Making Psychology’s Hidden Figures Visible Using Open Educational Resources: A Replication and Extension Study von Kelly, Alison E., Laurin, Jenna N., Clinton-Lisell, Virginia

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Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31 von Laurin, Nancy, Brown, Jacques P., Lemainque, Arnaud, Duchesne, Annie, Huot, Denys, Lacourcière, Yves, Drapeau, Gervais, Verreault, Jean, Raymond, Vincent, Morissette, Jean

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Estrogen receptor-related receptor-α (ERR-α) is dysregulated in inflammatory arthritis von Bonnelye, E., Laurin, N., Jurdic, P., Hart, D. A., Aubin, J. E.

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Estrogen receptor-related receptor-a (ERR-α) is dysregulated in inflammatory arthritis von BONNELYE, E, LAURIN, N, JURDIC, P, HART, D. A, AUBIN, J. E

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Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems von Luca, P, Laurin, N, Misener, V L, Wigg, K G, Anderson, B, Cate-Carter, T, Tannock, R, Humphries, T, Lovett, M W, Barr, C L

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Effect of a series of triorganotins on the immune function of human natural killer cells von Gomez, Fabiola D, Apodaca, Paula, Holloway, Laurin N, Pannell, Keith H, Whalen, Margaret M

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Association of the calcyon gene (DRD1IP) with attention deficit/hyperactivity disorder von Laurin, N, Misener, V L, Crosbie, J, Ickowicz, A, Pathare, T, Roberts, W, Malone, M, Tannock, R, Schachar, R, Kennedy, J L, Barr, C L

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No preferential transmission of paternal alleles at risk genes in attention-deficit hyperactivity disorder von Laurin, N, Feng, Y, Ickowicz, A, Pathare, T, Malone, M, Tannock, R, Schachar, R, Kennedy, J L, Barr, C L

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Recurrent Mutation of the Gene Encoding sequestosome 1 ( SQSTM1/p62) in Paget Disease of Bone von Laurin, Nancy, Brown, Jacques P., Morissette, Jean, Raymond, Vincent

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Sequestosome 1: Mutation Frequencies, Haplotypes, and Phenotypes in Familial Paget's Disease of Bone von Morissette, Jean, Laurin, Nancy, Brown, Jacques P

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Effects of a series of triorganotins on ATP levels in human natural killer cells von Holloway, Laurin N, Pannell, Keith H, Whalen, Margaret M

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The hormone-sensitive lipase gene is transcribed from at least five alternative first exons in mouse adipose tissue von Laurin, N N, Wang, S P, Mitchell, G A

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p53 protein expression in ulcerative colitis-associated colorectal dysplasia and carcinoma von Harpaz, Noam, Peck, Allan L., Yin, Jing, Fiel, Isabel, Hontanosas, Maria, Tong, Tommy R., Laurin, Jacqueline N., Abraham, John M., Greenwald, Bruce D., Meltzer, Stephen J.

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The Adipose Tissue Phenotype of Hormone‐Sensitive Lipase Deficiency in Mice von Wang, Shu Pei, Laurin, Nancy, Himms‐Hagen, Jean, Rudnicki, Michael A., Levy, Emile, Robert, Marie‐France, Pan, Linghe, Oligny, Luc, Mitchell, Grant A.

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Cerebral Perfusion Imaging with Technetium-99m HM-PAO in Brain Death and Severe Central Nervous System Injury von Laurin, Norman R, Driedger, Albert A, Hurwitz, Gilbert A, Mattar, Adel G, Powe, John E, Chamberlain, Michael J, Zabel, Pamela L, Pavlosky, William F

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Le démantèlement des institutions intermédiaires de la régulation sociale : Vers une nouvelle forme de domination : Citoyenneté et identité sociale von LAURIN, N

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Human hormone-sensitive lipase (HSL): expression in white fat corrects the white adipose phenotype of HSL-deficient mice von Fortier, Melanie, Soni, Krishnakant, Laurin, Nancy, Wang, Shu Pei, Mauriege, Pascale, Jirik, Frank R, Mitchell, Grant A

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Association study of the nicotinic acetylcholine receptor α4 subunit gene, CHRNA4, in attention‐deficit hyperactivity disorder von Lee, J., Laurin, N., Crosbie, J., Ickowicz, A., Pathare, T., Malone, M., Kennedy, J. L., Tannock, R., Schachar, R., Barr, C. L.

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Le Canadien de Montréal: Une légende repensée von Laurin-Lamothe, Audrey, Moreau, Nicolas

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Cours de droit maritime / par M. Cresp ; annoté, complété et mis au courant de la jurisprudence la plus récente, par Auguste Laurin,... von Cresp, Pierre Philippe (1788-1869). Auteur du texte

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