Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Lili Magyari"'
Autor:
Zsolt Bánfai, Erzsébet Kövesdi, Katalin Sümegi, Gergely Büki, András Szabó, Lili Magyari, Valerián Ádám, Ferenc Pálos, Attila Miseta, Miklós Kásler, Béla Melegh
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background German-derived ethnicities are one of the largest ethnic groups in Hungary, dating back to the formation of the Kingdom of Hungary, which took place at the beginning of the 11th century. Germans arrived in Hungary in many waves. T
Externí odkaz:
https://doaj.org/article/800fd80deb8c4610a9d248e581b683f2
Autor:
Gábor Ternák, Gergely Márovics, Katalin Sümegi, Zsolt Bánfai, Gergely Büki, Lili Magyari, András Szabó, Béla Melegh
Publikováno v:
Antibiotics, Vol 12, Iss 6, p 1029 (2023)
Down syndrome (DS) is a leading human genomic abnormality resulting from the trisomy of chromosome 21. The genomic base of the aneuploidy behind this disease is complex, and this complexity poses formidable challenges to understanding the underlying
Externí odkaz:
https://doaj.org/article/5d4ecc5d2ef84b1faaecd223f999d0e8
Autor:
Valerián Ádám, Zsolt Bánfai, Katalin Sümegi, Gergely Büki, András Szabó, Lili Magyari, Attila Miseta, Miklós Kásler, Béla Melegh
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Genome-wide genotype data from 48 carefully selected population samples of Transylvania-living Szeklers and non-Szekler Hungarians were analyzed by comparative analysis. Our analyses involved contemporary Hungarians living in Hungary, other Europeans
Externí odkaz:
https://doaj.org/article/46fcf08729ed41d18ca4250e3d46eab0
Autor:
Melegh, Gábor Ternák, Gergely Márovics, Katalin Sümegi, Zsolt Bánfai, Gergely Büki, Lili Magyari, András Szabó, Béla
Publikováno v:
Antibiotics; Volume 12; Issue 6; Pages: 1029
Down syndrome (DS) is a leading human genomic abnormality resulting from the trisomy of chromosome 21. The genomic base of the aneuploidy behind this disease is complex, and this complexity poses formidable challenges to understanding the underlying
Autor:
Ternák Gábor, Gergely Márovics, Katalin Sümegi, Zsolt Bánfai, Gergely Büki, Lili Magyari, András Szabó, Bela Melegh
Down syndrome (DS) is a leading human genomic abnormality resulting from the trisomy of chromosome 21. The genomic base of the aneuploidy behind this disease is complex, and this complexity poses formidable challenges to understanding the underlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::280bc6bf6246bda1cfbc5513a81b21b7
https://doi.org/10.20944/preprints202305.0838.v1
https://doi.org/10.20944/preprints202305.0838.v1
Autor:
Zsolt Bánfai, Erzsébet Kövesdi, Katalin Sümegi, Gergely Büki, András Szabó, Lili Magyari, Valerián Ádám, Ferenc Pálos, Attila Miseta, Miklós Kásler, Béla Melegh
Background German-derived ethnicities are one of the largest ethnic groups in Hungary, dating back to the formation of the Kingdom of Hungary, which took place at the beginning of the 11th century. Germans arrived in Hungary in many waves. The most s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf474dd1f0f2ef8ba6caf72d943d62f4
https://doi.org/10.21203/rs.3.rs-1407483/v2
https://doi.org/10.21203/rs.3.rs-1407483/v2
Autor:
Reka Ripszam, Emese Beatrix Horvath, Katalin Sumegi, Anna Kelemen, Etelka Pöstyéni, Lili Magyari, Pilar Moreno, Viktor Farkas, Peter O. Bauer, Beata Fabos, Kinga Hadzsiev, Béla Melegh, Erzsebet Kovesdi
Publikováno v:
Genes, Vol 12, Iss 1401, p 1401 (2021)
Genes; Volume 12; Issue 9; Pages: 1401
Genes; Volume 12; Issue 9; Pages: 1401
Background: Approximately fifteen percent of patients with tuberous sclerosis complex (TSC) phenotype do not have any genetic disease-causing mutations which could be responsible for the development of TSC. The lack of a proper diagnosis significantl
Autor:
Erzsebet, Kovesdi, Reka, Ripszam, Etelka, Postyeni, Emese Beatrix, Horvath, Anna, Kelemen, Beata, Fabos, Viktor, Farkas, Kinga, Hadzsiev, Katalin, Sumegi, Lili, Magyari, Pilar Guatibonza, Moreno, Peter, Bauer, Bela, Melegh
Publikováno v:
Genes
Background: Approximately fifteen percent of patients with tuberous sclerosis complex (TSC) phenotype do not have any genetic disease-causing mutations which could be responsible for the development of TSC. The lack of a proper diagnosis significantl
Autor:
Katalin Komlósi, Judit Bene, Etelka Pöstyéni, Renata Szalai, Lili Magyari, Petra Matyas, Béla Melegh, Kinga Hadzsiev
Publikováno v:
Pathology & Oncology Research. 25:1349-1355
Age-related hearing impairment (ARHI) is the most frequent sensory disease in the elderly, which is caused by an interaction between genetic and environmental factors. Here we examined the ethnic differences, allele and genotype frequencies of the NA
Publikováno v:
Drug Metabolism and Pharmacokinetics. 30:453-456
Taxanes are widely used microtubule-stabilizing chemotherapeutic agents in the treatment of cancers. Several cytochrome P450 gene variants have been proven to influence taxane metabolism and therapy. The purpose of this work was to determine the dist