نتایج جستجو برای: thalassemic

تعداد نتایج: 1036  

Journal: :Haematologica 2010
Pathrapol Lithanatudom Amporn Leecharoenkiat Tirawat Wannatung Saovaros Svasti Suthat Fucharoen Duncan R Smith

BACKGROUND Cells respond to stress stimuli through a number of response pathways, of which one of the most important and well characterized is the unfolded protein response. Despite a large body of work which suggests that stress in erythroblasts may play a pivotal role in the pathogenesis of beta-thalassemia/Hb E disease, this pathway remains uninvestigated. DESIGN AND METHODS Day 10 erythro...

Journal: :Blood 2012
Eugene Khandros Christopher S Thom Janine D'Souza Mitchell J Weiss

Cells remove unstable polypeptides through protein quality-control (PQC) pathways such as ubiquitin-mediated proteolysis and autophagy. In the present study, we investigated how these pathways are used in β-thalassemia, a common hemoglobinopathy in which β-globin gene mutations cause the accumulation and precipitation of cytotoxic α-globin subunits. In β-thalassemic erythrocyte precursors, free...

Journal: :The Southeast Asian journal of tropical medicine and public health 2004
Piyada Jittangprasert Prapin Wilairat Pensri Pootrakul

This paper describes a comparison of two analytical techniques, one employing bathophenanthrolinedisulfonate (BPT), a most commonly-used reagent for Fe (II) determination, as chromogen and an electrothermal atomic absorption spectroscopy (ETAAS) for the quantification of non-transferrin bound iron (NTBI) in sera from thalassemic patients. Nitrilotriacetic acid (NTA) was employed as the ligand f...

Journal: :medical journal of islamic republic of iran 0
h foroutan from the department of1nternal medicine.imom hospital. tehran university of medical sciences, h ghofrani sh . mirmomen s kazemi asl mj farahvash m nasiri tousi

hepatitis c virus (hcv) infection is highly prevalent in thalassemic patients, and this may decrease the serum antibody response to hepatitis b virus (hbv) vaccine. there is also some alteration of the immune system in multi-transfused thalassemic patients, as a consequence of iron overload. we investigated whether hcy infection may reduce the effectiveness of hby vaccine in multi - transfused ...

Journal: :Asian Pacific journal of tropical biomedicine 2014
Kanokwan Kulprachakarn Nittaya Chansiw Kanjana Pangjit Chada Phisalaphong Suthat Fucharoen Robert C Hider Sineenart Santitherakul Somdet Srichairatanakool

OBJECTIVE To evaluate the iron-chelating properties and free-radical scavenging activities of 1-(N-acetyl-6-aminohexyl)-3-hydroxy-2-methylpyridin-4-one (CM1) treatment in chronic iron-loaded β-thalassemic (BKO) mice. METHODS The BKO mice were fed with a ferrocene-rich diet and were orally administered with CM1 [50 mg/(kg.day)] for 6 months. Blood levels of non-transferrin bound iron, labile p...

H FOROUTAN, H GHOFRANI, M NASIRI TOUSI, MJ FARAHVASH, S KAZEMI ASL, SH . MIRMOMEN,

Hepatitis C virus (HCV) infection is highly prevalent in thalassemic patients, and this may decrease the serum antibody response to hepatitis B virus (HBV) vaccine. There is also some alteration of the immune system in multi-transfused thalassemic patients, as a consequence of iron overload. We investigated whether HCY infection may reduce the effectiveness of HBY vaccine in multi - transf...

Journal: :Blood 1999
K Pattanapanyasat K Yongvanitchit P Tongtawe K Tachavanich W Wanachiwanawin S Fucharoen D S Walsh

Certain red blood cell (RBC) disorders, including thalassemia, have been associated with an innate protection against malaria infection. However, many in vitro correlative studies have been inconclusive. To better understand the relationship between human RBCs with thalassemia hemoglobinopathies and susceptibility to in vitro infection, we used an in vitro coculture system that involved biotin ...

Journal: :Blood 2004
Pietro Sodani David Gaziev Paola Polchi Buket Erer Claudio Giardini Emanuele Angelucci Donatella Baronciani Marco Andreani Marisa Manna Sonia Nesci Barbarella Lucarelli Reginald A Clift Guido Lucarelli

When prepared for transplantation with busulfan (BU) 14 mg/kg and cyclophosphamide (CY) 120 to 160 mg/kg, patients with thalassemia in risk class 3, aged younger than 17 years, who receive transplants from HLA-identical donors, had a 30% incidence of transplant rejection with recurrence of thalassemia. This, relatively poor, outcome was ascribed to insufficient immune suppression or to inadequa...

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