Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pierre Bedoucha"'
Publikováno v:
Computers & graphics
When studying the function of proteins, biochemists utilize normal mode decomposition to enable the analysis of structural changes on time scales that are too long for molecular dynamics simulation. Such a decomposition yields a high-dimensional para
Publikováno v:
Computational and Structural Biotechnology Journal
Computational and Structural Biotechnology Journal, Vol 18, Iss, Pp 532-547 (2020)
Computational and Structural Biotechnology Journal, Vol 18, Iss, Pp 532-547 (2020)
Graphical abstract
N-terminal acetyltransferases (NATs) belong to the superfamily of acetyltransferases. They are enzymes catalysing the transfer of an acetyl group from acetyl coenzyme A to the N-terminus of polypeptide chains. N-terminal acety
N-terminal acetyltransferases (NATs) belong to the superfamily of acetyltransferases. They are enzymes catalysing the transfer of an acetyl group from acetyl coenzyme A to the N-terminus of polypeptide chains. N-terminal acety
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::694de509c94a1ec057001a596b857080
https://hdl.handle.net/11250/2754693
https://hdl.handle.net/11250/2754693
N-terminal acetyltransferases (NATs) are enzymes catalysing the transfer of the acetyl from Ac-CoA to the N-terminus of proteins, one of the most common protein modifications. Unlike NATs, lysine acetyltransferases (KATs) transfer an acetyl onto the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d51e491abe37603e57d138b7fbef502e
Autor:
Etienne Levavasseur, Jean-Louis Laplanche, Philippe Derreumaux, Human Rezaei, Céline Chapuis, Nicolas Privat, Katell Peoc'h, M. Borg, Isabelle Laffont-Proust, Pierre Bedoucha, Yassmine Chebaro, Annie Laquerrière, Stéphane Haïk, Jean-Jacques Hauw, Alfonso De Simone, Jean-Louis Kemeny, Jean-Philippe Brandel, Emilien Delmont
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, 2012, 21 (26), pp.5417--5428. ⟨10.1093/hmg/dds377⟩
Human Molecular Genetics 26 (21), 5417-5428. (2012)
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (26), pp.5417--5428. ⟨10.1093/hmg/dds377⟩
Hum. Mol. Genet.
Hum. Mol. Genet., 2012, 21 (26), pp.5417--5428. 〈10.1093/hmg/dds377〉
Human Molecular Genetics, 2012, 21 (26), pp.5417--5428. ⟨10.1093/hmg/dds377⟩
Human Molecular Genetics 26 (21), 5417-5428. (2012)
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (26), pp.5417--5428. ⟨10.1093/hmg/dds377⟩
Hum. Mol. Genet.
Hum. Mol. Genet., 2012, 21 (26), pp.5417--5428. 〈10.1093/hmg/dds377〉
Human prion diseases are a heterogeneous group of fatal neurodegenerative disorders, characterized by the deposition of the partially protease-resistant prion protein (PrPres), astrocytosis, neuronal loss and spongiform change in the brain. Among inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e351c19f516b7b777c862ed92ede2cc
https://hal.science/hal-01498095/document
https://hal.science/hal-01498095/document
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 18, Iss , Pp 532-547 (2020)
N-terminal acetyltransferases (NATs) belong to the superfamily of acetyltransferases. They are enzymes catalysing the transfer of an acetyl group from acetyl coenzyme A to the N-terminus of polypeptide chains. N-terminal acetylation is one of the mos
Externí odkaz:
https://doaj.org/article/c0bab6a947cb4e70817490881c617cf5
Publikováno v:
Cerebrovascular Diseases. 14:264-265
Autor:
T. Nakamura, Pierre Bedoucha, José M. Ferro, Zvi R. Cohen, Birgitta Lundgren-Lindquist, Steven M. Greenberg, J. van Gijn, Tobias Neumann-Haefelin, Achim Gass, Carolina Araújo, Marcel Chatel, T. Erkinjuntti, Anne Desmet, J. Bogousslavsky, Joachim Röther, C. Schleime, S. Osthaus, Karen L. Furie, R. Gilberto Gonzalez, Konstantinos Spengos, Andreas Terént, Ynte M. Ruigrok, Markku Kaste, Lisbeth Claesson, Sarah L. Keir, Gabriel J.E. Rinkel, V. Oliveira, Lee H. Schwamm, Jamary Oliveira-Filho, Zaza Katsarava, Antoine Dunac, F. Soares, Ester S. Bitanga, Yasuhiro Fjino, Nachshon Knoller, James F. Meschia, Kazuo Yamada, Mathias Hoehn, M. Jauss, Ingegerd Nydevik, J.M. Ferro, Moshe Hadani, Stephen J. Victor, Athanassios Grivas, R. Vataja, Walter J. Koroshetz, Eun Jung Choi, Peter D. Schellinger, M.G. Hennerici, Clifford J. Eskey, M. Iwata, Jong S. Kim, Einat Peles, Zvi Ram, Maire-Hélène Mahagne, Isabel Henriques, Robert Gan, Yasuhiko Baba, Tatsuo Yamada, Christian Blomstrand, Atsushi Umemura, Marianne Kloke, Cesare Fieschi, M. Kaste, Ferdinando S. Buonanno, Naoki Shimazu, Peter Sandercock, Yuchiao Chang, A. Leppävuori, P. Batista, M. Hügens-Penzel, Jean-Marc Orgogozo, H. Traupe, Leila Florento, Mario Siebler, T. Pohjasvaara, Hans-Christoph Diener, Guy Rordorf, Charalambos Pavlopoulos, Assia Jaillard, M. Kaps, Andrew J. Catto, Masashi Nakajima, Åke Seiger, Gunilla Gosman-Hedström, Zhengming Chen, S. Uchiyama, Gabriela C. Lopes, Rosalia A. Teleg, Atsuo Masago, Björn Fagerberg, M. Yamazaki, Joanna M. Wardlaw, Christian Weimar, Yoshio Tsuboi, Hakan Ay, Jonathan Rosand, Yoshie Kanda, Pamela W. Schaefer, Jochen B. Fiebach, Kaori Sakiyama, Geoffrey A. Donnan, Jens Fiehler, Martina Schlott, Julien Bogousslavsky, Peter J. Grant, Peter Appelros, Eliseo O. Salinas, Thomas Kucinski, Ángel Chamorro, Maria José Rosas, Arno Villringer, B. Rosengarten, Alastair J. Lansbury, Takashi Matsumoto, Rüdiger von Kummer, Allan Pallay
Publikováno v:
Cerebrovascular Diseases. 14:277-277
Autor:
Christian Blomstrand, Peter D. Schellinger, Walter J. Koroshetz, Karen L. Furie, Sarah L. Keir, M.G. Hennerici, Tobias Neumann-Haefelin, Steven M. Greenberg, P. Batista, Alastair J. Lansbury, J. van Gijn, Atsuo Masago, Åke Seiger, Ferdinando S. Buonanno, Anne Desmet, C. Schleime, Peter Appelros, Yasuhiro Fjino, Hans-Christoph Diener, Guy Rordorf, Jean-Marc Orgogozo, Atsushi Umemura, Maire-Hélène Mahagne, Eliseo O. Salinas, Assia Jaillard, Takashi Matsumoto, Ynte M. Ruigrok, M. Yamazaki, Achim Gass, Robert Gan, Mathias Hoehn, Joachim Röther, Mario Siebler, Jamary Oliveira-Filho, Ingegerd Nydevik, Isabel Henriques, H. Traupe, Thomas Kucinski, Allan Pallay, R. Gilberto Gonzalez, Rosalia A. Teleg, Einat Peles, Clifford J. Eskey, Arno Villringer, B. Rosengarten, S. Osthaus, Kazuo Yamada, T. Pohjasvaara, Leila Florento, Jong S. Kim, Marianne Kloke, James F. Meschia, Pierre Bedoucha, Peter J. Grant, M. Kaste, Lisbeth Claesson, Geoffrey A. Donnan, Charalambos Pavlopoulos, Gabriela C. Lopes, Jens Fiehler, Yasuhiko Baba, T. Erkinjuntti, Zhengming Chen, Eun Jung Choi, M. Iwata, S. Uchiyama, J. Bogousslavsky, José M. Ferro, Carolina Araújo, Marcel Chatel, Birgitta Lundgren-Lindquist, Martina Schlott, Christian Weimar, Björn Fagerberg, Zvi R. Cohen, Andrew J. Catto, Hakan Ay, Masashi Nakajima, Stephen J. Victor, F. Soares, Jochen B. Fiebach, Kaori Sakiyama, Andreas Terént, Gabriel J.E. Rinkel, Zvi Ram, M. Hügens-Penzel, Nachshon Knoller, Naoki Shimazu, J.M. Ferro, Moshe Hadani, Yoshie Kanda, Joanna M. Wardlaw, Yoshio Tsuboi, Jonathan Rosand, Konstantinos Spengos, Rüdiger von Kummer, M. Kaps, Zaza Katsarava, Ángel Chamorro, Julien Bogousslavsky, Tatsuo Yamada, Maria José Rosas, Cesare Fieschi, Yuchiao Chang, A. Leppävuori, Antoine Dunac, Peter Sandercock, T. Nakamura, Pamela W. Schaefer, Gunilla Gosman-Hedström, Markku Kaste, V. Oliveira, Lee H. Schwamm, Ester S. Bitanga, M. Jauss, Athanassios Grivas, R. Vataja
Publikováno v:
Cerebrovascular Diseases. 14:276-276