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2017

Functional implications of microbial and viral gut metagenome changes in early stage L-DOPA-naive Parkinson's disease patients.
Bedarf, J.R. and Hildebrand, F. and Coelho, L.P. and Sunagawa, S. and Bahram, M. and Goeser, F. and Bork, P. and Wuellner, U.
Genome Medicine 9 (1): 39. 28 April 2017

Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells.
Middelkamp, S. and van Heesch, S. and Braat, A.K. and de Ligt, J. and van Iterson, M. and Simonis, M. and van Roosmalen, M.J. and Kelder, M.J.E. and Kruisselbrink, E. and Hochstenbach, R. and Verbeek, N.E. and Ippel, E.F. and Adolfs, Y. and Pasterkamp, R.J. and Kloosterman, W.P. and Kuijk, E.W. and Cuppen, E.
Genome Medicine 9 (1): 9. 26 January 2017

2016

The IL-4/STAT6 signaling axis establishes a conserved microRNA signature in human and mouse macrophages regulating cell survival via miR-342-3p.
Czimmerer, Z. and Varga, T. and Kiss, M. and Vazquez, C.O. and Doan-Xuan, Q.M. and Rueckerl, D. and Tattikota, S.G. and Yan, X. and Nagy, Z.S. and Daniel, B. and Poliska, S. and Horvath, A. and Nagy, G. and Varallyay, E. and Poy, M.N. and Allen, J.E. and Bacso, Z. and Abreu-Goodger, C. and Nagy, L.
Genome Medicine 8 (1): 63. 31 May 2016

A roadmap of constitutive NF-κB activity in Hodgkin lymphoma: dominant roles of p50 and p52 revealed by genome-wide analyses.
de Oliveira, K.A.P. and Kaergel, E. and Heinig, M. and Fontaine, J.F. and Patone, G. and Muro, E.M. and Mathas, S. and Hummel, M. and Andrade-Navarro, M.A. and Hübner, N. and Scheidereit, C.
Genome Medicine 8 (1): 28. 17 March 2016

2014

Modules, networks and systems medicine for understanding disease and aiding diagnosis.
Gustafsson, M. and Nestor, C.E. and Zhang, H. and Barabási, A.L. and Baranzini, S. and Brunak, S. and Chung, K.F. and Federoff, H.J. and Gavin, A.C. and Meehan, R.R. and Picotti, P. and Pujana, M.À. and Rajewsky, N. and Smith, K.G.C. and Sterk, P.J. and Villoslada, P. and Benson, M.
Genome Medicine 6 (10): 82. 17 October 2014

2013

De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome.
Bainbridge, M.N. and Hu, H. and Muzny, D.M. and Musante, L. and Lupski, J.R. and Graham, B.H. and Chen, W. and Gripp, K.W. and Jenny, K. and Wienker, T.F. and Yang, Y. and Sutton, V.R. and Gibbs, R.A. and Ropers, H.H.
Genome Medicine 5 (2): 11. 5 February 2013

2012

Mining the literature: new methods to exploit keyword profiles.
Andrade-Navarro, M.A.
Genome Medicine 4 (10): 81. 30 October 2012

2009

Linking genes to diseases: it's all in the data.
Tiffin, N. and Andrade-Navarro, M.A. and Perez-Iratxeta, C.
Genome Medicine 1 (8): 77. 7 August 2009

Novel insights into proteomic technologies and their clinical perspective.
Dittmar, G. and Selbach, M.
Genome Medicine 1 (5): 53. 21 May 2009

This list was generated on Wed Oct 17 02:27:41 2018 CEST.
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