Zeitschriftenartikel (1249)
941.
Zeitschriftenartikel
10 (10), S. 1579 - 1585 (2013)
The long non-coding RNA Fendrr links epigenetic control mechanisms to gene regulatory networks in mammalian embryogenesis. RNA Biology 942.
Zeitschriftenartikel
22 (18), S. 3789 - 3797 (2013)
A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndrome. Human Molecular Genetics 943.
Zeitschriftenartikel
154 (6), S. 1190 - 1193 (2013)
Long noncoding RNAs usher in a new era in the biology of enhancers. Cell 944.
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5, S. 5:34 - 5:34 (2013)
DNA sequencing methods in human genetics and disease research. F1000Prime Rep 945.
Zeitschriftenartikel
91 (9), S. 1095 - 1107 (2013)
The enzymatic activity of the VEGFR2-receptor for the biosynthesis of dinucleoside polyphosphates. Journal of Molecular Medicine 946.
Zeitschriftenartikel
45 (9), S. 984 - 995 (2013)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics 947.
Zeitschriftenartikel
5 (9), S. 1431 - 1442 (2013)
Integrative analysis revealed the molecular mechanism underlying RBM10-mediated splicing regulation. EMBO Molecular Medicine 948.
Zeitschriftenartikel
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 949.
Zeitschriftenartikel
20 (8), S. 1044 - 1054 (2013)
Synaptic MAGUK multimer formation is mediated by PDZ domains and promoted by ligand binding. Chemistry & Biology 950.
Zeitschriftenartikel
14 (8), S. R84 - R84 (2013)
PROmiRNA: a new miRNA promoter recognition method uncovers the complex regulation of intronic miRNAs. Genome Biology 951.
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 952.
Zeitschriftenartikel
2 (8), S. 771 - 778 (2013)
An integrative computational analysis provides evidence for FBN1-associated network de-regulation in trisomy 21. Biology Open 953.
Zeitschriftenartikel
23 (8), S. 1307 - 1318 (2013)
Comprehensive prediction in 78 human cell lines reveals rigidity and compactness of transcription factor dimers. Genome Research 954.
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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 955.
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 956.
Zeitschriftenartikel
10 (4), S. 305 - 307 (2013)
Protein set analyses: how could this impact the clinic? Expert Review of Proteomics 957.
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 958.
Zeitschriftenartikel
4, 4:2156 (2013)
Genome sequence and functional genomic analysis of the oil-degrading bacterium Oleispira antarctica. Nature Communications 959.
Zeitschriftenartikel
8 (6) (2013)
Soluble Alpha-APP (sAPPalpha) Regulates CDK5 Expression and Activity in Neurons. PLoS One 960.
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