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32199 publications found in the database

*2011 (1784)

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

2011 Publications

Mutations in the Mitochondrial Seryl-tRNA Synthetase Cause Hyperuricemia, Pulmonary Hypertension, Renal Failure in Infancy and Alkalosis, HUPRA Syndrome
Belostotsky, R. et al. American Journal of Human Genetics 88(2), 193-200, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
Heeringa, S. F. et al. Journal of Clinical Investigation 121(5), 2013-24, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome
Rooryck, C. et al. Nature Genetics 43(3), NPG, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

Genetic architecture of open angle glaucoma and related determinants
Ramdas, W. D. et al. Journal of Medical Genetics 48(3), 190-6, 2011, Human Mapping 500K Array SetMapping 500K  PubMed

Acute Endotoxin-Induced Thymic Atrophy Is Characterized By Intrathymic Inflammatory and Wound Healing Responses
Billard, M. J. et al. Plos One 6(3), NPG, 2011, Mouse Genome 430 2.0 Array  PubMed

A Novel Role of RASSF9 in Maintaining Epidermal Homeostasis
Lee, C. M. et al. Plos One 6(3), NPG, 2011, Mouse Genome 430 2.0 Array  PubMed

Network analysis of skin tumor progression identifies a rewired genetic architecture affecting inflammation and tumor susceptibility
Quigley, D. A. et al. Genome Biology 12(1), NPG, 2011, Mouse Genome 430 2.0 Array  PubMed

Evi1 represses PTEN expression and activates PI3K/AKT/mTOR via interactions with polycomb proteins
Yoshimi, A. et al. Blood 117(13), 3617-28, 2011, Mouse Genome 430 2.0 Array  PubMed

Evaluating Gene Expression in C57BL/6J and DBA/2J Mouse Striatum Using RNA-Seq and Microarrays
Bottomly, D. et al. Plos One 6(3), NPG, 2011, Mouse Genome 430 2.0 Array  PubMed

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