Canlyniadau Chwilio - Markus Munter

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  1. 1
    Inactivation of anoctamin-6/Tmem16f, a regulator of phosphatidylserine scrambling in osteoblasts, leads to decreased mineral deposition in skeletal tissues

    Inactivation of anoctamin-6/Tmem16f, a regulator of phosphatidylserine scrambling in osteoblasts, leads to decreased mineral deposition in skeletal tissues gan Harald W.A. Ehlen, Milana Chinenkova, Markus Moser, Hans-Markus Munter, Yvonne Krause, Stefanie Groß, Bent Brachvogel, Manuela Wuelling, Uwe Kornak, Andrea Vortkamp

    Cyhoeddwyd 2012
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  2. 2
    Loss of the APP regulator RHBDL4 preserves memory in an Alzheimer’s disease mouse model

    Loss of the APP regulator RHBDL4 preserves memory in an Alzheimer’s disease mouse model gan Ylauna Christine Mégane Penalva, Sandra Paschkowsky, Jingyun Yang, Sherilyn Junelle Recinto, Jessica Cinkornpumin, Marina Ruelas, Bin Xiao, Albert Nitu, Sin Young Kwon, Helen Yee-Li Wu, Hans Markus Münter, Bernadeta Michalski, Margaret Fahnestock, William A. Pastor, David A. Bennett, Lisa Marie Munter

    Cyhoeddwyd 2025
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  3. 3
    Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity

    Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity gan Satoshi Yoshiji, Guillaume Butler‐Laporte, Tianyuan Lu, Julian Daniel Sunday Willett, Chen‐Yang Su, Tomoko Nakanishi, David Morrison, Yiheng Chen, Kevin Y. H. Liang, Michael Hultström, Yann Ilboudo, Zaman Afrasiabi, Shanshan Lan, Naomi Duggan, Chantal DeLuca, Mitra Vaezi, Chris Tselios, Xiaoqing Xue, Meriem Bouab, Fangyi Shi, Lætitia Laurent, Hans Markus Münter, Marc Afilalo, Jonathan Afilalo, Vincent Mooser, Nicholas J. Timpson, Hugo Zeberg, Sirui Zhou, Vincenzo Forgetta, Yossi Farjoun, J. Brent Richards

    Cyhoeddwyd 2023
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  4. 4
    Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

    Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons gan Gaël Nicolas, David Wallon, Camille Charbonnier, Olivier Quenez, Stéphane Rousseau, Anne‐Claire Richard, Anne Rovelet‐Lecrux, Sophie Coutant, Kilan Le Guennec, Delphine Bacq, Jean-Guillaume Garnier, Robert Olaso, Anne Boland, Vincent Meyer, Jean‐François Deleuze, Hans Markus Münter, Guillaume Bourque, Daniel Auld, Alexandre Montpetit, Mark Lathrop, Lucie Guyant‐Maréchal, Olivier Martinaud, Jérémie Pariente, Adeline Rollin‐Sillaire, Florence Pasquier, Isabelle Le Ber, Marie Sarazin, Bernard Croisile, Claire Boutoleau‐Bretonnière, Catherine Thomas-Antérion, Claire Paquet, Mathilde Sauvée, Olivier Moreaud, Audrey Gabelle, François Sellal, Mathieu Ceccaldi, Ludivine Chamard, Fréderic Blanc, Thierry Frébourg, Dominique Campion, Didier Hannequin

    Cyhoeddwyd 2015
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  5. 5
    Association of <i>FADS1/2</i> Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis

    Association of <i>FADS1/2</i> Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis gan Hao Yu Chen, Benjamin J. Cairns, Aeron Small, Hannah A. Burr, Athithan Ambikkumar, Andreas Martinsson, Sébastien Thériault, Hans Markus Münter, Brian T. Steffen, Richard Zhang, Rebecca T. Levinson, Christian M. Shaffer, Jian Rong, Emily Sonestedt, Line Dufresne, Johan Ljungberg, Ulf Näslund, Bengt Johansson, Dilrini K. Ranatunga, Rachel A. Whitmer, Matthew J. Budoff, Albert Nguyen, Ramachandran S. Vasan, Martin G. Larson, William S. Harris, Scott M. Damrauer, Ken D. Stark, S. Matthijs Boekholdt, Nicholas J. Wareham, Philippe Pîbarot, Benoît J. Arsenault, Patrick Mathieu, Vilmundur Guðnason, Christopher J. O’Donnell, Jerome I. Rotter, Michael Y. Tsai, Wendy S. Post, Robert Clarke, Stefan Söderberg, Yohan Bossé, Quinn S. Wells, J. G. Smith, Daniel J. Rader, Mark Lathrop, James C. Engert, George Thanassoulis

    Cyhoeddwyd 2020
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  6. 6
    Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

    Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study gan Hao Yu Chen, Christian Dina, Aeron Small, Christian M. Shaffer, Rebecca T. Levinson, Anna Helgadóttir, Romain Capoulade, Hans Markus Münter, Andreas Martinsson, Benjamin J. Cairns, Linea C. Trudsø, Mary Hoekstra, Hannah A. Burr, Thomas W. Marsh, Scott M. Damrauer, Line Dufresne, Solena Le Scouarnec, David Messika‐Zeitoun, Dilrini K. Ranatunga, Rachel A. Whitmer, Amélie Bonnefond, Garðar Sveinbjörnsson, Ragnar Daníelsen, Davíð O. Arnar, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Hilma Hólm, Jonas Ghouse, Morten S. Olesen, Alex Hørby Christensen, Susan Mikkelsen, Rikke Louise Jacobsen, Joseph Dowsett, Ole Birger Pedersen, Christian Erikstrup, Sisse Rye Ostrowski, Christopher J. O’Donnell, Matthew J. Budoff, Vilmundur Guðnason, Wendy S. Post, Jerome I. Rotter, Mark Lathrop, Henning Bundgaard, Bengt Johansson, Johan Ljungberg, Ulf Näslund, Thierry Le Tourneau, J. G. Smith, Quinn S. Wells, Stefan Söderberg, Kāri Stefánsson, Jean‐Jacques Schott, Daniel J. Rader, Robert Clarke, James C. Engert, George Thanassoulis

    Cyhoeddwyd 2023
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  7. 7
    <i>ABCA7</i> rare variants and Alzheimer disease risk

    <i>ABCA7</i> rare variants and Alzheimer disease risk gan Kilan Le Guennec, Gaël Nicolas, Olivier Quenez, Camille Charbonnier, David Wallon, Céline Bellenguez, Benjamin Grenier‐Boley, Stéphane Rousseau, Anne‐Claire Richard, Anne Rovelet‐Lecrux, Delphine Bacq, Jean-Guillaume Garnier, Robert Olaso, Anne Boland, Vincent Meyer, Jean‐François Deleuze, Philippe Amouyel, Hans Markus Münter, Guillaume Bourque, Mark Lathrop, Thierry Frébourg, Richard Redon, Luc Letenneur, Jean‐François Dartigues, Florence Pasquier, Adeline Rollin‐Sillaire, Emmanuelle Génin, Jean‐Charles Lambert, Didier Hannequin, Dominique Campion, Didier Hannequin, Dominique Campion, David Wallon, Olivier Martinaud, Gaël Nicolas, Adeline Rollin‐Sillaire, Stéphanie Bombois, Marie‐Anne Mackowiak, Vincent Deramecourt, Florence Pasquier, Agnès Michon, Isabelle Le Ber, Bruno Dubois, Charles Duyckaerts, Olivier Godefroy, Frédérique Etcharry‐Bouyx, Valérie Chauviré, Ludivine Chamard, Eric Berger, Éloi Magnin, Jean‐François Dartigues, Sophie Auriacombe, François Tison, Cyril Goizet, Vincent de la Sayette, Fausto Viader, Dominique Castan, Elsa Dionet, François Sellal, Olivier Rouaud, Christel Thauvin, Olivier Moreaud, Mathilde Sauvée, Maïté Formaglio, Hélène Mollion, Isabelle Roullet-Solignac, Alain Vighetto, Bernard Croisile, Mira Didic, Olivier Félician, Lejla Koric, Mathieu Ceccaldi, Audrey Gabelle, Cecilia Marelli, Jacques Touchon, Pierre Labauge, Thérèse Jonveaux, Martine Vercelletto, Claire Boutoleau‐Bretonnière, Giovanni Castelnovo, D.L. Renaud, Philippe Robert, Claire Paquet, Julien Dumurgier, Jacques Hugon, Foucauld De Boisgueheneuc, Serge Belliard, Serge Bakchine, Marie Sarazin, Marie‐Odile Barrellon, Bernard Laurent, Fréderic Blanc, Christine Tranchant, Jérémie Pariente, Michèle Puel, Caroline Hommet, Karl Mondon

    Cyhoeddwyd 2016
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  8. 8
    Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

    Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome gan Najim Lahrouchi, Rafik Tadros, Lia Crotti, Yuka Mizusawa, Pieter G. Postema, Leander Beekman, Roddy Walsh, Kanae Hasegawa, Julien Barc, Marko Ernsting, Kari L. Turkowski, Andrea Mazzanti, Britt M. Beckmann, Keiko Shimamoto, Ulla-Britt Diamant, Yanushi D. Wijeyeratne, Yu Kucho, Tomas Robyns, Taisuke Ishikawa, Elena Arbelo, Michael Christiansen, Annika Winbo, Reza Jabbari, Steven A. Lubitz, Johannes Steinfurt, Boris Rudic, Bart Loeys, Moore B. Shoemaker, Peter Weeke, Ryan Pfeiffer, Brianna Davies, Antoine Andorin, Nynke Hofman, Federica Dagradi, Matteo Pedrazzini, David J. Tester, J. Martijn Bos, Geòrgia Sarquella-Brugada, Òscar Campuzano, Pyotr G. Platonov, Birgit Stallmeyer, Sven Zumhagen, Eline A. Nannenberg, Jan H. Veldink, Leonard H. van den Berg, Ammar Al‐Chalabi, Christopher E. Shaw, Pamela J. Shaw, Karen Morrison, Peter M. Andersen, Martina Müller‐Nurasyid, Daniele Cusi, Cristina Barlassina, Pilar Galán, Mark Lathrop, Markus Munter, Thomas Werge, Marta Ribasés, Tin Aung, Chiea Chuen Khor, Mineo Ozaki, Peter Lichtner, Thomas Meitinger, J. Peter van Tintelen, Yvonne M. Hoedemaekers, Isabelle Denjoy, Antoine Leenhardt, Carlo Napolitano, Wataru Shimizu, Jean‐Jacques Schott, Jean‐Baptiste Gourraud, Takeru Makiyama, Seiko Ohno, Hideki Itoh, Andrew D. Krahn, Charles Antzelevitch, Dan M. Roden, Johan Saenen, Martin Borggrefe, Katja E. Odening, Patrick T. Ellinor, Jacob Tfelt‐Hansen, Jonathan R. Skinner, Maarten P. van den Berg, Morten S. Olesen, Josép Brugada, Ramón Brugada, Naomasa Makita, Jeroen Breckpot, Masao Yoshinaga, Elijah R. Behr, Annika Rydberg, Takeshi Aiba, Stefan Kääb, Silvia G. Priori, Pascale Guicheney, Hanno L. Tan, Christopher Newton‐Cheh, Michael Ackerman, Peter J. Schwartz

    Cyhoeddwyd 2020
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