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Multiple Sclerosis (Houndmills, Basingstoke, England)|March 10, 2018
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trialsDorothea Buck, Till Fm Andlauer, Wilmar Igl, et al.
American Journal of Human Genetics|April 17, 2012
Genetic adaptation of fatty-acid metabolism: a human-specific haplotype increasing the biosynthesis of long-chain omega-3 and omega-6 fatty acidsAdam Ameur, Stefan Enroth, Asa Johansson, et al.
Human Molecular Genetics|September 13, 2011
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adultsJennifer E Huffman, Ana Knezevic, Veronique Vitart, et al.
Plos Genetics|October 3, 2009
Genetic determinants of circulating sphingolipid concentrations in European populationsAndrew A Hicks, Peter P Pramstaller, Asa Johansson, et al.
Plos Genetics|February 24, 2012
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrationsAyşe Demirkan, Cornelia M van Duijn, Peter Ugocsai, et al.
Plos Genetics|July 26, 2012
Evidence of inbreeding depression on human heightRuth McQuillan, Niina Eklund, Nicola Pirastu, et al.
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