Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sander Pajusalu"'
Autor:
Sally C. Fletcher, Charlotte Hall, Tristan J. Kennedy, Sander Pajusalu, Monica H. Wojcik, Uncaar Boora, Chan Li, Kaisa Teele Oja, Eline Hendrix, Christian A.E. Westrip, Regina Andrijes, Sonia K. Piasecka, Mansi Singh, Mohammed E. El-Asrag, Anetta Ptasinska, Vallo Tillmann, Martin R. Higgs, Deanna A. Carere, Andrew D. Beggs, John Pappas, Rachel Rabin, Stephen J. Smerdon, Grant S. Stewart, Katrin Õunap, Mathew L. Coleman
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 7 (2023)
Although protein hydroxylation is a relatively poorly characterized posttranslational modification, it has received significant recent attention following seminal work uncovering its role in oxygen sensing and hypoxia biology. Although the fundamenta
Externí odkaz:
https://doaj.org/article/a5976c6079974ce1ba5fd035f60800a3
Autor:
Marios P. Stavridis, Mehmet Gundogdu, Sergio G. Bartual, Daan M. F. van Aalten, Andrew T. Ferenbach, Riina Žordania, Katrin Õunap, Veronica M. Pravata, Monica H. Wojcik, Sander Pajusalu
Publikováno v:
Febs Letters
'FEBS Letters ', vol: 594, pages: 717-727 (2020)
'FEBS Letters ', vol: 594, pages: 717-727 (2020)
X‐linked intellectual disabilities (XLID) are common developmental disorders. The enzyme O‐GlcNAc transferase encoded by OGT, a recently discovered XLID gene, attaches O‐GlcNAc to nuclear and cytoplasmic proteins. As few missense mutations have
Autor:
Olga Fjodorova, Natalia H. Revelo, Eveline C F Gerretsen, Richard Arts, Kimiyo Raymond, Fokje Zijlstra, Martin ter Beest, Karin Huijben, Rinse de Boer, Angel Ashikov, Katrin Õunap, Mari-Anne Vals, Kai Muru, Geert van den Bogaart, Melissa Baerenfaenger, Peter T. A. Linders, Dirk Lefeber, Sander Pajusalu
Publikováno v:
Nature Communications, 12
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications, 12, 1
Nature Communications, 12(1):6227. Nature Publishing Group
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications, 12, 1
Nature Communications, 12(1):6227. Nature Publishing Group
The SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) protein syntaxin-5 (Stx5) is essential for Golgi transport. In humans, the STX5 mRNA encodes two protein isoforms, Stx5 Long (Stx5L) from the first starting methionine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37a224e59f6199469bd35cf1f6d3b7e5
http://hdl.handle.net/2066/239969
http://hdl.handle.net/2066/239969
Autor:
Sander Pajusalu, Inga Talvik, Raymond Y. Wang, Daniel L. Kastner, Achim Werner, Mohammed Abul Basar, Precilla D'Souza, Katrin Õunap, Yutaka Nishimura, Johji Inazawa, Ken Saida, Ellen Macnamara, David B. Beck, Anthony J. Asmar, Kristin W. Barañano, Hirotsugu Oda, Marlies Kempers, Weiyi Mu, Naomichi Matsumoto, Joann Bodurtha, Tomoki Kosho, Joyce J. Thompson, Pedro P. Rocha, Ivona Aksentijevich, Apratim Mitra, Magdalena Walkiewicz, Tomoko Tamada, Ryan K. Dale, Satoshi Okada, Daniela Tiaki Uehara, Noriko Miyake, Cynthia J. Tifft
Publikováno v:
Science Advances, 7, 4
Science Advances
Science Advances, 7
Science Advances
Science Advances, 7
Disease-causing mutations in a linkage-specific deubiquitylase provide insights into chromatin remodeling during embryogenesis.
Reversible modification of proteins with linkage-specific ubiquitin chains is critical for intracellular signaling. I
Reversible modification of proteins with linkage-specific ubiquitin chains is critical for intracellular signaling. I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::685f6090f52ead44cd34ca0941bfa4a1
https://hdl.handle.net/2066/230561
https://hdl.handle.net/2066/230561
Autor:
Geert van den Bogaart, Karin Huijben, Katrin Õunap, Olga Fjodorova, Eveline C F Gerretsen, Natalia H. Revelo, Fokje Zijlstra, Richard Arts, Mari-Anne Vals, Kimiyo Raymond, Dirk Lefeber, Angel Ashikov, Sander Pajusalu, Peter T. A. Linders, Kai Muru, Martin ter Beest, Melissa Baerenfaenger
The SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor) protein syntaxin-5 (Stx5) is essential for Golgi transport. In humans, theSTX5mRNA encodes two protein isoforms, Stx5 Long (Stx5L) from the first starting methionine an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8868b7432023872fd3fe8b1cdd32eaa
https://doi.org/10.1101/2020.03.30.20044438
https://doi.org/10.1101/2020.03.30.20044438
Autor:
Giuseppe Matullo, Brett H. Graham, Elisa Coluzzi, Karit Reinson, Antonella Sgura, Monica H. Wojcik, Luca Pannone, Melissa P. Wasserstein, Lucia Pedace, Seema R. Lalani, Elena Carcarino, Daniela Q.C.M. Barge-Schaapveld, Anke Van Dijck, Austin Larson, Giovanna Carpentieri, Alessandro Bruselles, Simona Petrucci, Simone Pizzi, Elisabetta Flex, Cornelia Di Gaetano, Francesca Clementina Radio, Bruno Dallapiccola, Serena Cecchetti, Clara Viberti, Enrico Bertini, Chieko Chijiwa, Emilia K. Bijlsma, Elisabetta Ferretti, William J. Craigen, Cristina Andreoli, Brian G. Skotko, Daan J. Kamphuis, Alessandro De Luca, J. Louw Roos, Giuseppina Catanzaro, Sandra Kenis, Mariëtte J.V. Hoffer, Katrin Õunap, Maria Karayiorgou, Gijs W. E. Santen, Annette P.M. van den Elzen, Kathleen Brown, Haley Streff, M. E. Suzanne Lewis, Claudia A. L. Ruivenkamp, Xiaoyan Ge, Andrea Ciolfi, Nathalie Van der Aa, Marco Tartaglia, Rossella Rota, Amber Begtrup, Richard E. Person, Simone Martinelli, Koen L.I. van Gassen, R. Frank Kooy, Marije Meuwissen, Magdalena Walkiewicz, Evelina Miele, Marije Koopmans, Sander Pajusalu
Publikováno v:
The American journal of human genetics
American Journal of Human Genetics, 105(3), 493. Cell Press
American Journal of Human Genetics, 105(3), 493-508. CELL PRESS
American Journal of Human Genetics, 105(3), 493. Cell Press
American Journal of Human Genetics, 105(3), 493-508. CELL PRESS
Histones mediate dynamic packaging of nuclear DNA in chromatin, a process that is precisely controlled to guarantee efficient compaction of the genome and proper chromosomal segregation during cell division and to accomplish DNA replication, transcri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b4aede8a428ff2cc48fd476c697e3a3
http://hdl.handle.net/11573/1383117
http://hdl.handle.net/11573/1383117
Autor:
Olivier Vanakker, Maria Kirchhoff, Christian Gilissen, Jenny Morton, Ineke van der Burgt, Kelly Radtke, Tugce Aktas, Sarah Vergult, Diana Johnson, Tobias Rumpf, Tony Roscioli, André Reis, Alan Fryer, Salima El Chehadeh, Christel Thauvin-Robinet, Ange Line Bruel, Rolph Pfundt, Sander Pajusalu, David Francis, Asifa Akhtar, Iben Bache, Tiong Yang Tan, Vera M. Kalscheuer, Meredith Wilson, Björn Menten, Giuseppe Semplicio, Julien Thevenon, Richard Fisher, Yannis Duffourd, Gerhard Mittler, Witold G. Szymanski, M. Felicia Basilicata, Victoria McKay, Kristin Lindstrom, Han G. Brunner, Katrin Õunap, Jaya Ganesh, Claudia Isabelle Keller Valsecchi, Megan T. Cho, Laurence Faivre
Publikováno v:
Nature Genetics, 50, 1442-1451
Nature Genetics, 50(10), 1442-1451. Nature Publishing Group
Nature Genetics, 50, 10, pp. 1442-1451
Nature Genetics
Nature Genetics, Nature Publishing Group, 2018, 50 (10), pp.1442-1451. ⟨10.1038/s41588-018-0220-y⟩
Nat Genet
Nature Genetics, 50(10), 1442-1451. Nature Publishing Group
Nature Genetics, 50, 10, pp. 1442-1451
Nature Genetics
Nature Genetics, Nature Publishing Group, 2018, 50 (10), pp.1442-1451. ⟨10.1038/s41588-018-0220-y⟩
Nat Genet
International audience; The etiological spectrum of ultra-rare developmental disorders remains to be fully defined. Chromatin regulatory mechanisms maintain cellular identity and function, where misregulation may lead to developmental defects. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eaa71589cbe2fa7af4514c06198a58d
http://hdl.handle.net/2066/196095
http://hdl.handle.net/2066/196095