Zeitschriftenartikel (1266)
Zeitschriftenartikel
5, S. 7 - 13 (2012)
Characteristics of fads2 gene expression and putative promoter in European sea bass (Dicentrarchus labrax): Comparison with salmonid species and analysis of CpG methylation. Marine Genomics
Zeitschriftenartikel
40 (6), S. 2426 - 2431 (2012)
The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process. Nucleic Acids Research (London)
Zeitschriftenartikel
78 (4-5), S. 393 - 405 (2012)
Survey of sugar beet (Beta vulgaris L.) hAT transposons and MITE-like hATpin derivatives. Plant Molecular Biology
Zeitschriftenartikel
45 (4), S. 567 - 580 (2012)
Dynamic protein-protein interaction wiring of the human spliceosome. Molecular Cell
Zeitschriftenartikel
287 (9), S. 6318 - 6325 (2012)
Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome. The Journal of Biological Chemistry
Zeitschriftenartikel
335 (6070), S. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science
Zeitschriftenartikel
2012, S. e - e (2012)
Neurocognitive impairments in non-deprived smokers-results from a population-based multi-center study on smoking-related behavior. Addiction Biology
Zeitschriftenartikel
49 (2), S. 119 - 125 (2012)
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics (London)
Zeitschriftenartikel
8 (2), S. 495 - 503 (2012)
Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse. Molecular BioSystems
Zeitschriftenartikel
12 (12), S. 38 (2012)
Hsp90 inhibition differentially destabilises MAP kinase and TGF-beta signalling components in cancer cells revealed by kinase-targeted chemoproteomics. BMC Cancer
Zeitschriftenartikel
27 (2), S. 429 - 442 (2012)
New insights into the molecular mechanism of multiple synostoses syndrome (SYNS): mutation within the GDF5 knuckle epitope causes noggin-resistance. Journal of Bone and Mineral Research
Zeitschriftenartikel
13 Suppl 1, S. S2 - S2 (2012)
Detection of interacting transcription factors in human tissues using predicted DNA binding affinity. BMC Genomics
Zeitschriftenartikel
48 (1), S. 62 - 67 (2012)
High levels of brain-type creatine kinase activity in human platelets and leukocytes: a genetic anomaly with autosomal dominant inheritance. Blood Cells Molecules and Diseases
Zeitschriftenartikel
90 (1), S. 61 - 8 (2012)
Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin. The American Journal of Human Genetics
Zeitschriftenartikel
7 (1), e30140 (2012)
Modeling of miRNA and drug action in the EGFR signaling pathway. PLoS One
Zeitschriftenartikel
30 (3), S. 224 - 226 (2012)
BLUEPRINT to decode the epigenetic signature written in blood. Nature biotechnology
Zeitschriftenartikel
20 (3), S. 271 - 276 (2012)
Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. European journal og human genetics: EJHG ; the official journal of the European Society of Human Genetics
Zeitschriftenartikel
7 (1), S. e29365 - e29365 (2012)
Long-term survival of hydrated resting eggs from Brachionus plicatilis. PLoS One
Zeitschriftenartikel
56 (10-11-12), S. 789 - 797 (2012)
Comparative molecular portraits of human unfertilized oocytes and primordial germ cells at 10 weeks of gestation. International Journal of Developmental Biology
Zeitschriftenartikel
8, S. 119 - 126 (2012)
Construction of a pig physical interactome using sequence homology and a comprehensive reference human interactome. Evolutionary Bioinformatics