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of 3
pro vyhledávání: '"Ina Kirchberg"'
Autor:
Ina Kirchberg, Elke Lainka, Andrea Gangfuß, Alma Kuechler, Fabian Baertling, Lea D. Schlieben, Dominic Lenz, Eva Tschiedel
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Background/purposeMEGDHEL syndrome is a rare autosomal recessive metabolic disorder, which is characterized by 3-methylglutaconic aciduria with deafness-dystonia, hepatopathy, encephalopathy and Leigh-like syndrome. It is caused by biallelic pathogen
Externí odkaz:
https://doaj.org/article/7f48da23cd244ccda1488ac164242ba9
Autor:
Stefanie Albrecht, Ann-Katrin Fleck, Ina Kirchberg, Stephanie Hucke, Marie Liebmann, Luisa Klotz, Tanja Kuhlmann
Publikováno v:
Journal of Neuroinflammation, Vol 14, Iss 1, Pp 1-10 (2017)
Abstract Background The nuclear receptor farnesoid-X-receptor (FXR; NR1H4) is expressed not only in the liver, gut, kidney and adipose tissue but also in the immune cells. FXR has been shown to confer protection in several animal models of inflammati
Externí odkaz:
https://doaj.org/article/fdd7d50a3a1d4c60b2ba14a2a64615da
Autor:
Tanja Kuhlmann, Marie Liebmann, Stephanie Hucke, Ina Kirchberg, Ann-Katrin Fleck, Stefanie Albrecht, Luisa Klotz
Publikováno v:
Journal of Neuroinflammation, Vol 14, Iss 1, Pp 1-10 (2017)
Journal of Neuroinflammation
Journal of Neuroinflammation
Background The nuclear receptor farnesoid-X-receptor (FXR; NR1H4) is expressed not only in the liver, gut, kidney and adipose tissue but also in the immune cells. FXR has been shown to confer protection in several animal models of inflammation, inclu