X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (159786) 159786
Newspaper Article (9617) 9617
Newsletter (2426) 2426
Book Chapter (801) 801
Dissertation (219) 219
Book / eBook (196) 196
Magazine Article (154) 154
Conference Proceeding (66) 66
Trade Publication Article (61) 61
Publication (50) 50
Web Resource (38) 38
Government Document (35) 35
Transcript (34) 34
Book Review (33) 33
Reference (19) 19
Journal / eJournal (8) 8
Streaming Video (6) 6
Data Set (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
lipids (81998) 81998
humans (64270) 64270
animals (62363) 62363
male (37910) 37910
female (30295) 30295
biochemistry & molecular biology (29816) 29816
mice (28610) 28610
proteins (26488) 26488
metabolism (23525) 23525
research (23073) 23073
cholesterol (22011) 22011
lipid metabolism (21042) 21042
physiological aspects (20053) 20053
cell biology (18342) 18342
analysis (18171) 18171
gene expression (18123) 18123
research article (18091) 18091
oxidative stress (17870) 17870
multidisciplinary sciences (17430) 17430
fatty acids (16437) 16437
medicine (15359) 15359
expression (13588) 13588
adult (13430) 13430
life sciences (13406) 13406
middle aged (13246) 13246
rats (12919) 12919
science (12852) 12852
enzymes (12829) 12829
studies (12772) 12772
biochemistry (12192) 12192
genetic aspects (11977) 11977
obesity (11126) 11126
inflammation (10814) 10814
rodents (10760) 10760
risk factors (10724) 10724
microbiology (10591) 10591
genes (10236) 10236
mutation (10225) 10225
lipid-peroxidation (10200) 10200
liver (10190) 10190
health aspects (10103) 10103
physiology (10056) 10056
biology (9914) 9914
cardiovascular disease (9864) 9864
genetics (9828) 9828
lipid peroxidation (9797) 9797
atherosclerosis (9507) 9507
lipids - blood (9465) 9465
diet (9415) 9415
signal transduction (9273) 9273
antioxidants (8899) 8899
molecular sequence data (8723) 8723
mice, inbred c57bl (8621) 8621
endocrinology & metabolism (8529) 8529
diabetes (8433) 8433
apoptosis (8338) 8338
cells (8192) 8192
liver - metabolism (7937) 7937
aged (7845) 7845
nutrition & dietetics (7633) 7633
glucose (7557) 7557
lipoproteins (7456) 7456
biosynthesis (7422) 7422
triglycerides (7350) 7350
carbohydrates (7293) 7293
insulin resistance (7282) 7282
gene-expression (7154) 7154
cancer (7003) 7003
protein (6971) 6971
mice, knockout (6892) 6892
disease (6859) 6859
cells, cultured (6805) 6805
pharmacology & pharmacy (6804) 6804
cell line (6753) 6753
biotechnology & applied microbiology (6720) 6720
amino acid sequence (6691) 6691
immunology (6672) 6672
activation (6652) 6652
plant sciences (6625) 6625
genetics & heredity (6476) 6476
insulin (6448) 6448
insulin-resistance (6430) 6430
biology and life sciences (6333) 6333
identification (6084) 6084
homeostasis (6055) 6055
medicine, research & experimental (6051) 6051
nutrition (6046) 6046
bacteria (6044) 6044
kinases (6030) 6030
protein binding (5858) 5858
membranes (5773) 5773
gene (5737) 5737
disease models, animal (5628) 5628
growth (5484) 5484
neurosciences (5480) 5480
biophysics (5267) 5267
metabolites (5229) 5229
biotechnology (5219) 5219
biochemistry, general (5194) 5194
oncology (5182) 5182
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (61) 61
Online Resources - Online (28) 28
Collection Dvlpm't (Acquisitions) - Vendor file (11) 11
UofT at Mississauga - Stacks (11) 11
Earth Sciences (Noranda) - Stacks (10) 10
UofT at Scarborough - Stacks (8) 8
Chemistry (A D Allen) - Stacks (3) 3
UTL at Downsview - May be requested (3) 3
Collection Dvlpm't (Acquisitions) - Closed Orders (2) 2
Engineering & Comp. Sci. - Stacks (2) 2
St. Michael's Hospital - Stacks (2) 2
Chemistry (A D Allen) - May be requested in 6-10 wks (1) 1
Gerstein Science - Bindery (1) 1
Gerstein Science - Periodical Stacks (1) 1
Gerstein Science - Theses (1) 1
Scarborough Hospital - Online (1) 1
St Josephs Health Centre - Stacks (1) 1
St. Michael's College (John M. Kelly) - Circulation Desk (1) 1
Sunnybrook Health Sciences Centre - Online (1) 1
UTL at Downsview - Bindery (1) 1
UTL at Downsview - Periodical Stacks (1) 1
University Archives - Archives (1) 1
UofT at Mississauga - Missing (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (171725) 171725
Japanese (839) 839
Chinese (419) 419
Russian (389) 389
German (360) 360
French (291) 291
Spanish (159) 159
Portuguese (136) 136
Polish (80) 80
Czech (59) 59
Italian (42) 42
Hungarian (18) 18
Korean (16) 16
Ukrainian (14) 14
Dutch (13) 13
Turkish (12) 12
Norwegian (10) 10
Slovak (9) 9
Romanian (8) 8
Serbian (8) 8
Danish (6) 6
Bulgarian (5) 5
Finnish (5) 5
Arabic (4) 4
Persian (4) 4
Hebrew (3) 3
Catalan (2) 2
Lithuanian (1) 1
Slovenian (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


International Journal of Dermatology, ISSN 0011-9059, 12/2017, Volume 56, Issue 12, pp. 1406 - 1413
Background Genodermatoses represent genetic anomalies of skin tissues including hair follicles, sebaceous glands, eccrine glands, nails, and teeth... 
KINDLER-SYNDROME | KINDLIN-1 | PROTEIN | MUTATION | VII COLLAGEN | SPECTRUM | DYSTROPHIC EPIDERMOLYSIS-BULLOSA | IDENTIFICATION | DERMATOLOGY | Rare Diseases - genetics | 1-Acylglycerol-3-Phosphate O-Acyltransferase - genetics | Endonucleases - genetics | Lipid Metabolism, Inborn Errors - genetics | Sjogren-Larsson Syndrome - genetics | Xeroderma Pigmentosum - genetics | Humans | Male | Mitochondrial Proteins - genetics | Ichthyosis Vulgaris - genetics | INDEL Mutation | Skin Diseases, Genetic - genetics | Exome | Epidermolysis Bullosa - genetics | DNA Mutational Analysis | Intermediate Filament Proteins - genetics | Female | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Periodontal Diseases - genetics | Protoporphyrinogen Oxidase - genetics | Porphyria, Variegate - genetics | Photosensitivity Disorders - genetics | Epidermolysis Bullosa Simplex - genetics | Flavoproteins - genetics | Membrane Proteins - genetics | Collagen Type VII - genetics | Aldehyde Oxidoreductases - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Blister - genetics | Keratin-14 - genetics | Homozygote | Phenotype | Ichthyosis, Lamellar - genetics | Pedigree | Lipoxygenase - genetics | Consanguinity | Epidermolysis Bullosa Dystrophica - genetics | Muscular Diseases - genetics | Ichthyosiform Erythroderma, Congenital - genetics | Genetic research | Skin | Nucleotide sequencing | Genes | DNA sequencing | Sebaceous glands | Nails | Glands | Teeth | Disorders | Homozygosity | Tissues | Follicles | Gene sequencing | Genodermatosis | Gene mapping
Journal Article
Neuron, ISSN 0896-6273, 04/2013, Volume 78, Issue 1, pp. 57 - 64
Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. VCP mutations are the cause of inclusion body myopathy,... 
LIPID-PEROXIDATION | SPINAL-CORD PATHOLOGY | MOUSE MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | DYSFUNCTION | BONE | NEUROSCIENCES | PAGET-DISEASE | TRANSGENIC MICE | REVEALS | RNA, Small Interfering - genetics | Humans | Middle Aged | Male | Frontotemporal Dementia - metabolism | Neurons - ultrastructure | Muscular Dystrophies, Limb-Girdle - genetics | Adenosine Triphosphate - metabolism | Membrane Potential, Mitochondrial - genetics | Muscular Dystrophies, Limb-Girdle - pathology | NAD - metabolism | Fibroblasts - metabolism | Animals, Newborn | Frontotemporal Dementia - genetics | Magnesium - metabolism | Mitochondria - pathology | Fibroblasts - pathology | Mutation - genetics | Myositis, Inclusion Body - genetics | Osteitis Deformans - pathology | Muscular Dystrophies, Limb-Girdle - metabolism | Analysis of Variance | Luminescent Proteins - genetics | Adenosine Triphosphatases - genetics | Mice | Lipid Peroxidation - genetics | RNA, Small Interfering - metabolism | Valosin Containing Protein | Osteitis Deformans - metabolism | Family Health | Cerebral Cortex - cytology | Case-Control Studies | Osteitis Deformans - genetics | Transfection | Mitochondria - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Adult | Female | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Adenosine Triphosphatases - deficiency | Mice, Inbred C57BL | Cells, Cultured | Cell Cycle Proteins - deficiency | Mitochondria - metabolism | Animals | Oxygen Consumption - genetics | Myositis, Inclusion Body - metabolism | Aged | Nervous system diseases | Neurosciences | Genes | Amyotrophic lateral sclerosis | Genetic aspects | Adenosine triphosphatase | Dementia | Proteins | Medical research | Phosphorylation | Biomedical research | Disease | Rodents | Respiration | Experiments | Patients | Report
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 5, p. e10693
...; however, non-genetic variations, alone or in combination with genetics, may also influence expression traits and have a critical role in physiological and disease processes... 
VARIANTS | MACROPHAGES | MULTIDISCIPLINARY SCIENCES | GENES | RISK | LOCI | SMOKING | EXPRESSION PROFILES | HAPLOTYPE | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Smoking - adverse effects | Monocytes - cytology | Atherosclerosis - genetics | Humans | Middle Aged | Male | Monocytes - metabolism | Gene Expression Profiling | Cell Movement - genetics | Genetic Variation | Base Sequence | DNA Probes - metabolism | Adult | Female | Genetic Predisposition to Disease | Genome-Wide Association Study | Quantitative Trait, Heritable | Risk Factors | Gene Expression Regulation | Smoking - genetics | Chromosomes, Human, Pair 21 - genetics | Genome, Human - genetics | Phenotype | Polymorphism, Single Nucleotide - genetics | Aged | Immunity - genetics | Quantitative Trait Loci - genetics | Medical research | Genomics | Genes | Disease susceptibility | Gene expression | Mediation | Risk factors | Quantitative genetics | Analysis | Atherosclerosis | Physiological aspects | Medicine, Experimental | Genetic aspects | Cardiovascular diseases | Smoking | Genetic variability | Pathogenesis | Variability | Colorectal cancer | Lipids | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Immunity | Medical schools | Body mass index | Risk assessment | Genetic analysis | Genetics | Blood pressure | Cytokines | Phenotypic variations | Health risks | Genetic diversity | Risk analysis | Cigarette smoking | Loci | Quantitative trait loci | Studies | Monocytes | Body mass | Attention Deficit Hyperactivity Disorder | Arteriosclerosis | Body size | Chemokines
Journal Article
PLoS genetics, ISSN 1553-7404, 2017, Volume 13, Issue 10, p. e1007079
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 02/2011, Volume 52, Issue 2, pp. 189 - 206
Journal Article
by Kilpeläinen, Tuomas O and Bentley, Amy R and Noordam, Raymond and Sung, Yun Ju and Schwander, Karen and Winkler, Thomas W and Jakupović, Hermina and Chasman, Daniel I and Manning, Alisa and Ntalla, Ioanna and Aschard, Hugues and Brown, Michael R and de las Fuentes, Lisa and Franceschini, Nora and Guo, Xiuqing and Vojinovic, Dina and Aslibekyan, Stella and Feitosa, Mary F and Kho, Minjung and Musani, Solomon K and Richard, Melissa and Wang, Heming and Wang, Zhe and Bartz, Traci M and Bielak, Lawrence F and Campbell, Archie and Dorajoo, Rajkumar and Fisher, Virginia and Hartwig, Fernando P and Horimoto, Andrea R. V. R and Li, Changwei and Lohman, Kurt K and Marten, Jonathan and Sim, Xueling and Smith, Albert V and Tajuddin, Salman M and Alver, Maris and Amini, Marzyeh and Boissel, Mathilde and Chai, Jin Fang and Chen, Xu and Divers, Jasmin and Evangelou, Evangelos and Gao, Chuan and Graff, Mariaelisa and Harris, Sarah E and He, Meian and Hsu, Fang-Chi and Jackson, Anne U and Zhao, Jing Hua and Kraja, Aldi T and Kühnel, Brigitte and Laguzzi, Federica and Lyytikäinen, Leo-Pekka and Nolte, Ilja M and Rauramaa, Rainer and Riaz, Muhammad and Robino, Antonietta and Rueedi, Rico and Stringham, Heather M and Takeuchi, Fumihiko and van der Most, Peter J and Varga, Tibor V and Verweij, Niek and Ware, Erin B and Wen, Wanqing and Li, Xiaoyin and Yanek, Lisa R and Amin, Najaf and Arnett, Donna K and Boerwinkle, Eric and Brumat, Marco and Cade, Brian and Canouil, Mickaël and Chen, Yii-Der Ida and Concas, Maria Pina and Connell, John and de Mutsert, Renée and de Silva, H. Janaka and de Vries, Paul S and Demirkan, Ayşe and Ding, Jingzhong and Eaton, Charles B and Faul, Jessica D and Friedlander, Yechiel and Gabriel, Kelley P and Ghanbari, Mohsen and Giulianini, Franco and Gu, Chi Charles and Gu, Dongfeng and Harris, Tamara B and He, Jiang and Heikkinen, Sami and Heng, Chew-Kiat and Hunt, Steven C and Ikram, M. Arfan and Jonas, Jost B and Koh, Woon-Puay and Komulainen, Pirjo and Krieger, Jose E and ... and Lifelines Cohort Study and et al
Nature communications, ISSN 2041-1723, 2019, Volume 10, Issue 1, pp. 1 - 11
Journal Article
PLoS biology, ISSN 1545-7885, 2011, Volume 9, Issue 2, p. e1000595
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2014, Volume 111, Issue 31, pp. 11491 - 11496
.... Genetic transfer of these mutations into the human TB agent, Mycobacterium tuberculosis, resulted in downregulation of the PhoP regulon, with loss of biologically active lipids, reduced secretion... 
Mycobacterium | Tuberculosis | Mycobacterium tuberculosis | Mycobacterium bovis | Secretion | Humans | Virulence | Alleles | Lipids | Genetic mutation | Evolution | Phylogeny | Zoonosis | Adaptation | MYCOBACTERIUM-TUBERCULOSIS | COMPLEX | UNITED-KINGDOM | MULTIDISCIPLINARY SCIENCES | CATTLE | adaptation | evolution | IDENTIFICATION | zoonosis | LIPID BIOSYNTHESIS | GENE-CLUSTER | BOVIS | phylogeny | INFECTION | SECRETION | Conserved Sequence - genetics | Bacterial Proteins - genetics | Tuberculosis - microbiology | Antigens, Bacterial | Bacterial Proteins - secretion | Mutation - genetics | Mycobacterium - genetics | Biological Evolution | Host-Pathogen Interactions | Mycobacterium tuberculosis - pathogenicity | Animals | Tuberculosis - genetics | Virulence - genetics | Cattle | Gene Deletion | Polymorphism, Single Nucleotide - genetics | Mutagenesis, Insertional | Mycobacterium bovis - pathogenicity | Mycobacterium bovis - genetics | Mycobacterium tuberculosis - genetics | Tuberculosis in cattle | Microbiological research | Research | Natural history | Microbial mutation | Mycobacterium tuberculosis / pathogenicity | Tuberculosis / microbiology | Life Sciences | Bacterial Proteins / genetics | Conserved Sequence / genetics | Bacterial Proteins / metabolism | Virulence / genetics | Mycobacterium bovis / pathogenicity | Tuberculosis / genetics | Mycobacterium tuberculosis / genetics | Bacteriology | Mycobacterium bovis / genetics | Microbiology and Parasitology | Polymorphism, Single Nucleotide / genetics | Mutation / genetics | Mycobacterium / genetics | Biological Sciences
Journal Article