Cargando…

Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction

Thromboembolic complication occurs frequently in β-thalassaemia/HbE patients, particularly in splenectomised patients. Endothelial cells play an important role in thrombosis. There is strong evidence of endothelial cell activation and dysfunction in β-thalassaemia. Microparticles (MPs) are associate...

Descripción completa

Detalles Bibliográficos
Autores principales:	Kheansaard, Wasinee, Phongpao, Kunwadee, Paiboonsukwong, Kittiphong, Pattanapanyasat, Kovit, Chaichompoo, Pornthip, Svasti, Saovaros
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2018
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115342/ https://www.ncbi.nlm.nih.gov/pubmed/30158562 http://dx.doi.org/10.1038/s41598-018-31386-6

Ejemplares similares

Impaired neutrophil extracellular trap formation in β-thalassaemia/HbE
por: Thubthed, Rattanawan, et al.
Publicado: (2022)

Platelet proteome reveals specific proteins associated with platelet activation and the hypercoagulable state in β-thalassmia/HbE patients
por: Chanpeng, Puangpaka, et al.
Publicado: (2019)

Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification
por: Chumworathayee, Worakawee, et al.
Publicado: (2023)

Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis
por: Chaichompoo, Pornthip, et al.
Publicado: (2022)

Restoration of correct β(IVS2-654)-globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cells
por: Nualkaew, Tiwaporn, et al.
Publicado: (2019)

The Roles of Mitophagy and Autophagy in Ineffective Erythropoiesis in β-Thalassemia
por: Chaichompoo, Pornthip, et al.
Publicado: (2022)

Plasma microRNA-451 as a novel hemolytic marker for β(0)-thalassemia/HbE disease
por: Leecharoenkiat, Kamonlak, et al.
Publicado: (2017)

Predictive SNPs for β(0)-thalassemia/HbE disease severity
por: Munkongdee, Thongperm, et al.
Publicado: (2021)

Deferiprone, an iron chelator, alleviates platelet hyperactivity in patients with β-thalassaemia/HbE
por: Tran, Ngan Thi, et al.
Publicado: (2022)

Clinical Severity of β-thalassaemia/Hb E Disease Is Associated with Differential Activities of the Calpain-Calpastatin Proteolytic System
por: Sukati, Suriyan, et al.
Publicado: (2012)

HBB Gene Mutations and Their Pathological Impacts on HbE/β-Thalassaemia in Kuala Terengganu, Malaysia
por: Saad, Hanan Kamel M., et al.
Publicado: (2023)

Decreased nitrite reductase activity of deoxyhemoglobin correlates with platelet activation in hemoglobin E/ß-thalassemia subjects
por: Chamchoi, Attaphon, et al.
Publicado: (2018)

A FACS Based Case Study on Two HbE-β Thalassaemia Members of a Family, Having Similar Mutational Background
por: Chatterjee, Tridip, et al.
Publicado: (2016)

Trienone analogs of curcuminoids induce fetal hemoglobin synthesis via demethylation at (G)γ-globin gene promoter
por: Nuamsee, Khanita, et al.
Publicado: (2021)

A comprehensive ethnic-based analysis of alpha thalassaemia allelle frequency in northern Thailand
por: Kulaphisit, Mattapong, et al.
Publicado: (2017)

Moyamoya syndrome in a child with HbEβ‐thalassemia
por: Zahra, Akmal, et al.
Publicado: (2022)

Altered profile of circulating microparticles in nonvalvular atrial fibrillation
por: Siwaponanan, Panjaree, et al.
Publicado: (2019)

Mitochondrial Changes in β(0)-Thalassemia/Hb E Disease
por: Khungwanmaythawee, Kornpat, et al.
Publicado: (2016)

Effect of Tumor Necrosis Factor-Alpha on Erythropoietin- and Erythropoietin Receptor-Induced Erythroid Progenitor Cell Proliferation in β-Thalassemia/Hemoglobin E Patients
por: Tanyong, Dalina I, et al.
Publicado: (2015)

Hb E/beta-thalassaemia: a common & clinically diverse disorder
por: Olivieri, Nancy F., et al.
Publicado: (2011)

Differential Thermal Stability and Oxidative Vulnerability of the Hemoglobin Variants, HbA(2) and HbE
por: Chakrabarti, Abhijit, et al.
Publicado: (2013)

High Prevalence of Antiphospholipid Antibodies in Children with Non-Transfusion Dependent Thalassemia and Possible Correlations with Microparticles
por: Chinsuwan, Jitlada, et al.
Publicado: (2020)

Genetic predictions of life expectancy in southern Thai patients with β(0)-thalassemia/Hb E
por: Nuinoon, Manit, et al.
Publicado: (2022)

Abstract 40: Adrenal insufficiency in patients with HbE/Beta thalassemia
por: Singh, Arijit, et al.
Publicado: (2022)

Update in Laboratory Diagnosis of Thalassemia
por: Munkongdee, Thongperm, et al.
Publicado: (2020)

Bubble-Induced Endothelial Microparticles Promote Endothelial Dysfunction
por: Yu, Xuhua, et al.
Publicado: (2017)

Status of HbE variant among Rabha tribe of West Bengal, India
por: Bhattacharyya, Deboshree M., et al.
Publicado: (2015)

A decision support scheme for beta thalassemia and HbE carrier screening
por: Das, Reena, et al.
Publicado: (2020)

Severe homozygous HbE disease: the first case report from Nepal
por: Bhattarai, Urza, et al.
Publicado: (2023)

Thalidomide-Induced Primary Amenorrhea in a Patient With HbE/Beta-Thalassemia
por: Singha, Arijit, et al.
Publicado: (2023)

A successful twin pregnancy in a patient with HbE-β-thalassemia in western India
por: Merchant, R, et al.
Publicado: (2015)

Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA(2) in β-thalassaemia carriers
por: Cyrus, Cyril, et al.
Publicado: (2019)

Endothelial Microparticles as Potential Biomarkers in the Assessment of Endothelial Dysfunction in Hypercholesterolemia
por: Nik Ibrahim, Nik Nor Izah, et al.
Publicado: (2022)

Genetic modifiers of Hb E/β(0 )thalassemia identified by a two-stage genome-wide association study
por: Sherva, Richard, et al.
Publicado: (2010)

Relationship between Plasma Ferritin Level and Siderocyte Number in Splenectomized β-Thalassemia/HbE Patients
por: Tripatara, A., et al.
Publicado: (2012)

Impaired Terminal Erythroid Maturation in β(0)-Thalassemia/HbE Patients with Different Clinical Severity
por: Suriyun, Thunwarat, et al.
Publicado: (2022)

Endothelial microparticles are increased in congenital heart diseases and contribute to endothelial dysfunction
por: Lin, Ze-Bang, et al.
Publicado: (2017)

α-thalassaemia
por: Harteveld, Cornelis L, et al.
Publicado: (2010)

The effect of cryopreservation media on the quality of β-thalassemia mouse spermatozoa
por: Buranaamnuay, Kakanang, et al.
Publicado: (2022)

A Suspected Case of Cerebral Fat Embolism Triggering a Drug-resistant Status Epilepticus in a HbS/β(+)-Thalassaemia Patient
por: Bortolotti, Marta, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_bdlh17jbkehs92b3doj9pnis5k