    Hertfelder HJ; Bös M; Weber D; Winkler K; Hanfland P; Preusse CJ
    Semin Thromb Hemost; 2005; 31(4):426-40. PubMed ID: 16149021
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A study of platelet aggregation, thromboxane A2 and prostacyclin in central aortic and coronary sinus blood in ischemic heart disease.
    Narain VS; Bhargava B; Chandra N; Puri VK; Hasan M
    Indian Heart J; 1994; 46(4):149-52. PubMed ID: 7875701
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.
    Su K; Jin Y; Miao Z; Cheng X; Yang L; Wang M
    Hematology; 2017 Jul; 22(6):380-385. PubMed ID: 28196451
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders.
    Leo VC; Morgan NV; Bem D; Jones ML; Lowe GC; Lordkipanidzé M; Drake S; Simpson MA; Gissen P; Mumford A; Watson SP; Daly ME;
    J Thromb Haemost; 2015 Apr; 13(4):643-50. PubMed ID: 25556537
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ridogrel inhibits systemic and renal formation of thromboxane A2 and antagonizes platelet thromboxane A2/prostaglandin endoperoxide receptors upon chronic administration to man.
    Weber C; Beetens JR; Tegtmeier F; Van Rooy P; Vercammen E; Wouters L; De Clerck F
    Thromb Haemost; 1992 Aug; 68(2):214-20. PubMed ID: 1412169
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Receptor homodimerization plays a critical role in a novel dominant negative P2RY12 variant identified in a family with severe bleeding.
    Mundell SJ; Rabbolini D; Gabrielli S; Chen Q; Aungraheeta R; Hutchinson JL; Kilo T; Mackay J; Ward CM; Stevenson W; Morel-Kopp MC
    J Thromb Haemost; 2018 Jan; 16(1):44-53. PubMed ID: 29117459
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Congenital disorders associated with platelet dysfunctions.
    Nurden P; Nurden AT
    Thromb Haemost; 2008 Feb; 99(2):253-63. PubMed ID: 18278172
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.