These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

136 related articles for article (PubMed ID: 33626581)

  • 1. Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model.
    Marín-Quílez A; García-Tuñón I; Fernández-Infante C; Hernández-Cano L; Palma-Barqueros V; Vuelta E; Sánchez-Martín M; González-Porras JR; Guerrero C; Benito R; Rivera J; Hernández-Rivas JM; Bastida JM
    Thromb Haemost; 2021 Sep; 121(9):1193-1205. PubMed ID: 33626581
    [No Abstract]   [Full Text] [Related]  

  • 2. Defective acid hydrolase secretion in RUNX1 haplodeficiency: Evidence for a global platelet secretory defect.
    Rao AK; Poncz M
    Haemophilia; 2017 Sep; 23(5):784-792. PubMed ID: 28662545
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A mouse model of the protease-activated receptor 4 Pro310Leu variant has reduced platelet reactivity.
    Han X; Knauss EA; Fuente M; Li W; Conlon RA; LePage DF; Jiang W; Renna SA; McKenzie SE; Nieman MT
    J Thromb Haemost; 2024 Jun; 22(6):1715-1726. PubMed ID: 38508397
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mechanisms underlying platelet function defect in a pedigree with familial platelet disorder with a predisposition to acute myelogenous leukemia: potential role for candidate RUNX1 targets.
    Glembotsky AC; Bluteau D; Espasandin YR; Goette NP; Marta RF; Marin Oyarzun CP; Korin L; Lev PR; Laguens RP; Molinas FC; Raslova H; Heller PG
    J Thromb Haemost; 2014 May; 12(5):761-72. PubMed ID: 24606315
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Effects of the ITGA2B Nonsense Mutation (c.2659C > T, p.Q887X) on Platelet Function in a Mouse Model of Glanzmann's Thrombasthenia Generated with CRISPR/Cas9 Technology].
    Yang F; Jiang M; Lin ZH; Xie ZL; Ma ZN; Yang L; Liu H; Wang ZY; Zhou L
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Apr; 30(2):559-564. PubMed ID: 35395997
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Regulation of platelet myosin light chain (MYL9) by RUNX1: implications for thrombocytopenia and platelet dysfunction in RUNX1 haplodeficiency.
    Jalagadugula G; Mao G; Kaur G; Goldfinger LE; Dhanasekaran DN; Rao AK
    Blood; 2010 Dec; 116(26):6037-45. PubMed ID: 20876458
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.
    Glembotsky AC; Sliwa D; Bluteau D; Balayn N; Marin Oyarzún CP; Raimbault A; Bordas M; Droin N; Pirozhkova I; Washington V; Goette NP; Marta RF; Favier R; Raslova H; Heller PG
    Haematologica; 2019 Jun; 104(6):1244-1255. PubMed ID: 30545930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Thrombocytopathy leading to impaired in vivo haemostasis and thrombosis in platelet type von Willebrand disease.
    Kaur H; Corscadden K; Ware J; Othman M
    Thromb Haemost; 2017 Feb; 117(3):543-555. PubMed ID: 28004055
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Impaired Platelet Function in Sept8-Deficient Mice In Vitro.
    Neubauer K; Jurk K; Petermann V; Kumm E; Zieger B
    Thromb Haemost; 2021 Apr; 121(4):484-494. PubMed ID: 33202444
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NLRP3 regulates platelet integrin αIIbβ3 outside-in signaling, hemostasis and arterial thrombosis.
    Qiao J; Wu X; Luo Q; Wei G; Xu M; Wu Y; Liu Y; Li X; Zi J; Ju W; Fu L; Chen C; Wu Q; Zhu S; Qi K; Li D; Li Z; Andrews RK; Zeng L; Gardiner EE; Xu K
    Haematologica; 2018 Sep; 103(9):1568-1576. PubMed ID: 29794149
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.
    Badin MS; Iyer JK; Chong M; Graf L; Rivard GE; Waye JS; Paterson AD; Pare G; Hayward CPM
    Haemophilia; 2017 May; 23(3):e204-e213. PubMed ID: 28181366
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Platelet transcriptome analysis in patients with germline RUNX1 mutations.
    Palma-Barqueros V; Bastida JM; López Andreo MJ; Zámora-Cánovas A; Zaninetti C; Ruiz-Pividal JF; Bohdan N; Padilla J; Teruel-Montoya R; Marín-Quilez A; Revilla N; Sánchez-Fuentes A; Rodriguez-Alen A; Benito R; Vicente V; Iturbe T; Greinacher A; Lozano ML; Rivera J; ;
    J Thromb Haemost; 2023 May; 21(5):1352-1365. PubMed ID: 36736831
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alterations in Platelet Alpha-Granule Secretion and Adhesion on Collagen under Flow in Mice Lacking the Atypical Rho GTPase RhoBTB3.
    Berger M; Lutz DRJ; Lutz J; Khalil JS; Aburima A; Naseem KM; Rivero F
    Cells; 2019 Feb; 8(2):. PubMed ID: 30754723
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.
    Latger-Cannard V; Philippe C; Bouquet A; Baccini V; Alessi MC; Ankri A; Bauters A; Bayart S; Cornillet-Lefebvre P; Daliphard S; Mozziconacci MJ; Renneville A; Ballerini P; Leverger G; Sobol H; Jonveaux P; Preudhomme C; Nurden P; Lecompte T; Favier R
    Orphanet J Rare Dis; 2016 Apr; 11():49. PubMed ID: 27112265
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dysregulation of PLDN (pallidin) is a mechanism for platelet dense granule deficiency in RUNX1 haplodeficiency.
    Mao GF; Goldfinger LE; Fan DC; Lambert MP; Jalagadugula G; Freishtat R; Rao AK
    J Thromb Haemost; 2017 Apr; 15(4):792-801. PubMed ID: 28075530
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The catalytic subunit of protein phosphatase 1 gamma regulates thrombin-induced murine platelet alpha(IIb)beta(3) function.
    Gushiken FC; Hyojeong H; Pradhan S; Langlois KW; Alrehani N; Cruz MA; Rumbaut RE; Vijayan KV
    PLoS One; 2009 Dec; 4(12):e8304. PubMed ID: 20016849
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of two novel mutations in RASGRP2 affecting platelet CalDAG-GEFI expression and function in patients with bleeding diathesis.
    Sevivas T; Bastida JM; Paul DS; Caparros E; Palma-Barqueros V; Coucelo M; Marques D; Ferrer-Marín F; González-Porras JR; Vicente V; Hernández-Rivas JM; Watson SP; Lozano ML; Bergmeier W; Rivera J
    Platelets; 2018 Mar; 29(2):192-195. PubMed ID: 28762304
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Full activation of mouse platelets requires ADP secretion regulated by SERCA3 ATPase-dependent calcium stores.
    Elaïb Z; Adam F; Berrou E; Bordet JC; Prévost N; Bobe R; Bryckaert M; Rosa JP
    Blood; 2016 Aug; 128(8):1129-38. PubMed ID: 27301859
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Restoration of responsiveness of phospholipase Cγ2-deficient platelets by enforced expression of phospholipase Cγ1.
    Zheng Y; Adams T; Zhi H; Yu M; Wen R; Newman PJ; Wang D; Newman DK
    PLoS One; 2015; 10(3):e0119739. PubMed ID: 25793864
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of Integrin αIIbβ3-Mediated Outside-in Signaling by Protein Kinase Cδ in Platelets.
    Chaudhary PK; Kim S; Jee Y; Lee SH; Kim S
    Int J Mol Sci; 2020 Sep; 21(18):. PubMed ID: 32911704
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.