Results 51 to 60 of about 320,664 (149)
Molecular Oncology, Volume 19, Issue S1, Page 1-940, June 2025.Abstracts submitted to the ‘EACR 2025 Congress: Innovative Cancer Science’, from 16–19 June 2025 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
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Anne HFE, H63D gen polimorfizminin plasental kurşun düzeyine etkisi
, 2020 Hemakromatozis (HFE) geni bir transmembran proteinidir. Bu gen β2 mikroglobulinle etkileşime girer ve transferin reseptörüne (TR) bağlanarak intestinal demir emiliminin düzenlenmesinde görev almaktadır. HFE geni ayrıca plasentanın sinsitotrofoblast hücrelerinde sentezlenmektedir. Bu şekilde anne fötüs arasındaki demir geçişi sağlanabilmektedir.
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Kriptojenik sirozlarda ve HBV ilişkili sirozlarda HFE gen mutasyonları
, 2008 Gastroenteroloji Yan Dal Tezi olarak hazırlanmıştır.Giriş ve amaç: HFE gen mutasyonları ile ilişkili herediter hemokromatozis, Avrupa populasyonunda yaygın görülen otozomal resesif geçişli bir hastalıktır.
Tüzün, Ahmet Yekta
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HLA and hemochromatosis disease association in São Miguel Island [PDF]
, 2008 Mestrado em Biologia Molecular e CelularA hemocromatose hereditária uma doença autossómica recessiva do metabolismo do ferro, geralmente associada à mutação C282Y no gene HFE. Presume-se que a origem desta mutação tenha ocorrido por acaso no haplótipo
Gomes, Cidália Maria Teixeira
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HFE in Biophilic Design: Human Connections with Nature
, 2018 Human Factors and Ergonomics (HFE) pays insufficient attention to nature based solutions for workplace issues, despite evidence for its effectiveness, while also being relatively inexpensive to implement. Lumber, Richardson and Albertsen discuss research
Lumber, R. +8 more
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Talasemi hastalarinda HFE gen polimorfizminin kan metal düzeylerine etkisi
, 2020 There are many genetic factors that play a role in iron metabolism. One of them, HFE (hemochromatosis-causing gene) gene. The aim of this study; is to determine the polymorphism of HFE gene H63D polimorphism in beta thalassemia major patients and investigate whether this polymorphism has an effect on whole blood Fe, Pb and Cd levels and Ferritin, Hct ...
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Kriptojenik sirozlarda ve HBV ilişkili sirozlarda HFE gen mutasyonları
, 2017 Backround and aim: Mutations of HFE gene are associated with hereditary hemochomatosis (HH), the most common autosomal recessive disorder in European population. To early detection, population screening is not currently advocated because of the discrepancy betweenthe common mutation prevalence and apparently lower frequency of clinical disease.
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A study of zinc transporter 1 and its role in Type 3 Haemochromatosis [PDF]
, 2009 Hereditary haemochromatosis is an autosomal recessive disorder of iron metabolism, characterised by increased iron absorption and progressive iron accumulation particularly in the liver.
Parkinson, Liza
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Standard Poster Abstracts for the 17th Asia Pacific Heart Rhythm Society (APHRS) Scientific Sessions
Journal of Arrhythmia, Volume 41, Issue 2, April 2025.
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Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2
, 2011 The induction of the iron-regulatory peptide hepcidin by proinflammatory cytokines is thought to result in the withholding of iron from invading pathogens.
Wallace, Daniel F. +11 more
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