Search Results - "Moore, S. H."

Evaluation of USDA Soybean Germplasm Accessions for Resistance to Soybean Rust in the Southern United States by Walker, D.R, Boerma, H.R, Phillips, D.V, Schneider, R.W, Buckley, J.B, Shipe, E.R, Mueller, J.D, Weaver, D.B, Sikora, E.J, Moore, S.H, Hartman, G.L, Miles, M.R, Harris, D.K, Wright, D.L, Marois, J.J, Nelson, R.L

“…Soybean [Glycine max (L.) Merr.] resistance to soybean rust (SBR) caused by Phakopsora pachyrhizi could reduce reliance on fungicides to manage this disease…”
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Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events by Helgason, Hannes, Eiriksdottir, Thjodbjorg, Ulfarsson, Magnus O, Choudhary, Abhishek, Lund, Sigrun H, Ivarsdottir, Erna V, Hjorleifsson Eldjarn, Grimur, Einarsson, Gudmundur, Ferkingstad, Egil, Moore, Kristjan H. S, Honarpour, Narimon, Liu, Thomas, Wang, Huei, Hucko, Thomas, Sabatine, Marc S, Morrow, David A, Giugliano, Robert P, Ostrowski, Sisse Rye, Pedersen, Ole Birger, Bundgaard, Henning, Erikstrup, Christian, Arnar, David O, Thorgeirsson, Gudmundur, Masson, Gísli, Magnusson, Olafur Th, Saemundsdottir, Jona, Gretarsdottir, Solveig, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Helgadottir, Anna, Sulem, Patrick, Thorsteinsdottir, Unnur, Holm, Hilma, Gudbjartsson, Daniel, Stefansson, Kari

“…IMPORTANCE: Whether protein risk scores derived from a single plasma sample could be useful for risk assessment for atherosclerotic cardiovascular disease…”
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Further neurochemical and behavioural investigation of Brattleboro rats as a putative model of schizophrenia by Cilia, J., Gartlon, JE, Shilliam, C., Dawson, LA, Moore, SH, Jones, DNC

“…Brattleboro (BRAT) rats are a mutant variant of the Long-Evans (LE) strain deficient in the neurohormone vasopressin. BRAT rats show behavioural alterations…”
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The genetic structure of Norway by Mattingsdal, Morten, Ebenesersdóttir, S Sunna, Moore, Kristjan H S, Andreassen, Ole A, Hansen, Thomas F, Werge, Thomas, Kockum, Ingrid, Olsson, Tomas, Alfredsson, Lars, Helgason, Agnar, Stefánsson, Kári, Hovig, Eivind

“…The aim of the present study was to describe the genetic structure of the Norwegian population using genotypes from 6369 unrelated individuals with detailed…”
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Learning Chronobiology by Improving Wikipedia by Chiang, C.D., Lewis, C.L., Wright, M.D.E., Agapova, S., Akers, B., Azad, T.D., Banerjee, K., Carrera, P., Chen, A., Chen, J., Chi, X., Chiou, J., Cooper, J., Czurylo, M., Downs, C., Ebstein, S.Y., Fahey, P.G., Goldman, J.W., Grieff, A., Hsiung, S., Hu, R., Huang, Y., Kapuria, A., Li, K., Marcu, I., Moore, S.H., Moseley, A.C., Nauman, N., Ness, K.M., Ngai, D.M., Panzer, A., Peters, P., Qin, E.Y., Sadhu, S., Sariol, A., Schellhase, A., Schoer, M.B., Steinberg, M., Surick, G., Tsai, C.A., Underwood, K., Wang, A., Wang, M.H., Wang, V.M., Westrich, D., Yockey, L.J., Zhang, L., Herzog, E.D.

“…Although chronobiology is of growing interest to scientists, physicians, and the general public, access to recent discoveries and historical perspectives is…”
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Ancient genomes from Iceland reveal the making of a human population by Ebenesersdóttir, S Sunna, Sandoval-Velasco, Marcela, Gunnarsdóttir, Ellen D, Jagadeesan, Anuradha, Guðmundsdóttir, Valdís B, Thordardóttir, Elísabet L, Einarsdóttir, Margrét S, Moore, Kristjan H S, Sigurðsson, Ásgeir, Magnúsdóttir, Droplaug N, Jónsson, Hákon, Snorradóttir, Steinunn, Hovig, Eivind, Møller, Pål, Kockum, Ingrid, Olsson, Tomas, Alfredsson, Lars, Hansen, Thomas F, Werge, Thomas, Cavalleri, Gianpiero L, Gilbert, Edmund, Lalueza-Fox, Carles, Walser, 3rd, Joe W, Kristjánsdóttir, Steinunn, Gopalakrishnan, Shyam, Árnadóttir, Lilja, Magnússon, Ólafur Þ, Gilbert, M Thomas P, Stefánsson, Kári, Helgason, Agnar

“…Opportunities to directly study the founding of a human population and its subsequent evolutionary history are rare. Using genome sequence data from 27 ancient…”
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Physical Properties and Bonding in RE3TiSb5 (RE = La, Ce, Pr, Nd, Sm) by MOORE, S. H. Devon, DEAKIN, Laura, FERGUSON, Michael J., MAR, Arthur

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Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease by Saevarsdottir, Saedis, Bjarnadottir, Kristbjörg, Markusson, Thorsteinn, Berglund, Jonas, Olafsdottir, Thorunn A., Halldorsson, Gisli H., Rutsdottir, Gudrun, Gunnarsdottir, Kristbjorg, Arnthorsson, Asgeir Orn, Lund, Sigrun H., Stefansdottir, Lilja, Gudmundsson, Julius, Johannesson, Ari J., Sturluson, Arni, Oddsson, Asmundur, Halldorsson, Bjarni, Ludviksson, Björn R., Ferkingstad, Egil, Ivarsdottir, Erna V., Sveinbjornsson, Gardar, Grondal, Gerdur, Masson, Gisli, Eldjarn, Grimur Hjorleifsson, Thorisson, Gudmundur A., Kristjansdottir, Katla, Knowlton, Kirk U., Moore, Kristjan H. S., Gudjonsson, Sigurjon A., Rognvaldsson, Solvi, Knight, Stacey, Nadauld, Lincoln D., Holm, Hilma, Magnusson, Olafur T., Sulem, Patrick, Gudbjartsson, Daniel F., Rafnar, Thorunn, Thorleifsson, Gudmar, Melsted, Pall, Norddahl, Gudmundur L., Jonsdottir, Ingileif, Stefansson, Kari

“…Autoimmune thyroid disease (AITD) is a common autoimmune disease. In a GWAS meta-analysis of 110,945 cases and 1,084,290 controls, 290 sequence variants at 225…”
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G159(P) Cerebral infarction in paediatric diabetic ketoacidosis by Parmar, RS, Moore, HS, Paul, P

“…Aims/IntroductionDiabetic Ketoacidosis (DKA) is a potentially fatal complication of Type 1 Diabetes Mellitus (T1DM). Cerebral complications affect 0.3%–1% of…”
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Cardiomyopathy in the congenital disorders of glycosylation (CDG): a case of late presentation and literature review by Footitt, E. J., Karimova, A., Burch, M., Yayeh, T., Dupré, T., Vuillaumier-Barrot, S., Chantret, I., Moore, S. E. H., Seta, N., Grunewald, S.

“…Summary The congenital disorders of glycosylation (CDG) are a recently described group of inherited multisystem disorders characterized by defects…”
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HaploGrouper: a generalized approach to haplogroup classification by Jagadeesan, Anuradha, Ebenesersdóttir, S Sunna, Guðmundsdóttir, Valdis B, Thordardottir, Elisabet Linda, Moore, Kristjan H S, Helgason, Agnar

“…Abstract Motivation We introduce HaploGrouper, a versatile software to classify haplotypes into haplogroups on the basis of a known phylogenetic tree. A…”
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The rate and nature of mitochondrial DNA mutations in human pedigrees by Árnadóttir, Erla R, Moore, Kristján H S, Guðmundsdóttir, Valdís B, Ebenesersdóttir, S Sunna, Guity, Kamran, Jónsson, Hákon, Stefánsson, Kári, Helgason, Agnar

“…We examined the rate and nature of mitochondrial DNA (mtDNA) mutations in humans using sequence data from 64,806 contemporary Icelanders from 2,548 matrilines…”
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Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency by Oddsson, Asmundur, Steinthorsdottir, Valgerdur, Oskarsson, Gudjon R., Styrkarsdottir, Unnur, Moore, Kristjan H. S., Isberg, Salvor, Halldorsson, Gisli H., Sveinbjornsson, Gardar, Westergaard, David, Nielsen, Henriette Svarre, Fridriksdottir, Run, Jensson, Brynjar O., Arnadottir, Gudny A., Jonsson, Hakon, Sturluson, Arni, Snaebjarnarson, Audunn S., Andreassen, Ole A., Walters, G. Bragi, Nyegaard, Mette, Erikstrup, Christian, Steingrimsdottir, Thora, Lie, Rolv T., Melsted, Pall, Jonsdottir, Ingileif, Halldorsson, Bjarni V., Thorleifsson, Gudmar, Saemundsdottir, Jona, Magnusson, Olafur Th, Banasik, Karina, Sorensen, Erik, Masson, Gisli, Pedersen, Ole Birger, Tryggvadottir, Laufey, Haavik, Jan, Ostrowski, Sisse Rye, Stefansson, Hreinn, Holm, Hilma, Rafnar, Thorunn, Gudbjartsson, Daniel F., Sulem, Patrick, Stefansson, Kari

“…Age at menopause (AOM) has a substantial impact on fertility and disease risk. While many loci with variants that associate with AOM have been identified…”
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Author Correction: The Anglo-Saxon migration and the formation of the early English gene pool by Gretzinger, Joscha, Sayer, Duncan, Justeau, Pierre, Altena, Eveline, Pala, Maria, Dulias, Katharina, Edwards, Ceiridwen J., Jodoin, Susanne, Lacher, Laura, Sabin, Susanna, Vågene, Åshild J., Haak, Wolfgang, Ebenesersdóttir, S. Sunna, Moore, Kristjan H. S., Radzeviciute, Rita, Schmidt, Kara, Brace, Selina, Bager, Martina Abenhus, Patterson, Nick, Papac, Luka, Broomandkhoshbacht, Nasreen, Callan, Kimberly, Harney, Éadaoin, Iliev, Lora, Lawson, Ann Marie, Michel, Megan, Stewardson, Kristin, Zalzala, Fatma, Rohland, Nadin, Kappelhoff-Beckmann, Stefanie, Both, Frank, Winger, Daniel, Neumann, Daniel, Saalow, Lars, Krabath, Stefan, Beckett, Sophie, Van Twest, Melanie, Faulkner, Neil, Read, Chris, Barton, Tabatha, Caruth, Joanna, Hines, John, Krause-Kyora, Ben, Warnke, Ursula, Schuenemann, Verena J., Barnes, Ian, Dahlström, Hanna, Clausen, Jane Jark, Richardson, Andrew, Popescu, Elizabeth, Dodwell, Natasha, Ladd, Stuart, Phillips, Tom, Mortimer, Richard, Sayer, Faye, Swales, Diana, Stewart, Allison, Powlesland, Dominic, Kenyon, Robert, Ladle, Lilian, Peek, Christina, Grefen-Peters, Silke, Ponce, Paola, Daniels, Robin, Spall, Cecily, Woolcock, Jennifer, Jones, Andy M., Roberts, Amy V., Symmons, Robert, Rawden, Anooshka C., Cooper, Alan, Bos, Kirsten I., Booth, Tom, Schroeder, Hannes, Thomas, Mark G., Helgason, Agnar, Richards, Martin B., Reich, David, Krause, Johannes, Schiffels, Stephan

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Temporal candidate gene expression in the sow placenta and embryo during early gestation and effect of maternal Progenos supplementation on embryonic and placental development by Novak, S, Paradis, F, Patterson, J L, Pasternak, J A, Oxtoby, K, Moore, H S, Hahn, M, Dyck, M K, Dixon, W T, Foxcroft, G R

“…The present study characterised gene expression associated with embryonic muscle development and placental vascularisation during early gestation in the pig…”
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A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity by Sabry, S, Vuillaumier-Barrot, S, Mintet, E, Fasseu, M, Valayannopoulos, V, Héron, D, Dorison, N, Mignot, C, Seta, N, Chantret, I, Dupré, T, Moore, S E H

“…Type I congenital disorders of glycosylation (CDG-I) are mostly complex multisystemic diseases associated with hypoglycosylated serum glycoproteins. A subgroup…”
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Actionable Genotypes and Their Association with Life Span in Iceland by Jensson, Brynjar O., Arnadottir, Gudny A., Katrinardottir, Hildigunnur, Fridriksdottir, Run, Helgason, Hannes, Oddsson, Asmundur, Sveinbjornsson, Gardar, Eggertsson, Hannes P., Halldorsson, Gisli H., Atlason, Bjarni A., Jonsson, Hakon, Oskarsson, Gudjon R., Sturluson, Arni, Gudjonsson, Sigurjon A., Thorisson, Gudmundur A., Zink, Florian, Moore, Kristjan H.S., Palsson, Gunnar, Sigurdsson, Asgeir, Jonasdottir, Adalbjorg, Jonasdottir, Aslaug, Magnusson, Magnus K., Helgadottir, Anna, Steinthorsdottir, Valgerdur, Gudmundsson, Julius, Stacey, Simon N., Hilmarsson, Rafn, Olafsson, Isleifur, Johannsson, Oskar T., Arnar, David O., Saemundsdottir, Jona, Magnusson, Olafur T., Masson, Gisli, Halldorsson, Bjarni V., Helgason, Agnar, Stefansson, Hreinn, Jonsdottir, Ingileif, Holm, Hilma, Rafnar, Thorunn, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Stefansson, Kari, Sulem, Patrick

“…This study examines the relationship of pathogenic and likely pathogenic variants for which preventive or therapeutic measures are available to life span and…”
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Ternary rare-earth titanium antimonides : Phase equilibria in the RE-Ti-Sb (RE = La, Er) systems and crystal structures of RE2Ti7Sb12 (RE = La, Ce, Pr, Nd) and RETi3(SnxSb1_ x)4 (RE = Nd, Sm) by HAIYING BIE, DEVON MOORE, S. H, PIERCEY, Davin G, TKACHUK, Andriy V, ZELINSKA, Oksana Ya, MAR, Arthur

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Registration of 'Secretariat LA495' oat by Harrison, S.A, Mascagni, H.J, Moore, S.H

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Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations by Dupré, T, Vuillaumier-Barrot, S, Chantret, I, Sadou Yayé, H, Yayé, H S, Le Bizec, C, Afenjar, A, Altuzarra, C, Barnérias, C, Burglen, L, de Lonlay, P, Feillet, F, Napuri, S, Seta, N, Moore, S E H

“…In type I congenital disorders of glycosylation (CDG I), proteins necessary for the biosynthesis of the lipid-linked oligosaccharide (LLO) required for protein…”
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