Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Maria Sasvari-Szekely"'
Autor:
Sigurdur Boðvarsson, Maria Sasvari-Szekely, Zsolt Ronai, G.J. Arason, George Füst, Perla Thorbjornsdottir, Ragnhildur Kolka, Zoltán Prohászka, Sigurður Thór Sigurðarson, G. Thorgeirsson, Margit Kovács, Garðar Sigurðsson, Bernadett Blaskó
Publikováno v:
International Immunology. 20:31-37
Background and Objectives: Some recent data indicate that risk of death after acute coronary syndrome is under genetic control. Previously, we found that the C4B*Q0 genotype (low copy number of the C4B gene that encodes the fourth component of comple
Publikováno v:
Clinical Chemistry. 52:1756-1762
Background: Investigation of the genetic background of complex traits is the focus of recent interest, as several common diseases or the individual response to treatments of various illnesses have not yet been explored. These studies require the deve
Autor:
Ágnes Szilágyi, Zsolt Ronai, Maria Sasvari-Szekely, András Guttman, Bernadett Blaskó, György Füst
Publikováno v:
ELECTROPHORESIS. 27:1437-1443
Complement component 4 (C4) is an important plasma protein playing a major role in the human defense mechanism against infectious diseases and inflammatory processes. The C4A and C4B genes, encoding the two isoforms of complement 4, are located in th
Autor:
Zsolt Ronai, Maria Sasvari-Szekely, Zsolt Csapó, Éva Kereszturi, Orsolya Király, Zsofia Nemoda, Eszter Szantai, Judit Gervai
Publikováno v:
Psychiatric Genetics. 15:259-270
OBJECTIVES: Polymorphic regions of the dopamine D4 receptor gene and its promoter region are in the focus of psychogenetic association studies. Besides the accurate phenotype characterization, highly reliable genotyping methods are also of outstandin
Autor:
Ibolya Varga, Maria Sasvari-Szekely, Nikolette Szücs, Attila Patócs, Miklós Tóth, Csaba Barta, Edit Gláz, Csilla Jakab, Károly Rácz
Publikováno v:
European Journal of Endocrinology. :349-355
OBJECTIVE: The aims of the present study were (a) to examine the occurrence of 21-hydroxylase gene (CYP21) mutations in patients with unilateral and bilateral adrenal incidentalomas and (b) to correlate the results of mutation screening with hormonal
Autor:
Zsolt Ronai, Maria Sasvari-Szekely, Erika Kovács, Anna Szekely, Zsofia Nemoda, András Guttman, Sarah Shandrick
Publikováno v:
ELECTROPHORESIS. 22:4008-4011
Large-scale genotyping of the repeat polymorphism in the regulatory region of the serotonin transporter gene (5-HTTLPR) was attempted by polymerase chain reaction (PCR) amplification followed by gel microchip electrophoresis analysis. The multilane (
Publikováno v:
ELECTROPHORESIS. 22:779-782
Rapid molecular diagnosis of 21-hydroxylase deficiency by detecting the most common mutation in the 21-hydroxylase gene is presented using primer extension and capillary electrophoresis with a polyvinyl pyrrolidone matrix. DNA samples were subjected
Publikováno v:
Journal of Chromatography A. 853:519-525
Ultrathin-layer agarose gel electrophoresis is a novel combination of the established methodologies of slab gel electrophoresis and capillary gel electrophoresis. This new format provides a multilane separation platform with rapid analysis time and e
Publikováno v:
Journal of Chromatography A. 828:481-487
Ultra-thin-layer agarose gel electrophoresis, a novel combination of agarose slab gel electrophoresis and capillary gel electrophoresis was introduced in conjunction with laser-induced fluorescence (LIF) scanning detection for the analysis of polymer
Publikováno v:
Journal of Chromatography A. 817:281-286
A detailed study is presented on the detection of various known point mutations using polymerase chain reaction (PCR) based multi-allele specific amplification (MASA) in conjunction with capillary gel electrophoresis (CGE) separation. The resulting P