Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dipeptidyl Peptidase 4/genetics"'
Autor:
Jelte van der Vaart, Bart L. Haagmans, Anna Z Mykytyn, Georg A. Busslinger, Tim I Breugem, Mart M. Lamers, Maarten H. Geurts, Wim de Lau, Cayetano Pleguezuelos-Manzano, Joep Beumer, Jingshu Zhang, Debby Schipper, Petra B. van den Doel, Hans Clevers, Jens Puschhof, Samra Riesebosch
Publikováno v:
Nature Communications
Nature Communications, 12(1):5498. Nature Publishing Group
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
Nature Communications, 12(1). Nature Publishing Group
Nature Communications, 12(1):5498. Nature Publishing Group
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
Nature Communications, 12(1). Nature Publishing Group
Rapid identification of host genes essential for virus replication may expedite the generation of therapeutic interventions. Genetic screens are often performed in transformed cell lines that poorly represent viral target cells in vivo, leading to di
Autor:
Nicola D. Kerrison, Carlos González, Mark Walker, Adam S. Butterworth, Martina Müller-Nurasyid, Mark I. McCarthy, Jarmo Virtamo, Nilesh J. Samani, Daniel F. Freitag, Jennifer Wessel, Inês Barroso, Jette Bork-Jensen, Marit E. Jørgensen, Torben Hansen, Nita G. Forouhi, Jennifer A. Smith, Peter Vollenweider, Douglas F. Easton, Heiner Boeing, Helena M. Earl, Laufey T. Amundadottir, Annette Peters, Ingrid B. Borecki, L. Adrienne Cupples, Li Li, Josée Dupuis, Sara Benlloch Garcia, J. Wouter Jukema, Shuai Wang, Veikko Salomaa, Jukka Kontto, Timothy J. Key, Yuning Chen, Sune F. Nielsen, Robin Young, Jing Hua Zhao, Andrew P. Morris, Larraitz Arriola, Claudia Langenberg, Joshua C. Bis, Nisa M. Maruthur, Ele Ferrannini, Joanna M. M. Howson, Marcel den Hoed, Jeanette Erdmann, Rosalind A. Eeles, Daphne L. van der A, Panos Deloukas, Eric Boerwinkle, Sara M. Willems, Elio Riboli, Markku Laakso, Gina M. Peloso, Muriel J. Caslake, Nadia Slimani, Zsofia Kote-Jarai, Paul W. Franks, EPIC-InterAct, Dominique Arveiler, Sarah Bowden, Janet A. Dunn, Jan-Håkan Jansson, Carlos Cruchaga, Audrey Y. Chu, James S. Pankow, Rudolf Kaaks, Jerome I. Rotter, Jaspal S. Kooner, Ailith Pirie, Johanna Kuusisto, Hanieh Yaghootkar, Niels Grarup, Danish Saleheen, Thomas Foltynie, Jean Abraham, Stefan Blankenberg, Mark O. Goodarzi, Markus Perola, Olov Rolandsson, Chris J. Packard, Praveen Surendran, Allan Linneberg, Beverley Balkau, Christopher J. Poole, Frank Kee, Carmen Navarro, Nicholas J. Wareham, Oluf Pedersen, Heribert Schunkert, Domenico Palli, Patricia B. Munroe, Sven J. van der Lee, Chunyu Liu, Rebecca Sims, Georg Ehret, Michael Boehnke, Stephen J. Sharp, Peter M. Nilsson, Salvatore Panico, Børge G. Nordestgaard, Aldi T. Kraja, Sara Grioni, Sekar Kathiresan, Dawn M. Waterworth, Francesco Gianfagna, Jacek Czajkowski, Naveed Sattar, Margaret G. Ehm, Christopher J. Gillson, Karen L. Mohlke, Stella Trompet, John Danesh, Carlotta Sacerdote, Gaëlle Marenne, Jian'an Luan, Timothy M. Frayling, J. Ramón Quirós, Iciar Aviles-Olmos, Robert A. Scott, Yvonne T. van der Schouw, Jennifer L. Aponte, María José Sánchez, Deborah J. Thompson, Klaudia Walter, James B. Meigs, Tibor V. Varga, Kari Kuulasmaa, Torben Jørgensen, Rosario Tumino, Kyriaki Michailidou, Kenneth Muir, Philippe Amouyel, Ian Ford, Aurelio Barricarte, Stephen O'Rahilly, Ali Amin Al Olama, Louise Hiller, Alena Stančáková, Carlos Caldas, Jean Ferrières
Publikováno v:
341ra76
Scott, R A, Freitag, D F, Li, L, Chu, A Y, Surendran, P, Young, R, Grarup, N, Stancáková, A, Chen, Y, Varga, T V, Yaghootkar, H, Luan, J, Zhao, J H, Willems, S M, Wessel, J, Wang, S, Maruthur, N, Michailidou, K, Pirie, A, van der Lee, S J, Gillson, C, Al Olama, A A, Amouyel, P, Arriola, L, Arveiler, D, Aviles-Olmos, I, Balkau, B, Barricarte, A, Barroso, I, Garcia, S B, Bis, J C, Blankenberg, S, Boehnke, M, Boeing, H, Boerwinkle, E, Borecki, I B, Bork-Jensen, J, Bowden, S, Caldas, C, Caslake, M, Cupples, L A, Cruchaga, C, Czajkowski, J, den Hoed, M, Dunn, J A, Earl, H M, Ehret, G B, Ferrannini, E, Ferrieres, J, Jørgensen, T & CVD50 consortium 2016, ' A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ', Science Translational Medicine, vol. 8, no. 341, 341ra76 . https://doi.org/10.1126/scitranslmed.aad3744
Scott, R A, Freitag, D F, Li, L, Chu, A Y, Surendran, P, Young, C R, Grarup, N, Stancakova, A, Chen, Y, Varga, T V, Yaghootkar, H, Luan, J, Zhao, J H, Willems, S M, Wessel, J, Wang, S, Maruthur, N M, Michailidou, K, Pirie, A, Van Der Lee, S J, Gillson, C J, Amin Al Olama, A, Amouyel, P, Arriola, L, Arveiler, D, Aviles-Olmos, I, Balkau, B, Barricarte, A, Barroso, I, Garcia, S B, Bis, J C, Blankenberg, S, Boehnke, M, Boeing, H, Boerwinkle, E, Borecki, I B, Bork-Jensen, J, Bowden, S, Caldas, C, Caslake, M, Cupples, L A, Cruchaga, C, Czajkowski, J, den Hoed, M, Dunn, J A, Earl, H M, Ehret, G B, Ferrannini, E, Ferrieres, J, Foltynie, T, Ford, I, Forouhi, N G, Gianfagna, F, Gonzalez, C A, Grioni, S, Hiller, L, Jansson, J H, Jørgensen, M E, Jukema, J W, Kaaks, R, Kee, F, Kerrison, N D, J. Key, T, Kontto, J, Kote-Jarai, Z, Kraja, A T, Kuulasmaa, K, Kuusisto, J, Linneberg, A, Liu, C, Marenne, G, Mohlke, K L, Morris, A P, Muir, K, Müller-Nurasyid, M, Munroe, P B, Navarro, C, Nielsen, S F, Nilsson, P M, Nordestgaard, B G, Packard, C J, Palli, D, Panico, S, Peloso, G M, Perola, M, Peters, A, Poole, C J, Quiros, J R, Rolandsson, O, Sacerdote, C, Salomaa, V, Sánchez, M-J, Sattar, N, Sharp, S J, Sims, R, Slimani, N, Smith, J A, Thompson, J D, Trompet, S, Tumino, R, van der A, D L, van der Schouw, Y T, Virtamo, J, Walker, M, Walter, K, Abraham, J E, Amundadottir, L T, Butterworth, A S, Aponte, J L, Dupuis, J, Easton, D F, Eeles, R A, Erdmann, J, Franks, P W, Frayling, T M, Hansen, T, Howson, J M M, Jørgensen, T, Kooner, J, Laakso, M, McCarthy, M I, Pankow, J S, Pedersen, O, Riboli, E, Rotter, J I, Saleheen, D, Samani, N J, Schunkert, H, Vollenweider, P, O'Rahilly, S, Deloukas, P, Danesh, J, Goodarzi, M O, Kathiresan, S, Meigs, J B, Ehm, M G, Wareham, N J & Waterworth, D M 2016, ' A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ', Science Translational Medicine, bind 8, nr. 341 . https://doi.org/10.1126/scitranslmed.aad3744
SCIENCE TRANSLATIONAL MEDICINE
Scott, R A, Freitag, D F, Li, L, Chu, A Y, Surendran, P, Young, R, Grarup, N, Stancáková, A, Chen, Y, Varga, T V, Yaghootkar, H, Luan, J, Zhao, J H, Willems, S M, Wessel, J, Wang, S, Maruthur, N, Michailidou, K, Pirie, A, van der Lee, S J, Gillson, C, Al Olama, A A, Amouyel, P, Arriola, L, Arveiler, D, Aviles-Olmos, I, Balkau, B, Barricarte, A, Barroso, I, Garcia, S B, Bis, J C, Blankenberg, S, Boehnke, M, Boeing, H, Boerwinkle, E, Borecki, I B, Bork-Jensen, J, Bowden, S, Caldas, C, Caslake, M, Cupples, L A, Cruchaga, C, Czajkowski, J, den Hoed, M, Dunn, J A, Earl, H M, Ehret, G B, Ferrannini, E & Ferrieres, J & Foltynie, T 2016, ' A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ', Science Translational Medicine, vol. 8, no. 341, pp. 341ra76 . https://doi.org/10.1126/scitranslmed.aad3744
Science Translational Medicine, 8(341)
Science Translational Medicine, 8(341):341ra76. American Association for the Advancement of Science
Science Translational Medicine, Vol. 8, No 341 (2016) P. 341ra76
Science Translational Medicine, 8(341). American Association for the Advancement of Science
Scott, R A, Freitag, D F, Li, L, Chu, A Y, Surendran, P, Young, R, Grarup, N, Stancáková, A, Chen, Y, Varga, T V, Yaghootkar, H, Luan, J, Zhao, J H, Willems, S M, Wessel, J, Wang, S, Maruthur, N, Michailidou, K, Pirie, A, van der Lee, S J, Gillson, C, Al Olama, A A, Amouyel, P, Arriola, L, Arveiler, D, Aviles-Olmos, I, Balkau, B, Barricarte, A, Barroso, I, Garcia, S B, Bis, J C, Blankenberg, S, Boehnke, M, Boeing, H, Boerwinkle, E, Borecki, I B, Bork-Jensen, J, Bowden, S, Caldas, C, Caslake, M, Cupples, L A, Cruchaga, C, Czajkowski, J, den Hoed, M, Dunn, J A, Earl, H M, Ehret, G B, Ferrannini, E, Ferrieres, J, Jørgensen, T & CVD50 consortium 2016, ' A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ', Science Translational Medicine, vol. 8, no. 341, 341ra76 . https://doi.org/10.1126/scitranslmed.aad3744
Scott, R A, Freitag, D F, Li, L, Chu, A Y, Surendran, P, Young, C R, Grarup, N, Stancakova, A, Chen, Y, Varga, T V, Yaghootkar, H, Luan, J, Zhao, J H, Willems, S M, Wessel, J, Wang, S, Maruthur, N M, Michailidou, K, Pirie, A, Van Der Lee, S J, Gillson, C J, Amin Al Olama, A, Amouyel, P, Arriola, L, Arveiler, D, Aviles-Olmos, I, Balkau, B, Barricarte, A, Barroso, I, Garcia, S B, Bis, J C, Blankenberg, S, Boehnke, M, Boeing, H, Boerwinkle, E, Borecki, I B, Bork-Jensen, J, Bowden, S, Caldas, C, Caslake, M, Cupples, L A, Cruchaga, C, Czajkowski, J, den Hoed, M, Dunn, J A, Earl, H M, Ehret, G B, Ferrannini, E, Ferrieres, J, Foltynie, T, Ford, I, Forouhi, N G, Gianfagna, F, Gonzalez, C A, Grioni, S, Hiller, L, Jansson, J H, Jørgensen, M E, Jukema, J W, Kaaks, R, Kee, F, Kerrison, N D, J. Key, T, Kontto, J, Kote-Jarai, Z, Kraja, A T, Kuulasmaa, K, Kuusisto, J, Linneberg, A, Liu, C, Marenne, G, Mohlke, K L, Morris, A P, Muir, K, Müller-Nurasyid, M, Munroe, P B, Navarro, C, Nielsen, S F, Nilsson, P M, Nordestgaard, B G, Packard, C J, Palli, D, Panico, S, Peloso, G M, Perola, M, Peters, A, Poole, C J, Quiros, J R, Rolandsson, O, Sacerdote, C, Salomaa, V, Sánchez, M-J, Sattar, N, Sharp, S J, Sims, R, Slimani, N, Smith, J A, Thompson, J D, Trompet, S, Tumino, R, van der A, D L, van der Schouw, Y T, Virtamo, J, Walker, M, Walter, K, Abraham, J E, Amundadottir, L T, Butterworth, A S, Aponte, J L, Dupuis, J, Easton, D F, Eeles, R A, Erdmann, J, Franks, P W, Frayling, T M, Hansen, T, Howson, J M M, Jørgensen, T, Kooner, J, Laakso, M, McCarthy, M I, Pankow, J S, Pedersen, O, Riboli, E, Rotter, J I, Saleheen, D, Samani, N J, Schunkert, H, Vollenweider, P, O'Rahilly, S, Deloukas, P, Danesh, J, Goodarzi, M O, Kathiresan, S, Meigs, J B, Ehm, M G, Wareham, N J & Waterworth, D M 2016, ' A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ', Science Translational Medicine, bind 8, nr. 341 . https://doi.org/10.1126/scitranslmed.aad3744
SCIENCE TRANSLATIONAL MEDICINE
Scott, R A, Freitag, D F, Li, L, Chu, A Y, Surendran, P, Young, R, Grarup, N, Stancáková, A, Chen, Y, Varga, T V, Yaghootkar, H, Luan, J, Zhao, J H, Willems, S M, Wessel, J, Wang, S, Maruthur, N, Michailidou, K, Pirie, A, van der Lee, S J, Gillson, C, Al Olama, A A, Amouyel, P, Arriola, L, Arveiler, D, Aviles-Olmos, I, Balkau, B, Barricarte, A, Barroso, I, Garcia, S B, Bis, J C, Blankenberg, S, Boehnke, M, Boeing, H, Boerwinkle, E, Borecki, I B, Bork-Jensen, J, Bowden, S, Caldas, C, Caslake, M, Cupples, L A, Cruchaga, C, Czajkowski, J, den Hoed, M, Dunn, J A, Earl, H M, Ehret, G B, Ferrannini, E & Ferrieres, J & Foltynie, T 2016, ' A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease ', Science Translational Medicine, vol. 8, no. 341, pp. 341ra76 . https://doi.org/10.1126/scitranslmed.aad3744
Science Translational Medicine, 8(341)
Science Translational Medicine, 8(341):341ra76. American Association for the Advancement of Science
Science Translational Medicine, Vol. 8, No 341 (2016) P. 341ra76
Science Translational Medicine, 8(341). American Association for the Advancement of Science
Regulatory authorities have indicated that new drugs to treat type 2 diabetes (T2D) should not be associated with an unacceptable increase in cardiovascular risk. Human genetics may be able to guide development of antidiabetic therapies by predicting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b2df1af35c1e4c46ac1448dacdbce98
http://hdl.handle.net/11588/650489
http://hdl.handle.net/11588/650489
Autor:
Rosa Barreira da Silva, Melissa E Laird, Nader Yatim, Laurence Fiette, Molly A Ingersoll, Matthew L Albert
Publikováno v:
Nature Immunology
Nature Immunology, 2015, 16 (8), pp.850-858. ⟨10.1038/ni.3201⟩
Nature Immunology, Nature Publishing Group, 2015, 16 (8), pp.850-858. ⟨10.1038/ni.3201⟩
Nature Immunology, 2015, 16 (8), pp.850-858. ⟨10.1038/ni.3201⟩
Nature Immunology, Nature Publishing Group, 2015, 16 (8), pp.850-858. ⟨10.1038/ni.3201⟩
International audience; The success of antitumor immune responses depends on the infiltration of solid tumors by effector T cells, a process guided by chemokines. Here we show that in vivo post-translational processing of chemokines by dipeptidylpept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e2ab8828a29afd88e17c54fdc280cd
https://hal-pasteur.archives-ouvertes.fr/pasteur-01380810
https://hal-pasteur.archives-ouvertes.fr/pasteur-01380810
Autor:
Darragh Duffy, Eric G. Meissner, Henry Masur, Shyam Kottilil, Matthew L. Albert, Jérémie Decalf, Armanda Casrouge
Publikováno v:
PLoS ONE
PLoS ONE, 2015, 10 (7), pp.e0133236. ⟨10.1371/journal.pone.0133236⟩
PLoS ONE, Vol 10, Iss 7, p e0133236 (2015)
PLoS ONE, Public Library of Science, 2015, 10 (7), pp.e0133236. ⟨10.1371/journal.pone.0133236⟩
PLoS ONE, 2015, 10 (7), pp.e0133236. ⟨10.1371/journal.pone.0133236⟩
PLoS ONE, Vol 10, Iss 7, p e0133236 (2015)
PLoS ONE, Public Library of Science, 2015, 10 (7), pp.e0133236. ⟨10.1371/journal.pone.0133236⟩
Serum levels of the interferon (IFN)-stimulated chemokine CXCL10 are increased during chronic HCV infection and associate with outcome of IFN-based therapy. Elevated levels of NH2-terminal truncated CXCL10 (3-77aa), produced by DPP4 cleavage, negativ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34288c84d102b5e0fb82496371553986
https://hal-pasteur.archives-ouvertes.fr/pasteur-01380964/file/journal.pone.0133236.PDF
https://hal-pasteur.archives-ouvertes.fr/pasteur-01380964/file/journal.pone.0133236.PDF
Autor:
Rocío Ramos-Medina, Bárbara Alonso, Armanda Casrouge, Janet Vega, Matthew L. Albert, Marta Tejera-Alhambra, Silvia Sánchez-Ramón, Clara de Andrés
Publikováno v:
Clinical Immunology
Clinical Immunology, Elsevier, 2014, 150 (2), pp.170-183. ⟨10.1016/j.clim.2013.11.011⟩
Clinical Immunology, 2014, 150 (2), pp.170-183. ⟨10.1016/j.clim.2013.11.011⟩
Clinical Immunology, Elsevier, 2014, 150 (2), pp.170-183. ⟨10.1016/j.clim.2013.11.011⟩
Clinical Immunology, 2014, 150 (2), pp.170-183. ⟨10.1016/j.clim.2013.11.011⟩
International audience; Multiple sclerosis (MS) is a prototypic Th1/Th17 chronic autoimmune disease of the central nervous system. Dipeptidyl peptidase 4 (DPP4 or CD26) is a multifunctional molecule involved in autoimmune diseases' pathophysiology. W
Autor:
Massimo Locati, Elena Monica Borroni, Raffaella Bonecchi, Paul Proost, Alberto Mantovani, Benedetta Savino, Nina Machado Torres, Sofie Struyf, Anneleen Mortier
The chemokine decoy receptor D6 controls inflammatory responses by selective recognition and degradation of most CCR1 to CCR5 agonistic ligands. CCL14 is a homeostatic chemokine present at high concentrations in the serum with a weak agonist activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::654dfb1c35edc3f328766f781dd42a7b
https://doi.org/10.1074/jbc.m109.029249
https://doi.org/10.1074/jbc.m109.029249