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High resolution oligonucleotide CGH using DNA from archived prostatetissuePARIS, Pamela L; SRIDHARAN, Shivaranjani; SCHEFFER, Alicia et al.The Prostate. 2007, Vol 67, Num 13, pp 1447-1455, issn 0270-4137, 9 p.Article

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males : implications for association studies of complex diseasesDE SMITHL, Adam J; TSALENKO, Anya; LADERMAN, Stephen et al.Human molecular genetics (Print). 2007, Vol 16, Num 23, pp 2783-2794, issn 0964-6906, 12 p.Article

lincRNAs act in the circuitry controlling pluripotency and differentiationGUTTMAN, Mitchell; DONAGHEY, Julie; XIAOPING YANG et al.Nature (London). 2011, Vol 477, Num 7364, pp 295-300, issn 0028-0836, 6 p.Article

Population-Genetic Properties of Differentiated Human Copy-Number PolymorphismsCAMPBELL, Catarina D; SAMPAS, Nick; EICHLER, Evan E et al.American journal of human genetics. 2011, Vol 88, Num 3, pp 317-332, issn 0002-9297, 16 p.Article

Molecular signatures determining coronary artery and saphenous vein smooth muscle cell phenotypes : Distinct responses to stimuliDENG, David Xing-Fei; SPIN, Joshua M; TSALENKO, Anya et al.Arteriosclerosis, thrombosis, and vascular biology. 2006, Vol 26, Num 5, pp 1058-1065, issn 1079-5642, 8 p.Article

Diversity of Human Copy Number Variation and Multicopy GenesSUDMANT, Peter H; KITZMAN, Jacob O; ANTONACCI, Francesca et al.Science (Washington, D.C.). 2010, Vol 330, Num 6004, pp 641-646, issn 0036-8075, 6 p.Article

The Fine-Scale and Complex Architecture of Human Copy-Number VariationPERRY, George H; BEN-DOR, Amir; HAN SOO PARK et al.American journal of human genetics. 2008, Vol 82, Num 3, pp 685-695, issn 0002-9297, 11 p.Article

Novel role for the potent endogenous inotrope apelin in human cardiac dysfunctionCHEN, Mary M; ASHLEY, Euan A; FOWLER, Michael et al.Circulation (New York, N.Y.). 2003, Vol 108, Num 12, pp 1432-1439, issn 0009-7322, 8 p.Article

Mapping and sequencing of structural variation from eight human genomesKIDD, Jeffrey M; COOPER, Gregory M; HAUGEN, Eric et al.Nature genetics. 2009, Vol SEP, issn 1061-4036, S22-S30, SUPArticle

Mapping and sequencing of structural variation from eight human genomesKIDD, Jeffrey M; COOPER, Gregory M; HAUGEN, Eric et al.Nature (London). 2008, Vol 452, Num 7191, pp 56-64, issn 0028-0836, 9 p.Article

Differences in vascular bed disease susceptibility reflect differences in gene expression response to atherogenic stimuliDENG, David Xing-Fei; TSALENKO, Anya; QUERTERMOUS, Thomas et al.Circulation research. 2006, Vol 98, Num 2, pp 200-208, issn 0009-7330, 9 p.Article

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