Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Gyula Hadlaczky"'
Autor:
Anna Tóth, Katalin Fodor, Tünde Praznovszky, Vilmos Tubak, Andor Udvardy, Gyula Hadlaczky, Robert L Katona
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e85565 (2014)
Mammalian artificial chromosomes are natural chromosome-based vectors that may carry a vast amount of genetic material in terms of both size and number. They are reasonably stable and segregate well in both mitosis and meiosis. A platform artificial
Externí odkaz:
https://doaj.org/article/f4273f10e4a3495b9e5d460d1935b20b
Autor:
Ruttachuk Rungsiwiwut, Erika Csonka, Julianna Kobolák, Andras Dinnyes, Gyula Hadlaczky, Olga Ujhelly, Solomon Mamo
Publikováno v:
Cellular Reprogramming. 14:56-67
Embryonic stem cells derived from nuclear transfer embryos (ntESCs) are particularly valuable for regenerative medicine, as they are a patient-specific and histocompatible cell source for the treatment of varying diseases. However, currently, little
Autor:
Erika Csonka, Gyula Hadlaczky, Andor Udvardy, Tünde Praznovszky, J. Kereső, Imre Cserpán, K. Székely Szűcs, Barnabas Szakal, Robert L. Katona, Péter Blazsó, Ildikó Sinkó, Gy. Holló, Katalin Fodor
Publikováno v:
Cellular and Molecular Life Sciences. 65:3830-3838
Mammalian artificial chromosomes (MACs) are safe, stable, non-integrating genetic vectors with almost unlimited therapeutic transgene-carrying capacity. The combination of MAC and stem cell technologies offers a new strategy for stem cell-based thera
Autor:
Katalin Fodor, Katalin Bajnóczky, Erika Csonka, István Andó, Gyula Hadlaczky, Györgyi Bujdosó, Imre Cserpán
Publikováno v:
Hungarian Medical Journal. 2:365-380
We analyzed the 15p-15q11.2 region of human chromosome 15 that was tetrasomic in a three-generation family with a chromosome 15-derived small supernumerary marker chromosome (der15, sSMC). This stable, inherited sSMC was present in four family member
Autor:
András Rusz, Orsolya Bellovits, Imre Romics, Erika Csonka, Györgyi Bujdosó, Péter Sótonyi, Gyula Hadlaczky
Publikováno v:
International Journal of Human Genetics. 6:171-176
The aim of this study was to estimate the prevalence of chromosome abnormalities in patients with azoospermia, in our material. Preoperative evaluation included routine andrological investigations with 2 semen analysis, ultrasound, hormonal and genet
Publikováno v:
Acta Biologica Hungarica. 56:67-74
Transgenic mice are suitable model animals for testing the in vivo functionality of custom-tailored ribozymes. Transgenic experiments can demonstrate whether a ribozyme is able to cleave any RNA transcript of the host animal or not. Most probably, th
Publikováno v:
Gene. 343:271-279
We report here the isolation, cloning and characterization of two abundant centromeric satellite sequences (Rsat I and Rsat II) what are not related to each other, and that of a divergent subfamily (Rsat IIE) of rabbit (Oryctolagus cuniculus). The Rs
Publikováno v:
Chromosome Research. 12:483-493
The Chinese hamster is one of the few mammalian species that are characterized by relatively poor heterochromatin content. It was intriguing to test whether or not the lack of large blocks of heterochromatin in the hamster chromosomes could be correl
Autor:
Erika Csonka, Edit Novák, Robert L. Katona, Mónika Mórocz, Márta Rózsavölgyi, Imre Cserpán, Tünde Praznovszky, Gyula Hadlaczky, Katalin Fodor
Publikováno v:
Nucleic Acids Research. 30:2899-2905
We have investigated the large-scale organization of the human chAB4-related long-range multisequence family, a low copy-number repetitive DNA located in the pericentromeric heterochromatin of several human chromosomes. Analysis of genomic clones rev
Autor:
Robert L. Katona, Katalin Fodor, Tünde Praznovszky, Vilmos Tubak, Andor Udvardy, Anna Tóth, Gyula Hadlaczky, Péter Blazsó, Imre Cserpán
Publikováno v:
Acta biologica Hungarica. 65(3)
Direct reprogramming of mouse fibroblasts into induced pluripotent stem cells (iPS) was achieved recently by overexpression of four transcription factors encoded by retroviral vectors. Most of the virus vectors, however, may cause insertional mutagen