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32199 publications found in the database

*2013 (2117)

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

2013 Publications

Association of genes with physiological functions by comparative analysis of pooled expression microarray data
Chen, I. B. D. et al. Physiological Genomics 45(2), 69-78, 2013, Mouse Genome 430A 2.0 Array  PubMed

Wide Clinical Variability in Conditions with Coarse Facial Features and Hypertrichosis Caused by Mutations in ABCC9
Czeschik, J. C. et al. American Journal of Medical Genetics Part a 161A(2), 295-300, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Molecular Analysis of Precursor Lesions in Familial Pancreatic Cancer
Crnogorac-Jurcevic, T. et al. Plos One 8(1), NPG, 2013, Human Genome U133 Set  PubMed

Non-Apoptotic Toxicity of Pseudomonas aeruginosa toward Murine Cells
Roy, S. et al. Plos One 8(1), NPG, 2013, Mouse Gene 1.0 ST array  PubMed

N-Cadherin Dependent Collective Cell Invasion of Prostate Cancer Cells Is Regulated by the N-Terminus of alpha-Catenin
Cui, Y. Y. et al. Plos One 8(1), NPG, 2013, Human Gene 1.0 ST Array  PubMed

NR2F1 Haploinsufficiency is Associated With Optic Atrophy, Dysmorphism and Global Developmental Delay
Al-Kateb, H. et al. American Journal of Medical Genetics Part a 161A(2), 377-81, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Nuclear genome transfer in human oocytes eliminates mitochondrial DNA variants
Paull, D. et al. Nature 493(7434), NPG, 2013  PubMed

FOXM1 Is an Oncogenic Mediator in Ewing Sarcoma
Christensen, L. et al. Plos One 8(1), NPG, 2013, Human Exon Array  PubMed

A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia
Szklarczyk, R. et al. Human Molecular Genetics 22(4), 656-67, 2013, Mouse Genome 430 2.0 Array  PubMed

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