134 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. miR-15a-5p regulates expression of multiple proteins in the megakaryocyte GPVI signaling pathway.
Basak I; Bhatlekar S; Manne BK; Stoller M; Hugo S; Kong X; Ma L; Rondina MT; Weyrich AS; Edelstein LC; Bray PF
J Thromb Haemost; 2019 Mar; 17(3):511-524. PubMed ID: 30632265
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]