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32199 publications found in the database

*2015 (1336)

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

2015 Publications

Mutation of SLC9A1, encoding the major Na(+)/H(+) exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome
Guissart, C. et al. Human Molecular Genetics 24(2), 463-70, 2015, Mapping 100K Set  PubMed

Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans
Li, J. et al. Human Molecular Genetics 24(2), 572-81, 2015, Genome-Wide Human SNP Array 6.0  PubMed

Identification of Specific mRNA Signatures as Fingerprints for Carcinogenesis in Mice Induced by Genotoxic and Nongenotoxic Hepatocarcinogens
Kossler, N. et al. Toxicological Sciences 143(2), 277-95, 2015, Mouse Genome 430 2.0 Array  PubMed

DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions
Chen, Y. H. et al. Nucleic Acids Research 43(2), 1268-82, 2015, Mouse Gene 1.0 ST array  PubMed

CACNA1B mutation is linked to unique myoclonus-dystonia syndrome
Groen, J. L. et al. Human Molecular Genetics 24(4), 987-93, 2015, Human Mapping 500K Array SetMapping 500K  PubMed

Potentiation of neurotoxicity in double-mutant mice with Pink1 ablation and A53T-SNCA overexpression
Gispert, S. et al. Human Molecular Genetics 24(4), 1061-76, 2015, Mouse Genome 430 2.0 Array  PubMed

Expression of progerin in aging mouse brains reveals structural nuclear abnormalities without detectible significant alterations in gene expression, hippocampal stem cells or behavior
Baek, J. H. et al. Human Molecular Genetics 24(5), 1305-21, 2015, Human Exon Array  PubMed

Indications for distinct pathogenic mechanisms of asbestos and silica through gene expression profiling of the response of lung epithelial cells
Perkins, T. N. et al. Human Molecular Genetics 24(5), 1374-89, 2015, Human Genome U133A 2.0 Array  PubMed

Genetic control of gene expression at novel and established chronic obstructive pulmonary disease loci
Castaldi, P. J. et al. Human Molecular Genetics 24(4), 1200-10, 2015, Human Genome U133 Plus 2.0 Array  PubMed

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