Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Maria Sasvari-Szekely"'
Publikováno v:
ELECTROPHORESIS. 35:379-384
The 25 kDa synaptosomal-associated protein (SNAP-25) is a crucial component of the soluble N-ethylmaleimide-sensitive factor attachment protein receptor complex and plays an important role in neurotransmission in the central nervous system. SNAP-25 h
Autor:
Gabor Faludi, Omar Abdul Rahman, Anna Szekely, Maria Sasvari-Szekely, András Guttman, Zsofia Nemoda
Publikováno v:
ELECTROPHORESIS. 31:1790-1795
The recent discovery of post-transcriptional regulation by microRNAs (miRNAs) drew our attention to SNPs of putative miRNA target sites in candidate genes of depression-related psychiatric disorders. The P2RX7 (purinergic receptor P2X, ligand-gated i
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, 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 (
Autor:
Zsolt Ronai, Maria Sasvari-Szekely, András Guttman, Judit Gervai, Maria Staub, Csaba Barta, Krisztina Lakatos
Publikováno v:
ELECTROPHORESIS. 22:1102-1105
The -521C/Tsingle nucleotide polymorphism (SNP) in the promoter region of the dopamine D4 receptor gene (DRD4) has recently been detected in oriental (Japanese) individuals and related to novelty seeking and schizophrenia. Here, we report the analysi
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:
ELECTROPHORESIS. 22:294-299
Applicability of modern microfabrication technology to electrophoresis microchips initiated a rapidly moving interdisciplinary field in analytical chemistry. Electric field mediated separations in microfabricated devices (electrophoresis microchips)
Autor:
Zsolt Ronai, Jimmy Hu, Reka Kovacs-Nagy, Maria Sasvari-Szekely, Peter Sarkozy, András Guttman
Publikováno v:
Electrophoresis. 32(15)
Synaptosomal-associated protein 25 (SNAP-25) plays a crucial role in exocitosis. Single nucleotide polymorphisms (rs3746544 and rs1051312) in the 3' un-translated region of the SNAP-25 gene have been described to be in association with attention-defi
Autor:
Omar Abdul, Rahman, Maria, Sasvari-Szekely, Anna, Szekely, Gabor, Faludi, Andras, Guttman, Zsofia, Nemoda
Publikováno v:
Electrophoresis. 31(11)
The recent discovery of post-transcriptional regulation by microRNAs (miRNAs) drew our attention to SNPs of putative miRNA target sites in candidate genes of depression-related psychiatric disorders. The P2RX7 (purinergic receptor P2X, ligand-gated i
Publikováno v:
Electrophoresis. 30(7)
Genetic polymorphisms are often considered as risk factors of complex diseases serving as valuable and easily detectable biomarkers, also stable during the whole lifespan. A novel type of genetic polymorphism has been identified just recently, referr