Zeitschriftenartikel (1248)
1141.
Zeitschriftenartikel
8 (3), S. e1002548 (2012)
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database. PLoS Genetics 1142.
Zeitschriftenartikel
107 (3), S. 186 - 196 (2012)
Structural distance and evolutionary relationship of networks. Biosystems 1143.
Zeitschriftenartikel
4 (3), S. 218 - 233 (2012)
Hedgehog-EGFR cooperation response genes determine the oncogenic phenotype of basal cell carcinoma and tumour-initiating pancreatic cancer cells. EMBO Molecular Medicine 1144.
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 1145.
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) 1146.
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 1147.
Zeitschriftenartikel
45 (4), S. 567 - 580 (2012)
Dynamic protein-protein interaction wiring of the human spliceosome. Molecular Cell 1148.
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 1149.
Zeitschriftenartikel
335 (6070), S. 823 - 828 (2012)
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes. Science 1150.
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 1151.
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) 1152.
Zeitschriftenartikel
8 (2), S. 495 - 503 (2012)
Dynamics of Srf, p300 and histone modifications during cardiac maturation in mouse. Molecular BioSystems 1153.
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 1154.
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 1155.
Zeitschriftenartikel
13 Suppl 1, S. S2 - S2 (2012)
Detection of interacting transcription factors in human tissues using predicted DNA binding affinity. BMC Genomics 1156.
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 1157.
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 1158.
Zeitschriftenartikel
7 (1), e30140 (2012)
Modeling of miRNA and drug action in the EGFR signaling pathway. PLoS One 1159.
Zeitschriftenartikel
30 (3), S. 224 - 226 (2012)
BLUEPRINT to decode the epigenetic signature written in blood. Nature biotechnology 1160.
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