Publikationen

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Bisher wurden 687 Paper veröffentlicht (Stand 11.12.2017).

 

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Aktuelle e:Med Publikationen

Dezember 2017

  • Juniorverbund SYMBOL-HF

Meyer, P., Maity, P., Burkovski, A., Schwab, J., Müssel, C., Singh, K., Ferreira, F.F., Krug, L., Maier, H.J., Wlaschek, M., Wirth, T., Kestler, H.A., Scharffetter-Kochanek, K., 2017. A model of the onset of the senescence associated secretory phenotype after DNA damage induced senescence. PLoS Comput. Biol. 13, e1005741. doi.org/10.1371/journal.pcbi.1005741

  • Konsortium SYSIMIT

Nava-Sedeño, J.M., Hatzikirou, H., Klages, R., Deutsch, A., 2017. Cellular automaton models for time-correlated random walks: derivation and analysis. Sci Rep 7, 16952. doi.org/10.1038/s41598-017-17317-x

  • Konsortium SysMedAlcoholism

Ruggeri, B., Macare, C., Stopponi, S., Jia, T., Carvalho, F.M., Robert, G., Banaschewski, T., Bokde, A.L.W., Bromberg, U., Büchel, C., Cattrell, A., Conrod, P.J., Desrivières, S., Flor, H., Frouin, V., Gallinat, J., Garavan, H., Gowland, P., Heinz, A., Ittermann, B., Martinot, J.L., Martinot, M.-L.P., Nees, F., Papadopoulos-Orfanos, D., Paus, T., Poustka, L., Smolka, M.N., Vetter, N.C., Walter, H., Whelan, R., Sommer, W.H., Bakalkin, G., Ciccocioppo, R., Schumann, G., IMAGEN consortium, 2017. Methylation of OPRL1 mediates the effect of psychosocial stress on binge drinking in adolescents. J Child Psychol Psychiatry. doi.org/10.1111/jcpp.12843

November 2017

  • Konsortium CAPSyS

Arakelyan, A., Nersisyan, L., Poghosyan, D., Khondkaryan, L., Hakobyan, A., Löffler-Wirth, H., Melanitou, E., Binder, H., 2017. Autoimmunity and autoinflammation: A systems view on signaling pathway dysregulation profiles. PLoS ONE 12, e0187572. doi.org/10.1371/journal.pone.0187572

Gutbier, B., Jiang, X., Dietert, K., Ehrler, C., Lienau, J., Van Slyke, P., Kim, H., Hoang, V.C., Maynes, J.T., Dumont, D.J., Gruber, A.D., Weissmann, N., Mitchell, T.J., Suttorp, N., Witzenrath, M., 2017. Vasculotide reduces pulmonary hyperpermeability in experimental pneumococcal pneumonia. Crit Care 21, 274. doi.org/10.1186/s13054-017-1851-6

  • Konsortium e:Athero-Sysmed

Benedetti, E., Pučić-Baković, M., Keser, T., Wahl, A., Hassinen, A., Yang, J.-Y., Liu, L., Trbojević-Akmačić, I., Razdorov, G., Štambuk, J., Klarić, L., Ugrina, I., Selman, M.H.J., Wuhrer, M., Rudan, I., Polasek, O., Hayward, C., Grallert, H., Strauch, K., Peters, A., Meitinger, T., Gieger, C., Vilaj, M., Boons, G.-J., Moremen, K.W., Ovchinnikova, T., Bovin, N., Kellokumpu, S., Theis, F.J., Lauc, G., Krumsiek, J., 2017. Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway. Nat Commun 8, 1483. doi.org/10.1038/s41467-017-01525-0

  • Konsortium IntegraMent

International Consortium on Lithium Genetics (ConLi+Gen), Amare, A.T., Schubert, K.O., Clark, S.R., Papiol, S., Heilbronner, U., Degenhardt, F., Tekola-Ayele, F., Hsu, Y.-H., Shekhtman, T., Adli, M., Akula, N., Akiyama, K., Ardau, R., Arias, B., Aubry, J.-M., Backlund, L., Bhattacharjee, A.K., Bellivier, F., Benabarre, A., Bengesser, S., Biernacka, J.M., Birner, A., Brichant-Petitjean, C., Cervantes, P., Chen, H.-C., Chillotti, C., Cichon, S., Cruceanu, C., Czerski, P.M., Dalkner, N., Dayer, A., Del Zompo, M., DePaulo, J.R., Étain, B., Falkai, P., Forstner, A.J., Frisen, L., Frye, M.A., Fullerton, J.M., Gard, S., Garnham, J.S., Goes, F.S., Grigoroiu-Serbanescu, M., Grof, P., Hashimoto, R., Hauser, J., Herms, S., Hoffmann, P., Hofmann, A., Jamain, S., Jiménez, E., Kahn, J.-P., Kassem, L., Kuo, P.-H., Kato, T., Kelsoe, J., Kittel-Schneider, S., Kliwicki, S., König, B., Kusumi, I., Laje, G., Landén, M., Lavebratt, C., Leboyer, M., Leckband, S.G., Tortorella, A., Manchia, M., Martinsson, L., McCarthy, M.J., McElroy, S., Colom, F., Mitjans, M., Mondimore, F.M., Monteleone, P., Nievergelt, C.M., Nöthen, M.M., Novák, T., O’Donovan, C., Ozaki, N., Ösby, U., Pfennig, A., Potash, J.B., Reif, A., Reininghaus, E., Rouleau, G.A., Rybakowski, J.K., Schalling, M., Schofield, P.R., Schweizer, B.W., Severino, G., Shilling, P.D., Shimoda, K., Simhandl, C., Slaney, C.M., Squassina, A., Stamm, T., Stopkova, P., Maj, M., Turecki, G., Vieta, E., Volkert, J., Witt, S., Wright, A., Zandi, P.P., Mitchell, P.B., Bauer, M., Alda, M., Rietschel, M., McMahon, F.J., Schulze, T.G., Baune, B.T., 2017. Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study. JAMA Psychiatry. doi.org/10.1001/jamapsychiatry.2017.3433

Mühleisen, T.W., Reinbold, C.S., Forstner, A.J., Abramova, L.I., Alda, M., Babadjanova, G., Bauer, M., Brennan, P., Chuchalin, A., Cruceanu, C., Czerski, P.M., Degenhardt, F., Fischer, S.B., Fullerton, J.M., Gordon, S.D., Grigoroiu-Serbanescu, M., Grof, P., Hauser, J., Hautzinger, M., Herms, S., Hoffmann, P., Kammerer-Ciernioch, J., Khusnutdinova, E., Kogevinas, M., Krasnov, V., Lacour, A., Laprise, C., Leber, M., Lissowska, J., Lucae, S., Maaser, A., Maier, W., Martin, N.G., Mattheisen, M., Mayoral, F., McKay, J.D., Medland, S.E., Mitchell, P.B., Moebus, S., Montgomery, G.W., Müller-Myhsok, B., Oruc, L., Pantelejeva, G., Pfennig, A., Pojskic, L., Polonikov, A., Reif, A., Rivas, F., Rouleau, G.A., Schenk, L.M., Schofield, P.R., Schwarz, M., Streit, F., Strohmaier, J., Szeszenia-Dabrowska, N., Tiganov, A.S., Treutlein, J., Turecki, G., Vedder, H., Witt, S.H., Schulze, T.G., Rietschel, M., Nöthen, M.M., Cichon, S., 2017. Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. J Affect Disord 228, 20–25. doi.org/10.1016/j.jad.2017.11.068

Rietschel, L., Streit, F., Zhu, G., McAloney, K., Kirschbaum, C., Frank, J., Hansell, N.K., Wright, M.J., McGrath, J.J., Witt, S.H., Rietschel, M., Martin, N.G., 2016. Hair Cortisol and Its Association With Psychological Risk Factors for Psychiatric Disorders: A Pilot Study in Adolescent Twins. Twin Res Hum Genet 19, 438–446. doi.org/10.1017/thg.2016.50

Schulz, H., Ruppert, A.-K., Herms, S., Wolf, C., Mirza-Schreiber, N., Stegle, O., Czamara, D., Forstner, A.J., Sivalingam, S., Schoch, S., Moebus, S., Pütz, B., Hillmer, A., Fricker, N., Vatter, H., Müller-Myhsok, B., Nöthen, M.M., Becker, A.J., Hoffmann, P., Sander, T., Cichon, S., 2017. Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. Nat Commun 8, 1511. doi.org/10.1038/s41467-017-01818-4

Van der Auwera, S., Peyrot, W.J., Milaneschi, Y., Hertel, J., Baune, B., Breen, G., Byrne, E., Dunn, E.C., Fisher, H., Homuth, G., Levinson, D., Lewis, C., Mills, N., Mullins, N., Nauck, M., Pistis, G., Preisig, M., Rietschel, M., Ripke, S., Sullivan, P., Teumer, A., Völzke, H., Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Boomsma, D.I., Wray, N.R., Penninx, B., Grabe, H., 2017. Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD. Am. J. Med. Genet. B Neuropsychiatr. Genet. doi.org/10.1002/ajmg.b.32593

Xiao, X., Zhang, C., Grigoroiu-Serbanescu, M., Wang, L., Li, L., Zhou, D., Yuan, T.-F., Wang, C., Chang, H., Wu, Y., Li, Y., Wu, D.-D., Yao, Y.-G., Li, M., 2017. The cAMP responsive element-binding (CREB)-1 gene increases risk of major psychiatric disorders. Mol. Psychiatry. doi.org/10.1038/mp.2017.243

  • Konsortium IntegraMent & SysMedAlcoholism

Bernardi, R.E., Broccoli, L., Hirth, N., Justice, N.J., Deussing, J.M., Hansson, A.C., Spanagel, R., 2017. Dissociable Role of Corticotropin Releasing Hormone Receptor Subtype 1 on Dopaminergic and D1 Dopaminoceptive Neurons in Cocaine Seeking Behavior. Front Behav Neurosci 11, 221. doi.org/10.3389/fnbeh.2017.00221

  • Juniorverbund mitOmics

Charif, M., Nasca, A., Thompson, K., Gerber, S., Makowski, C., Mazaheri, N., Bris, C., Goudenège, D., Legati, A., Marrofian, R., Shariati, G., Lamantea, E., Hopton, S., Ardissone, A., Moroni, I., Giannotta, M., Siegel, C., Strom, T.M., Prokisch, H., Vignal-Clermont, C., Derrien, S., Zanlonghi, X., Kaplan, J., Hamel, C.P., Leruez, S., Procaccio, V., Bonneau, D., Reynier, P., White, F.E., Hardy, S.A., Barbosa, I.A., Simpson, M.A., Vara, R., Perdomo Trujillo, Y., Galehdari, H., Deshpande, C., Haack, T.B., Rozet, J.-M., Taylor, R.W., Ghezzi, D., Amati-Bonneau, P., Lenaers, G., 2017. Neurologic Phenotypes Associated With Mutations in RTN4IP1 (OPA10) in Children and Young Adults. JAMA Neurol. doi.org/10.1001/jamaneurol.2017.2065

  • Konsortium Multiscale HCC

Frey, N., Venturelli, S., Zender, L., Bitzer, M., 2017. Cellular senescence in gastrointestinal diseases: from pathogenesis to therapeutics. Nat Rev Gastroenterol Hepatol. doi.org/10.1038/nrgastro.2017.146

  • Konsortium PANC-STRAT

Jabs, J., Zickgraf, F.M., Park, J., Wagner, S., Jiang, X., Jechow, K., Kleinheinz, K., Toprak, U.H., Schneider, M.A., Meister, M., Spaich, S., Sütterlin, M., Schlesner, M., Trumpp, A., Sprick, M., Eils, R., Conrad, C., 2017. Screening drug effects in patient-derived cancer cells links organoid responses to genome alterations. Mol. Syst. Biol. 13, 955.

  • Konsortium SMOOSE

Doerr, F., George, J., Schmitt, A., Beleggia, F., Rehkämper, T., Hermann, S., Walter, V., Weber, J.-P., Thomas, R.K., Wittersheim, M., Büttner, R., Persigehl, T., Reinhardt, H.C., 2017. Targeting a non-oncogene addiction to the ATR/CHK1 axis for the treatment of small cell lung cancer. Sci Rep 7, 15511. doi.org/10.1038/s41598-017-15840-5

  • Juniorverbund SymAtrial

Yan, X., Wang, Z., Schmidt, V., Gauert, A., Willnow, T.E., Heinig, M., Poy, M.N., 2017a. Cadm2 regulates body weight and energy homeostasis in mice. Molecular Metabolism. doi.org/10.1016/j.molmet.2017.11.010

  • Konsortium SYSIMIT

Alfonso, J.C.L., Talkenberger, K., Seifert, M., Klink, B., Hawkins-Daarud, A., Swanson, K.R., Hatzikirou, H., Deutsch, A., 2017. The biology and mathematical modelling of glioma invasion: a review. J R Soc Interface 14. doi.org/10.1098/rsif.2017.0490

  • Konsortium SysINFLAME

Dand, N., Mucha, S., Tsoi, L.C., Mahil, S.K., Stuart, P.E., Arnold, A., Baurecht, H., Burden, A.D., Callis Duffin, K., Chandran, V., Curtis, C.J., Das, S., Ellinghaus, D., Ellinghaus, E., Enerback, C., Esko, T., Gladman, D.D., Griffiths, C.E.M., Gudjonsson, J.E., Hoffman, P., Homuth, G., Hüffmeier, U., Krueger, G.G., Laudes, M., Lee, S.H., Lieb, W., Lim, H.W., Löhr, S., Mrowietz, U., Müller-Nurayid, M., Nöthen, M., Peters, A., Rahman, P., Reis, A., Reynolds, N.J., Rodriguez, E., Schmidt, C.O., Spain, S.L., Strauch, K., Tejasvi, T., Voorhees, J.J., Warren, R.B., Weichenthal, M., Weidinger, S., Zawistowski, M., Nair, R.P., Capon, F., Smith, C.H., Trembath, R.C., Abecasis, G.R., Elder, J.T., Franke, A., Simpson, M.A., Barker, J.N., 2017b. Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Hum. Mol. Genet. 26, 4301–4313. doi.org/10.1093/hmg/ddx328

  • Nachwuchsgruppe SysMedOs

Ni, Z., Angelidou, G., Hoffmann, R., Fedorova, M., 2017. LPPtiger software for lipidome-specific prediction and identification of oxidized phospholipids from LC-MS datasets. Sci Rep 7, 15138. doi.org/10.1038/s41598-017-15363-z

  • Konsortium SYS-Stomach

Fichter, C.D., Przypadlo, C.M., Buck, A., Herbener, N., Riedel, B., Schäfer, L., Nakagawa, H., Walch, A., Reinheckel, T., Werner, M., Lassmann, S., 2017. A new model system identifies epidermal growth factor receptor-human epidermal growth factor receptor 2 (HER2) and HER2-human epidermal growth factor receptor 3 heterodimers as potent inducers of oesophageal epithelial cell invasion. J. Pathol. 243, 481–495. doi.org/10.1002/path.4987

Oktober 2017

  • Konsortium CancerTelSys

Bonetti, D., Longhese, M.P., 2017. Analysis of De Novo Telomere Addition by Southern Blot. Methods Mol. Biol. 1672, 363–373. https://doi.org/10.1007/978-1-4939-7306-4_25

  • Konsortium CAPSyS

Lisboa, M.P., Khan, N., Martin, C., Xu, F.-F., Reppe, K., Geissner, A., Govindan, S., Witzenrath, M., Pereira, C.L., Seeberger, P.H., 2017. Semisynthetic glycoconjugate vaccine candidate against Streptococcus pneumoniae serotype 5. Proc. Natl. Acad. Sci. U.S.A. doi.org/10.1073/pnas.1706875114

  • Nachwuchsgruppe ComorbSysMed

Degenhardt, F., Seifert, S., Szymczak, S., 2017. Evaluation of variable selection methods for random forests and omics data sets. Brief. Bioinformatics. https://doi.org/10.1093/bib/bbx124

  • Konsortium e:Athero-Sysmed

Steinegger, M., Söding, J., 2017. MMseqs2 enables sensitive protein sequence searching for the analysis of massive data sets. Nat. Biotechnol. 35, 1026–1028. https://doi.org/10.1038/nbt.3988

Vilne, B., Skogsberg, J., Foroughi Asl, H., Talukdar, H.A., Kessler, T., Björkegren, J.L.M., Schunkert, H., 2017. Network analysis reveals a causal role of mitochondrial gene activity in atherosclerotic lesion formation. Atherosclerosis 267, 39–48. doi.org/10.1016/j.atherosclerosis.2017.10.019

Wilson, R., Wahl, S., Pfeiffer, L., Ward-Caviness, C.K., Kunze, S., Kretschmer, A., Reischl, E., Peters, A., Gieger, C., Waldenberger, M., 2017. The dynamics of smoking-related disturbed methylation: a two time-point study of methylation change in smokers, non-smokers and former smokers. BMC Genomics 18, 805. https://doi.org/10.1186/s12864-017-4198-0

  • Demonstrator Her2Low

Bernhardt, S., Bayerlová, M., Vetter, M., Wachter, A., Mitra, D., Hanf, V., Lantzsch, T., Uleer, C., Peschel, S., John, J., Buchmann, J., Weigert, E., Bürrig, K.-F., Thomssen, C., Korf, U., Beissbarth, T., Wiemann, S., Kantelhardt, E.J., 2017. Proteomic profiling of breast cancer metabolism identifies SHMT2 and ASCT2 as prognostic factors. Breast Cancer Res. 19, 112. https://doi.org/10.1186/s13058-017-0905-7

  • Konsortium IntegraMent

Chan, M.K., Cooper, J.D., Heilmann-Heimbach, S., Frank, J., Witt, S.H., Nöthen, M.M., Steiner, J., Rietschel, M., Bahn, S., 2017. Associations between SNPs and immune-related circulating proteins in schizophrenia. Sci Rep 7, 12586. https://doi.org/10.1038/s41598-017-12986-0

Hertel, J., König, J., Homuth, G., Van der Auwera, S., Wittfeld, K., Pietzner, M., Kacprowski, T., Pfeiffer, L., Kretschmer, A., Waldenberger, M., Kastenmüller, G., Artati, A., Suhre, K., Adamski, J., Langner, S., Völker, U., Völzke, H., Nauck, M., Friedrich, N., Grabe, H.J., 2017. Evidence for Stress-like Alterations in the HPA-Axis in Women Taking Oral Contraceptives. Sci Rep 7, 14111. https://doi.org/10.1038/s41598-017-13927-7

Martin, J., Streit, F., Treutlein, J., Lang, M., Frank, J., Forstner, A.J., Degenhardt, F., Witt, S.H., Schulze, T.G., Cichon, S., Nöthen, M.M., Rietschel, M., Strohmaier, J., 2017. Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist. Psychiatr. Genet. 27, 187–196. doi.org/10.1097/YPG.0000000000000182

Metzger, M.W., Walser, S.M., Dedic, N., Aprile-Garcia, F., Jakubcakova, V., Adamczyk, M., Webb, K.J., Uhr, M., Refojo, D., Schmidt, M.V., Friess, E., Steiger, A., Kimura, M., Chen, A., Holsboer, F., Arzt, E., Wurst, W., Deussing, J.M., 2017. Heterozygosity for the mood disorder-associated variant Gln460Arg alters P2X7 receptor function and sleep quality. J. Neurosci. doi.org/10.1523/JNEUROSCI.3487-16.2017

Milaneschi, Y., Lamers, F., Peyrot, W.J., Baune, B.T., Breen, G., Dehghan, A., Forstner, A.J., Grabe, H.J., Homuth, G., Kan, C., Lewis, C., Mullins, N., Nauck, M., Pistis, G., Preisig, M., Rivera, M., Rietschel, M., Streit, F., Strohmaier, J., Teumer, A., Van der Auwera, S., Wray, N.R., Boomsma, D.I., Penninx, B.W.J.H., CHARGE Inflammation Working Group and the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, 2017. Genetic Association of Major Depression With Atypical Features and Obesity-Related Immunometabolic Dysregulations. JAMA Psychiatry. doi.org/10.1001/jamapsychiatry.2017.3016

  • Juniorverbund mitOmics

Glasgow, R.I.C., Thompson, K., Barbosa, I.A., He, L., Alston, C.L., Deshpande, C., Simpson, M.A., Morris, A.A.M., Neu, A., Löbel, U., Hall, J., Prokisch, H., Haack, T.B., Hempel, M., McFarland, R., Taylor, R.W., 2017. Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits. Neurogenetics. https://doi.org/10.1007/s10048-017-0526-4

  • Konsortium SMOOSE

Kaitsiotou, H., Keul, M., Hardick, J., Mühlenberg, T., Ketzer, J., Ehrt, C., Krüll, J., Medda, F., Koch, O., Giordanetto, F., Bauer, S., Rauh, D., 2017. Inhibitors to overcome secondary mutations in the stem cell factor receptor KIT. J. Med. Chem. https://doi.org/10.1021/acs.jmedchem.7b00841

  • Juniorverbund SYMBOL-HF

Lausser, L., Szekely, R., Schirra, L.-R., Kestler, H.A., 2017. The Influence of Multi-class Feature Selection on the Prediction of Diagnostic Phenotypes. Neural Process Lett 1–18. https://doi.org/10.1007/s11063-017-9706-3

  • Juniorverbund symAtrial

Magnussen, C., Niiranen, T.J., Ojeda, F.M., Gianfagna, F., Blankenberg, S., Njølstad, I., Vartiainen, E., Sans, S., Pasterkamp, G., Hughes, M., Costanzo, S., Donati, M.B., Jousilahti, P., Linneberg, A., Palosaari, T., de Gaetano, G., Bobak, M., den Ruijter, H.M., Mathiesen, E., Jørgensen, T., Söderberg, S., Kuulasmaa, K., Zeller, T., Iacoviello, L., Salomaa, V., Schnabel, R.B., BiomarCaRE Consortium, 2017. Sex Differences and Similarities in Atrial Fibrillation Epidemiology, Risk Factors, and Mortality in Community Cohorts: Results From the BiomarCaRE Consortium (Biomarker for Cardiovascular Risk Assessment in Europe). Circulation 136, 1588–1597. https://doi.org/10.1161/CIRCULATIONAHA.117.028981

  • Konsortium SysINFLAME

Howell, K.J., Kraiczy, J., Nayak, K.M., Gasparetto, M., Ross, A., Lee, C., Mak, T.N., Koo, B.-K., Kumar, N., Lawley, T., Sinha, A., Rosenstiel, P., Heuschkel, R., Stegle, O., Zilbauer, M., 2017. DNA Methylation and Transcription Patterns in Intestinal Epithelial Cells From Pediatric Patients With Inflammatory Bowel Diseases Differentiate Disease Subtypes and Associate With Outcome. Gastroenterology. https://doi.org/10.1053/j.gastro.2017.10.007

  • Konsortium SysMedAlcoholism

Bach, P., Zois, V., Vollstädt-Klein, S., Kirsch, M., Hoffmann, S., Jorde, A., Frank, J., Charlet, K., Treutlein, J., Beck, A., Heinz, A., Walter, H., Rietschel, M., Kiefer, F., 2017. Association of the alcohol dehydrogenase gene polymorphism rs1789891 with gray matter brain volume, alcohol consumption, alcohol craving and relapse risk. Addict Biol. doi.org/10.1111/adb.12571

  • Demonstrator SYS-GLIO

Silva, L.S., Poschet, G., Nonnenmacher, Y., Becker, H.M., Sapcariu, S., Gaupel, A.-C., Schlotter, M., Wu, Y., Kneisel, N., Seiffert, M., Hell, R., Hiller, K., Lichter, P., Radlwimmer, B., 2017. Branched-chain ketoacids secreted by glioblastoma cells via MCT1 modulate macrophage phenotype. EMBO Rep. https://doi.org/10.15252/embr.201744154

Gesamtliste der e:Med-Publikationen

2017

Agís-Balboa, R.C., Pinhero, P., Rebola, N., Kerimoglu, C., Benito, E., Gertig, M., Bahari-Javan, S., Jain, G., Burkhardt, S., Delalle, I., Jatzko, A., Dettenhofer, M., Zunszain, P.A., Schmitt, A., Falkai, P., Pape, J.C., Binder, E.B., Mulle, C., Fischer, A., Sananbenesi, F., 2017. Formin 2 links neuropsychiatric phenotypes at young age to an increased risk for dementia. EMBO J. doi.org/10.15252/embj.201796821

Aichler, M., Borgmann, D., Krumsiek, J., Buck, A., MacDonald, P.E., Fox, J.E.M., Lyon, J., Light, P.E., Keipert, S., Jastroch, M., Feuchtinger, A., Mueller, N.S., Sun, N., Palmer, A., Alexandrov, T., Hrabe de Angelis, M., Neschen, S., Tschöp, M.H., Walch, A., 2017. N-acyl Taurines and Acylcarnitines Cause an Imbalance in Insulin Synthesis and Secretion Provoking β Cell Dysfunction in Type 2 Diabetes. Cell Metab. 25, 1334–1347.e4. doi.org/10.1016/j.cmet.2017.04.012

Ait-El-Mkadem, S., Dayem-Quere, M., Gusic, M., Chaussenot, A., Bannwarth, S., François, B., Genin, E.C., Fragaki, K., Volker-Touw, C.L.M., Vasnier, C., Serre, V., van Gassen, K.L.I., Lespinasse, F., Richter, S., Eisenhofer, G., Rouzier, C., Mochel, F., De Saint-Martin, A., Abi Warde, M.-T., de Sain-van der Velde, M.G.M., Jans, J.J.M., Amiel, J., Avsec, Z., Mertes, C., Haack, T.B., Strom, T., Meitinger, T., Bonnen, P.E., Taylor, R.W., Gagneur, J., van Hasselt, P.M., Rötig, A., Delahodde, A., Prokisch, H., Fuchs, S.A., Paquis-Flucklinger, V., 2017. Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy. Am. J. Hum. Genet. 100, 151–159. doi.org/10.1016/j.ajhg.2016.11.014

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2013

Chubb, D., Weinhold, N., Broderick, P., Chen, B., Johnson, D.C., Försti, A., Vijayakrishnan, J., Migliorini, G., Dobbins, S.E., Holroyd, A., Hose, D., Walker, B.A., Davies, F.E., Gregory, W.A., Jackson, G.H., Irving, J.A., Pratt, G., Fegan, C., Fenton, J.A.L., Neben, K., Hoffmann, P., Nöthen, M.M., Mühleisen, T.W., Eisele, L., Ross, F.M., Straka, C., Einsele, H., Langer, C., Dörner, E., Allan, J.M., Jauch, A., Morgan, G.J., Hemminki, K., Houlston, R.S., Goldschmidt, H., 2013. Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nat. Genet. 45, 1221–1225. https://doi.org/10.1038/ng.2733

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