Results 11 to 20 of about 24,501 (221)
Non-HFE haemochromatosis [PDF]
World Journal of Gastroenterology, 2007 Non-HFE hereditary haemochromatosis (HH) refers to a genetically heterogeneous group of iron overload disorders that are unlinked to mutations in the HFE gene. The four main types of non-HFE HH are caused by mutations in the hemojuvelin, hepcidin, transferrin receptor 2 and ferroportin genes. Juvenile haemochromatosis is an autosomal recessive disorder
Wallace, Daniel, Subramaniam, V. Nathan
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Cryptanalysis of HFE, multi-HFE and variants for odd and even characteristic [PDF]
Designs, Codes and Cryptography, 2012 zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Luk Bettale +2 more
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Non- HFE hemochromatosis [PDF]
Hepatology, 2004 The term "non-HFE hemochromatosis" (non-HFE HC) refers to several phenotypically similar but genetically distinct forms of hereditary hemochromatosis affecting individuals without pathogenic mutations of HFE. The involved genes are, sinsu strictu, transferrin receptor 2 (TfR2), hemojuvelin (HJV), and hepcidin (HAMP).
PIETRANGELO, Antonello
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In situ proximity ligation assays indicate that hemochromatosis proteins Hfe and transferrin receptor 2 (Tfr2) do not interact. [PDF]
PLoS ONE, 2013 The hemochromatosis associated proteins HFE and Transferrin Receptor 2 (TFR2) have been shown to be important for the proper regulation of hepcidin. A number of in vitro studies using transient overexpression systems have suggested that an interaction ...
Gautam Rishi +3 more
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The structure and function of HFE
BioEssays, 2000 The iron overload disease hereditary haemochromatosis (HH) occurs in about 1 in 300 Caucasians; the protein mutated in this disorder is termed HFE.(1) HFE is homologous to major histocompatibility complex (MHC) class I proteins, but unlike MHC class I molecules, HFE does not present peptides to T cells.(2) The transferrin receptor (TfR) is a ligand for
Drakesmith, H, Townsend, A
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Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2011 Review on HFE (hemochromatosis), with data on DNA, on the protein encoded, and where the gene is implicated.
Dorak, MT, MT Dorak
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Estudi de les mutacions dels exons 2 i 4 del gen HFE en pacients amb porfiria cutània tarda esporàdica [PDF]
, 2006 [cat] La Porfíria Cutània Tarda (PCT) és una malaltia metabòlica que afecta a la pell i al fetge i que és desencadenada per la interacció de múltiples factors que inclouen l´herència, l´alcohol, el VHC, els estrògens i alguns agents tòxics, entre d ...
Toll Abelló, Agustí
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Degree of regularity for HFE Minus (HFE-)
Degree of regularity for HFE Minus (HFE-)In this paper, we prove a closed formula for the degree of regularity of the family of HFE- (HFE Minus) multivariate public key cryptosystems over a finite field of size q. The degree of regularity of the polynomial system derived from an HFE- system is less than or equal to ((q-1)(⌊log_q(D-1)⌋+a))/2+2 if q is even and r+a is odd, ((q-1)(⌊log_q(D-1)⌋+a+
ディン, ジンタイ +3 more
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Two-dimensional tellurium-based diodes for RF applications
npj 2D Materials and Applications, 2023 The research of two-dimensional (2D) Tellurium (Te) or tellurene is thriving to address current challenges in emerging thin-film electronic and optoelectronic devices.
Abdelrahman M. Askar +6 more
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Haematologica, 2000 HFE is a class-I MHC related protein which carries the C282Y mutation in most patients with hereditary hemochromatosis, an iron overload disease. HFE protein is expected to have a relevant role in the regulation of duodenal iron absorption, and HFE protein was immunohistochemically identified in the crypt cells.
L. Zuccon +9 more
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