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32199 publications found in the database

*2011 (1784)

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

2011 Publications

Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse
Lindfors, C. et al. Proceedings of the National Academy of Sciences of the United States of America 108(44), 18108-13, 2011, Mouse Genome 430 2.0 Array  PubMed

Interleukin-1 as an Injury Signal Mobilizes Retinyl Esters in Hepatic Stellate Cells through Down Regulation of Lecithin Retinol Acyltransferase
Kida, Y. et al. Plos One 6(11), NPG, 2011, Rat Expression Set 230  PubMed

Integrated Epigenetics of Human Breast Cancer: Synoptic Investigation of Targeted Genes, MicroRNAs and Proteins upon Demethylation Treatment
Radpour, R. et al. Plos One 6(11), NPG, 2011, Human Genome U133 Plus 2.0 Array  PubMed

Pontocerebellar Hypoplasia in Association With De Novo 19p13.11p13.12 Microdeletion
Gallant, N. M. et al. American Journal of Medical Genetics Part a 155A(11), 2871-8, 2011, Genome-Wide Human SNP Array 6.0  PubMed

De Novo 5q14.3 Translocation 121.5-kb Upstream of MEF2C in a Patient With Severe Intellectual Disability and Early-Onset Epileptic Encephalopathy
Saitsu, H. et al. American Journal of Medical Genetics Part a 155A(11), 2879-84, 2011  PubMed

Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to Mutations in the IFT-A Gene WDR19
Bredrup, C. et al. American Journal of Human Genetics 89(5), 634-43, 2011  PubMed

Whole-Exome-Sequencing Identifies Mutations in Histone Acetyltransferase Gene KAT6B in Individuals with the Say-Barber-Biesecker Variant of Ohdo Syndrome
Cayton-Smith, J. et al. American Journal of Human Genetics 89(5), 675-81, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping
Siemiatkowska, A. M. et al. Molecular Vision 17(325-26), 3013-24, 2011  PubMed

MII5 Is Required for Normal Spermatogenesis
Yap, D. B. et al. Plos One 6(11), NPG, 2011  PubMed

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