Zobrazeno 1 - 10
of 88
pro vyhledávání: '"aminoacid metabolism"'
Autor:
Ioannis M. Koukourakis, Kalliopi Platoni, Dina Tiniakos, Vassilis Kouloulias, Anna Zygogianni
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 5, Pp 4495-4517 (2023)
It is well-established that tumor antigens and molecules expressed and secreted by cancer cells trigger innate and adaptive immune responses. These two types of anti-tumor immunity lead to the infiltration of the tumor’s microenvironment by immune
Externí odkaz:
https://doaj.org/article/8afd12743bf843b2a293c4d8e8dc84bb
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
Externí odkaz:
https://doaj.org/article/ba47d03962bc47b68d7e9df99d7ec10b
Akademický článek
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Publikováno v:
Allelopathy Journal. 53:35-52
In bioassay guided extraction of pseudostem powder of Pisanglilin by organic solvents we found the larvicidal activity in acetone extract, whose column chromatography by methanol-chloroform mixture separated the extract into 9-fractions, of which the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05b559fa56827d7057c352345edfd694
https://doi.org/10.26651/allelo.j/2021-53-1-1326
https://doi.org/10.26651/allelo.j/2021-53-1-1326
Akademický článek
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Autor:
Aggeliki Tserga, Jerome Zoidakis, Irene Theochari, Harikleia Gakiopoulou, Joost P. Schanstra, Rafael Stroggilos, Manousos Makridakis, Jean Sébastien Saulnier-Blache, Despoina Pouloudi, Harald Mischak, Antonia Vlahou
BackgroundThe absence of efficient inhibitors for DKD progression reflects the gaps in our understanding of DKD molecular pathogenesis. A comprehensive proteomic analysis was performed on glomeruli and kidney cortex of diabetic mice with subsequent v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33f448f585fd157bf58727f94f2a1633
https://doi.org/10.1101/2021.10.21.465240
https://doi.org/10.1101/2021.10.21.465240
Publikováno v:
Frontiers Research Topics ISBN: 9782889661824
Frontiers in Physiology
Frontiers in Physiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb507cbc02852a1d6081fadb96aae490
https://doi.org/10.3389/978-2-88966-182-4
https://doi.org/10.3389/978-2-88966-182-4
Objectives Inborn errors of metabolism are generally autosomal recessive inherited disorders. The incidence and genetic features of neonatal metabolic disorders vary significantly by regions and populations. In this study, we aimed to determine the a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c66908b31873e2335cae5b499f0b47a
https://avesis.deu.edu.tr/publication/details/e6028ea9-d313-4e48-9607-93e923c047ce/oai
https://avesis.deu.edu.tr/publication/details/e6028ea9-d313-4e48-9607-93e923c047ce/oai
Autor:
F. A. Van Assche, Johan Verhaeghe
Publikováno v:
Perinatal Biochemistry ISBN: 9781003068624
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad0e0b30666d64815b09d996cb55ba73
https://doi.org/10.1201/9781003068624-3
https://doi.org/10.1201/9781003068624-3
Autor:
Susanne Hopf, Caroline Nowak, Julia B. Hennermann, Irene Schmidtmann, Norbert Pfeiffer, Susanne Pitz
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Background Phenylketonuria (PKU) is an inherited metabolic disorder characterized by reduced activity of phenylalanine hydroxylase resulting in elevated blood phenylalanine (Phe) concentration. Despite some obvious ocular changes, the disorder has be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::164a99249c56d51c14ac4814b4cf3fcd