Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Olga Brantova"'
Autor:
Olga Brantova, Jiri Kobr, Jan Hridel, Pavel Martásek, Olga Cerna, Václav Vobruba, Pavla Pokorná, Ivan Mikula, Oxana V. Klimenko
Publikováno v:
Experimental Lung Research. 39:1-8
The aim of this study was to investigate longitudinal changes of the pulmonary inflammatory process as a result of mechanical stress due to mechanical ventilation. The concentrations of IL-8, TNF-α, MIP-1β, nitrites/nitrates, and inducible nitric o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::501f09a64ea9d1f92fe85cd44d24dd65
https://doi.org/10.3109/01902148.2012.737404
https://doi.org/10.3109/01902148.2012.737404
Autor:
Jiri Zeman, Katerina Vesela, Jana Ledvinová, Martin Magner, Jana Sladkova, Marketa Tesarova, Hana Hansikova, Helena Poupetova, Befekadu Asfaw, Jan Zivny, Olga Brantova, Jan Krusek
Publikováno v:
Biologia. 64:394-401
α-Mannosidosis is a lysosomal storage disorder caused by α-mannosidase deficiency. Clinical course of the disease ranges from severe infantile to milder juvenile type and includes mental retardation, skeletal deformities, coarse facies, hepatomegal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4710ad31d3d36a03ceb5bee2e2ab9af5
https://doi.org/10.2478/s11756-009-0054-2
https://doi.org/10.2478/s11756-009-0054-2
Autor:
Hana Hansikova, Tomas Honzik, Lukas Stiburek, Marketa Tesarova, Laszlo Wenchich, Evzenie Tietzeova, Olga Brantova, Daniela Fornuskova, Jiri Zeman
Publikováno v:
Biochimica et Biophysica Acta-Molecular Basis of Disease
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2008, 1782 (5), pp.317. ⟨10.1016/j.bbadis.2008.02.001⟩
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2008, 1782 (5), pp.317. ⟨10.1016/j.bbadis.2008.02.001⟩
The impact of point mutations in mitochondrial tRNA genes on the amount and stability of respiratory chain complexes and ATP synthase (OXPHOS) has been broadly characterized in cultured skin fibroblasts, skeletal muscle samples, and mitochondrial cyb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ec4c604c6a1bb653f920be1b23217b5
https://doi.org/10.1016/j.bbadis.2008.02.001
https://doi.org/10.1016/j.bbadis.2008.02.001
Publikováno v:
Ultrastructural Pathology. 30:239-245
Mitochondrial disorders represent a heterogeneous group of multisystem diseases with extreme variability in clinical phenotype. The diagnosis of mitochondrial disorders relies heavily on extensive biochemical and molecular analyses combined with morp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::582a4fbd64ccfc3055a0ae9616d4ee78
https://doi.org/10.1080/01913120600820112
https://doi.org/10.1080/01913120600820112