Results 31 to 40 of about 24,501 (221)
HFE variants in colorectal cancer and their clinicopathological correlations.
BACKGROUND: The study aimed to screen mutation of human homeostatic iron regulator (HFE) in colorectal carcinoma (CRC) and detect their associations with clinicopathological parameters.
Lee, Katherine TW +9 more
core +1 more source
A family of weak keys in HFE and the corresponding practical key-recovery
The HFE (hidden field equations) cryptosystem is one of the most interesting public-key multivariate schemes. It has been proposed more than 10 years ago by Patarin and seems to withstand the attacks that break many other multivariate schemes, since ...
Bouillaguet Charles +3 more
doaj +1 more source
Mutations in HFE cause hereditary hemochromatosis type I hallmarked by increased iron absorption, iron accumulation in hepatocytes and iron deficiency in myeloid cells.
Manfred Nairz +13 more
doaj +1 more source
Inverting HFE Is Quasipolynomial [PDF]
In the last ten years, multivariate cryptography has emerged as a possible alternative to public key cryptosystems based on hard computational problems from number theory. Notably, the HFE scheme [17] appears to combine efficiency and resistance to attacks, as expected from any public key scheme.
Louis Granboulan +2 more
openaire +1 more source
Alternative polyadenylation and nonsense-mediated decay coordinately regulate the human HFE mRNA levels. [PDF]
Nonsense-mediated decay (NMD) is an mRNA surveillance pathway that selectively recognizes and degrades defective mRNAs carrying premature translation-termination codons.
Rute Martins +6 more
doaj +1 more source
A chemically defined PEG‐based microgel platform enables scalable, reproducible production of three‐dimensional microgel‐iPSC constructs in multiple sizes. The system is compatible with high‐throughput automation and supports human iPSC expansion and differentiation within a single construct, including directed differentiation into cardiac organoids ...
Laura Klasen +8 more
wiley +1 more source
BACKGROUND: β-thalassemia major (βTM) is a genetic disorder characterized by a deficiency in hemoglobin production, ineffective erythropoiesis, chronic hemolysis, lifelong blood transfusions, iron overload, and increased risk of cardiac complications ...
Hussein Yaqoub Hamza +2 more
doaj +1 more source
Glaucoma, a major cause of blindness, involves retinal ganglion cell (RGC) degeneration. This study shows growth hormone‐releasing hormone receptor (GHRHR) deficiency preserves RGC survival and restores vision, unlike activation which only aids survival.
Yan Tong +24 more
wiley +1 more source
Liver disorder and the HFE locus [PDF]
Hereditary haemochromatosis (HH) is the most common inherited disease in Northern Europeans, with a prevalence of around 1 in 300.1 When Feder et al . identified a mutation in a novel MHC‐class‐I‐like gene, HFE , that was present in over 80% of these patients, it was evident that there was potential to improve not only patient diagnosis, but also the ...
S F, Stewart, C P, Day
openaire +2 more sources
Differential HFE gene expression is regulated by alternative splicing in human tissues. [PDF]
The pathophysiology of HFE-derived Hereditary Hemochromatosis and the function of HFE protein in iron homeostasis remain uncertain. Also, the role of alternative splicing in HFE gene expression regulation and the possible function of the corresponding ...
Rute Martins +3 more
doaj +1 more source

