Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tamas Szommer"'
Autor:
Sabrina R. Mackinnon, Gustavo A. Bezerra, Tobias Krojer, Tamas Szommer, Frank von Delft, Paul E. Brennan, Wyatt W. Yue
Publikováno v:
Frontiers in Chemistry, Vol 10 (2022)
Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. A build-up of the enzyme’s substrate, glyoxylate, results in excessive deposition of calcium oxalate c
Externí odkaz:
https://doaj.org/article/dfd6aa5544794ca1b1e7cb0be889d771
Autor:
Adrienne M. Flanagan, Udo Oppermann, Richard G. Jenner, Nischalan Pillay, Paul E. Brennan, Catrine Johansson, Tamas Szommer, Edward S. Hookway, Patrick Lombard, Anthony Tumber, Martin Philpott, Lorena Ligammari, Graham Wells, Garima Khandelwal, Adam P. Cribbs, Lucia Cottone
Chordoma RNAseq_all cell lines_gene lists
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6578577fc25599f576ad85a99627634
https://doi.org/10.1158/0008-5472.22426561
https://doi.org/10.1158/0008-5472.22426561
Autor:
Adrienne M. Flanagan, Udo Oppermann, Richard G. Jenner, Nischalan Pillay, Paul E. Brennan, Catrine Johansson, Tamas Szommer, Edward S. Hookway, Patrick Lombard, Anthony Tumber, Martin Philpott, Lorena Ligammari, Graham Wells, Garima Khandelwal, Adam P. Cribbs, Lucia Cottone
Supplementary Information
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c485bbf1b953bd1304c5c3572926d52
https://doi.org/10.1158/0008-5472.22426555.v1
https://doi.org/10.1158/0008-5472.22426555.v1
Autor:
Adrienne M. Flanagan, Udo Oppermann, Richard G. Jenner, Nischalan Pillay, Paul E. Brennan, Catrine Johansson, Tamas Szommer, Edward S. Hookway, Patrick Lombard, Anthony Tumber, Martin Philpott, Lorena Ligammari, Graham Wells, Garima Khandelwal, Adam P. Cribbs, Lucia Cottone
Expression of the transcription factor brachyury (TBXT) is normally restricted to the embryo, and its silencing is epigenetically regulated. TBXT promotes mesenchymal transition in a subset of common carcinomas, and in chordoma, a rare cancer showing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8212a639932c9ee33a88afa370634f22
https://doi.org/10.1158/0008-5472.c.6512377
https://doi.org/10.1158/0008-5472.c.6512377
Autor:
Sabrina R. Mackinnon, Gustavo A. Bezerra, Tobias Krojer, Tamas Szommer, Frank von Delft, Paul E. Brennan, Wyatt W. Yue
Publikováno v:
Frontiers in chemistry. 10
Primary hyperoxaluria type I (PH1) is caused by AGXT gene mutations that decrease the functional activity of alanine:glyoxylate aminotransferase. A build-up of the enzyme’s substrate, glyoxylate, results in excessive deposition of calcium oxalate c