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32199 publications found in the database

*2014 (1694)

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

2014 Publications

Transcriptomic Changes Triggered by Hypoxia: Evidence for HIF-1alpha -Independent, [Na(+)](i)/[K(+)](i)-Mediated, Excitation-Transcription Coupling
Koltsova, S. V. et al. Plos One 9(11), NPG, 2014  PubMed

Exercise-Mediated Wall Shear Stress Increases Mitochondrial Biogenesis in Vascular Endothelium
Kim, B. et al. Plos One 9(11), NPG, 2014  PubMed

Caspase-1/ASC Inflammasome-Mediated Activation of IL-1beta-ROS-NF-kappaB Pathway for Control of Trypanosoma cruzi Replication and Survival Is Dispensable in NLRP3(-/-) Macrophages
Dey, N. et al. Plos One 9(11), NPG, 2014, Human Genome U133 Plus 2.0 Array  PubMed

MYC and EGR1 synergize to trigger tumor cell death by controlling NOXA and BIM transcription upon treatment with the proteasome inhibitor bortezomib
Wirth, M. et al. Nucleic Acids Research 42(16), 10433-47, 2014  PubMed

Isolation of Specific Neurons from C. elegans Larvae for Gene Expression Profiling
Spencer, W. C. et al. Plos One 9(11), NPG, 2014  PubMed

Dectin-1-mediated Signaling Leads to Characteristic Gene Expressions and Cytokine Secretion via Spleen Tyrosine Kinase (Syk) in Rat Mast Cells
Kimura, Y. et al. Journal of Biological Chemistry 289(45), 31565-75, 2014, Rat Gene 1.0 ST Array  PubMed

NDST1 Missense Mutations in Autosomal Recessive Intellectual Disability
Reuter, M. S. et al. American Journal of Medical Genetics Part a 164(11), 2753-63, 2014  PubMed

Definition of 5q11.2 Microdeletion Syndrome Reveals Overlap with CHARGE Syndrome and 22q11 Deletion Syndrome Phenotypes
Blok, C. S. et al. American Journal of Medical Genetics Part a 164(11), 2843-8, 2014, Human Mapping 500K Array SetMapping 500K  PubMed

A Terminal 3p26.3 Deletion Is Not Associated With Dysmorphic Features and Intellectual Disability in a Four- Generation Family
Moghadasi, S. et al. American Journal of Medical Genetics Part a 164(11), 2863-8, 2014  PubMed

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