Pages that link to "Q48067239"

The following pages link to Mutation analysis in hereditary hemochromatosis (Q48067239):

Displaying 50 items.

• Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum (Q22001443) (← links)
• The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding (Q24309651) (← links)
• The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression (Q24323216) (← links)
• HLA-H and Associated Proteins in Patients with Hemochromatosis (Q24654613) (← links)
• Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population (Q24799853) (← links)
• Hepatocellular carcinoma and the penetrance of HFE C282Y mutations: a cross sectional study (Q24811285) (← links)
• HFE H63D mutation frequency shows an increase in Turkish women with breast cancer (Q25256743) (← links)
• Multicentric origin of hemochromatosis gene (HFE) mutations (Q28139525) (← links)
• Genotypic and phenotypic heterogeneity of African Americans with primary iron overload (Q28187076) (← links)
• Global prevalence of putative haemochromatosis mutations (Q28237178) (← links)
• Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis (Q28254820) (← links)
• HFE gene knockout produces mouse model of hereditary hemochromatosis (Q28263309) (← links)
• Haemochromatosis protein is expressed on the terminal web of enterocytes in proximal small intestine of the rat (Q28581175) (← links)
• The twin questions of personalized medicine: who are you and whom do you most resemble? (Q28755234) (← links)
• Incidence of liver disease in people with HFE mutations. (Q30652113) (← links)
• High-performance multiplex SNP analysis of three hemochromatosis-related mutations with capillary array electrophoresis microplates (Q30982529) (← links)
• A simple combined microdissection and aspiration device for the rapid procurement of single cells from clinical peripheral blood smears (Q31931772) (← links)
• Cloning of the hereditary hemochromatosis gene: implications for pathogenesis, diagnosis, and screening (Q33540057) (← links)
• Interrelationships of alcohol and iron in liver disease with particular reference to the iron-binding proteins, ferritin and transferrin (Q33590854) (← links)
• Hereditary haemochromatosis: diagnosis and management in the gene era. (Q33603907) (← links)
• Screening for hemochromatosis. A public health perspective (Q33644877) (← links)
• Hereditary hemochromatosis (HFE) genotypes in heart failure: relation to etiology and prognosis (Q33644914) (← links)
• Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis (Q33679433) (← links)
• Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis (Q33681573) (← links)
• Should all patients with diabetes mellitus be screened for hemochromatosis? (Q33729647) (← links)
• The haemochromatosis gene: a global perspective and implications for the Asia-Pacific region (Q33760038) (← links)
• The hereditary hemochromatosis gene (HFE): a MHC class I-like gene that functions in the regulation of iron homeostasis (Q33784079) (← links)
• Long-term follow-up after liver transplantation in patients with hepatic iron overload (Q33873371) (← links)
• The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22. (Q33901224) (← links)
• Hereditary hemochromatosis (Q33927510) (← links)
• Regulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis (Q34016565) (← links)
• Population screening for hemochromatosis: has the time finally come? (Q34027952) (← links)
• Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry (Q34082863) (← links)
• Sequence variation and haplotype structure at the human HFE locus (Q34146092) (← links)
• The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populations (Q34385747) (← links)
• EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). (Q34483947) (← links)
• The influence of iron status and genetic polymorphisms in the HFE gene on the risk for postoperative complications after bariatric surgery: a prospective cohort study in 1,064 patients (Q34540883) (← links)
• Molecular pathogenesis of iron overload. (Q34739178) (← links)
• Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants. (Q34750501) (← links)
• Mutation analysis of the HLA-H gene in Italian hemochromatosis patients (Q35238695) (← links)
• Mutations in the hereditary haemochromatosis gene HFE in professional endurance athletes. (Q35329531) (← links)
• The significance of haemochromatosis gene mutations in the general population: implications for screening (Q35353437) (← links)
• Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis (Q35359395) (← links)
• Is genetic screening for hemochromatosis worthwhile? (Q35742155) (← links)
• Iron overload states (Q35960826) (← links)
• Targeted disruption of the HFE gene (Q36060569) (← links)
• Magnetic resonance imaging quantification of liver iron (Q36197679) (← links)
• Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with β 2 -microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells (Q36809964) (← links)
• Genetic background of Japanese patients with adult-onset storage diseases in the liver (Q36828253) (← links)
• Hyperferritinemia is a risk factor for steatosis in chronic liver disease. (Q37182959) (← links)