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32199 publications found in the database

*2015 (1336)

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

2015 Publications

Consequences of a Deficit in Vitamin B(6) Biosynthesis de Novo for Hormone Homeostasis and Root Development in Arabidopsis
Boycheva, S. et al. Plant Physiology 167(1), 102-17, 2015, Arabidopsis ATH1 Genome Array  PubMed

The Arabidopsis Vacuolar Sorting Receptor1 Is Required for Osmotic Stress-Induced Abscisic Acid Biosynthesis
Wang, Z. Y. et al. Plant Physiology 167(1), 137-52, 2015, Arabidopsis ATH1 Genome Array  PubMed

Promotion of Testa Rupture during Garden Cress Germination Involves Seed Compartment-Specific Expression and Activity of Pectin Methylesterases
Scheler, C. et al. Plant Physiology 167(1), 200-15, 2015, Arabidopsis ATH1 Genome Array  PubMed

Decreasing Electron Flux through the Cytochrome and/or Alternative Respiratory Pathways Triggers Common and Distinct Cellular Responses Dependent on Growth Conditions
Kuhn, K. et al. Plant Physiology 167(1), 228-50, 2015, Arabidopsis ATH1 Genome Array  PubMed

Phage-Encoded Colanic Acid-Degrading Enzyme Permits Lytic Phage Infection of a Capsule-Forming Resistant Mutant Escherichia coli Strain
Kim, M. S. et al. Applied and Environmental Microbiology 81(3), 900-9, 2015, E. coli Genome 2.0 Array  PubMed

The Novel Small Leucine-rich Protein Chondroadherin-like (CHADL) Is Expressed in Cartilage and Modulates Chondrocyte Differentiation
Tillgren, V. et al. Journal of Biological Chemistry 290(2), 918-25, 2015  PubMed

Appearance and disappearance of the mRNA signature characteristic of T(reg) cells in visceral adipose tissue: Age, diet, and PPARgamma effects
Cipolletta, D. et al. Proceedings of the National Academy of Sciences of the United States of America 112(2), 482-7, 2015, Mouse Gene 1.0 ST array  PubMed

Gene Expression Variation in Drosophila melanogaster Due to Rare Transposable Element Insertion Alleles of Large Effect
Cridland, J. M. et al. Genetics 199(1), NPG, 2015, Drosophila Genome 2.0 Array  PubMed

CRB2 Mutations Produce a Phenotype Resembling Congenital Nephrosis, Finnish Type, with Cerebral Ventriculomegaly and Raised Alpha-Fetoprotein
Slavotinek, A. et al. American Journal of Human Genetics 96(1), 162-9, 2015, CytoScan  PubMed

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