Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Bence Acs"'
Autor:
George Füst, Ágnes Szilágyi, Judit Majnik, Zsófia Bánlaki, Márton Doleschall, Bence Acs, Attila Patócs, Károly Rácz, György Raizer
Publikováno v:
Clinical Endocrinology. 76:478-484
Summary Objective According to our previous findings, carriers of the C4B*Q0 genotype, which means zero or one copy of the C4B gene, which is located in the RCCX copy number variation region on chromosome 6, have a significantly shorter life-expectan
Autor:
Károly Rácz, Bence Acs, Karolina Feldmann, Peter Gergics, Andrea Kerti, Attila Patócs, Miklós Tóth, Ágnes Szappanos, Rita Bertalan
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 123:79-84
Objective The type 1 and type 2 isoenzymes of the 11β-hydroxysteroid dehydrogenase (HSD11B) play an important role in the prereceptor regulation of glucocorticoid bioavailability and action. The potential importance of gene variants coding HSD11B ha
Autor:
Alexa Marta, Karolina Feldman, Zsolt Nagy, Károly Rácz, Attila Patócs, Bence Acs, Henriett Butz, Kornélia Baghy, Péter Szabó, István Likó, Tamas Pazmany
Publikováno v:
The Journal of steroid biochemistry and molecular biology. 155
The glucocorticoid receptor (GR) plays a crucial role in inflammatory responses. GR has several isoforms, of which the most deeply studied are the GRα and GRs. Recently it has been suggested that in addition to its negative dominant effect on GRα,
Autor:
Judit Majnik, Miklós Tóth, Károly Rácz, István Likó, Ágnes Szappanos, Nikolette Szücs, Attila Patocs, Karolina Feldman-Kovacs, Bence Acs, Orsolya Acs
Publikováno v:
Endocrine Abstracts.
Autor:
Bence Acs, Szilvia Mészáros, Csaba Horváth, Emoke Csupor, Viktória Ferencz, Gabor Farkas, Orsolya Acs, Edit Tóth
Publikováno v:
Endocrine Abstracts.
Autor:
Zsófia, Bánlaki, György, Raizer, Bence, Acs, Judit, Majnik, Márton, Doleschall, Agnes, Szilágyi, Karoly, Rácz, George, Füst, Attila, Patócs
Publikováno v:
Clinical endocrinology. 76(4)
According to our previous findings, carriers of the C4B*Q0 genotype, which means zero or one copy of the C4B gene, which is located in the RCCX copy number variation region on chromosome 6, have a significantly shorter life-expectancy and higher risk
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