Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Katja Wiechmann"'
Publikováno v:
WE_OS-Jahrbuch, Vol 4, Iss 1 (2021)
Der Ausgangspunkt für die pädagogische Entwicklung an der Universitätsschule Dresden ist die Bestimmung, dass Lernen sich, wie es die kulturhistorische Theorie (u.a. Vygotskij, 2002) bestimmt, im Dialog vollzieht, bzw. wird das Lernen dem Konstruk
Externí odkaz:
https://doaj.org/article/5c60e38961f5410e81e557f36d9f61f1
Autor:
Sarah K Oettl, Jana Gerstmeier, Shafaat Y Khan, Katja Wiechmann, Julia Bauer, Atanas G Atanasov, Clemens Malainer, Ezzat M Awad, Pavel Uhrin, Elke H Heiss, Birgit Waltenberger, Daniel Remias, Johannes M Breuss, Joel Boustie, Verena M Dirsch, Hermann Stuppner, Oliver Werz, Judith M Rollinger
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e76929 (2013)
In vitro screening of 17 Alpine lichen species for their inhibitory activity against 5-lipoxygenase, microsomal prostaglandin E2 synthase-1 and nuclear factor kappa B revealed Cetrelia monachorum (Zahlbr.) W.L. Culb. & C.F. Culb. As conceivable sourc
Externí odkaz:
https://doaj.org/article/f45fc10753c74c9f9eca974ae82417db
Publikováno v:
Apoptosis. 20:1508-1517
The acylphloroglucinols hyperforin (Hypf) and myrtucommulone A (MC A) induce death of cancer cells by triggering the intrinsic/mitochondrial pathway of apoptosis, accompanied by a loss of the mitochondrial membrane potential and release of cytochrome
Publikováno v:
European Journal of Medicinal Chemistry. 101:133-149
The natural acylphloroglucinol myrtucommulone A (1) inhibits microsomal prostaglandin E2 synthase (mPGES)-1 and 5-lipoxygenase (5-LO), and induces apoptosis of cancer cells. Starting from 1 as lead, 28 analogues were synthesized following a straightf
Autor:
Stefanie König, Oliver Werz, Hans Müller, Katja Wiechmann, Aleš Svatoš, Johann Jauch, Natalie Wielsch
Publikováno v:
Cell chemical biology. 24(5)
The acylphloroglucinol myrtucommulone A (MC) causes mitochondrial dysfunctions by direct interference leading to apoptosis in cancer cells, but the molecular targets involved are unknown. Here, we reveal the chaperonin heat-shock protein 60 (HSP60) a
Autor:
Hermann Stuppner, Gerhard Wolber, Judith M. Rollinger, Daniela Schuster, Julia Bauer, Oliver Werz, Stefan M. Noha, Patrick Markt, Katja Wiechmann, Birgit Waltenberger
Publikováno v:
Journal of Medicinal Chemistry. 54:3163-3174
Microsomal prostaglandin E2 synthase-1 (mPGES-1) catalyzes prostaglandin E2 formation and is considered as a potential anti-inflammatory pharmacological target. To identify novel chemical scaffolds active on this enzyme, two pharmacophore models for
Autor:
Oliver Werz, Olga Scherer, Markus Bohnert, Dirk Hoffmeister, Hans-Martin Dahse, Stefanie König, Katja Wiechmann
Publikováno v:
Bioorganicmedicinal chemistry. 22(15)
The melleolides are structurally unique and bioactive natural products of the basidiomycete genus Armillaria. Here, we report on cytotoxic effects of melleolides from Armillaria mellea towards non-transformed human primary monocytes and human cancer
Autor:
Atanas G. Atanasov, Katja Wiechmann, Judith M. Rollinger, Sarah K. Oettl, Verena M. Dirsch, Elke H. Heiss, Joël Boustie, J Gerstmeier, H Stuppner, Birgit Waltenberger, Oliver Werz, Julia Bauer
Publikováno v:
Planta Medica. 79
Autor:
Jeffrey S. Barrett, Antonietta Rossi, Katja Wiechmann, Mona Abdel-Tawab, Jan Hüsch, Lidia Sautebin, Jürgen Meins, Carsten Skarke, Kathleen Gerbeth, Oliver Werz, Manfred Schubert-Zsilavecz
Nonsteroidal anti-inflammatory drug intake is associated with a high prevalence of gastrointestinal side effects, and severe cardiovascular adverse reactions challenged the initial enthusiasm in cyclooxygenase-2 inhibitors. Recently, it was shown tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e3fb5d5efb58e3389e9085641d058fb
http://hdl.handle.net/11588/558328
http://hdl.handle.net/11588/558328
Autor:
Birgit, Waltenberger, Katja, Wiechmann, Julia, Bauer, Patrick, Markt, Stefan M, Noha, Gerhard, Wolber, Judith M, Rollinger, Oliver, Werz, Daniela, Schuster, Hermann, Stuppner
Publikováno v:
Journal of Medicinal Chemistry
Microsomal prostaglandin E(2) synthase-1 (mPGES-1) catalyzes prostaglandin E(2) formation and is considered as a potential anti-inflammatory pharmacological target. To identify novel chemical scaffolds active on this enzyme, two pharmacophore models