Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Oksana Nadzemova"'
Autor:
Matthias Weiand, Vanessa Sandfort, Oksana Nadzemova, Robert Schierwagen, Jonel Trebicka, Bernhard Schlevogt, Iyad Kabar, Hartmut Schmidt, Andree Zibert
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract SEC61A1 encodes a central protein of the mammalian translocon and dysfunction results in severe disease. Recently, mutation R236C was identified in patients having autosomal dominant polycystic liver disease (ADPLD). The molecular phenotype
Externí odkaz:
https://doaj.org/article/cedbb668342747488178467fcfa116d3
Autor:
Sarah Guttmann, Oksana Nadzemova, Inga Grünewald, Malte Lenders, Eva Brand, Andree Zibert, Hartmut H Schmidt
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0230025 (2020)
Intestinal cells control delivery of lipids to the body by adsorption, storage and secretion. Copper (Cu) is an important trace element and has been shown to modulate lipid metabolism. Mutation of the liver Cu exporter ATP7B is the cause of Wilson di
Externí odkaz:
https://doaj.org/article/151f7ce376c84391bfcf6f190e687253
Autor:
Michael Pöhler, Sarah Guttmann, Oksana Nadzemova, Malte Lenders, Eva Brand, Andree Zibert, Hartmut H Schmidt, Vanessa Sandfort
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0239411 (2020)
Wilson's disease (WD) is a monogenetic liver disease that is based on a mutation of the ATP7B gene and leads to a functional deterioration in copper (Cu) excretion in the liver. The excess Cu accumulates in various organs such as the liver and brain.
Externí odkaz:
https://doaj.org/article/706fad175a1d41b39f76ed6dd808173b
Autor:
Matthias Weiand, Vanessa Sandfort, Oksana Nadzemova, Iyad Kabar, Jonel Trebicka, Hartmut Schmidt, Andree Zibert
Publikováno v:
39. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::411767b46b1897a19698288dca20efc6
https://doi.org/10.1055/s-0042-1759915
https://doi.org/10.1055/s-0042-1759915
Publikováno v:
39. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::534ce5d3ca629947972c8fb546d7ea72
https://doi.org/10.1055/s-0042-1759922
https://doi.org/10.1055/s-0042-1759922
The novel class of compounds represented by lipid nanoparticle (LNP)-encapsulated siRNA formulations has an enormous potential to target disease, notably of the liver. Endocytosis of LNPs is believed to be mediated by APOE, an important serum protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04f37165514defb3a4432a30b7fc0cdb
Autor:
Hartmut Schmidt, Andree Zibert, Malte Lenders, Eva Brand, S Guttmann, Oksana Nadzemova, Inga Grünewald
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 3, p e0230025 (2020)
PLoS ONE, Vol 15, Iss 3, p e0230025 (2020)
Intestinal cells control delivery of lipids to the body by adsorption, storage and secretion. Copper (Cu) is an important trace element and has been shown to modulate lipid metabolism. Mutation of the liver Cu exporter ATP7B is the cause of Wilson di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37135d1f5eb1b50aa5155bbc20675726
https://doi.org/10.1371/journal.pone.0230025
https://doi.org/10.1371/journal.pone.0230025