Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maria Sasvari-Szekely"'
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
Autor:
Iannis Talianidis, Zsolt Csapó, Tatjana Spasokoukotskaja, Maria Staub, Staffan Eriksson, Maria Sasvari-Szekely
Publikováno v:
Biochemical Pharmacology. 61:191-197
Deoxycytidine kinase (dCK, EC.2.7.1.74) is a key enzyme in the intracellular metabolism of 2-chlorodeoxyadenosine, 1-β- d -arabinofuranosylcytosine, difluorodeoxycytidine, and other drugs used in chemotherapy of different leukaemias and solid tumour
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
Autor:
Péter Gaszner, Maria Sasvari-Szekely, Zsolt Ronai, András Guttman, Krisztina Boór, Zsofia Nemoda, Huba Kalász
Publikováno v:
Current medicinal chemistry. 9(8)
A noninvasive DNA sampling method has been implemented collecting buccal mucosa cells by cotton wool swabs. An amount of 0.2 2 microg DNA per patient was obtained after the phenol-extraction procedure and 0.2 2 ng DNA template was sufficient for PCR
Autor:
Zsolt Ronai, András Guttman, Zsofia Nemoda, Erika Kovács, Csaba Barta, Maria Sasvari-Szekely, Anna Szekely
Publikováno v:
Journal of chromatography. A. 924(1-2)
A microfabricated electrophoresis device was used for rapid polymerase chain reaction product analysis in genotyping the dopamine D4 receptor gene (DRD4) 48 base pairs repeat polymorphism. An allelic ladder, prepared from homozygous individuals, was
Publikováno v:
Electrophoresis. 21(10)
Prior studies have revealed possible association between the presence of a seven repeat of the 48 bp variable number tandem repeat polymorphism of the human dopamine D4 receptor gene (DRD4) and some normal and pathological human traits, such as novel
Publikováno v:
Electrophoresis. 21(4)
We report a novel, high-throughput genotyping method by single nucleotide polymorphism (SNP) analysis using bidirectional allele-specific amplification with polymerase chain reaction (PCR) in a single-step/single-tube format. Blood coagulation factor
Publikováno v:
Scopus-Elsevier
The polymorphic human DNA sequence in the promoter region of the dopamine D4 receptor gene has been investigated by means of non-invasive DNA sampling, amplification by means of the polymerase chain reaction, and subsequent separation of the reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60444060790d36aefeae661429d7edf7
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036084159&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036084159&partnerID=MN8TOARS