Zeitschriftenartikel (71)
41.
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216 (6), S. 1567 - 1577 (2017)
Oncogenic ß-catenin and PIK3CA instruct network states and cancer phenotypes in intestinal organoids. The Journal of Cell Biology: JCB 42.
Zeitschriftenartikel
46, S. 72 - 80 (2017)
Pause & go: from the discovery of RNA polymerase pausing to its functional implications. Current Opinion in Cell Biology 43.
Zeitschriftenartikel
38 (6), S. 621 - 636 (2017)
Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability. Human Mutations 44.
Zeitschriftenartikel
8 (3), S. 179 - 184 (2017)
Two possible modes of pioneering associated with combinations of H2A.Z and p300/CBP at nucleosome-occupied enhancers. Transcription 45.
Zeitschriftenartikel
3 (3), e148 (2017)
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlation. Neurology Genetics 46.
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20 (5), S. 706 - 719 (2017)
DUSP9 Modulates DNA Hypomethylation in Female Mouse Pluripotent Stem Cells. Cell Stem Cell 47.
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20 (5), e9, S. 659 - 674 (2017)
Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders. Cell Stem Cell 48.
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13 (4), e1006746 (2017)
Homozygous ARHGEF2 mutation causes intellectual disability and midbrain-hindbrain malformation. PLoS Genetics 49.
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2, 2:17062 (2017)
Structural basis for λN-dependent processive transcription antitermination. Nature Microbiology 50.
Zeitschriftenartikel
2017, 17:237 (2017)
Transcriptomic and proteomic insight into the effects of a defined European mistletoe extract in Ewing sarcoma cells reveals cellular stress responses. BMC Complementary and Alternative Medicine 51.
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419, S. 227 - 237 (2017)
The information capacity of the genetic code: Is the natural code optimal? Journal of Theoretical Biology 52.
Zeitschriftenartikel
18, E879 (2017)
ρ⁰ Cells Feature De-Ubiquitination of SLC Transporters and Increased Levels and Fluxes of Amino Acids. International Journal of Molecular Sciences 53.
Zeitschriftenartikel
45 (6), e44 (2017)
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments. Nucleic Acids Research (London) 54.
Zeitschriftenartikel
20 (4), S. 426 - 428 (2017)
"Neural Killer" Cells: Autologous Cytotoxic Neural Stem Cells for Fighting Glioma. Cell Stem Cell 55.
Zeitschriftenartikel
20 (4), S. 547 - 557 (2017)
Induced Pluripotent Stem Cell Differentiation Enables Functional Validation of GWAS Variants in Metabolic Disease. Cell Stem Cell 56.
Zeitschriftenartikel
38 (4), S. 409 - 425 (2017)
EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO. Human Mutation 57.
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605, S. 92 - 98 (2017)
Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. Gene 58.
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8, 8:14536 (2017)
Epilepsy and intellectual disability linked protein Shrm4 interaction with GABABRs shapes inhibitory neurotransmission. Nature Communications 59.
Zeitschriftenartikel
27 (3), S. 479 - 490 (2017)
Reciprocal insulation analysis of Hi-C data shows that TADs represent a functionally but not structurally privileged scale in the hierarchical folding of chromosomes. Genome Research 60.
Zeitschriftenartikel
45 (4), S. 1805 - 1819 (2017)
Role of the chromatin landscape and sequence in determining cell type-specific genomic glucocorticoid receptor binding and gene regulation. Nucleic Acids Research (London)