tallózása szerző szerint "Törőcsik, Beáta"

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Alterations in voltage-sensing of the mitochondrial permeability transition pore in ANT1-deficient cells

Dóczi, Judit; Törőcsik, Beáta; Echaniz-Laguna A; Mousson de Camaret B; Starkov A; Starkova N; Gál, Anikó; Molnár, Mária Judit; Kawamata H; Manfredi G; Ádám, Veronika; Chinopoulos, Christos (2016)

The probability of mitochondrial permeability transition (mPT) pore opening is inversely related to the magnitude of the proton electrochemical gradient. The module conferring sensitivity of the pore to this gradient has ...
Asymmetry of movements in CFTR's two ATP sites during pore opening serves their distinct functions

Sorum, Ben; Törőcsik, Beáta; Csanády, László (2017)

CFTR, the chloride channel mutated in cystic fibrosis (CF) patients, is opened by ATP binding to two cytosolic nucleotide binding domains (NBDs), but pore-domain mutations may also impair gating. ATP-bound NBDs dimerize ...
Formation of reactive oxygen species by human and bacterial pyruvate and 2- oxoglutarate dehydrogenase multienzyme complexes reconstituted from recombinant components

Ambrus, Attila; Nemeria, Natália S; Törőcsik, Beáta; Tretter, László; Nilsson, Mattias; Frank, Jordan; Ádám, Veronika (2015)
Secretagogin expression in the vertebrate brainstem with focus on the noradrenergic system and implications for Alzheimer's disease

Zahola, Péter; Hanics, János; Pintér, Anna; Máté, Zoltán; Gáspárdy, Anna; Hevesi, Zsófia; Echevarria, Diego; Adori, Csaba; Barde, Swapnali; Törőcsik, Beáta; Erdélyi, Ferenc; Szabó, Gábor; Wagner, Ludwig; Kovács, Gábor Géza; Hökfelt, Tomas; Harkany, Tibor; Alpár, Alán (2019)

Calcium-binding proteins are widely used to distinguish neuronal subsets in the brain. This study focuses on secretagogin, an EF-hand calcium sensor, to identify distinct neuronal populations in the brainstem of several ...
Structural alterations induced by ten disease-causing mutations of human dihydrolipoamide dehydrogenase analyzed by hydrogen/deuterium-exchange mass spectrometry: Implications for the structural basis of E3 deficiency

Ambrus, Attila; Wang Junjie; Mizsei, Réka; Zámbó, Zsófia; Törőcsik, Beáta; Jordan Frank; Ádám-Vizi, Veronika (2016)

Pathogenic amino acid substitutions of the common E3 component (hE3) of the human alpha-ketoglutarate dehydrogenase and the pyruvate dehydrogenase complexes lead to severe metabolic diseases (E3 deficiency), which usually ...
Structure-activity analysis of a CFTR channel potentiator: Distinct molecular parts underlie dual gating effects.

Csanády, László; Törőcsik, Beáta (2014)

The cystic fibrosis (CF) transmembrane conductance regulator (CFTR) is a member of the ATP-binding cassette transporter superfamily that functions as an epithelial chloride channel. Gating of the CFTR ion conduction pore ...

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tallózása szerző szerint "Törőcsik, Beáta"

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