Zobrazeno 1 - 10 of 27 pro vyhledávání: '"N Q Hanson"'
1
Influence of 699C→T and 1080C→T polymorphisms of the cystathionine β-synthase gene on plasma homocysteine levels
Autor: Feng Yang, N Q Hanson, Michael Y. Tsai, O Aras
Publikováno v: Clinical Genetics. 58:455-459
The association of moderately elevated total homocysteine (tHcy) levels with coronary artery disease is increasingly being recognized. However, the role of genetic influence on plasma tHcy levels is not completely understood. We studied 1,055 individ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::26c038a921d50aac740f479e88bfefe2
https://doi.org/10.1034/j.1399-0004.2000.580605.x
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3
Cystatin C is an independent predictor of fasting and post-methionine load total homocysteine concentrations among stable renal transplant recipients
Autor: Aras O, M Y, Tsai, N Q, Hanson, R, Bailey, G, Rao, D B, Hunninghake
Publikováno v: Clinical chemistry. 47(7)
An increased prevalence of hyperhomocysteinemia with an increased incidence of cardiovascular disease events has been reported among stable renal transplant recipients (RTRs). Preliminary studies in a small number of these individuals have shown that
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0b71206f4df9951900cb08e87f847fab
https://pubmed.ncbi.nlm.nih.gov/11427458
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4
C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease
Autor: N Q, Hanson, O, Aras, F, Yang, M Y, Tsai
Publikováno v: Clinical chemistry. 47(4)
Moderately increased plasma concentrations of total homocysteine (tHcy) have been shown to be an important risk factor for vascular diseases. Two common polymorphisms of the methylenetetrahydrofolate reductase (MTHFR) gene, the thermolabile C677T and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b086803fbb01c237c58385262fdd7081
https://pubmed.ncbi.nlm.nih.gov/11274015
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5
Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: a single nucleotide substitution in the second repeat prevents multiple alternate splicing
Autor: F, Yang, N Q, Hanson, K, Schwichtenberg, M Y, Tsai
Publikováno v: American journal of medical genetics. 95(4)
We studied a large number of individuals with respect to the 31-bp variable number tandem repeat (VNTR) in the cystathionine beta-synthase (CBS) gene. The number of repeats varies from 15-20, with 17 repeats the most common allele. Significantly, we
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ae88bcc40a295fbb6c75582d22361a8d
https://pubmed.ncbi.nlm.nih.gov/11186895
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6
Influence of 699C--T and 1080C--T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels
Autor: O, Aras, N Q, Hanson, F, Yang, M Y, Tsai
Publikováno v: Clinical genetics. 58(6)
The association of moderately elevated total homocysteine (tHcy) levels with coronary artery disease is increasingly being recognized. However, the role of genetic influence on plasma tHcy levels is not completely understood. We studied 1,055 individ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fbcd87846b270617c8e657e1b192d4f5
https://pubmed.ncbi.nlm.nih.gov/11149614
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7
High prevalence of a mutation in the cystathionine beta-synthase gene
Autor: M Y, Tsai, M, Bignell, K, Schwichtenberg, N Q, Hanson
Publikováno v: American journal of human genetics. 59(6)
We found that a mutation previously described by Sebastio et al., involving a 68-bp insertion in the coding region of exon 8 of the cystathionine-beta-synthase (CBS) gene in a single patient with homocystinuria, is highly prevalent. In our control po
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::110a6776f215bf70e5059b79c5cfd1fe
https://pubmed.ncbi.nlm.nih.gov/8940271
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9
Determination of a T/G polymorphism at nucleotide 3206 of the apolipoprotein C III gene by amplification refractory mutation system
Autor: M Y, Tsai, N Q, Hanson, K R, Copeland, I, Beheshti, U, Garg
Publikováno v: Clinical chemistry. 40(12)
We used the amplification refractory mutation system (ARMS)--a polymerase-chain-reaction-based method--to determine the 3206 T-to-G polymorphism on exon 4 of the apolipoprotein (apo) C III gene. Apo C III is an inhibitor of the enzyme lipoprotein lip
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2a81461276e14f32bf09333d17af93cd
https://pubmed.ncbi.nlm.nih.gov/7988011
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