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[PDF] Top 20 Ancestral association between HLA and HFE H63D and C282Y gene

Has 10000 "Ancestral association between HLA and HFE H63D and C282Y gene" found on our website. Below are the top 20 most common "Ancestral association between HLA and HFE H63D and C282Y gene".

Ancestral association between HLA and HFE H63D and C282Y gene

Ancestral association between HLA and HFE H63D and C282Y gene

... the H63D mutation is less cer- tain and because the highest H63D frequency was detected in Spain, Aguilar-Martinez et ...the H63D mutation emerged in the Iberian Peninsula. Al- ternatively, ... See full document

6

Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis

Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis

... are C282Y ho- mozygotes or C282Y and H63D compound heterozygotes (5,20-25), but agree with re- cent data reported for Italy, where approxi- mately one third of the patients with HH showed ... See full document

7

Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR

Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR

... primer and probe set employed by Bernard et ...the HFE gene, but with a 1.5°C difference in Tm between S65C and C282Y mutant alleles, which may pose some risk of a false-positive ... See full document

6

Analysis of the induction of the cytoprotective Nrf2 signalling pathway in reticuloendothelial cells from iron-treated mice and HFE Haemochromatosis patients

Analysis of the induction of the cytoprotective Nrf2 signalling pathway in reticuloendothelial cells from iron-treated mice and HFE Haemochromatosis patients

... overload and multiorgan dysfunction. The most common mutation of HFE–HH is the missense mutation where a cysteine is replaced for a tyrosine at amino acid 282 ...for C282Y and H63D ... See full document

86

HFE gene mutation and oxidative damage biomarkers in patients with  syndromes and its relation to transfusional iron oload : an observational crosssectional study

HFE gene mutation and oxidative damage biomarkers in patients with syndromes and its relation to transfusional iron oload : an observational crosssectional study

... failure and a variable propensity to evolve into acute myeloid ...disease and many develop transfusion dependence and consequent iron overload (IOL), considered to be a negative inde- pendent ... See full document

7

Rev. Bras. Hematol. Hemoter.  vol.30 número5

Rev. Bras. Hematol. Hemoter. vol.30 número5

... to C282Y and H63D mutations in the HFE ...on HFE gene mutation frequencies are rare, mainly in regards to a representative sample ...of C282Y and H63D ... See full document

5

Estudo das mutações C282Y, H63D e S65C do gene HFE em doentes brasileiros com sobrecarga de ferro.

Estudo das mutações C282Y, H63D e S65C do gene HFE em doentes brasileiros com sobrecarga de ferro.

... of C282Y, H63D and S65C mutations of the HFE gene in Brazilian patients with iron overload, to verify the coexistence of chronic hemolytic anemia, hepatitis C and excessive ... See full document

10

Alterações moleculares associadas à hemocromatose hereditária.

Alterações moleculares associadas à hemocromatose hereditária.

... 3 and 4, when the iron overload is associated to the HFE, HJV, HAMP, TFR2 and SLC40A1 genes, ...three HFE gene mutations (C282Y, H63D and S65C) in the Brazilian ... See full document

11

Arq. Gastroenterol.  vol.49 número1

Arq. Gastroenterol. vol.49 número1

... (86.4%) and 6 genotype 2 ...5) and F4 (n = ...55-516). HFE gene mutations were detected in 16 patients (36%), with the following distribution: heterozygous H63D (n = 11); heterozygous ... See full document

5

HFE gene mutations in Brazilian

HFE gene mutations in Brazilian

... intake and progressive storage and is related to mutations in the HFE ...Interactions between thalassemia and hemochromatosis may further increase iron ...heterogeneous and ... See full document

6

Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload

Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload

... the C282Y mutation were: 5’ – TGC CTC CTT TGG TGA AGG TGA CAC – 3’ and 5’ – CTC AGG CAC TCC TCT CAA CC – ...the H63D and S65C HFE gene mutations, the following primers were used: ... See full document

6

Interplay between temperature gradients field and C - E transformation in solidifying rolls

Interplay between temperature gradients field and C - E transformation in solidifying rolls

... A comparison of temperature field created at 5.5 hour of solidification progress and that at 8.0 hour indicates that practically temperature field is not changed significantly. The only decrease of temperature is ... See full document

7

Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia.

Association between protective and deleterious HLA alleles with multiple sclerosis in Central East Sardinia.

... on HLA loci, these last results need to be confirmed both on our population and replicated in ...studying HLA main loci only could not be enough as other HLA genes may be involved and ... See full document

9

Associação do alelo HLA-DRB1 com suscetibilidade a artrite reumatoide e gravidade da doença na Síria.

Associação do alelo HLA-DRB1 com suscetibilidade a artrite reumatoide e gravidade da doença na Síria.

... alelos HLA-DRB1 com a suscetibilidade a AR e sua gravidade na ...alelos HLA-DRB1 *01, *04 e *10 mostraram forte associação com suscetibilidade à doença (OR = 2,29, IC 95% = 1,11–4,75, P = 0,022; OR = 3,16, ... See full document

6

Common variants on cytotoxic T lymphocyte antigen-4 polymorphisms contributes to type 1 diabetes susceptibility: evidence based on 58 studies.

Common variants on cytotoxic T lymphocyte antigen-4 polymorphisms contributes to type 1 diabetes susceptibility: evidence based on 58 studies.

... published and thus can be included in the ...individuals, and these high-risk people are usually more likely to be included in small ...English and less likely to be cited in other ... See full document

9

HFE gene mutations in coronary atherothrombotic disease

HFE gene mutations in coronary atherothrombotic disease

... the HFE gene (Cys282Tyr and His63Asp) related to hereditary hemo- chromatosis provides an opportunity to address the question of the association between iron overload and ...of ... See full document

6

Health And Wellbeing Impact And Treatment of Nocturia – A Review of The Literature

Health And Wellbeing Impact And Treatment of Nocturia – A Review of The Literature

... Safety and eicacy of alfuzosin 10 mg once-daily in the treatment of lower urinary tract symptoms and clinical benign prostatic hyperplasia: a pooled analysis of three double-blind, placebo-controlled ... See full document

6

Rev. Bras. Reumatol.  vol.53 número1 en v53n1a05

Rev. Bras. Reumatol. vol.53 número1 en v53n1a05

... the association of HLA-DRB1 alleles with the susceptibility and severity of RA in ...Patients and methods: Eighty- six RA patients and 200 healthy controls from Syria were genotyped ... See full document

7

Rev. Bras. Hematol. Hemoter.  vol.32 número6

Rev. Bras. Hematol. Hemoter. vol.32 número6

... the HFE gene (C282Y homozygotes or C282Y/H63D compound heterozygotes) and is almost exclusively found in populations of northern European ...enterocytes and macrophages. ... See full document

7

Estudos de associação entre transtorno obsessivo-compulsivo e genes candidatos: uma revisão.

Estudos de associação entre transtorno obsessivo-compulsivo e genes candidatos: uma revisão.

... Objetivo: Nos últimos anos, o papel dos genes dos sistemas serotoninérgicos e dopaminérgicos tem sido sistematicamente investigado em pacientes FRP WUDQVWRUQR REVHVVLYRFRPSXOVLYR 72&  XPD YH] TXH HVVHV ... See full document

8

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