Sasvári-Székely M - Search Results

1

Screening for mutations of 21-hydroxylase gene in Hungarian patients with congenital adrenal hyperplasia.

Ferenczi A, Garami M, Kiss E, Pék M, Sasvári-Székely M, Barta C, Staub M, Sólyom J, Fekete G. Ferenczi A, et al. J Clin Endocrinol Metab. 1999 Jul;84(7):2369-72. doi: 10.1210/jcem.84.7.5835. J Clin Endocrinol Metab. 1999. PMID: 10404805 Free article.

2

Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification.

Theodoropoulou M, Barta C, Szoke M, Guttman A, Staub M, Niederland T, Sólyom J, Fekete G, Sasvari-Szekely M. Theodoropoulou M, et al. Fetal Diagn Ther. 2001 Jul-Aug;16(4):237-40. doi: 10.1159/000053918. Fetal Diagn Ther. 2001. PMID: 11399887

3

Analysis of mutations in the plasma cholinesterase gene of patients with a history of prolonged neuromuscular block during anesthesia.

Barta C, Sasvari-Szekely M, Devai A, Kovacs E, Staub M, Enyedi P. Barta C, et al. Mol Genet Metab. 2001 Dec;74(4):484-8. doi: 10.1006/mgme.2001.3251. Mol Genet Metab. 2001. PMID: 11749053

4

Simultaneous analysis of various mutations on the 21-hydroxylase gene by multi-allele specific amplification and capillary gel electrophoresis.

Barta C, Sasvári-Székely M, Guttman A. Barta C, et al. J Chromatogr A. 1998 Aug 21;817(1-2):281-6. doi: 10.1016/s0021-9673(98)00457-9. J Chromatogr A. 1998. PMID: 9764500

5

Rapid genotyping of factor V Leiden mutation using single-tube bidirectional allele-specific amplification and automated ultrathin-layer agarose gel electrophoresis.

Sasvari-Szekely M, Gerstner A, Ronai Z, Staub M, Guttman A. Sasvari-Szekely M, et al. Electrophoresis. 2000 Mar;21(4):816-21. doi: 10.1002/(SICI)1522-2683(20000301)21:4<816::AID-ELPS816>3.0.CO;2-Y. Electrophoresis. 2000. PMID: 10733227

6

Genotyping the -521C/T functional polymorphism in the promoter region of dopamine D4 receptor (DRD4) gene.

Ronai Z, Barta C, Guttman A, Lakatos K, Gervai J, Staub M, Sasvari-Szekely M. Ronai Z, et al. Electrophoresis. 2001 Apr;22(6):1102-5. doi: 10.1002/1522-2683()22:6<1102::AID-ELPS1102>3.0.CO;2-3. Electrophoresis. 2001. PMID: 11358133

7

Rapid single nucleotide polymorphism analysis by primer extension and capillary electrophoresis using polyvinyl pyrrolidone matrix.

Barta C, Ronai Z, Sasvari-Szekely M, Guttman A. Barta C, et al. Electrophoresis. 2001;22(4):779-82. doi: 10.1002/1522-2683(200102)22:4<779::AID-ELPS779>3.0.CO;2-4. Electrophoresis. 2001. PMID: 11296934

8

Deoxyribocytidine is salvaged not only into DNA but also into phospholipid precursors. IV. Exogenous deoxyribocytidine can be used with the same efficacy as (ribo)cytidine for lipid activation.

Sasvári-Székely M, Spasokukotskaja T, Staub M. Sasvári-Székely M, et al. Biochem Biophys Res Commun. 1993 Jul 30;194(2):966-72. doi: 10.1006/bbrc.1993.1915. Biochem Biophys Res Commun. 1993. PMID: 8343176

9

Nucleoside transport and metabolism in lymphocytes, polymorphonuclear cells and cerebral synaptosomes.

Staub M, Sasvari-Szekely M, Solymossy M, Szikla K. Staub M, et al. Adv Exp Med Biol. 1994;370:769-74. doi: 10.1007/978-1-4615-2584-4_161. Adv Exp Med Biol. 1994. PMID: 7661018

10

Deoxycytidine kinase can be also potentiated by the G-protein activator NaF in cells.

Staub M, Csapó Z, Spasokukotskaja T, Sasvári-Székely M. Staub M, et al. Adv Exp Med Biol. 1998;431:425-8. doi: 10.1007/978-1-4615-5381-6_83. Adv Exp Med Biol. 1998. PMID: 9598103

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