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Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy. [electronic resource] by
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- Zhu, Xiaoxi
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- Koch, Susanne
- Krebs, Martin
- Schulz, Herbert
- Lodka, Doerte
- Saar, Kathrin
- Labeit, Siegfried
- Spies, Claudia
- Hubner, Norbert
- Spranger, Joachim
- Spuler, Simone
- Boschmann, Michael
- Dittmar, Gunnar
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HEART DISEASE. Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy. [electronic resource] by
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- Swist, Sandra
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- Schafer, Sebastian
- Sheng, Calvin C
- Haghighi, Alireza
- Homsy, Jason
- Hubner, Norbert
- Church, George
- Cook, Stuart A
- Linke, Wolfgang A
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Science (New York, N.Y.) vol. 349
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A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism. [electronic resource] by
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- Meder, Benjamin
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- Hubner, Norbert
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Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy. [electronic resource] by
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- Price, Mareike
- Hansen, Gesine
- Seidenberg, Jürgen
- Röblitz, Holger
- Yürek, Songül
- Tschirner, Sebastian
- Hong, Xiumei
- Wang, Xiaobin
- Homuth, Georg
- Schmidt, Carsten O
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- Hübner, Norbert
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- Lee, Young-Ae
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Genetical genomic determinants of alcohol consumption in rats and humans. [electronic resource] by
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- Bell, Richard L
- Hübner, Norbert
- Heinig, Matthias
- Pravenec, Michal
- Mangion, Jonathan
- Legault, Lucie
- Dongier, Maurice
- Conigrave, Katherine M
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Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease. [electronic resource] by
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- Monti, Jan
- Zidek, Vaclav
- Musilova, Alena
- Kren, Vladimir
- Causton, Helen
- Game, Laurence
- Born, Gabriele
- Schmidt, Sabine
- Müller, Anita
- Cook, Stuart A
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Ndufc2 Gene Inhibition Is Associated With Mitochondrial Dysfunction and Increased Stroke Susceptibility in an Animal Model of Complex Human Disease. [electronic resource] by
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- Falak, Samreen
- Stanzione, Rosita
- Marchitti, Simona
- Scarpino, Stefania
- Giusti, Betti
- Kura, Ada
- Gensini, Gian Franco
- Peyvandi, Flora
- Mannucci, Pier Mannuccio
- Rasura, Maurizia
- Sciarretta, Sebastiano
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A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity. [electronic resource] by
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- Kittler, Ralf
- Junqueira, Magno
- Shevchenko, Andrej
- Schulz, Herbert
- Hubner, Norbert
- Doss, Michael Xavier
- Sachinidis, Agapios
- Hescheler, Juergen
- Iacone, Roberto
- Anastassiadis, Konstantinos
- Stewart, A Francis
- Pisabarro, M Teresa
- Caldarelli, Antonio
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- Buchholz, Frank
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Tumour ischaemia by interferon-γ resembles physiological blood vessel regression. [electronic resource] by
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- Patone, Giannino
- Kunz, Severine
- Sommermeyer, Daniel
- Engels, Boris
- Leisegang, Matthias
- Textor, Ana
- Fehling, Hans Joerg
- Fruttiger, Marcus
- Lohoff, Michael
- Herrmann, Andreas
- Yu, Hua
- Weichselbaum, Ralph
- Uckert, Wolfgang
- Hübner, Norbert
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Eleven loci with new reproducible genetic associations with allergic disease risk. [electronic resource] by
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- Ullemar, Vilhelmina
- Lu, Yi
- Rüschendorf, Franz
- Hinds, David A
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- Weidinger, Stephan
- Magnusson, Patrik K E
- Jorgenson, Eric
- Lee, Young-Ae
- Boomsma, Dorret I
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- Almqvist, Catarina
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The Journal of allergy and clinical immunology vol. 143
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Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease. [electronic resource] by
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- Schulz, Herbert
- Gösele, Claudia
- Heuser, Arnd
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- Schmidt, Cosima
- Schirdewan, Alexander
- Gross, Volkmar
- Hummel, Oliver
- Maatz, Henrike
- Patone, Giannino
- Saar, Kathrin
- Vingron, Martin
- Weldon, Steven M
- Lindpaintner, Klaus
- Hammock, Bruce D
- Rohde, Klaus
- Dietz, Rainer
- Cook, Stuart A
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In:
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Recessive TTN truncating mutations define novel forms of core myopathy with heart disease. [electronic resource] by
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- Kho, Ay Lin
- Marks, Harold
- Talim, Beril
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- Uro-Coste, Emmanuelle
- Alexandrovich, Alexander
- Vihola, Anna
- Schafer, Sebastian
- Kaufmann, Beth
- Medne, Livija
- Hübner, Norbert
- Foley, A Reghan
- Santi, Mariarita
- Udd, Bjarne
- Topaloglu, Haluk
- Moore, Steven A
- Gotthardt, Michael
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In:
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A common variant on chromosome 11q13 is associated with atopic dermatitis. [electronic resource] by
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- Fölster-Holst, Regina
- Bauerfeind, Anja
- Ruschendorf, Franz
- Patone, Giannino
- Rohde, Klaus
- Marenholz, Ingo
- Schulz, Florian
- Kerscher, Tamara
- Hubner, Norbert
- Wahn, Ulrich
- Schreiber, Stefan
- Franke, Andre
- Vogler, Rainer
- Heath, Simon
- Baurecht, Hansjörg
- Novak, Natalija
- Rodriguez, Elke
- Illig, Thomas
- Lee-Kirsch, Min-Ae
- Ciechanowicz, Andrzej
- Kurek, Michael
- Piskackova, Tereza
- Macek, Milan
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A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis. [electronic resource] by
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- Kretschmer, Anja
- Baurecht, Hansjörg
- Lipinski, Simone
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- Harder, Jürgen
- Lieb, Wolfgang
- Novak, Natalija
- Fölster-Holst, Regina
- Esparza-Gordillo, Jorge
- Marenholz, Ingo
- Ruschendorf, Franz
- Hubner, Norbert
- Reischl, Eva
- Waldenberger, Melanie
- Gieger, Christian
- Illig, Thomas
- Kabesch, Michael
- Zhang, Xue-Jun
- Xiao, Feng-Li
- Lee, Young-Ae
- Franke, Andre
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Producer: 20151125
In:
The Journal of allergy and clinical immunology vol. 136
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Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus. [electronic resource] by
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- Chowdhury, Dipanjan
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- Engel, Kerstin
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- Bailey, Suzanna L
- Witte, Torsten
- Vyse, Timothy J
- Kere, Juha
- Pfeiffer, Christiane
- Harvey, Scott
- Wong, Andrew
- Koskenmies, Sari
- Hummel, Oliver
- Rohde, Klaus
- Schmidt, Reinhold E
- Dominiczak, Anna F
- Gahr, Manfred
- Hollis, Thomas
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Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. [electronic resource] by
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- Castagne, Raphaele
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- Lackner, Karl
- Rossmann, Heidi
- Eleftheriadis, Medea
- Sinning, Christoph R
- Schnabel, Renate B
- Lubos, Edith
- Mennerich, Detlev
- Rust, Werner
- Perret, Claire
- Proust, Carole
- Nicaud, Viviane
- Loscalzo, Joseph
- Hübner, Norbert
- Tregouet, David
- Münzel, Thomas
- Ziegler, Andreas
- Tiret, Laurence
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Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. [electronic resource] by
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- Sabeh, M Khaled
- Plovie, Eva R
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- Klopocki, Eva
- Musso, Gabriel
- Werdich, Andreas A
- Kalwa, Hermann
- Heinig, Matthias
- Padera, Robert F
- Wassilew, Katharina
- Bluhm, Julia
- Harnack, Christine
- Martitz, Janine
- Barton, Paul J
- Greutmann, Matthias
- Berger, Felix
- Hubner, Norbert
- Siebert, Reiner
- Kramer, Hans-Heiner
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- Klaassen, Sabine
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In:
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The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance. [electronic resource] by
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- Birol, Inanç
- Guryev, Victor
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- Hummel, Oliver
- Morrissey, Catherine
- Behmoaras, Jacques
- Fernandez-Suarez, Xose M
- Johnson, Michelle D
- McLaren, William M
- Patone, Giannino
- Petretto, Enrico
- Plessy, Charles
- Rockland, Kathleen S
- Rockland, Charles
- Saar, Kathrin
- Zhao, Yongjun
- Carninci, Piero
- Flicek, Paul
- Kurtz, Ted
- Cuppen, Edwin
- Pravenec, Michal
- Hubner, Norbert
- Jones, Steven J M
- Birney, Ewan
- Aitman, Timothy J
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In:
Genome research vol. 20
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Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular mass. [electronic resource] by
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- Sarwar, Rizwan
- Grieve, Ian
- Lu, Han
- Kumaran, Mande K
- Muckett, Phillip J
- Mangion, Jonathan
- Schroen, Blanche
- Benson, Matthew
- Punjabi, Prakash P
- Prasad, Sanjay K
- Pennell, Dudley J
- Kiesewetter, Chris
- Tasheva, Elena S
- Corpuz, Lolita M
- Webb, Megan D
- Conrad, Gary W
- Kurtz, Theodore W
- Kren, Vladimir
- Fischer, Judith
- Hubner, Norbert
- Pinto, Yigal M
- Pravenec, Michal
- Aitman, Timothy J
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Wars2 is a determinant of angiogenesis. [electronic resource] by
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- Sips, Patrick
- Khin, Ester
- Rotival, Maxime
- Sun, Ximing
- Ahmed, Rizwan
- Widjaja, Anissa Anindya
- Schafer, Sebastian
- Yusoff, Permeen
- Choksi, Pervinder Kaur
- Ko, Nicole Shi Jie
- Singh, Manvendra K
- Epstein, David
- Guan, Yuguang
- Houštěk, Josef
- Mracek, Tomas
- Nuskova, Hana
- Mikell, Brittney
- Tan, Jessie
- Pesce, Francesco
- Kolar, Frantisek
- Bottolo, Leonardo
- Mancini, Massimiliano
- Hubner, Norbert
- Pravenec, Michal
- Petretto, Enrico
- MacRae, Calum
- Cook, Stuart A
Producer: 20180822
In:
Nature communications vol. 7
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