BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 25876182)

  • 21. 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]  

  • 22. Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family.
    Perez Botero J; Chen D; He R; Viswanatha DS; Majerus JA; Coon LM; Nguyen PL; Reichard KK; Oliveira JL; Tefferi A; Gangat N; Pruthi RK; Patnaik MM
    Platelets; 2016 Nov; 27(7):712-715. PubMed ID: 27123948
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling.
    Marín-Quílez A; Vuelta E; Díaz-Ajenjo L; Fernández-Infante C; García-Tuñón I; Benito R; Palma-Barqueros V; Hernández-Rivas JM; González-Porras JR; Rivera J; Bastida JM
    J Thromb Haemost; 2022 May; 20(5):1248-1255. PubMed ID: 35170221
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Pedigree Analysis of ACTN1-Related Thrombocytopenia Attributed to A Novel Mutation].
    Liu JX; Wang CJ; Dai JH; Zhang MX; Lyu M; Sun YQ; Jiang B
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Apr; 30(2):565-570. PubMed ID: 35395998
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency.
    Faioni EM; Razzari C; Zulueta A; Femia EA; Fenu L; Trinchera M; Podda GM; Pugliano M; Marongiu F; Cattaneo M
    Thromb Haemost; 2014 Dec; 112(6):1182-9. PubMed ID: 25102815
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The role of platelets in bleeding in patients with thrombocytopenia and hematological disease.
    Vinholt PJ
    Clin Chem Lab Med; 2019 Nov; 57(12):1808-1817. PubMed ID: 31465290
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Levels of procoagulant microparticles expressing phosphatidylserine contribute to bleeding phenotype in patients with inherited thrombocytopenia.
    Brøns N; Leinøe E; Salado-Jimena JA; Rossing M; Ostrowski SR
    Blood Coagul Fibrinolysis; 2021 Oct; 32(7):480-490. PubMed ID: 34475331
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A clinical and molecular study of a Bedouin family with dysmegakaryopoiesis, mild anemia, and neutropenia cured by bone marrow transplantation.
    Tamary H; Yaniv I; Stein J; Dgany O; Shalev Z; Shechter T; Resnitzky P; Shaft D; Zoldan M; Kornreich L; Levy R; Cohen A; Moser RA; Kapelushnik J; Shalev H
    Eur J Haematol; 2003 Sep; 71(3):196-203. PubMed ID: 12930321
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Reduced platelet count, but no major platelet function abnormalities, are associated with loss-of-function ATP-binding cassette-1 gene mutations.
    Minuz P; Meneguzzi A; Femia EA; Fava C; Calabria S; Scavone M; Benati D; Poli G; Zancanaro C; Calandra S; Lucchi T; Cattaneo M
    Clin Sci (Lond); 2017 Aug; 131(16):2095-2107. PubMed ID: 28634189
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Platelet kinetics in autosomal dominant macrothrombocytopenia.
    Erslev AJ; Palascak JE; Shaikh BS; Martinez J
    J Lab Clin Med; 1998 Jun; 131(6):488-95; discussion 487. PubMed ID: 9626983
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A new familial 'giant platelet syndrome' with structural, metabolic and functional abnormalities of platelets due to a primary megakaryocyte defect.
    Greaves M; Pickering C; Martin J; Cartwright I; Preston FE
    Br J Haematol; 1987 Apr; 65(4):429-35. PubMed ID: 3580299
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Congenital macrothrombocytopenia is a heterogeneous disorder in India.
    Ali S; Ghosh K; Daly ME; Hampshire DJ; Makris M; Ghosh M; Mukherjee L; Bhattacharya M; Shetty S
    Haemophilia; 2016 Jul; 22(4):570-82. PubMed ID: 27291889
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Inherited thrombocytopenia caused by reduced platelet production in mice with the gunmetal pigment gene mutation.
    Novak EK; Reddington M; Zhen L; Stenberg PE; Jackson CW; McGarry MP; Swank RT
    Blood; 1995 Apr; 85(7):1781-9. PubMed ID: 7703484
    [TBL] [Abstract][Full Text] [Related]  

  • 35. International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country.
    Glembotsky AC; Marta RF; Pecci A; De Rocco D; Gnan C; Espasandin YR; Goette NP; Negro F; Noris P; Savoia A; Balduini CL; Molinas FC; Heller PG
    J Thromb Haemost; 2012 Aug; 10(8):1653-61. PubMed ID: 22672365
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Alterations of the platelet proteome in type I Glanzmann thrombasthenia caused by different homozygous delG frameshift mutations in ITGA2B.
    Loroch S; Trabold K; Gambaryan S; Reiß C; Schwierczek K; Fleming I; Sickmann A; Behnisch W; Zieger B; Zahedi RP; Walter U; Jurk K
    Thromb Haemost; 2017 Feb; 117(3):556-569. PubMed ID: 28078347
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Progress in understanding the diagnosis and molecular genetics of macrothrombocytopenias.
    Favier R; Raslova H
    Br J Haematol; 2015 Sep; 170(5):626-39. PubMed ID: 25944497
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.
    Song WJ; Sullivan MG; Legare RD; Hutchings S; Tan X; Kufrin D; Ratajczak J; Resende IC; Haworth C; Hock R; Loh M; Felix C; Roy DC; Busque L; Kurnit D; Willman C; Gewirtz AM; Speck NA; Bushweller JH; Li FP; Gardiner K; Poncz M; Maris JM; Gilliland DG
    Nat Genet; 1999 Oct; 23(2):166-75. PubMed ID: 10508512
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan.
    Johnson B; Fletcher SJ; Morgan NV
    Platelets; 2016 Sep; 27(6):519-25. PubMed ID: 27025194
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel splice site mutation of CDHR1 in a consanguineous Israeli Christian Arab family segregating autosomal recessive cone-rod dystrophy.
    Cohen B; Chervinsky E; Jabaly-Habib H; Shalev SA; Briscoe D; Ben-Yosef T
    Mol Vis; 2012; 18():2915-21. PubMed ID: 23233793
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.