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Alan F Wright

Showing results (131-140 of 239) with videos related to

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Molecular & Cellular Proteomics : MCP|April 11, 2014
Comparative performance of four methods for high-throughput glycosylation analysis of immunoglobulin G in genetic and epidemiological researchJennifer E Huffman, Maja Pučić-Baković, Lucija Klarić, et al.
Human Molecular Genetics|April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachmentMirna Kirin, Aman Chandra, David G Charteris, et al.
Human Molecular Genetics|December 15, 2010
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsKonrad Oexle, Janina S Ried, Andrew A Hicks, et al.
Plos Genetics|January 5, 2011
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylationGordan Lauc, Abdelkader Essafi, Jennifer E Huffman, et al.
Genome Medicine|March 9, 2017
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participantsReka Nagy, Thibaud S Boutin, Jonathan Marten, et al.
Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, 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.
Circulation. Genomic and Precision Medicine|July 16, 2019
Lipidomics, Atrial Conduction, and Body Mass IndexFabiola Del Greco M, Luisa Foco, Alexander Teumer, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysisMatthias Olden, Tanguy Corre, Caroline Hayward, et al.
Human Molecular Genetics|July 16, 2015
Homozygous loss-of-function variants in European cosmopolitan and isolate populationsVera B Kaiser, Victoria Svinti, James G Prendergast, et al.
Pageof 24

Showing results (131-140 of 239) with videos related to

Sort By:
Pageof 24
Molecular & Cellular Proteomics : MCP|April 11, 2014
Comparative performance of four methods for high-throughput glycosylation analysis of immunoglobulin G in genetic and epidemiological researchJennifer E Huffman, Maja Pučić-Baković, Lucija Klarić, et al.
Human Molecular Genetics|April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachmentMirna Kirin, Aman Chandra, David G Charteris, et al.
Human Molecular Genetics|December 15, 2010
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levelsKonrad Oexle, Janina S Ried, Andrew A Hicks, et al.
Plos Genetics|January 5, 2011
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylationGordan Lauc, Abdelkader Essafi, Jennifer E Huffman, et al.
Genome Medicine|March 9, 2017
Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participantsReka Nagy, Thibaud S Boutin, Jonathan Marten, et al.
Plos Genetics|April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatednessJared O'Connell, Deepti Gurdasani, Olivier Delaneau, 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.
Circulation. Genomic and Precision Medicine|July 16, 2019
Lipidomics, Atrial Conduction, and Body Mass IndexFabiola Del Greco M, Luisa Foco, Alexander Teumer, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysisMatthias Olden, Tanguy Corre, Caroline Hayward, et al.
Human Molecular Genetics|July 16, 2015
Homozygous loss-of-function variants in European cosmopolitan and isolate populationsVera B Kaiser, Victoria Svinti, James G Prendergast, et al.
Pageof 24