Clinically relevant mutations in the ABCG2 transporter uncovered by genetic analysis linked to erythrocyte membrane protein expression

por Zámbó, Boglárka, Bartos, Zsuzsa, Mózner, Orsolya, Szabó, Edit, Várady, György, Poór, Gyula, Pálinkás, Márton, Andrikovics, Hajnalka, Hegedűs, Tamás, Homolya, László, Sarkadi, Balázs
Publicado 2018

Pattern of SQSTM1 Gene Variants in a Hungarian Cohort of Paget’s Disease of Bone

por Donáth, Judit, Balla, Bernadett, Pálinkás, Márton, Rásonyi, Rita, Vastag, Gyula, Alonso, Nerea, Prieto, Beatriz Larraz, Vallet, Mahéva, Ralston, Stuart H., Poór, Gyula
Publicado 2020

Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia

por Pálinkás, Márton, Szabó, Edit, Kulin, Anna, Mózner, Orsolya, Rásonyi, Rita, Juhász, Péter, Nagy, Krisztina, Várady, György, Vörös, Dóra, Zámbó, Boglárka, Sarkadi, Balázs, Poór, Gyula
Publicado 2022