Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ion C Cirstea"'
Autor:
Si-Cai Zhang, Lothar Gremer, Henrike Heise, Petra Janning, Aliaksei Shymanets, Ion C Cirstea, Eberhard Krause, Bernd Nürnberg, Mohammad Reza Ahmadian
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e102425 (2014)
Small Rho GTPases are well known to regulate a variety of cellular processes by acting as molecular switches. The regulatory function of Rho GTPases is critically dependent on their posttranslational modification at the carboxyl terminus by isoprenyl
Externí odkaz:
https://doaj.org/article/fcd4875f56614d2eabdbcf0693029d43
Autor:
Melanie Haffner-Luntzer, Anita Ignatius, Sayantan Nandi, Attila Aszodi, Miriam Tschaffon, Ion C. Cirstea, Astrid Schoppa, Stefan O. Reber
Publikováno v:
Endocrine
Purpose Endochondral ossification, which involves transdifferentiation of chondrocytes into osteoblasts, is an important process involved in the development and postnatal growth of most vertebrate bones as well as in bone fracture healing. To study t
Publikováno v:
Trends in Cell Biology.
Constitutively activated rat sarcoma (RAS) GTPases are one of the major drivers of tumor growth and are difficult drug targets. The glucocorticoid receptor (GR), a nuclear receptor primarily acting in the nucleus, is a potent modulator of inflammatio
Publikováno v:
Methods in Molecular Biology ISBN: 9781071611890
Costello syndrome (CS), characterized by a developmental delay and a failure to thrive, is also associated with an impaired lipid and energy metabolism. White adipose tissue is a central sensor of whole-body energy homeostasis, and HRAS hyperactivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c42f9f802945226324c98da32b68627
https://doi.org/10.1007/978-1-0716-1190-6_24
https://doi.org/10.1007/978-1-0716-1190-6_24
Publikováno v:
Endogenous locus-driven H-Ras G12V expression induces senescence-like phenotype in primary fibroblasts of the Costello syndrome mouse model. :3-14
Autor:
Mohammad Reza Ahmadian, Stefano Paolacci, Dorit Lev, Ion C. Cirstea, Francesca Pantaleoni, Serena Cecchetti, Alessandra Carè, Antonio Novelli, Marco Tartaglia, Elisabetta Flex, Marialetizia Motta, Lisabianca Bottero, Ilan Linger, Francesca Romana Lepri, Emilia Stellacci
Publikováno v:
Human Mutation. 38:798-804
RASopathies are a group of rare, clinically related conditions affecting development and growth, and are caused by germline mutations in genes encoding signal transducers and modulators with a role in the RAS signaling network. These disorders share
Autor:
Ion C. Cirstea, Konstantin Schneider-Heieck, Francesca Pantaleoni, Emanuele Bellacchio, Simona Coppola, Miray Fidan, Guntram Borck, Martin Zenker, Leonardo Salviati, Marco Tartaglia, Marialetizia Motta
Noonan syndrome (NS), the most common RASopathy, is caused by mutations affecting signaling through RAS and the MAPK cascade. Recently, genome scanning has discovered novel genes implicated in NS, whose function in RAS-MAPK signaling remains obscure,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2034afdd233750056fe3289e8200b96f
http://hdl.handle.net/11577/3384318
http://hdl.handle.net/11577/3384318
Publikováno v:
Mechanisms of Ageing and Development. 194:111411
Senescence is a biological process that induces a permanent cell cycle arrest and a specific gene expression program in response to various stressors. Following studies over the last few decades, the concept of senescence has evolved from an antiprol
Autor:
Claus Kordes, Mohammad Reza Ahmadian, Radovan Dvorsky, Philippe I. H. Bastiaens, Malte Schmick, Saeideh Nakhaei-Rad, Dieter Häussinger, Hossein Nakhaeizadeh, Ion C. Cirstea
Publikováno v:
Journal of Biological Chemistry. 290:15892-15903
E-RAS is a member of the RAS family specifically expressed in embryonic stem cells, gastric tumors, and hepatic stellate cells. Unlike classical RAS isoforms (H-, N-, and K-RAS4B), E-RAS has, in addition to striking and remarkable sequence deviations
Autor:
Sarah L. Risse, Dieter Häussinger, Katja T. Koessmeier, Mamta Jaiswal, Eyad K. Fansa, Saeideh Nakhaei-Rad, Radovan Dvorsky, Monilola A. Olayioye, Ion C. Cirstea, Ehsan Amin, Mohamed S. Taha, Sicai Zhang, Claus Kordes, Mohammad Reza Ahmadian, Aziz Gauhar
Publikováno v:
Journal of Biological Chemistry. 289:6839-6849
The three deleted in liver cancer genes (DLC1–3) encode Rho-specific GTPase-activating proteins (RhoGAPs). Their expression is frequently silenced in a variety of cancers. The RhoGAP activity, which is required for full DLC-dependent tumor suppress