Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Eliška Marklová"'
Autor:
Eliška Marklová
Publikováno v:
Acta Medica, Vol 50, Iss 1, Pp 17-21 (2007)
Inflammation is a protective immune response to infection, trauma, or injury; however, only a subset of patients develops inflammation, suggesting other contributing factors involved, such as the environment and genes. Inflammationassociated genes in
Externí odkaz:
https://doaj.org/article/66a5c3b56b3443cbaee1be81c762747c
Autor:
Ziad Albahri, Eliška Marklová, Hubert Vaníček, Lenka Minxová, Petr Dědek, Sylva Skálová, Marika Talábová, Jaroslava Vávrová, Eva Rencová
Publikováno v:
Acta Medica, Vol 47, Iss 4, Pp 267-272 (2004)
The aim of this study is to report our 3years experience with the screening of congenital disorders of glycosylation. A common isoelectric focusing method with immunofixation was used for analysis of serum transferrin and α1-antitrypsin, apart from
Externí odkaz:
https://doaj.org/article/10cb0e0e5ddc440ba60e6d1d45ceeb56
Autor:
Eliška Marklová
Publikováno v:
Acta Medica, Vol 45, Iss 4, Pp 129-133 (2002)
In addition to the main groups of inherited metabolic diseases, including mitochondrial, peroxisomal and lysosomal defects, organic acidurias, porphyrias, defects of amino acids, saccharides and fatty acids metabolism, disorders of transport and util
Externí odkaz:
https://doaj.org/article/e3fe6b5a1f4c4958876930ae1c425344
Autor:
Eliška Marklová
Publikováno v:
Acta Medica, Vol 44, Iss 1, Pp 3-6 (2001)
Practically all types of diabetes mellitus (DM) result from complex interactions of genetic and environmental factors. Multifactorial and polygenic Type 1 DM is strongly influenced by genes controlling the immune system, mainly HLA-DQ and DR. In addi
Externí odkaz:
https://doaj.org/article/5e8b2b888f2a4c61ac08382235b0bdbb
Autor:
Jaroslav Dršata, Eliška Marklová
Publikováno v:
Acta Medica, Vol 43, Iss 1, Pp 15-17 (2000)
Decarboxylation of aromatic amino acid in mammalian tissues is catalyzed by aromatic amino acid decarboxylase (EC. 4.1.1.28, AAD). The enzyme differs in its affinity to individual aromatic amino acids, the best substrates being 3,4-dihydroxyphenylala
Externí odkaz:
https://doaj.org/article/770e10c76d5448db8521858145e42c3a
Publikováno v:
Acta Medica, Vol 40, Iss 1, Pp 17-19 (1997)
The detection of organic acidurias is a part of our screening programme for inherited metabolic diseases. Adapted procedure is differentiated and involves several steps: 1) thin-layer chromatography (TLC) in the case of an abnormal finding followed b
Externí odkaz:
https://doaj.org/article/763034b9269448a09adf1c3b8ba3096f
Autor:
Eliška Marklová, Ziad Albahri
Publikováno v:
Journal of Clinical Laboratory Analysis. 23:77-81
Congenital disorders of glycosylation are a rapidly growing group of inherited (neuro)metabolic disorders characterized by defects in glycosylation of proteins and lipids. This study discusses an analytical problem in the differentiation between hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da5bc4b8a73aec4a4746b248ccd5177
https://doi.org/10.1002/jcla.20293
https://doi.org/10.1002/jcla.20293
Publikováno v:
Journal of Inherited Metabolic Disease. 31:457-461
Genetic polymorphism of serum transferrin (Tf) was studied in order to differentiate between protein genetic variants and congenital disorders of glycosylation (CDG), further focusing on unusual findings.Screening of Tf hypoglycosylation was carried
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef8401fbafa8009c684037b71aaef176
https://doi.org/10.1007/s10545-008-0733-0
https://doi.org/10.1007/s10545-008-0733-0
Autor:
Eliška Marklová, Alena Fojtášková
Publikováno v:
Journal of Chromatography A. 730:133-137
Indolylacryloylglycine (IAcrGly) is one of the physiological components of urine, although its source and its role in the human organism have not yet been unambiguously established. Changes in the IAcrGly excretion level have been found under some ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17bd8543762d84f4cb9e3f3f20a8713d
https://doi.org/10.1016/0021-9673(95)00943-4
https://doi.org/10.1016/0021-9673(95)00943-4
Publikováno v:
Journal of the neurological sciences. 314(1-2)
article Background: Participation of protein polymorphism is often considered in the pathogenesis of various diseases. Aberrant protein glycosylation has been recognized to play major roles in human disorders, including neurodegenerative diseases. Ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3733894b46341dd05e69ab3684be782f
https://pubmed.ncbi.nlm.nih.gov/22118861
https://pubmed.ncbi.nlm.nih.gov/22118861