Zobrazeno 1 - 10
of 324
pro vyhledávání: '"Pfeufer Arne"'
Autor:
Arnold Matthias, Hartsperger Mara L, Baurecht Hansjörg, Rodríguez Elke, Wachinger Benedikt, Franke Andre, Kabesch Michael, Winkelmann Juliane, Pfeufer Arne, Romanos Marcel, Illig Thomas, Mewes Hans-Werner, Stümpflen Volker, Weidinger Stephan
Publikováno v:
BMC Genomics, Vol 13, Iss 1, p 490 (2012)
Abstract Background Genome-wide association studies (GWAS) have provided a large set of genetic loci influencing the risk for many common diseases. Association studies typically analyze one specific trait in single populations in an isolated fashion
Externí odkaz:
https://doaj.org/article/6cadd4efe8ed4d738e9da9b2e6ab2709
Autor:
Hopfner Franziska, Schormair Barbara, Knauf Franziska, Berthele Achim, Tölle Thomas R, Baron Ralf, Maier Christoph, Treede Rolf-Detlef, Binder Andreas, Sommer Claudia, Maihöfner Christian, Kunz Wolfram, Zimprich Friedrich, Heemann Uwe, Pfeufer Arne, Näbauer Michael, Kääb Stefan, Nowak Barbara, Gieger Christian, Lichtner Peter, Trenkwalder Claudia, Oexle Konrad, Winkelmann Juliane
Publikováno v:
BMC Neurology, Vol 11, Iss 1, p 134 (2011)
Abstract Background Action myoclonus-renal failure syndrome is a hereditary form of progressive myoclonus epilepsy associated with renal failure. It is considered to be an autosomal-recessive disease related to loss-of-function mutations in SCARB2. W
Externí odkaz:
https://doaj.org/article/b2f9b98b1e8f4fc5bd7bdb2e985fc066
Publikováno v:
BMC Evolutionary Biology, Vol 9, Iss 1, p 188 (2009)
Abstract Background KCNE1 represents the regulatory beta-subunit of the slowly activating delayed rectifier potassium channel (IKs). Variants of KCNE1 have repeatedly been linked to the long-QT syndrome (LQTS), a disorder which predisposes to deafnes
Externí odkaz:
https://doaj.org/article/34a6df8a34274e9b8b1c709ea4bb837c
Publikováno v:
BMC Genomics, Vol 8, Iss 1, p 159 (2007)
Abstract Background New technologies have enabled genome-wide association studies to be conducted with hundreds of thousands of genotyped SNPs. Several different first-generation genome-wide panels of SNPs have been commercialized. The total amount o
Externí odkaz:
https://doaj.org/article/cf545128facc44d08aad63c853f98494
Autor:
Mock, Andreas, Heilig, Christoph E, Kreutzfeldt, Simon, Huebschmann, Daniel, Heining, Christoph, Schröck, Evelin, Brors, Benedikt, Stenzinger, Albrecht, Jäger, Dirk, Schlenk, Richard, Glimm, Hanno, Fröhling, Stefan, Horak, Peter, Apostolidis, Leonidas, Augustin, Marinela, Aust, Daniela, Bhatti, Irfan Ahmed, Bloehdorn, Johannes, Brendel, Cornelia, Britschgi, Christian, Braess, Jan, Burdach, Stefan, Busch, Elena, Casuscelli, Jozefina, Desuki, Alexander, Deutsch, Thomas, Dietrich, Mareike, Ehmer, Ursula, Ettrich, Thomas J, Falkenhorst, Johanna, Fehm, Tanja, Flörcken, Anne, Forschner, Andrea, Fuxius, Stefan, Gonzales-Carmona, Maria, Griesinger, Frank, Grill, Sabine, Gröschel, Stefan, Haag, Georg Martin, Haag, Ulrich, Halama, Niels, Hebart, Holger, Heidger, Nina, Hermes, Barbara, Hess, Georg, Hettmer, Simone, Hoechstetter, Manuela, Hoffmann, Martin, Hüttner, Felix J, Illert, Anna L, Jenzer, Maximilian, Kasper, Bernd, Kasper-Virchow, Stefan, Kindler, Thomas, Koscielniak, Ewa, Krönke, Jan, Kühn, Michael, Kunzmann, Volker, Lang, Alois, Leichsenring, Jonas, Livingstone, Elisabeth, Liotta, Lucia, Luley, Kim, Mack, Elisabeth, Martens, Uwe M, Metzeler, Klaus, Middeke, Jan Moritz, Möhrmann, Lino, Jayarama-Naidu, Roopa, Pape, Ulrich-Frank, Perkhofer, Lukas, Pfeufer, Arne, Pixberg, Constantin, Quante, Michael, Rendenbach, Bernhard, Rieke, Damian, Rothermundt, Christian, Sagerer, Andre Norbert, Salzmann, Martin, Saur, Dieter, Schilling, Bastian, Schleicher, Jan, Schlenska-Lange, Anke, Schmidt, Thomas, Schmitz, Sophia, Schölch, Sebastian, Shah, Rajiv, Shoumariyeh, Khalid, Siebenhüner, Alexander, Singh, Martin, Siveke, Jens, Springfeld, Christoph, Starke, Helen, Strobel, Sophia, Teleanu, Veronica, Thon, Niklas, Wagner, Sebastian, Walle, Thomas, Westphalen, Benedikt, Whitlock, Bettina, Winkler, Eva, Wirsik, Naita Maren, Woydack, Lena, Bois, Angelika Zabel-du, Zschäbitz, Stefanie
Publikováno v:
In ESMO Open 2019 4(6)
Autor:
Herbert, Alan, Gerry, Norman P., McQueen, Matthew B., Heid, Iris M., Pfeufer, Arne, Illig, Thomas, Meitinger, Thomas, Hunter, David, Hu, Frank B., Colditz, Graham, Hinney, Anke, Hebebrand, Johannes, Koberwitz, Kerstin, Zhu, Xiaofeng, Cooper, Richard, Ardlie, Kristin, Lyon, Helen, Hirschhorn, Joel N., Laird, Nan M., Lenburg, Marc E., Lange, Christoph, Christman, Michael F.
Publikováno v:
Science, 2006 Apr . 312(5771), 279-283.
Externí odkaz:
https://www.jstor.org/stable/3846050
Autor:
Gibson, Jane, Tapper, William, Cox, David, Zhang, Weihua, Pfeufer, Arne, Gieger, Christian, Wichmann, H.-Erich, Kääb, Stefan, Collins, Andrew R., Meitinger, Thomas, Morton, Newton
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2008 Feb . 105(7), 2592-2597.
Externí odkaz:
https://www.jstor.org/stable/25451511
Autor:
Hinterseer, Martin, Beckmann, Britt-Maria, Thomsen, Morten B., Pfeufer, Arne, Ulbrich, Michael, Sinner, Moritz F., Perz, Siegfried, Wichmann, H.-Erich, Lengyel, Csaba, Schimpf, Rainer, Maier, Sebastian K.G., Varró, András, Vos, Marc A., Steinbeck, Gerhard, Kääb, Stefan
Publikováno v:
In The American Journal of Cardiology 2010 106(2):216-220
Autor:
Hinterseer, Martin, Beckmann, Britt-Maria, Thomsen, Morten B., Pfeufer, Arne, Dalla Pozza, Robert, Loeff, Markus, Netz, Heinrich, Steinbeck, Gerhard, Vos, Marc A., Kääb, Stefan
Publikováno v:
In The American Journal of Cardiology 2009 103(9):1244-1248
Autor:
Eichenlaub, Martin1,2,3, Pfeufer, Arne4, Behrens, Lars5, Klauss, Volker6, Roettinger, Michael5, Brodherr, Turgut1, Lewalter, Thorsten1,2,3 th.lewalter@uni-bonn.de
Publikováno v:
Journal of Cardiovascular Electrophysiology. Mar2018, Vol. 29 Issue 3, p365-374. 10p. 2 Diagrams, 5 Charts, 1 Graph.