Zeitschriftenartikel (124)
21.
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154 (6), S. 1190 - 1193 (2013)
Long noncoding RNAs usher in a new era in the biology of enhancers. Cell 22.
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5, S. 5:34 - 5:34 (2013)
DNA sequencing methods in human genetics and disease research. F1000Prime Rep 23.
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91 (9), S. 1095 - 1107 (2013)
The enzymatic activity of the VEGFR2-receptor for the biosynthesis of dinucleoside polyphosphates. Journal of Molecular Medicine 24.
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45 (9), S. 984 - 995 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 25.
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5 (9), S. 1431 - 1442 (2013)
Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation. EMBO Molecular Medicine 26.
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10 (3), S. 303 - 315 (2013)
Zebrafish Expression Ontology of Gene Sets (ZEOGS): a tool to analyze enrichment of zebrafish anatomical terms in large gene sets. Zebrafish 27.
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20 (8), S. 1044 - 1054 (2013)
Synaptic MAGUK multimer formation is mediated by PDZ domains and promoted by ligand binding. Chemistry & Biology 28.
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14 (8), S. R84 - R84 (2013)
PROmiRNA: a new miRNA promoter recognition method uncovers the complex regulation of intronic miRNAs. Genome Biology 29.
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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 30.
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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 31.
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23 (8), S. 1307 - 1318 (2013)
Comprehensive prediction in 78 human cell lines reveals rigidity and compactness of transcription factor dimers. Genome Research 32.
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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 33.
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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 34.
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10 (4), S. 305 - 307 (2013)
Protein set analyses: how could this impact the clinic? Expert Review of Proteomics 35.
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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 36.
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4, 4:2156 (2013)
Genome sequence and functional genomic analysis of the oil-degrading bacterium Oleispira antarctica. Nature Communications 37.
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8 (6) (2013)
Soluble Alpha-APP (sAPPalpha) Regulates CDK5 Expression and Activity in Neurons. PLoS One 38.
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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 39.
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45 (7), S. 767 - 775 (2013)
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats. Nature Genetics 40.
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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