نتایج جستجو برای: h63d

تعداد نتایج: 365  

2011
Ruth Blanco-Rojo Carlos Baeza-Richer Ana M López-Parra Ana M Pérez-Granados Anna Brichs Stefania Bertoncini Alfonso Buil Eduardo Arroyo-Pardo Jose M Soria M Pilar Vaquero

BACKGROUND Iron deficiency anaemia is a worldwide health problem in which environmental, physiologic and genetic factors play important roles. The associations between iron status biomarkers and single nucleotide polymorphisms (SNPs) known to be related to iron metabolism were studied in menstruating women. METHODS A group of 270 Caucasian menstruating women, a population group at risk of iro...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005
James P Robinson Victoria L Johnson Pauline A Rogers Richard S Houlston Earmonn R Maher D Timothy Bishop D Gareth R Evans Huw J W Thomas Ian P M Tomlinson Andrew R J Silver

Whereas a recent study reported an increased risk of colorectal cancer associated with any HFE germ line mutation (C282Y or H63D), other investigators have concluded there is no increased risk, or that any increase is dependent on polymorphisms in HFE-interacting genes such as the transferrin receptor (TFR). We have established the frequency of HFE mutations in colorectal cancer patients (n = 3...

Journal: :Clinical chemistry 2000
E Rossi J K Olynyk D J Cullen G Papadopoulos M Bulsara L Summerville L W Powell

BACKGROUND Women who inherit heterozygosity for the C282Y mutation of the HFE gene may have increased serum iron indices and hemoglobin and are less likely to develop iron deficiency compared with women with the wild-type genotype. METHODS We performed a cross-sectional analysis of 497 women 20-44 years of age and 830 women >51 years of age drawn from the Busselton (Australia) population stud...

Journal: :Diabetes care 2006
Ronald T Acton James C Barton Leah V Passmore Paul C Adams Mark R Speechley Fitzroy W Dawkins Phyliss Sholinsky David M Reboussin Gordon D McLaren Emily L Harris Thomas C Bent Thomas M Vogt Oswaldo Castro

OBJECTIVE We evaluated the associations of self-reported diabetes with serum ferritin concentration, transferrin saturation (TfSat), and HFE C282Y and H63D mutations in six racial/ethnic groups recruited at five field centers in the Hemochromatosis and Iron Overload Screening (HEIRS) study. RESEARCH DESIGN AND METHODS Analyses were conducted on 97,470 participants. Participants who reported a...

Journal: :The American journal of medicine 2002
Jill Waalen Vincent Felitti Terri Gelbart Ngoc J Ho Ernest Beutler

PURPOSE Mutations of the HFE gene that cause hereditary hemochromatosis may be associated with an increased risk of cardiovascular disease. We examined the relation between two HFE mutations (C282Y and H63D), indicators of iron homeostasis, and the prevalence of coronary heart disease in a large population of white adults. SUBJECTS AND METHODS We conducted a cross-sectional study of 30,916 wh...

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