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32199 publications found in the database

*2015 (1336)

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

2015 Publications

SOCS3-mediated regulation of inflammatory cytokines in PTEN and p53 inactivated triple negative breast cancer model
Kim, G. et al. Oncogene 34(6), 671-80, 2015, Human Genome U219 Array  PubMed

Intellectual Disability Secondary to a 16p13 Duplication in a 1;16 Translocation. Extended Phenotype in a Four-Generation Family
Mohamed, A. M. et al. American Journal of Medical Genetics Part a 167A(1), 128-36, 2015, CytoScan  PubMed

Prader-Willi Syndrome and Tay-Sachs Disease in Association with Mixed Maternal Uniparental Isodisomy and Heterodisomy 15 in a Girl Who Also had Isochromosome Xq
Zeesman, S. et al. American Journal of Medical Genetics Part a 167A(1), 180-4, 2015, CytoScan  PubMed

A 12Q24.31 Interstitial Deletion in an Adult Male With MODY3: Neuropsychiatric and Neuropsychological Characteristics
Verhoeven, W. M. A. et al. American Journal of Medical Genetics Part a 167A(1), 169-73, 2015, CytoScan  PubMed

Distal 22q11.2 Microduplication Combined With Typical 22q11.2 Proximal Deletion: A Case Report
Molck, M. C. et al. American Journal of Medical Genetics Part a 167A(1), 215-20, 2015  PubMed

Transcriptome analysis of hen preadipocytes treated with an adipogenic cocktail (DMIOA) with or without 20(S)- hydroxylcholesterol
Regassa, A. et al. BMC Genomics 16(), NPG, 2015, Chicken Genome Array  PubMed

Lysyl hydroxylase 2 induces a collagen cross-link switch in tumor strorna
Chen, Y. L. et al. Journal of Clinical Investigation 125(3), 1147-62, 2015, Mouse Genome 430 2.0 Array  PubMed

Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminus
Byrska-Bishop, M. et al. Journal of Clinical Investigation 125(3), 993-1005, 2015  PubMed

Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits
Zhu, Z. H. et al. American Journal of Human Genetics 96(3), 377-85, 2015, Genome-Wide Human SNP Array 6.0  PubMed

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