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32199 publications found in the database

*2015 (1336)

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

2015 Publications

Characterization of the Intrarenal Renin-Angiotensin System in Experimental Alport Syndrome
Bae, E. H. et al. American Journal of Pathology 185(5), 1423-35, 2015  PubMed

During Drosophila disc regeneration, JAK/STAT coordinates cell proliferation with Dilp8-mediated developmental delay
Katsuyama, T. et al. Proceedings of the National Academy of Sciences of the United States of America 112(18), E2327-36, 2015, Drosophila Genome 2.0 Array  PubMed

MEL-18 loss mediates estrogen receptor-alpha downregulation and hormone independence
Lee, J. Y. et al. Journal of Clinical Investigation 125(5), 1801-14, 2015  PubMed

An Examination of the Relationship between Lipid Levels and Associated Genetic Markers across Racial/Ethnic Populations in the Multi-Ethnic Study of Atherosclerosis
Johnson, L. et al. Plos One 10(5), NPG, 2015, Genome-Wide Human SNP Array 6.0  PubMed

Effect of BRAF mutational status on expression profiles in conventional papillary thyroid carcinomas
Schulten, H. J. et al. BMC Genomics 16(Supplement 1), NPG, 2015, Human Gene 1.0 ST Array  PubMed

Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development
Chan, Y. L. et al. American Journal of Human Genetics 96(5), 695-708, 2015  PubMed

Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination
Nakayama, T. et al. American Journal of Human Genetics 96(5), 709-19, 2015, Genome-Wide Human SNP Array 6.0  PubMed

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome
Mlynarski, E. E. et al. American Journal of Human Genetics 96(5), 753-64, 2015, Genome-Wide Human SNP Array 6.0  PubMed

A Potential Contributory Role for Ciliary Dysfunction in the 16p11.2 600 kb BP4-BP5 Pathology
Migliavacca, E. et al. American Journal of Human Genetics 96(5), 784-96, 2015  PubMed

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