tallózása szerző szerint "Illes, A"

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A teljesexom-szekvenálás jelentősége a ritka neurológiai betegségek diagnosztikájában – saját tapasztalatok egy ataxiás eset kapcsán

Balicza, P; Grosz, Z; Bencsik, R; Illes, A; Gal, A; Gezsi, A; Molnar, MJ (2018)

Next generation sequencing (NGS) technologies reshape the diagnostics of rare neurological diseases. In the background of certain neurological symptoms, such as ataxia, many acquired and genetic causes may be present. ...
Tight co-twin similarity of monozygotic twins for hTERT protein level of T cell subsets, for telomere length and mitochondrial DNA copy number, but not for telomerase activity.

Melicher, D; Illes, A; Pallinger, E; Kovacs, AF; Littvay, L; Tarnoki, AD; Tarnoki, DL; Bikov, A; Molnar, MJ; Buzas, EI; Falus, A (2018)

Our study analyzed lymphocyte subpopulations of 32 monozygotic twins and compared the level of the catalytic reverse transcriptase protein subunit (hTERT) in T lymphocytes (Tly), helper- (Th), cytotoxic- (Tc) and regulatory ...

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