نتایج جستجو برای: hemojuvelin mutation

تعداد نتایج: 291556  

Journal: :Haematologica 2008
Alessia Pagani Laura Silvestri Antonella Nai Clara Camaschella

BACKGROUND Hemojuvelin is a glycosylphosphatidylinositol-anchored protein, expressed in liver, skeletal muscle and heart. As a co-receptor of bone morphogenetic protein, membrane hemojuvelin positively modulates the iron regulator hepcidin. Mutations of the gene encoding for hemojuvelin cause juvenile hemochromatosis, characterized by hepcidin deficiency and severe iron overload. We have previo...

Journal: :Physiological research 2010
J Krijt Y Fujikura L Sefc M Vokurka T Hlobenová E Necas

Hepcidin is a key regulator of iron homeostasis, while hemojuvelin is an important component of the hepcidin regulation pathway. It has been recently proposed that soluble hemojuvelin, produced from hemojuvelin by the protease furin, decreases hepcidin expression. The aim of the presented study was to examine the downregulation of hepcidin by chronic bleeding in hemojuvelin-mutant mice. Male mi...

Journal: :Journal of medical genetics 2004
K J H Robson A T Merryweather-Clarke E Cadet V Viprakasit M G Zaahl J J Pointon D J Weatherall J Rochette

Mutations in the hepcidin gene HAMP and the hemojuvelin gene HJV have recently been shown to result in juvenile haemochromatosis (JH). Hepcidin is an antimicrobial peptide that plays a key role in regulating intestinal iron absorption. Hepcidin levels are reduced in patients with haemochromatosis due to mutations in the HFE and HJV genes. Digenic inheritance of mutations in HFE and HAMP can res...

Journal: :Haematologica 2007
Luca Valenti Edoardo A Pulixi Paolo Arosio Laura Cremonesi Giorgio Biasiotto Paola Dongiovanni Marco Maggioni Silvia Fargion Anna Ludovica Fracanzani

BACKGROUND AND OBJECTIVES Hepatitis C virus (HCV) chronic hepatitis predisposes to iron overload, which negatively influences the prognosis of this infection. Since the underlying mechanisms of this iron overload are undefined, we analyzed the prevalence of altered iron parameters, and the relative contribution of viral, metabolic, and genetic factors in Italian patients. DESIGN AND METHODS W...

Journal: :Haematologica 2012
Thomas B Bartnikas Mark D Fleming

Here we investigate the regulation of hepcidin, a hormone that inhibits dietary iron absorption and macrophage iron recycling, by the serum iron-binding protein transferrin. Mice deficient in transferrin (Tf(hpx/hpx)) and hemojuvelin (Hjv(-/-)), a gene mutated in juvenile hemochromatosis, a disease of hepcidin deficiency and iron overload, were generated. While Tf(hpx/hpx) Hjv(+/+) and Tf(hpx/h...

2017
Jana Frýdlová Zuzana Rychtarčíková Iuliia Gurieva Martin Vokurka Jaroslav Truksa Jan Krijt

Tmprss6-mutated mask mice display iron deficiency anemia and high expression of hepcidin. The aim of the study was to determine the effect of erythropoietin administration on proteins participating in the control of iron homeostasis in the liver and spleen in C57BL/6 and mask mice. Administration of erythropoietin for four days at 50 IU/mouse/day increased hemoglobin and hematocrit in C57BL/6 m...

Journal: :Blood 2009
Laura Silvestri Flavia Guillem Alessia Pagani Antonella Nai Claire Oudin Muriel Silva Fabienne Toutain Caroline Kannengiesser Carole Beaumont Clara Camaschella Bernard Grandchamp

Matriptase-2 is a transmembrane serine protease that negatively regulates hepcidin expression by cleaving membrane-bound hemojuvelin. Matriptase-2 has a complex ectodomain, including a C-terminal serine protease domain and its activation requires an autocatalytic cleavage. Matriptase-2 mutations have been reported in several patients with iron-refractory iron deficiency anemia. Here we describe...

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