Zeitschriftenartikel (82)
61.
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36 (6), S. 1794 - 1796 (2016)
Studying Mesodiencephalic Dopaminergic Neuron Development In Vivo to Improve Stem Cell Therapy in Parkinson’s Disease. The Journal of Neuroscience 62.
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14 (5), S. 1246 - 1257 (2016)
Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs. Cell Reports 63.
Zeitschriftenartikel
530 (7588), S. 57 - 62 (2016)
Active medulloblastoma enhancers reveal subgroup-specific cellular origins. Nature 64.
Zeitschriftenartikel
2016, 15030 (2016)
The metabolic background is a global player in Saccharomyces gene expression epistasis. Nature Microbiology 65.
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26 (2), S. 183 - 191 (2016)
Exome Sequencing and CRISPR/Cas Genome Editing Identify Mutations of ZAK as a Cause of Limb Defects in Humans and Mice. Genome Research 66.
Zeitschriftenartikel
2016, S. 1 - 8 (2016)
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis. Famillial Cancer 67.
Zeitschriftenartikel
8, 8:85 (2016)
Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family. Frontiers in Molecular Neuroscience 68.
Zeitschriftenartikel
575 (2 Pt 2), S. 438 - 451 (2016)
Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 69.
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13 (6), S. 1183 - 1193 (2016)
Time-Dependent Gene Network Modelling by Sequential Monte Carlo. IEEE ACM Transactions on Computational Biology and Bioinformatics 70.
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167 (5), e24, S. 1398 - 1414 (2016)
Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. Cell 71.
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12 (5), e1006022 (2016)
BOD1 Is Required for Cognitive Function in Humans and Drosophila. PLoS Genetics 72.
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170 (1), S. 94 - 102 (2016)
Tentative clinical diagnosis of Lujan-Fryns syndrome-A conglomeration of different genetic entities? American Journal of Medical Genetics Part A 73.
Zeitschriftenartikel
5, e16078 (2016)
Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation. eLife 74.
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12 (12), e1005249 (2016)
Improved Prediction of Non-methylated Islands in Vertebrates Highlights Different Characteristic Sequence Patterns. PLoS Computational Biology 75.
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17, 67 (2016)
sciReptor: analysis of single-cell level immunoglobulin repertoires. BMC Bioinformatics 76.
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33 (1), S. 185 - 200 (2016)
Evolution of DNA-Binding Sites of a Floral Master Regulatory Transcription Factor. Molecular Biology and Evolution 77.
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89 (1), S. 120 - 127 (2016)
New insights into Brunner syndrome and potential for targeted therapy. Clinical Genetics: an international journal of genetics in medicine 78.
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33 (5), S. 1231 - 1244 (2016)
Human Lineage-Specific Transcriptional Regulation through GA-Binding Protein Transcription Factor Alpha (GABPa). Molecular Biology and Evolution 79.
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7, 13784 (2016)
Corrigendum: Sequences flanking the core-binding site modulate glucocorticoid receptor structure and activity. Nature Communications 80.
Zeitschriftenartikel
7, 12621 (2016)
Sequences flanking the core-binding site modulate glucocorticoid receptor structure and activity. Nature Communications