X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (68) 68
Publication (11) 11
Book / eBook (10) 10
Trade Publication Article (7) 7
Newspaper Article (5) 5
Dissertation (2) 2
Magazine Article (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (31) 31
humans (28) 28
genetic aspects (21) 21
female (18) 18
research (17) 17
genetics (16) 16
risk factors (16) 16
male (15) 15
polymorphism, single nucleotide (14) 14
animals (13) 13
genome-wide association study (13) 13
abridged index medicus (10) 10
genomes (10) 10
dogs (9) 9
genetic predisposition to disease (9) 9
genetic variation (9) 9
epidemiology (8) 8
gene expression (8) 8
physiological aspects (8) 8
genetics & heredity (7) 7
genotype (7) 7
medicine (7) 7
middle aged (7) 7
case-control studies (6) 6
genome-wide association (6) 6
health aspects (6) 6
lipoproteins (6) 6
medical research (6) 6
mice (6) 6
mutation (6) 6
studies (6) 6
adult (5) 5
aged (5) 5
article (5) 5
biography (5) 5
cardiovascular disease (5) 5
disease (5) 5
genes (5) 5
genomics (5) 5
medical and health sciences (5) 5
medicin och hälsovetenskap (5) 5
myocardial-infarction (5) 5
peripheral vascular disease (5) 5
risk (5) 5
usage (5) 5
analysis (4) 4
association (4) 4
atherosclerosis (4) 4
biology (4) 4
biology and life sciences (4) 4
chromosome mapping (4) 4
coronary artery disease - genetics (4) 4
coronary heart disease (4) 4
diabetes (4) 4
diseases (4) 4
dog diseases - genetics (4) 4
european continental ancestry group (4) 4
expression (4) 4
lipids (4) 4
medicine and health sciences (4) 4
multidisciplinary sciences (4) 4
nucleotide sequencing (4) 4
phenotype (4) 4
positron-emission tomography (4) 4
proteins (4) 4
radiology, nuclear medicine & medical imaging (4) 4
research article (4) 4
science (4) 4
tumors (4) 4
xenograft model antitumor assays (4) 4
zoology (4) 4
alleles (3) 3
animal genetics (3) 3
articles (3) 3
asian continental ancestry group (3) 3
cancer (3) 3
cardiac & cardiovascular systems (3) 3
care and treatment (3) 3
cell biology (3) 3
cell line, tumor (3) 3
cholesterol (3) 3
cohort studies (3) 3
coronary artery disease (3) 3
coronary disease - genetics (3) 3
coronary-artery-disease (3) 3
critical care medicine (3) 3
diabetes mellitus, type 2 - genetics (3) 3
dna sequencing (3) 3
endocrinology & metabolism (3) 3
gene (3) 3
gene mutations (3) 3
gene-expression (3) 3
genetic research (3) 3
genome-wide association studies (3) 3
haplotypes (3) 3
heart-disease (3) 3
internal medicine (3) 3
life sciences (3) 3
medicine, general & internal (3) 3
metabolic disorders (3) 3
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (5) 5
Architecture Landscape (Shore + Moffat) - Stacks (1) 1
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Gerstein Science - Stacks (1) 1
Media Commons - Microtexts (1) 1
Online Resources - Online (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
UTL at Downsview - May be requested (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of the American Veterinary Medical Association, ISSN 0003-1488, 09/2018, Volume 253, Issue 6, pp. 774 - 780
CASE DESCRIPTION Two 12-week-old Norwegian Buhunds from a litter of 5 were evaluated because of slowly progressive cerebellar ataxia and fine head tremors. Two... 
PURKINJE-CELLS | CALCIUM-BINDING PROTEINS | CEREBELLAR CORTICAL DEGENERATION | SPINOCEREBELLAR ATAXIA | MOUSE MODEL | DOGS | GENE-EXPRESSION | VETERINARY SCIENCES | LABRADOR RETRIEVER | AUSTRALIAN KELPIE | GRANULOPRIVAL DEGENERATION
Journal Article
MOLECULAR VISION, ISSN 1090-0535, 02/2019, Volume 25, Issue 1, pp. 93 - 105
Purpose: To investigate the genetic basis of primary closed angle glaucoma (PCAG) in European Basset Hounds using genome-wide association and RNA sequencing... 
GONIODYSGENESIS | ENGLISH | TRABECULAR MESHWORK | CLOSURE GLAUCOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | PECTINATE LIGAMENT DYSPLASIA | OPHTHALMOLOGY | LINKAGE | TRAITS | DOG | EXPRESSION | IRIDOCORNEAL ANGLE | primary closed angle glaucoma | Genome-wide association studies
Journal Article
Canine genetics and epidemiology, ISSN 2052-6687, 2019, Volume 6, Issue 1, pp. 5 - 11
In humans, mutations are known to cause Weill-Marchesani-like syndrome, which is characterised by lenticular myopia, ectopia lentis, glaucoma, spherophakia,... 
Glaucoma | Genetic aspects | Research | Gene mutations | Patient outcomes | Dogs | Disease | Genes | Myopia | Alleles | Likelihood ratio | Genomes | Mutation | Females | Males | Continuity (mathematics) | Weill-Marchesani-like syndrome | Height | Primary open angle Glaucoma | ADAMTS17 | Primary Lens luxation
Journal Article
by Teslovich, Tanya M and Musunuru, Kiran and Smith, Albert V and Edmondson, Anew C and Stylianou, Ioannis M and Koseki, Masahiro and Pirruccello, James P and Ripatti, Samuli and Chasman, Daniel I and Willer, Cristen J and Johansen, Christopher T and Fouchier, Sigrid W and Isaacs, Aaron and Peloso, Gina M and Barbalic, Maja and Ricketts, Sally L and Bis, Joshua C and Aulchenko, Yurii S and Thorleifsson, Gudmar and Feitosa, Mary F and Chambers, John and Orho-Melander, Marju and Melander, Olle and Johnson, Toby and Li, Xiaohui and Guo, Xiuqing and Li, Mingyao and Shin Cho, Yoon and Jin Go, Min and Jin Kim, Young and Lee, Jong-Young and Park, Taesung and Kim, Kyunga and Sim, Xueling and Twee-Hee Ong, Rick and Croteau-Chonka, Damien C and Lange, Leslie A and Smith, Joshua D and Song, Kijoung and Hua Zhao, Jing and Yuan, Xin and Luan, Jian'an and Lamina, Claudia and Ziegler, Aneas and Zhang, Weihua and Zee, Robert Y. L and Wright, Alan F and Witteman, Jacqueline C. M and Wilson, James F and Willemsen, Gonneke and Wichmann, H.-Erich and Whitfield, John B and Waterworth, Dawn M and Wareham, Nicholas J and Waeber, Gérard and Vollenweider, Peter and Voight, Benjamin F and Vitart, Veronique and Uitterlinden, Ane G and Uda, Manuela and Tuomilehto, Jaakko and Thompson, John R and Tanaka, Toshiko and Surakka, Ida and Stringham, Heather M and Spector, Tim D and Soranzo, Nicole and Smit, Johannes H and Sinisalo, Juha and Silander, Kaisa and Sijbrands, Eric J. G and Scuteri, Angelo and Scott, James and Schlessinger, David and Sanna, Serena and Salomaa, Veikko and Saharinen, Juha and Sabatti, Chiara and Ruokonen, Aimo and Rudan, Igor and Rose, Lynda M and Roberts, Robert and Rieder, Mark and Psaty, Bruce M and Pramstaller, Peter P and Pichler, Irene and Perola, Markus and Penninx, Brenda W. J. H and Pedersen, Nancy L and Pattaro, Cristian and Parker, Alex N and Pare, Guillaume and Oostra, Ben A and O'Donnell, Christopher J and Nieminen, Markku S and Nickerson, Deborah A and Montgomery, Grant W and Meitinger, Thomas and McPherson, Ruth and McCarthy, Mark I and ... and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature, ISSN 0028-0836, 2010, Volume 466, Issue 7307, pp. 707 - 713
Journal Article
Lancet, The, ISSN 0140-6736, 2011, Volume 378, Issue 9791, pp. 584 - 594
Journal Article
by Dastani, Zari and Hivert, Marie-France and Timpson, Nicholas and Perry, John R. B and Yuan, Xin and Scott, Robert A and Henneman, Peter and Heid, Iris M and Kizer, Jorge R and Lyytikäinen, Leo-Pekka and Fuchsberger, Christian and Tanaka, Toshiko and Morris, Anew P and Small, Kerrin and Isaacs, Aaron and Beekman, Marian and Coassin, Stefan and Lohman, Kurt and Qi, Lu and Kanoni, Stavroula and Pankow, James S and Uh, Hae-Won and Wu, Ying and Bidulescu, Aurelian and Rasmussen-Torvik, Laura J and Greenwood, Celia M. T and Ladouceur, Martin and Grimsby, Jonna and Manning, Alisa K and Liu, Ching-Ti and Kooner, Jaspal and Mooser, Vincent E and Vollenweider, Peter and Kapur, Karen A and Chambers, John and Wareham, Nicholas J and Langenberg, Claudia and Frants, Rune and Willems-Vandijk, Ko and Oostra, Ben A and Willems, Sara M and Lamina, Claudia and Winkler, Thomas W and Psaty, Bruce M and Tracy, Russell P and Brody, Jennifer and Chen, Ida and Viikari, Jorma and Kähönen, Mika and Pramstaller, Peter P and Evans, David M and St Pourcain, Beate and Sattar, Naveed and Wood, Anew R and Bandinelli, Stefania and Carlson, Olga D and Egan, Josephine M and Böhringer, Stefan and van Heemst, Diana and Kedenko, Lyudmyla and Kristiansson, Kati and Nuotio, Marja-Liisa and Loo, Britt-Marie and Harris, Tamara and Garcia, Melissa and Kanaya, Alka and Haun, Margot and Klopp, Norman and Wichmann, H.-Erich and Deloukas, Panos and Katsareli, Efi and Couper, David J and Duncan, Bruce B and Kloppenburg, Margreet and Adair, Linda S and Borja, Judith B and Wilson, James G and Musani, Solomon and Guo, Xiuqing and Johnson, Toby and Semple, Robert and Teslovich, Tanya M and Allison, Matthew A and Redline, Susan and Buxbaum, Sarah G and Mohlke, Karen L and Meulenbelt, Ingrid and Ballantyne, Christie M and Dedoussis, George V and Hu, Frank B and Liu, Yongmei and Paulweber, Bernhard and Spector, Timothy D and Slagboom, P. Eline and Ferrucci, Luigi and Jula, Antti and Perola, Markus and Raitakari, Olli and Florez, Jose C and Salomaa, Veikko and ... and GLGC Investigators and DIAGRAM Consortium and MAGIC Consortium and MuTHER Consortium and Global B Pgen Consortium and MAGIC investigators and Procardis Consortium and DIAGRAM+ Consortium and GLGC Consortium and GIANT Consortium
PLoS genetics, ISSN 1553-7390, 2012, Volume 8, Issue 3, p. e1002607
Journal Article
by Sarwar, Nadeem and Sandhu, Manjinder S and Ricketts, Sally L and Butterworth, Adam S and Di Angelantonio, Emanuele and Boekholdt, S. Matthijs and Ouwehand, Willem and Watkins, Hugh and Samani, Nilesh J and Saleheen, Danish and Lawlor, Debbie and Reilly, Muredach P and Hingorani, Aroon D and Talmud, Philippa J and Danesh, John and Braund, P. S and Hall, A. S and Samani, N. J and Thompson, J and März, W and Ouwehand, W and Sivapalaratnam, S and Soranzo, N and Trip, M and Lawlor, D. A and Casas, J. P and Ebrahim, S and Arsenault, B. J and Khaw, K. T and Ricketts, S. L and Sandhu, M. S and Wareham, N. J and Grallert, H and Illig, T and Humphries, S. E and Talmud, Talmud and Rader, D. J and He, J and Reilly, M. P and Clarke, R and Hamsten, A and Hopewell, J. C and Watkins, H and Saleheen, D and Frossard, P and Deloukas, P and Danesh, J and Ye, S and Simpson, I. A and Onat, A and Kömürcü-Bayrak, E and Martinelli, N and Olivieri, O and Girelli, D and Hingorani, A. D and Kivimäki, M and Kumari, M and Aouizerat, B. E and Baum, L and Campos, H and Chaaba, R and Chen, B. S and Cho, E. Y and Evans, D and Hill, J and Hsu, L. A and Hubacek, J. A and Lai, C. Q and Lee, J. H and Klos, K and Liu, H and Masana, L and Melegh, B and Nabika, T and Ribalta, J and Ruiz-Narvaez, E and Thomas, G. N and Tomlinson, B and Szalai, C and Vaverkova, H and Yamada, Y and Yang, Y and Kastelein, J. J and Tipping, R. W and Ford, C. E and Pressel, S. L and Ballantyne, C and Brautbar, A and Knuiman, M and Whincup, P. H and Wannamethee, S. G and Morris, R. W and Kiechl, S and Willeit, J and Santer, P and Mayr, A and Wald, N and Yarnell, J. W. G and Gallacher, J and Casiglia, E and ... and Triglyceride Coronary Dis Genetics and Triglyceride Coronary Disease Genetics Consortium and Emerging Risk Factors Collaboration and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Lancet, The, ISSN 0140-6736, 2010, Volume 375, Issue 9726, pp. 1634 - 1639
Journal Article