Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cinthia Claudia Amaya Ramirez"'
Autor:
Xiangli Jiang, Ali Hyder Baig, Giuliana Palazzo, Rossella Del Pizzo, Toman Bortecen, Sven Groessl, Esther A. Zaal, Cinthia Claudia Amaya Ramirez, Alexander Kowar, Daniela Aviles-Huerta, Celia R. Berkers, Wilhelm Palm, Darjus Tschaharganeh, Jeroen Krijgsveld, Fabricio Loayza-Puch
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract Cellular senescence is characterized by a permanent growth arrest and is associated with tissue aging and cancer. Senescent cells secrete a number of different cytokines referred to as the senescence-associated secretory phenotype (SASP), wh
Externí odkaz:
https://doaj.org/article/a98264621b174e53a5059a5de6ea1f66
Autor:
Isabel Myriam Schopp, Cinthia Claudia Amaya Ramirez, Jerneja Debeljak, Elisa Kreibich, Merle Skribbe, Klemens Wild, Julien Béthune
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
The BioID approaches takes advantage of the promiscuous biotinylation enzyme (BirA*) to identify proteins that closely interact. Here the authors improve the resolution of BioID using a protein fragment complementation approach that allows the assign
Externí odkaz:
https://doaj.org/article/5f14accf245a4ad4ab177b2e58e2b7ee
Publikováno v:
Methods in Molecular Biology ISBN: 9781071611258
Proximity-dependent labeling techniques such as BioID and APEX2 allow the biotinylation of proteins proximal to a protein of interest in living cells. Following streptavidin pulldown and mass spectrometry analysis, this enables the identification of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::718f9e25aa64bd3a19cb8402d7e393ca
https://doi.org/10.1007/978-1-0716-1126-5_17
https://doi.org/10.1007/978-1-0716-1126-5_17
Publikováno v:
Nucleic Acids Research
Initially identified as a factor involved in tyrosine kinase receptor signaling, Grb10-interacting GYF protein 2 (GIGYF2) has later been shown to interact with the 5′ cap-binding protein 4EHP as part of a translation repression complex, and to medi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37a8f1627a4fed76b25aee32689b0707
https://doi.org/10.1093/nar/gky198
https://doi.org/10.1093/nar/gky198
Autor:
Merle Skribbe, Elisa Kreibich, Klemens Wild, Cinthia Claudia Amaya Ramirez, Julien Béthune, Jerneja Debeljak, Isabel Myriam Schopp
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
Nature Communications
Nature Communications
Understanding the function of the thousands of cellular proteins is a central question in molecular cell biology. As proteins are typically part of multiple dynamic and often overlapping macromolecular complexes exerting distinct functions, the ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3debb61b634a8fba249c06beebc40d47
https://doaj.org/article/5f14accf245a4ad4ab177b2e58e2b7ee
https://doaj.org/article/5f14accf245a4ad4ab177b2e58e2b7ee
Initially identified as a factor involved in tyrosine kinase receptor signalling, GRB10-interacting GYF protein 2 (GIGYF2) has later been shown to interact with the 5’ cap-binding protein m4EHP as part of a translation repression complex, and to me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::408cd6ecc94a39909c8bef6c8d562236
https://doi.org/10.1101/181776
https://doi.org/10.1101/181776