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science & technology (86) 86
life sciences & biomedicine (78) 78
humans (74) 74
female (48) 48
male (45) 45
adult (35) 35
inflammatory bowel disease (35) 35
crohn disease - genetics (34) 34
gastroenterology and hepatology (32) 32
middle aged (32) 32
gastroenterology & hepatology (30) 30
genetic predisposition to disease (30) 30
polymorphism, single nucleotide (27) 27
colitis, ulcerative - genetics (26) 26
case-control studies (25) 25
medicin och hälsovetenskap (25) 25
ulcerative colitis (24) 24
crohn's disease (23) 23
aged (22) 22
genetics (22) 22
genetics & heredity (22) 22
biological and medical sciences (21) 21
genetic aspects (21) 21
adolescent (20) 20
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genome-wide association study (18) 18
genotype (18) 18
inflammatory bowel diseases - genetics (18) 18
gastroenterology. liver. pancreas. abdomen (16) 16
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risk factors (16) 16
other diseases. semiology (15) 15
stomach. duodenum. small intestine. colon. rectum. anus (15) 15
child (14) 14
gene expression (14) 14
young adult (14) 14
inflammatory bowel diseases (13) 13
analysis (12) 12
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gene frequency (11) 11
genomics (11) 11
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abridged index medicus (10) 10
alleles (10) 10
biochemistry & molecular biology (10) 10
genes (10) 10
medical and health sciences (10) 10
studies (10) 10
genetic variation (9) 9
medicine (9) 9
phenotype (9) 9
achalasia (8) 8
clinical medicine (8) 8
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fundamental and applied biological sciences. psychology (8) 8
genomes (8) 8
klinisk medicin (8) 8
multidisciplinary sciences (8) 8
science & technology - other topics (8) 8
single nucleotide polymorphisms (8) 8
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gastroenterologi (7) 7
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genetic research (7) 7
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polymorphism, single nucleotide - genetics (7) 7
prognosis (7) 7
receptors, interleukin - genetics (7) 7
risk (7) 7
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biology (6) 6
crohn disease (6) 6
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genetics of eukaryotes. biological and molecular evolution (6) 6
linkage disequilibrium (6) 6
polymorphism, genetic (6) 6
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colitis, ulcerative - immunology (5) 5
crohn disease - pathology (5) 5
crohn’s disease (5) 5
gene expression profiling (5) 5
genetic predisposition to disease - genetics (5) 5
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logistic models (5) 5
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1. Full Text Do pancreatic cancer and chronic pancreatitis share the same genetic risk factors? A PANcreatic Disease ReseArch (PANDoRA) consortium investigation
by Campa, Daniele and Pastore, Manuela and Capurso, Gabriele and Hackert, Thilo and Di Leo, Milena and Izbicki, Jakob R and Khaw, Kay-Tee and Gioffreda, Domenica and Kupcinskas, Juozas and Pasquali, Claudio and Macinga, Peter and Kaaks, Rudolf and Stigliano, Serena and Peeters, Petra H and Key, Timothy J and Talar-Wojnarowska, Renata and Vodicka, Pavel and Valente, Roberto and Vashist, Yogesh K and Salvia, Roberto and Papaconstantinou, Ioannis and Shimizu, Yasuhiro and Valsuani, Chiara and Zambon, Carlo Federico and Gazouli, Maria and Valantiene, Irena and Niesen, Willem and Mohelnikova-Duchonova, Beatrice and Hara, Kazuo and Soucek, Pavel and Malecka-Panas, Ewa and Bueno-de-Mesquita, H. B. As and Johnson, Theron and Brenner, Herman and Tavano, Francesca and Fogar, Paola and Ito, Hidemi and Sperti, Cosimo and Butterbach, Katja and Latiano, Anna and Aniulli, Angelo and Cavestro, Giulia Martina and Busch, Olivier R. C and Dijk, Frederike and Greenhalf, William and Matsuo, Keitaro and Lombardo, Carlo and Strobel, Oliver and König, Anna-Katharina and Cuk, Katarina and Strothmann, Henik and Katzke, Verena and Cantore, Maurizio and Mambrini, Anea and Oliverius, Martin and Pezzilli, Raffaele and Landi, Stefano and Canzian, Federico
International journal of cancer, ISSN 0020-7136, 2018, Volume 142, Issue 2, pp. 290 - 296
association | genetic polymorphisms | Chronic pancreatitis | pancreatic ductal adenocarcinoma | Life Sciences & Biomedicine | Oncology | Science & Technology | Adenocarcinoma - pathology | Prognosis | Follow-Up Studies | Humans | Middle Aged | Pancreatic Neoplasms - pathology | Risk Factors | Male | Pancreatic Neoplasms - genetics | Pancreatitis, Chronic - genetics | Trypsinogen - genetics | Carcinoma, Pancreatic Ductal - pathology | Case-Control Studies | Carcinoma, Pancreatic Ductal - genetics | Pancreatitis, Chronic - pathology | Trypsin - genetics | Adult | Female | Adenocarcinoma - genetics | Aged | Biomarkers, Tumor - genetics | Polymorphism, Single Nucleotide | Retrospective Studies | Nuclear Proteins - genetics | Consortia | Oncology, Experimental | Pancreatic cancer | Pancreatitis | Genetic research | Disease susceptibility | Research | Investigations | Risk factors | Genetic polymorphisms | Cancer | Adenocarcinoma | Statistical analysis | Health risks | Single-nucleotide polymorphism | Inflammation | Risk analysis | Epidemiology | Loci | Studies | Health risk assessment | Pancreas | Genotypes | Index Medicus
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2. Full Text Genomewide Association Study of Severe Covid-19 with Respiratory Failure
by Ellinghaus, David and Degenhardt, Frauke and Bujanda, Luis and Buti, Maria and Albillos, Agustin and Invernizzi, Pietro and Fernandez, Javier and Prati, Daniele and Baselli, Guido and Asselta, Rosanna and Grimsrud, Marit M and Milani, Chiara and Aziz, Fatima and Kassens, Jan and May, Sandra and Wendorff, Mareike and Wienbrandt, Lars and Uellendahl-Werth, Florian and Zheng, Tenghao and Yi, Xiaoli and de Pablo, Raul and Chercoles, Adolfo G and Palom, Adriana and Garcia-Fernandez, Alba-Estela and Rodriguez-Frias, Francisco and Zanella, Alberto and Bandera, Alessandra and Protti, Alessandro and Aghemo, Alessio and Lleo, Ana and Biondi, Andrea and Caballero-Garralda, Andrea and Gori, Andrea and Tanck, Anja and Nolla, Anna Carreras and Latiano, Anna and Fracanzani, Anna Ludovica and Peschuck, Anna and Julia, Antonio and Pesenti, Antonio and Voza, Antonio and Jimenez, David and Mateos, Beatriz and Jimenez, Beatriz Nafria and Quereda, Carmen and Paccapelo, Cinzia and Gassner, Christoph and Angelini, Claudio and Cea, Cristina and Solier, Aurora and Pestana, David and Muniz-Diaz, Eduardo and Sandoval, Elena and Paraboschi, Elvezia M and Navas, Enrique and Sanchez, Felix Garcia and Ceriotti, Ferruccio and Martinelli-Boneschi, Filippo and Peyvandi, Flora and Blasi, Francesco and Tellez, Luis and Blanco-Grau, Albert and Hemmrich-Stanisak, Georg and Grasselli, Giacomo and Costantino, Giorgio and Cardamone, Giulia and Foti, Giuseppe and Aneli, Serena and Kurihara, Hayato and ElAbd, Hesham and My, Ilaria and Galvan-Femenia, Ivan and Martin, Javier and Erdmann, Jeanette and Ferrusquia-Acosta, Jose and Garcia-Etxebarria, Koldo and Izquierdo-Sanchez, Laura and Bettini, Laura R and Sumoy, Lauro and Terranova, Leonardo and Moreira, Leticia and Santoro, Luigi and Scudeller, Luigia and Mesonero, Francisco and Roade, Luisa and Ruhlemann, Malte C and Schaefer, Marco and Carrabba, Maria and Riveiro-Barciela, Mar and Basso, Maria E. Figuera and Valsecchi, Maria G and Hernandez-Tejero, Maria and Acosta-Herrera, Marialbert and D'Angio, Mariella and Baldini, Marina and Cazzaniga, Marina and Schulzky, Martin and Cecconi, Maurizio and Wittig, Michael and Ciccarelli, Michele and ... and The Severe Covid-19 GWAS Group and Severe Covid-19 GWAS Grp and Severe Covid-19 GWAS Group
The New England journal of medicine, ISSN 0028-4793, 10/2020, Volume 383, Issue 16, pp. 1522 - 1534
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Multigene Family | Pandemics | Humans | Middle Aged | Respiratory Insufficiency - etiology | Male | Genetic Loci | Case-Control Studies | COVID-19 | Chromosomes, Human, Pair 9 - genetics | SARS-CoV-2 | Pneumonia, Viral - genetics | Pneumonia, Viral - complications | ABO Blood-Group System - genetics | Betacoronavirus | Coronavirus Infections - complications | Female | Genetic Predisposition to Disease | Genome-Wide Association Study | Coronavirus Infections - genetics | Spain | Respiratory Insufficiency - genetics | Italy | Aged | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 3 - genetics | Disease susceptibility | Genetic aspects | Respiratory insufficiency | Epidemics | Blood group A | Disease | Pathogenesis | Association analysis | Single-nucleotide polymorphism | Ethics | Genetic factors | Blood groups | Drug dosages | Age | Ventilators | Medical research | Blood & organ donations | Susceptibility | Mortality | Phlebotomy | ABO system | RNA polymerase | Coronaviruses | Chromosome 3 | Severe acute respiratory syndrome coronavirus 2 | Blood group O | Hospitals | Chromosome 9 | Quality control | Informed consent | CCR9 protein | Index Medicus | Abridged Index Medicus | Medicin och hälsovetenskap
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3. Full Text microRNA‐mRNA network model in patients with achalasia
by Palmieri, Orazio and Mazza, Tommaso and Bassotti, Gabrio and Merla, Antonio and Tolone, Salvatore and Biagini, Tommaso and Cuttitta, Antonello and Bossa, Fabrizio and Martino, Giuseppina and Latiano, Tiziana and Corritore, Giuseppe and Gioffreda, Domenica and Palumbo, Orazio and Carella, Massimo and Panza, Anna and Andriulli, Angelo and Latiano, Anna
Neurogastroenterology and motility, ISSN 1350-1925, 03/2020, Volume 32, Issue 3, pp. e13764 - n/a
microRNA | mRNA | achalasia | expression profile | Gastroenterology & Hepatology | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | MicroRNAs | Achalasia | Nervous system | miRNA | Bioinformatics | Systems development | Index Medicus
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4. Full Text Gene expression of muscular and neuronal pathways is cooperatively dysregulated in patients with idiopathic Achalasia
by Palmieri, Orazio and Mazza, Tommaso and Merla, Antonio and Fusilli, Caterina and Cuttitta, Antonello and Martino, Giuseppina and Latiano, Tiziana and Corritore, Giuseppe and Bossa, Fabrizio and Palumbo, Orazio and Muscarella, Lucia Anna and Carella, Massimo and Graziano, Paolo and Andriulli, Angelo and Latiano, Anna
Scientific reports, ISSN 2045-2322, 08/2016, Volume 6, Issue 1, pp. 31549 - 31549
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Esophageal sphincter | Cytology | Smooth muscle | Genomes | TLR4 protein | Peristalsis | Sphincter | Gene expression | Muscle contraction | Skeletal muscle | Immune response (humoral) | Esophagus | Interleukin 18 | Neurological diseases | Enteric nervous system | DNA microarrays | Morphology | Interleukin 1 | Toll-like receptors | Achalasia | Myenteric plexus | Histocompatibility antigen HLA | Index Medicus
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5. Full Text Transcriptome and gene fusion analysis of synchronous lesions reveals LNCMRPS31P5 as a novel transcript involved in colorectal cancer
by Panza, Anna and Castellana, Stefano and Biscaglia, Giuseppe and Piepoli, Ada and Parca, Luca and Gentile, Annamaria and Latiano, Anna and Mazza, Tommaso and Perri, Francesco and Andriulli, Angelo and Palmieri, Orazio
International journal of molecular sciences, ISSN 1661-6596, 10/2020, Volume 21, Issue 19, pp. 1 - 15
Sporadic CRC | Fusion genes | RNA-Seq | MRPS31P5 | LncRNAs | Synchronous lesions | Biochemistry & Molecular Biology | Physical Sciences | Chemistry | Life Sciences & Biomedicine | Chemistry, Multidisciplinary | Science & Technology | RNA sequencing | Epigenetic inheritance | Scientific equipment and supplies industry | MicroRNA | Analysis | Genes | Development and progression | Genetic aspects | Instrument industry | Gene expression | Apoptosis | Cancer | Index Medicus | fusion genes | lncRNAs | synchronous lesions | sporadic CRC
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6. Full Text Replication of interleukin 23 receptor and autophagy-related 16-like 1 association in adult-and pediatric-onset inflammatory bowel disease in Italy
by Anna Latiano Orazio Palmieri Maria Rosa Valvano Renata Dtnca Salvatore Cucchiara Gabriele Riegler Anna Maria Staiano Sandro Ardizzone Salvatore Accomando Gian Luigi de Angelis Giuseppe Corritore Fabrizio Bossa Vito Annese
World journal of gastroenterology : WJG, ISSN 1007-9327, 2008, Volume 14, Issue 29, pp. 4643 - 4651
遗传因素 | 结肠疾病 | 肠溃疡 | Genetic predisposition | Inflammatory bowel disease | Autophagy-related 16-like 1 | Genome-wide association study | Pediatric inflammatory bowel disease | Crohn's disease | Interleukin 23 receptor | Ulcerative colitis | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Crohn Disease - genetics | Autophagy-Related Proteins | Humans | Middle Aged | Child, Preschool | Infant | Male | Nod2 Signaling Adaptor Protein - genetics | Crohn Disease - ethnology | Case-Control Studies | Young Adult | Solute Carrier Family 22 Member 5 | Inflammatory Bowel Diseases - genetics | Adult | Female | Child | Genetic Predisposition to Disease - genetics | Genotype | Logistic Models | Receptors, Interleukin - genetics | Carrier Proteins - genetics | Adolescent | Age of Onset | Polymorphism, Single Nucleotide - genetics | Italy | Aged | Organic Cation Transport Proteins - genetics | Inflammatory Bowel Diseases - ethnology | Index Medicus | Clinical Research | Crohn’s disease
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7. Full Text Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
by Rivas, Manuel A and Beaudoin, Mélissa and Gardet, Agnes and Stevens, Christine and Sharma, Yashoda and Zhang, Clarence K and Boucher, Gabrielle and Ripke, Stephan and Ellinghaus, David and Burtt, Noel and Fennell, Tim and Kirby, Anew and Latiano, Anna and Goyette, Philippe and Green, Todd and Halfvarson, Jonas and Haritunians, Talin and Korn, Joshua M and Kuruvilla, Finny and Lagacé, Caroline and Neale, Benjamin and Lo, Ken Sin and Schumm, Phil and Törkvist, Leif and Dubinsky, Marla C and Brant, Steven R and Silverberg, Mark S and Duerr, Richard H and Altshuler, David and Gabriel, Stacey and Lettre, Guillaume and Franke, Ane and D'Amato, Mauro and McGovern, Dermot P. B and Cho, Judy H and Rioux, John D and Xavier, Ramnik J and Daly, Mark J and United Kingdom Inflammatory Bowel and Natl Inst Diabet Digestive Kidney and Int Inflammatory Bowel Dis and United Kingdom Inflammatory Bowel Disease Genetics Consortium and National Institute of Diabetes and Digestive Kidney Diseases Inflammatory Bowel Disease Genetics Consortium (NIDDK IBDGC) and International Inflammatory Bowel Disease Genetics Consortium
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 11, pp. 1066 - 1073
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | Cell Line | Genetic Predisposition to Disease | Genome-Wide Association Study | RNA Splicing | Humans | Inflammatory Bowel Diseases - genetics | Nod2 Signaling Adaptor Protein - genetics | Receptors, Interleukin - genetics | Sequence Analysis, DNA | Case-Control Studies | Inflammatory bowel disease | Studies | Design | Medical research | Genealogy | Genes | Genetics | Data processing | Genomes | Grants | Diabetes | Twins | Index Medicus | Medicin och hälsovetenskap
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8. Full Text Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease
by Ventham, N.T and Kennedy, N.A and Adams, A.T and Kalla, R and Heath, S and O'Leary, K.R and Drummond, H and Wilson, D.C and Gut, I.G and Nimmo, E.R and Satsangi, J and Lauc, Gordan and Campbell, Harry and McGovern, Dermot P.B and Annese, Vito and Zoldoš, Vlatka and Permberton, Iain K and Wuhrer, Manfred and Kolarich, Daniel and Fernandes, Daryl L and Theorodorou, Evropi and Merrick, Victoria and Spencer, Daniel I and Gardner, Richard A and Doran, Ray and Shubhakar, Archana and Boyapati, Ray and Rudan, Igor and Lionetti, Paolo and Akmačić, Irena Trbojević and Krištić, Jasminka and Vučković, Frano and Štambuk, Jerko and Novokmet, Mislav and Pučić-Baković, Maja and Gornik, Olga and Andriulli, Angelo and Cantoro, Laura and Sturniolo, Giancarlo and Fiorino, Gionata and Manetti, Natalia and Latiano, Anna and Kohn, Anna and D'Incà, Renata and Danese, Silvio and Arnott, Ian D and Noble, Colin L and Lees, Charlie W and Shand, Alan G and Ho, Gwo-Tzer and Dunlop, Malcolm G and Murphy, Lee and Gibson, Jude and Evenden, Louise and Wrobel, Nicola and Gilchrist, Tamara and Fawkes, Angie and Kammeijer, Guinevere S.M and Clerc, Florent and De Haan, Noortje and Vojta, Aleksandar and Samaržija, Ivana and Markulin, Dora and Klasić, Marija and Dobrinić, Paula and Aulchenko, Yurii and Van Den Heuve, Tim and Jonkers, Daisy and Pierik, Marieke and Vatn, Simen and Ricanek, Petr and Jahnsen, Jørgen and You, Panpan and Sølvernes, Janne and Frengen, Anna B and Tannæs, Tone M and Moen, Aina E.F and Dahl, Fredrik A and Lindstrøm, Jonas Christoffer and Ekeland, Gunn S and Detlie, Trond Espen and Keita, Åsa V and Söderholm, Johan D and Hjortswang, Henrik and Halfvarson, Jonas and Bergemalm, Daniel and Gomollón, Fernando and D'Amato, Mauro and Törkvist, Leif and Hjelm, Fredrik and Gullberg, Mats and Nordberg, Niklas and Ocklind, Anette and Pettersson, Erik and Ekman, Daniel and Sundell, Mikael and Modig, Eddie and Veillard, Anne-Clémence and Schoemans, Renaud and Poncelet, Dominique and ... and IBD CHARACTER Consortiumw and IBD BIOM Consortium and IBD CHARACTER consortium and IBD BIOM consortium
Nature communications, ISSN 2041-1723, 11/2016, Volume 7, Issue 1, pp. 13507 - 13507
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Crohn Disease - genetics | Epigenesis, Genetic | Humans | Middle Aged | Colitis, Ulcerative - genetics | Male | Gene-Environment Interaction | Case-Control Studies | Protein-Tyrosine Kinases - genetics | Epigenomics - methods | Adult | Female | Promoter Regions, Genetic | Genetic Predisposition to Disease | Membrane Proteins - genetics | Gene Expression Profiling - methods | Genotype | DNA Methylation - genetics | Colitis, Ulcerative - blood | Linkage Disequilibrium | Crohn Disease - blood | MicroRNAs - genetics | Polymorphism, Single Nucleotide | Cohort Studies | Quantitative Trait Loci - genetics | Index Medicus | Medicin och hälsovetenskap
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