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32199 publications found in the database

*2011 (1784)

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

2011 Publications

Variation in Human Recombination Rates and Its Genetic Determinants
Fledel-Alon, A. et al. Plos One 6(6), NPG, 2011  PubMed

Impact of Cellular miRNAs on Circulating miRNA Biomarker Signatures
Duttagupta, R. et al. Plos One 6(6), NPG, 2011  PubMed

Paneth cell marker expression in intestinal villi and colon crypts characterizes dietary induced risk for mouse sporadic intestinal cancer
Wang, D. H. et al. Proceedings of the National Academy of Sciences of the United States of America 108(25), 10272-7, 2011, Mouse Genome 430 2.0 Array  PubMed

Expression of rice SUB1A and SUB1C transcription factors in Arabidopsis uncovers flowering inhibition as a submergence tolerance mechanism
Pena-Castro, J. M. et al. Plant Journal 67(3), 434-46, 2011, Arabidopsis ATH1 Genome Array  PubMed

Loss of BRCC3 Deubiquitinating Enzyme Leads to Abnormal Angiogenesis and Is Associated with Syndromic Moyamoya
Miskinyte, S. et al. American Journal of Human Genetics 88(6), 718-28, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Overexpression of Arabidopsis ACBP3 Enhances NPR1-Dependent Plant Resistance to Pseudomonas syringe pv tomato DC3000(1[W][OA])
Xiao, S. et al. Plant Physiology 156(4), 2069-81, 2011, Arabidopsis ATH1 Genome Array  PubMed

Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature
Abou Jamra, R. et al. American Journal of Human Genetics 88(6), 788-95, 2011  PubMed

X-Linked Congenital Hypertrichosis Syndrome Is Associated with Interchromosomal Insertions Mediated by a Human-Specific Palindrome near SOX3
Zhu, H. W. et al. American Journal of Human Genetics 88(6), 819-26, 2011, Genome-Wide Human SNP Array 6.0  PubMed

Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance
Wright, E. M. M. B. et al. American Journal of Human Genetics 88(6), 767-77, 2011  PubMed

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