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32199 publications found in the database

*2014 (1694)

*Starting in 2010, coverage has been refocused on core journals.

2014 Publications

The Incidence of Sexually Dimorphic Gene Expression Varies Greatly between Tissues in the Rat
Huby, R. D. J. et al. Plos One 9(12), NPG, 2014  PubMed

Mosaic Deletion of EXOC6B: Further Evidence for An Important Role of the Exocyst Complex in the Pathogenesis of Intellectual Disability
Evers, C. et al. American Journal of Medical Genetics Part a 164(12), 3088-94, 2014, CytoScan  PubMed

Disruption of the ARID1B and ADAMTS6 Loci due to a t(5;6)(q12.3;q25.3) in a Patient With Developmental Delay
Malli, T. et al. American Journal of Medical Genetics Part a 164(12), 3126-31, 2014  PubMed

Altered MicroRNA Expression Profile in Exosomes during Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
Xu, J. F. et al. Plos One 9(12), NPG, 2014, miRNA Array  PubMed

Amplicon rearrangements during the extrachromosomal and intrachromosomal amplification process in a glioma
Vogt, N. et al. Nucleic Acids Research 42(21), 13194-205, 2014, Genome-Wide Human SNP Array 6.0  PubMed

TRIM37 is a new histone H2A ubiquitin ligase and breast cancer oncoprotein
Bhatnagar, S. et al. Nature 515(7529), NPG, 2014  PubMed

Transcriptomic signatures of peroxisome proliferator- activated receptor a (PPARalpha) in different mouse liver models identify novel aspects of its biology
Szalowska, E. et al. BMC Genomics 15(), NPG, 2014, Mouse Genome 430 2.0 Array  PubMed

RNA-Seq gene expression profiling of HepG2 cells: the influence of experimental factors and comparison with liver tissue
Tyakht, A. V. et al. BMC Genomics 15(), NPG, 2014  PubMed

Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome
Haghighi, A. et al. Plos One 9(11), NPG, 2014, Genome-Wide Human SNP Array 6.0  PubMed

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