Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kristina, Tanneberger"'
Autor:
Martine Cohen-Solal, Robert Brommage, Filippo Massa, Wolfgang Hans, Martin Hrabé de Angelis, Aurelie Charlet, Agnès Boutet, Ana-Sofia Rocha, Thomas Funck-Brentano, Fariba Jian Motamedi, Clara Panzolini, Glenda Comai, Kristina Tanneberger, Christine Hartmann, Jürgen Behrens, Andreas Schedl
Publikováno v:
Journal of Bone and Mineral Research. 33:875-887
The X-linked WTX/AMER1 protein constitutes an important component of the β-catenin destruction complex that can both enhance and suppress canonical β-catenin signaling. Somatic mutations in WTX/AMER1 have been found in a proportion of the pediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a635409efb57c43d2624193eb01a13ad
https://doi.org/10.1002/jbmr.3387
https://doi.org/10.1002/jbmr.3387
Autor:
Glenda, Comai, Agnès, Boutet, Kristina, Tanneberger, Filippo, Massa, Ana-Sofia, Rocha, Aurelie, Charlet, Clara, Panzolini, Fariba, Jian Motamedi, Robert, Brommage, Wolfgang, Hans, Thomas, Funck-Brentano, Martin, Hrabe de Angelis, Christine, Hartmann, Martine, Cohen-Solal, Jürgen, Behrens, Andreas, Schedl
Publikováno v:
J. Bone Min. Res. 33, 875-887 (2018)
The X-linked WTX/AMER1 protein constitutes an important component of the β-catenin destruction complex that can both enhance and suppress canonical β-catenin signaling. Somatic mutations in WTX/AMER1 have been found in a proportion of the pediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::23acbabf529c4152c9cff66331866e87
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52717
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52717
Autor:
Michaela B.C. Kilander, Juergen Behrens, Vítězslav Bryja, Alois Kozubík, Vítězslav Kříž, Kristina Tanneberger, Gunnar Schulte, Jan Masek, Josef Slavík, Vendula Pospichalova, Miroslav Machala
Publikováno v:
The Journal of Biological Chemistry
Background: β-Arrestins are required for Wnt/β-catenin signaling, but the mechanism of their action is unclear. Results: β-Arrestins bind PtdInsP2-interacting protein Amer1, bind PtdInsP2-producing kinases, and control Wnt3a-induced PtdInsP2 produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64bba95e22852e31c78a19b13fd9cf01
http://europepmc.org/articles/PMC3887180
http://europepmc.org/articles/PMC3887180
Autor:
Jean Schneikert, Kristina Tanneberger, Katharina Brauburger, Vitezslav Kriz, Vitezslav Bryja, Michel V. Hadjihannas, Gunnar Schulte, Astrid S. Pfister, Jürgen Behrens
Publikováno v:
The EMBO Journal. 30:1433-1443
Phosphorylation of the Wnt receptor low-density lipoprotein receptor-related protein 6 (LRP6) by glycogen synthase kinase 3β (GSK3β) and casein kinase 1γ (CK1γ) is a key step in Wnt/β-catenin signalling, which requires Wnt-induced formation of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72c54359b29ff6de4a66cb80a94fa636
https://doi.org/10.1038/emboj.2011.28
https://doi.org/10.1038/emboj.2011.28
Wnt/β-catenin signaling is negatively controlled by the adenomatous polyposis coli (APC) tumor suppressor, which induces proteasomal degradation of β-catenin as part of the β-catenin destruction complex. Amer2 (APC membrane recruitment 2; FAM123A)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b75a4cead9e5233946fa92981b3174
https://europepmc.org/articles/PMC3265856/
https://europepmc.org/articles/PMC3265856/
Publikováno v:
Journal of cell science. 120(Pt 21)
APC is a multifunctional tumor suppressor protein that negatively controls Wnt signaling, but also regulates cell adhesion and migration by interacting with the plasma membrane and the microtubule cytoskeleton. Although the molecular basis for the mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413f7aad48a05d4b3742681124d6251e
https://pubmed.ncbi.nlm.nih.gov/17925383
https://pubmed.ncbi.nlm.nih.gov/17925383