Cargando…

Effect of iron overload on furin expression in wild-type and β-thalassemic mice

Furin is a proprotein convertase enzyme. In the liver, it cleaves prohepcidin to form active hepcidin-25, which regulates systemic iron homeostasis. Hepcidin deficiency is a component of several iron overload disorders, including β-thalassemia. Several studies have identified factors that repress he...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wichaiyo, Surasak, Yatmark, Paranee, Morales Vargas, Ronald Enrique, Sanvarinda, Pimtip, Svasti, Saovaros, Fucharoen, Suthat, Morales, Noppawan Phumala
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2015
Materias:	Short Communication
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598392/ https://www.ncbi.nlm.nih.gov/pubmed/28962376 http://dx.doi.org/10.1016/j.toxrep.2015.01.004

Ejemplares similares

Effects of green tea extract treatment on erythropoiesis and iron parameters in iron-overloaded β-thalassemic mice
por: Settakorn, Kornvipa, et al.
Publicado: (2022)

Iron Overload in Transfusion-Dependent Indonesian Thalassemic Patients
por: Fianza, Pandji Irani, et al.
Publicado: (2021)

Pathogen-Associated Molecules from Gut Translocation Enhance Severity of Cecal Ligation and Puncture Sepsis in Iron-Overload β-Thalassemia Mice
por: Sae-khow, Kritsanawan, et al.
Publicado: (2020)

Iron homeostasis in a mouse model of thalassemia intermedia is altered between adolescence and adulthood
por: Sanyear, Chanita, et al.
Publicado: (2020)

Increased susceptibility to dextran sulfate-induced mucositis of iron-overload β-thalassemia mice, another endogenous cause of septicemia in thalassemia
por: Visitchanakun, Peerapat, et al.
Publicado: (2021)

The hypoferremic response to acute inflammation is maintained in thalassemia mice even under parenteral iron loading
por: Sanyear, Chanita, et al.
Publicado: (2021)

Nephrectomy Does not Exacerbate Cancellous Bone loss in Thalassemic Mice
por: Lotinun, Sutada, et al.
Publicado: (2020)

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)

High phosphate intake induces bone loss in nephrectomized thalassemic mice
por: Wanna-udom, Sasithorn, et al.
Publicado: (2022)

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

Mild-intensity physical activity prevents cardiac and osseous iron deposition without affecting bone mechanical property or porosity in thalassemic mice
por: Charoenphandhu, Narattaphol, et al.
Publicado: (2022)

An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia
por: Theerajangkhaphichai, Wasan, et al.
Publicado: (2021)

Hemoglobin E Prevalence among Ethnic Groups Residing in Malaria-Endemic Areas of Northern Thailand and Its Lack of Association with Plasmodium falciparum Invasion In Vitro
por: Lithanatudom, Pathrapol, et al.
Publicado: (2016)

Correction: Hemoglobin E Prevalence among Ethnic Groups Residing in Malaria-Endemic Areas of Northern Thailand and Its Lack of Association with Plasmodium falciparum Invasion In Vitro
por: Lithanatudom, Pathrapol, et al.
Publicado: (2016)

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

Can we measure iron overload in the heart using in vivo MRI T2*?
por: He, Taigang, et al.
Publicado: (2009)

Author Correction: An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia
por: Theerajangkhaphichai, Wasan, et al.
Publicado: (2023)

Responses of primary osteoblasts and osteoclasts from hemizygous β-globin knockout thalassemic mice with elevated plasma glucose to 1,25-dihydroxyvitamin D(3)
por: Charoenphandhu, Narattaphol, et al.
Publicado: (2019)

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

Combined Iron Chelator and Antioxidant Exerted Greater Efficacy on Cardioprotection Than Monotherapy in Iron-Overloaded Rats
por: Wongjaikam, Suwakon, et al.
Publicado: (2016)

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)

Mitapivat, a pyruvate kinase activator, improves transfusion burden and reduces iron overload in β-thalassemic mice
por: Mattè, Alessandro, et al.
Publicado: (2023)

Comparative Plasma Protein Profiling of Hemoglobin H Disease
por: Leecharoenkiat, Kamonlak, et al.
Publicado: (2014)

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

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

Protective Effect of Lusianthridin on Hemin-Induced Low-Density Lipoprotein Oxidation
por: Thant, Su Wutyi, et al.
Publicado: (2021)

Ultrasonographic evaluation of the renal dimensions in captive tigers
por: HUAIJANTUG, Somkiat, et al.
Publicado: (2016)

A pure compound from Curcuma comosa Roxb. protects neurons against hydrogen peroxide-induced neurotoxicity via the activation of Nrf-2
por: Khin Aung, Zon Mie, et al.
Publicado: (2022)

Inhibition of LPS-Induced Microglial Activation by the Ethyl Acetate Extract of Pueraria mirifica
por: Jantaratnotai, Nattinee, et al.
Publicado: (2022)

Outcome of iron reduction therapy in ex-thalassemics
por: Aboobacker, Fouzia N., et al.
Publicado: (2021)

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

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

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

Can levels of antioxidants in synovial fluid predict the severity of primary knee osteoarthritis: a preliminary study
por: Angthong, Chayanin, et al.
Publicado: (2013)

Iron deposits in the knee joints of a thalassemic patient
por: Economides, Charalambos P, et al.
Publicado: (2012)

Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure
por: Wangkumhang, Pongsakorn, et al.
Publicado: (2013)

Assessment of Hepatic and Pancreatic Iron Overload in Pediatric Beta-Thalassemic Major Patients by T2* Weighted Gradient Echo Magnetic Resonance Imaging
por: Youssef, Doaa Mohammed, et al.
Publicado: (2013)

Inhibitory Effects of Erythrosine/Curcumin Derivatives/Nano-Titanium Dioxide-Mediated Photodynamic Therapy on Candida albicans
por: Kanpittaya, Kasama, et al.
Publicado: (2021)

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

Al-hijamah (wet cupping therapy of prophetic medicine) significantly and safely reduces iron overload and oxidative stress in thalassemic children: a novel pilot study
por: El-Shanshory, Mohamed, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_j3vuscfn0l4kdaf99n7jfk3bm6