scispace - formally typeset
T

Tamás Janáky

Researcher at University of Szeged

Publications -  122
Citations -  3004

Tamás Janáky is an academic researcher from University of Szeged. The author has contributed to research in topics: Vasopressin & In vivo. The author has an hindex of 28, co-authored 116 publications receiving 2732 citations. Previous affiliations of Tamás Janáky include Veterans Health Administration & Albert Szent-Györgyi Medical University.

Papers
More filters
Journal ArticleDOI

Biogenesis of cytosolic ribosomes requires the essential iron-sulphur protein Rli1p and mitochondria

TL;DR: The essential character of Fe/S clusters in Rli1p explains the indispensable character of mitochondria in eukaryotes and is associated with ribosomes and with Hcr1p, a protein involved in rRNA processing and translation initiation.
Journal ArticleDOI

Functional analyses of placental protein 13/galectin-13.

TL;DR: In this paper, a placenta-derived galectin-13 (PP13) was cloned from human term placentia and a specific monoclonal antibody to PP13 was developed, which showed its conserved structural and functional homology to members of the Galectin family.
Journal ArticleDOI

New antagonists of LHRH. II: Inhibition and potentiation of LHRH by closely related analogues

TL;DR: Modifications of the previously described LHRH antagonists and corresponding D-Hci6 analogue, were completely free of the toxic effects, such as cyanosis and respiratory depression leading to death, which have been observed in rats with the D-Trp3, D-Arg6 antagonist and related antagonists.
Journal ArticleDOI

Decreased serum and red blood cell kynurenic acid levels in Alzheimer's disease.

TL;DR: Findings indicate an altered peripheral KP in AD regardless of the APOE status of the probands, and no association has been found with the possession of the epsilon4 allele.
Journal ArticleDOI

Cholesterol Potentiates ABCG2 Activity in a Heterologous Expression System: Improved in Vitro Model to Study Function of Human ABCG2

TL;DR: An essential role of membrane cholesterol for the function of ABCG2 is indicated, as cholesterol loading significantly improved the drug transport into inside-out membrane vesicles prepared fromMXR-Sf9 cells and in cholesterol-depleted MXR-M membranes.