Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Martina Machková"'
Autor:
Barbara Rewerska, MD, Lawrence D. Sher, MD, Sady Alpizar, MD, Sylvia Pauser, MD, Grazyna Pulka, MD, Neelufar Mozaffarian, MD, PhD, Yacine Salhi, PhD, Camille Martinet, MS, Wafaa Jabert, MS, Girish Gudi, PhD, Vinu CA, MPharm, MSc, Sunitha GN, PhD, Julie Macoin, MSc, Victor Anstett, MS, Riccardo Turrini, PhD, Marie-Agnès Doucey, PhD, Stanislas Blein, PhD, Cyril Konto, MD, Martina Machkova, MD
Publikováno v:
Journal of Allergy and Clinical Immunology: Global, Vol 3, Iss 1, Pp 100195- (2024)
Background: Telazorlimab is a humanized anti-OX40 monoclonal antibody being studied for treatment of T-cell–mediated diseases. Objective: This randomized, placebo-controlled, phase 2b dose-range finding study investigated efficacy, safety, pharmaco
Externí odkaz:
https://doaj.org/article/f0ee145bd815434e8dd240eedfceb966
Autor:
Jana Lisyová, Ján Chandoga, Petra Jungová, Marcel Repiský, Mária Knapková, Martina Machková, Svetozár Dluholucký, Darina Behúlová, Jana Šaligová, Ľudmila Potočňáková, Miroslava Lysinová, Daniel Böhmer
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-12 (2018)
Abstract Background Short-chain acyl-CoA dehydrogenase deficiency (SCADD) represents a rare autosomal recessive inborn metabolic disorder of mitochondrial β-oxidation of monocarboxylic acids. Clinical symptoms can vary from a severe life-threatening
Externí odkaz:
https://doaj.org/article/2208620606eb4afeb4c756b1436fd715
Publikováno v:
Acta Chimica Slovaca. 9:28-35
The proposed work deals with the utilization of three carbon-based electrode substrates such as boron-doped diamond, glassy carbon and carbon paste for the preparation of in situ bismuth film modified electrodes. Such modified electrodes were subsequ
Autor:
Miroslava Lysinová, Svetozár Dluholucký, D. Behulova, Ján Chandoga, Petra Jungová, Mária Knapková, Jana Lisyová, Marcel Repiský, Martina Machková, Daniel Böhmer, Ľudmila Potočňáková, Jana Saligová
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-12 (2018)
BMC Medical Genetics
BMC Medical Genetics
Background Short-chain acyl-CoA dehydrogenase deficiency (SCADD) represents a rare autosomal recessive inborn metabolic disorder of mitochondrial β-oxidation of monocarboxylic acids. Clinical symptoms can vary from a severe life-threatening conditio
Publikováno v:
Acta Chimica Slovaca. 5:42-46
Utilization of electrochemical methods in determination of trace elements in beveragesElectrochemical methods have many inherent advantages such as simplicity, low cost and amenability to miniaturization. A new, sensitive and selective electrochemica