Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Petra Langerak"'
Publikováno v:
PLoS Genetics, Vol 11, Iss 9, p e1005517 (2015)
Phosphorylation of histone H2AX by ATM and ATR establishes a chromatin recruitment platform for DNA damage response proteins. Phospho-H2AX (γH2AX) has been most intensively studied in the context of DNA double-strand breaks caused by exogenous clast
Externí odkaz:
https://doaj.org/article/eb7e88a7149a48378439cfffe324d01b
Publikováno v:
PLoS Genetics, Vol 7, Iss 9, p e1002271 (2011)
The multifunctional Mre11-Rad50-Nbs1 (MRN) protein complex recruits ATM/Tel1 checkpoint kinase and CtIP/Ctp1 homologous recombination (HR) repair factor to double-strand breaks (DSBs). HR repair commences with the 5'-to-3' resection of DNA ends, gene
Externí odkaz:
https://doaj.org/article/fc71716de1324abba27736f0887b6d72
Autor:
Ayal Hendel, Peter H L Krijger, Noam Diamant, Zohar Goren, Petra Langerak, Jungmin Kim, Thomas Reissner, Kyoo-young Lee, Nicholas E Geacintov, Thomas Carell, Kyungjae Myung, Satoshi Tateishi, Alan D'Andrea, Heinz Jacobs, Zvi Livneh
Publikováno v:
PLoS Genetics, Vol 7, Iss 9, p e1002262 (2011)
Translesion DNA synthesis (TLS) is a DNA damage tolerance mechanism in which specialized low-fidelity DNA polymerases bypass replication-blocking lesions, and it is usually associated with mutagenesis. In Saccharomyces cerevisiae a key event in TLS i
Externí odkaz:
https://doaj.org/article/bd8b7458253a4fe6ac0abb4029cfcd8a
Autor:
Bruno Martoglio, Michael Young, Sherry Niessen, Petra Langerak, Michael P. Cooke, Daniel R. Beisner, Carol Dahlberg, S. Sutton, Benjamin F. Cravatt, Albert E. Parker, Ursula Bodendorf, Tim Wiltshire, Whitney Barnes, Francella Otero, Laurent Poirot
Publikováno v:
The Journal of Experimental Medicine
The protease Sppl2a cleaves the N-terminal fragment of invariant chain (CD74) and is required for efficient B cell development and function.
B cell development requires tight regulation to allow for the generation of a diverse repertoire while p
B cell development requires tight regulation to allow for the generation of a diverse repertoire while p
Autor:
Heinz Jacobs, Niels de Wind, Peter H.L. Krijger, Niek Wit, Claude-Agnès Reynaud, Petra Langerak, Jacob G. Jansen, Paul C.M. van den Berk
Publikováno v:
DNA Repair, 10(10), 1051-1059
The generation of high affinity antibodies in B cells critically depends on translesion synthesis (TLS) polymerases that introduce mutations into immunoglobulin genes during somatic hypermutation (SHM). The majority of mutations at A/T base pairs dur
Publikováno v:
The Journal of Experimental Medicine
During somatic hypermutation (SHM), B cells introduce mutations into their immunoglobulin genes to generate high affinity antibodies. Current models suggest a separation in the generation of G/C transversions by the Ung2-dependent pathway and the gen
Autor:
Heinz Jacobs, Paul C.M. van den Berk, Marinus R. Heideman, Petra Langerak, Peter H.L. Krijger
Publikováno v:
Philosophical Transactions of the Royal Society B: Biological Sciences
Proliferating cell nuclear antigen (PCNA) encircles DNA as a ring-shaped homotrimer and, by tethering DNA polymerases to their template, PCNA serves as a critical replication factor. In contrast to high-fidelity DNA polymerases, the activation of low
Publikováno v:
PLoS Genetics, Vol 11, Iss 9, p e1005517 (2015)
PLoS Genetics
PLoS Genetics
Phosphorylation of histone H2AX by ATM and ATR establishes a chromatin recruitment platform for DNA damage response proteins. Phospho-H2AX (γH2AX) has been most intensively studied in the context of DNA double-strand breaks caused by exogenous clast
Autor:
Heinz Jacobs, Niels de Wind, Anastasia Tsaalbi-Shtylik, Paul C.M. van den Berk, Petra Langerak, Jacob G. Jansen
Publikováno v:
The Journal of Experimental Medicine
Somatic hypermutation of Ig genes enables B cells of the germinal center to generate high-affinity immunoglobulin variants. Key intermediates in somatic hypermutation are deoxyuridine lesions, introduced by activation-induced cytidine deaminase. Thes
Autor:
P.H.J. Peters, Jan Lankelma, Petra Langerak, Hans V. Westerhoff, Jorrit J. Hornberg, Everardus J.J. van Zoelen, Henk L. Dekker
Publikováno v:
Molecular Biotechnology, 34, 101-108
Hornberg, J J, Dekker, H, Peters, P H J, Langerak, P, Westerhoff, H V, Lankelma, J & Zoelen, E J J 2006, ' Epidermal growth factor receptor-induced activato protein 1 activity controls density-dependent growht inhibition in normal rat kidney fibroblasts. ', Molecular Biotechnology, vol. 34, pp. 101-108 . https://doi.org/10.1385/MB:34:2:101
Molecular Biotechnology, 34, 101-108. Humana Press
Molecular Biotechnology, 34, 2, pp. 101-108
Hornberg, J J, Dekker, H, Peters, P H J, Langerak, P, Westerhoff, H V, Lankelma, J & Zoelen, E J J 2006, ' Epidermal growth factor receptor-induced activato protein 1 activity controls density-dependent growht inhibition in normal rat kidney fibroblasts. ', Molecular Biotechnology, vol. 34, pp. 101-108 . https://doi.org/10.1385/MB:34:2:101
Molecular Biotechnology, 34, 101-108. Humana Press
Molecular Biotechnology, 34, 2, pp. 101-108
Density-dependent growth inhibition secures tissue homeostasis. Dysfunction of the mechanisms, which regulate this type of growth control is a major cause of neoplasia. In confluent normal rat kidney (NRK) fibroblasts, epidermal growth factor (EGF) r