Search Results - "Paterson, A.D"

Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD Study by JAMES, P. D., PATERSON, A. D., NOTLEY, C., CAMERON, C., HEGADORN, C., TINLIN, S., BROWN, C., O'BRIEN, L., LEGGO, J., LILLICRAP, D.

“…Background: von Willebrand disease (VWD) is the most common bleeding disorder known in humans, with type 1 VWD representing the majority of cases. Unlike the…”
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Relationship of speed of slaughter on infected premises and intensity of culling of other premises to the rate of spread of the foot-and-mouth disease epidemic in Great Britain, 2001 by Honhold, N., Taylor, N.M., Mansley, L.M., Paterson, A.D.

“…During the foot-and-mouth disease epidemic in the UK in 2001, two major control policies were the rapid identification of cases and the culling of animals on…”
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Clinical and genetic study of a large Italian family linked to SPG12 locus by ORLACCHIO, A, KAWARAI, T, ROGAEVA, E, SONG, Y. Q, PATERSON, A. D, BERNARDI, G, ST. GEORGE-HYSLOP, P. H

“…Seven loci for autosomal dominant hereditary spastic paraplegia (ADHSP) have been mapped. To date, two families of SPG12 (chromosome 19q13) have been analyzed;…”
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Genome-wide association study of emotional empathy in children by Woodbury-Smith, M. R., Paterson, A. D., Szatmari, P., Scherer, S. W.

“…The genetic contribution to different aspects of empathy is now established, although the exact loci are unknown. We undertook a genome-wide association study…”
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Novel RUNX1 Mutation in a Family with an Uncharacterized Secretion Defect by Badin, M., Hayward, C. P.M., Tasneem, S., Pare, G., Paterson, A.D., Waye, J.

“…Background: Platelet function disorders are a common cause of a bleeding problem. While many rare and severe forms of platelet function disorders are well…”
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Bleeding Risks Associated with Confirmed Platelet Dense Granule Deficiency and/or Impaired Aggregation Responses by Iyer, Janaki, Badin, Matthew, Graf, Lucas, Rivard, Georges E., Paterson, A.D., Pare, Guillaume, Hayward, Catherine P.M.

“…Platelet function disorders represent a heterogeneous group of bleeding disorders with diverse molecular causes that are frequently associated with platelet…”
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The phenotypic manifestations of rare genic CNVs in autism spectrum disorder by Merikangas, A K, Segurado, R, Heron, E A, Anney, R J L, Paterson, A D, Cook, E H, Pinto, D, Scherer, S W, Szatmari, P, Gill, M, Corvin, A P, Gallagher, L

“…Significant evidence exists for the association between copy number variants (CNVs) and Autism Spectrum Disorder (ASD); however, most of this work has focused…”
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Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia by Sung, L., Dix, D., Cellot, S., Gillmeister, B., Ethier, M.C., Roslin, N.M., Johnston, D.L., Feusner, J., Mitchell, D., Lewis, V., Aplenc, R., Yanofsky, R., Portwine, C., Price, V., Zelcer, S., Silva, M., Bowes, L., Michon, B., Stobart, K., Traubici, J., Allen, U., Beyene, J., den Hollander, N., Paterson, A.D.

“…We evaluated single nucleotide polymorphisms (SNPs) associated with infection risk in children with newly diagnosed acute myeloid leukaemia (AML). We conducted…”
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Expanded repeat in canine epilepsy by Lohi, H, Young, E.J, Fitzmaurice, S.N, Rusbridge, C, Chan, E.M, Vervoort, M, Turnbull, J, Zhao, X.C, Ianzano, L, Paterson, A.D

“…Epilepsy afflicts 1% of humans and 5% of dogs. We report a canine epilepsy mutation and evidence for the existence of repeat-expansion disease outside humans…”
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Genetic dissection of Iddm26 in the spontaneously diabetic BBDP rat by Sarmiento, J, Wallis, R H, Ning, T, Marandi, L, Chao, G Y C, Paterson, A D, Poussier, P

“…The 40 Mb T1D susceptibility locus Iddm26 was mapped to chromosome 2 through linkage analysis of a conditioned cross-intercross between the diabetes-prone BBDP…”
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Effects of the plant host on the detergent sensitivity and viability of Rhizobium bacteroids by Sutton, W.D, Paterson, A.D

“…Bacteroids prepared from different legume species showed large differences in detergent sensitivity as judged by changes in turbidity and the release of…”
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Umbilical Vein and Placental Vessels from Newborns with Hereditary Haemorrhagic Telangiectasia Type 1 Genotype are Normal despite Reduced Expression of Endoglin by Chan, N.L.M, Bourdeau, A, Vera, S, Abdalla, S, Gross, M, Wong, J, Cymerman, U, Paterson, A.D, Mullen, B, Letarte, M

“…Hereditary haemorrhagic telangiectasia, HHT, is an autosomal dominant disorder that affects approximately 1 in 8000 people. HHT1 is associated with mutations…”
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Association study between the dopamine D4 receptor gene and schizophrenia by Petronis, A, Macciardi, F, Athanassiades, A, Paterson, A D, Verga, M, Meltzer, H Y, Cola, P, Buchanan, J A, Van Tol, H H, Kennedy, J L

“…The dopamine D4 receptor is of major interest in schizophrenia research due to its high affinity for the atypical neuroleptic clozapine and a high degree of…”
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Search for unstable DNA in schizophrenia by Petronis, A., Vincent, J.B., Paterson, A.D., Bassett, A.S., Honer, W.G., Gottesman, I.I., Fuller Torrey, E., Meltzer, H.Y., Lieberman, J., Kennedy, J.L.

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Diabetics and renal failure by Paterson, A D, Dornan, T L

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A comparison of fine needle aspiration cytology and tru-cut tissue biopsy in the diagnosis of acute renal allograft rejection by Reeve, R S, Cooksey, G, Wenham, P W, Bourne, L D, Paterson, A D, Blamey, R W, Burden, R P, Cotton, R E

“…Simultaneous Tru-cut biopsies and fine needle aspirations (FNAs) performed over a 2-year period on patients following renal transplantation were assessed by…”
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Platelet sialic acid in malignant disease by Martin, J F, Kilbey, R S, Paterson, A D

“…n-Acetylneuraminic acid (NANA) was measured in the platelets and serum of normal subjects, patients with malignant disease, and patients with acute myocardial…”
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Biochemical markers of bone turnover in Paget's disease by Russell, R G, Beard, D J, Cameron, E C, Douglas, D L, Forrest, A R, Guilland-Cumming, D, Paterson, A D, Poser, J, Preston, C J, Milford-Ward, A, Woodhead, S, Kanis, J A

“…The two most commonly used biochemical markers of bone turnover are the serum alkaline phosphatase and the urinary excretion of peptide-bound hydroxyproline,…”
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