Zeitschriftenartikel (1119)
821.
Zeitschriftenartikel
14 (8), S. R84 - R84 (2013)
PROmiRNA: a new miRNA promoter recognition method uncovers the complex regulation of intronic miRNAs. Genome Biology 822.
Zeitschriftenartikel
22 (16), S. 3306 - 3314 (2013)
Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth. Human Molecular Genetics 823.
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2 (8), S. 771 - 778 (2013)
An integrative computational analysis provides evidence for FBN1-associated network de-regulation in trisomy 21. Biology Open 824.
Zeitschriftenartikel
23 (8), S. 1307 - 1318 (2013)
Comprehensive prediction in 78 human cell lines reveals rigidity and compactness of transcription factor dimers. Genome Research 825.
Zeitschriftenartikel
161A (8), S. 1915 - 1922 (2013)
A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. American Journal of Medical Genetics Part A 826.
Zeitschriftenartikel
21 (8), S. 887 - 890 (2013)
A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring. European journal of human genetics: EJHG ; the official journal of the European Society of Human Genetics 827.
Zeitschriftenartikel
10 (4), S. 305 - 307 (2013)
Protein set analyses: how could this impact the clinic? Expert Review of Proteomics 828.
Zeitschriftenartikel
56 (8), S. 1802 - 1812 (2013)
Amorfrutin B is an efficient natural peroxisome proliferator-activated receptor gamma (PPARgamma) agonist with potent glucose-lowering properties. Diabetologia 829.
Zeitschriftenartikel
4, 4:2156 (2013)
Genome sequence and functional genomic analysis of the oil-degrading bacterium Oleispira antarctica. Nature Communications 830.
Zeitschriftenartikel
8 (6) (2013)
Soluble Alpha-APP (sAPPalpha) Regulates CDK5 Expression and Activity in Neurons. PLoS One 831.
Zeitschriftenartikel
8 (7), S. e67461 - e67461 (2013)
High-Throughput miRNA and mRNA Sequencing of Paired Colorectal Normal, Tumor and Metastasis Tissues and Bioinformatic Modeling of miRNA-1 Therapeutic Applications. PLoS One 832.
Zeitschriftenartikel
45 (7), S. 767 - 775 (2013)
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats. Nature Genetics 833.
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12 (7), S. 659 - 668 (2013)
Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study. Lancet Neurology 834.
Zeitschriftenartikel
34 (5), S. 838 - 844 (2013)
Familial aggregation of pure tone hearing thresholds in an aging European population. Otology & neurotology: official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 835.
Zeitschriftenartikel
56 (7), S. 379 - 382 (2013)
HUWE1 mutation explains phenotypic severity in a case of familial idiopathic intellectual disability. European Journal of Medical Genetics 836.
Zeitschriftenartikel
12 (7), S. 1965 - 1979 (2013)
Protein sets define disease states and predict in vivo effects of drug treatment. Molecular and Cellular Proteomics 837.
Zeitschriftenartikel
30 (7), S. 1700 - 1712 (2013)
Twisted signatures of GC-biased gene conversion embedded in an evolutionary stable karyotype. Molecular Biology and Evolution 838.
Zeitschriftenartikel
50 (6), S. 844 - 855 (2013)
Genome-wide Kinase-Chromatin Interactions Reveal the Regulatory Network of ERK Signaling in Human Embryonic Stem Cells. Molecular Cell 839.
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50 (6), S. 831 - 843 (2013)
Mutations in the intellectual disability gene Ube2a cause neuronal dysfunction and impair parkin-dependent mitophagy. Molecular Cell 840.
Zeitschriftenartikel
8 (6), S. e65403 - e65403 (2013)
Synergism between Hedgehog-GLI and EGFR Signaling in Hedgehog-Responsive Human Medulloblastoma Cells Induces Downregulation of Canonical Hedgehog-Target Genes and Stabilized Expression of GLI1. PLoS One