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science & technology (15) 15
cancer (10) 10
humans (10) 10
life sciences & biomedicine (10) 10
genomes (8) 8
research (8) 8
dna (7) 7
genetic aspects (7) 7
leukemia, lymphocytic, chronic, b-cell - genetics (7) 7
methylation (7) 7
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tumors (5) 5
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genètica (4) 4
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epigenetics (3) 3
gene expression (3) 3
gene mutations (3) 3
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hematologic and hematopoietic diseases (3) 3
high-throughput nucleotide sequencing (3) 3
leukemias. malignant lymphomas. malignant reticulosis. myelofibrosis (3) 3
lymphatic leukemia (3) 3
medical sciences (3) 3
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physiological aspects (3) 3
àrees temàtiques de la upc (3) 3
aged (2) 2
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cell differentiation (2) 2
ciències de la salut (2) 2
cohort studies (2) 2
cpg islands (2) 2
cpg islands - genetics (2) 2
dna methylation - genetics (2) 2
dna mutational analysis (2) 2
dna sequencing (2) 2
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fundamental and applied biological sciences. psychology (2) 2
gene sequencing (2) 2
genetics of eukaryotes. biological and molecular evolution (2) 2
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immunoglobulins (2) 2
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leukemia, lymphocytic, chronic, b-cell - pathology (2) 2
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parallel programming models (2) 2
promoter regions, genetic (2) 2
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signature analysis (2) 2
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studies (2) 2
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1. Full Text Epigenomic analysis detects aberrant super-enhancer DNA methylation in human cancer
by Heyn, Holger and Vidal, Enrique and Ferreira, Humberto J and Vizoso, Miguel and Sayols, Sergi and Gomez, Antonio and Moran, Sebastian and Boque-Sastre, Raquel and Guil, Sonia and Martinez-Cardus, Anna and Lin, Charles Y and Royo, Romina and Sanchez-Mut, Jose V and Martinez, Ramon and Gut, Marta and Torrents, David and Orozco, Modesto and Gut, Ivo and Young, Richard A and Esteller, Manel
Genome Biology, ISSN 1474-7596, 01/2016, Volume 17, Issue 1, pp. 11 - 11
DNA methylation | Super-enhancer | Epigenomics | Cancer | Genetics & Heredity | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Promoter Regions, Genetic | Neoplasms - genetics | Humans | CpG Islands - genetics | DNA Methylation - genetics | High-Throughput Nucleotide Sequencing | Genome, Human | Phenotypes | Transcription factors | Bisulfite | Nucleotide sequence | Lung cancer | Colorectal cancer | Genomes | Breast cancer | Regulatory sequences | Metastasis | Gene expression | Carcinogenesis | Gene silencing | Enhancers | Epigenetics | Deoxyribonucleic acid--DNA | Tumors | CpG islands | Index Medicus | Aspectes genètics | Càncer | Dany | Research | ADN | Enginyeria biomèdica | DNA | Analysis | Àrees temàtiques de la UPC
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2. Full Text Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia
by Kulis, Marta and Heath, Simon and Bibikova, Marina and Queirós, Ana C and Navarro, Alba and Clot, Guillem and Martínez-Trillos, Alejandra and Castellano, Giancarlo and Brun-Heath, Isabelle and Pinyol, Magda and Barberán-Soler, Sergio and Papasaikas, Panagiotis and Jares, Pedro and Beà, Sílvia and Rico, Daniel and Ecker, Simone and Rubio, Miriam and Royo, Romina and Ho, Vincent and Klotzle, Brandy and Hernández, Lluis and Conde, Laura and López-Guerra, Mónica and Colomer, Dolors and Villamor, Neus and Aymerich, Marta and Rozman, María and Bayes, Mónica and Gut, Marta and Gelpí, Josep L and Orozco, Modesto and Fan, Jian-Bing and Quesada, Víctor and Puente, Xose S and Pisano, David G and Valencia, Alfonso and López-Guillermo, Armando and Gut, Ivo and López-Otín, Carlos and Campo, Elías and Martín-Subero, José I
Nature genetics, ISSN 1061-4036, 11/2012, Volume 44, Issue 11, pp. 1236 - 1242
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Hematologic and hematopoietic diseases | Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Alternative Splicing | Humans | Middle Aged | Gene Expression Regulation | Male | DNA Methylation - genetics | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Epigenesis, Genetic - genetics | Aged, 80 and over | CpG Islands - genetics | Adult | Female | Aged | High-Throughput Nucleotide Sequencing | Genome, Human | B-Lymphocytes - metabolism | Chronic lymphocytic leukemia | DNA | Physiological aspects | Genetic aspects | Research | Methylation | Risk factors | Proteins | Cytokines | DNA methylation | Epigenetics | Genetics | Principal components analysis | Genomes | Experiments | Deoxyribonucleic acid--DNA | Index Medicus | Bisulfite
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3. Full Text A practical guide for mutational signature analysis in hematological malignancies
by Maura, Francesco and Degasperi, Andrea and Nadeu, Ferran and Leongamornlert, Daniel and Davies, Helen and Moore, Luiza and Royo, Romina and Ziccheddu, Bachisio and Puente, Xose S and Avet-Loiseau, Herve and Cambell, Peter J and Nik-Zainal, Serena and Campo, Elias and Munshi, Nikhil and Bolli, Niccolò
Nature communications, ISSN 2041-1723, 12/2019, Volume 10, Issue 1, pp. 2969 - 12
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Computational Biology - methods | Datasets as Topic | DNA Mutational Analysis - standards | Humans | Whole Genome Sequencing - standards | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Whole Genome Sequencing - methods | DNA Mutational Analysis - methods | High-Throughput Nucleotide Sequencing - standards | BRCA1 Protein - genetics | Mutation | Computational Biology - standards | High-Throughput Nucleotide Sequencing - methods | BRCA2 Protein - genetics | Multiple Myeloma - genetics | Leukemia, Myeloid, Acute - genetics | Practice Guidelines as Topic | BRCA2 protein | Chronic lymphatic leukemia | Hematology | BRCA1 protein | Myeloid leukemia | Pathogenesis | Leukemia | Homologous recombination | Genomics | Multiple myeloma | Homology | Breast cancer | Lymphatic leukemia | Decision analysis | Gene sequencing | Signature analysis | Signatures | Acute myeloid leukemia | Index Medicus | Immunological aspects | Càncer | Mutational signatures | Aspectes immunològics | Hematological malignancies | Àrees temàtiques de la UPC | Ciències de la salut | Cancer
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4. Full Text Minimal spatial heterogeneity in chronic lymphocytic leukemia at diagnosis
by Nadeu, Ferran and Royo, Romina and Maura, Francesco and Dawson, Kevin J and Dueso-Barroso, Ana and Aymerich, Marta and Pinyol, Magda and Bea, Silvia and Lopez-Guillermo, Armando and Delgado, Julio and Puente, Xose S and Campo, Elias
Leukemia, ISSN 0887-6924, 07/2020, Volume 34, Issue 7, pp. 1929 - 1933
Oncology | Life Sciences & Biomedicine | Hematology | Science & Technology | Leukocytes, Mononuclear - metabolism | Lymph Nodes - pathology | Prognosis | Follow-Up Studies | Humans | Middle Aged | Lymph Nodes - metabolism | Male | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Genetic Heterogeneity | Leukemia, Lymphocytic, Chronic, B-Cell - pathology | Whole Exome Sequencing | Whole Genome Sequencing | Leukocytes, Mononuclear - pathology | Spatial Analysis | Leukemia, Lymphocytic, Chronic, B-Cell - classification | Bone Marrow - metabolism | Bone Marrow - pathology | Aged, 80 and over | Female | Aged | Cohort Studies | B cells | Spatial heterogeneity | Heterogeneity | Chronic lymphatic leukemia | Lymphatic leukemia | Leukemia | Index Medicus
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5. Full Text Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads
by Moncunill, Valentí and Gonzalez, Santi and Beà, Sílvia and Andrieux, Lise O and Salaverria, Itziar and Royo, Cristina and Martinez, Laura and Puiggròs, Montserrat and Segura-Wang, Maia and Stütz, Adrian M and Navarro, Alba and Royo, Romina and Gelpí, Josep L and Gut, Ivo G and López-Otín, Carlos and Orozco, Modesto and Korbel, Jan O and Campo, Elias and Puente, Xose S and Torrents, David
Nature biotechnology, ISSN 1087-0156, 11/2014, Volume 32, Issue 11, pp. 1106 - 1112
Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Science & Technology | Genetic Variation | Neoplasms - genetics | Humans | Nucleotides - genetics | Chromosome Mapping | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Mutation | Genome, Human | Oncology, Experimental | Genetic research | Genetic aspects | Research | Nucleotide sequencing | Cancer | DNA sequencing | Genomics | Biomedical research | Index Medicus
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6. Full Text Non-coding recurrent mutations in chronic lymphocytic leukaemia
by Puente, X.S and Bea, S and Valdes-Mas, R and Villamor, N and Gutierrez-Abril, J and Martin-Subero, J.I and Munar, M and Rubio-Perez, C and Jares, P and Aymerich, M and Baumann, T and Beekman, R and Belver, L and Carrio, A and Castellano, G and Clot, G and Colado, E and Colomer, D and Costa, D and Delgado, J and Enjuanes, A and Estivill, X and Ferrando, A.A and Gelpi, J.L and Gonzalez, B and Gonzalez, S and Gonzalez, M and Gut, M and Hernandez-Rivas, J.M and Lopez-Guerra, M and Martin-Garcia, D and Navarro, A and Nicolas, P and Orozco, M and Payer, A.R and Pinyol, M and Pisano, D.G and Puente, D.A and Queiros, A.C and Quesada, V and Romeo-Casabona, C.M and Royo, C and Royo, R and Rozman, M and Russinol, N and Salaverria, I and Stamatopoulos, K and Stunnenberg, H.G and Tamborero, D and Terol, M.J and Valencia, A and Lopez-Bigas, N and Torrents, D and Gut, I and Lopez-Guillermo, A and Lopez-Otin, C and Campo, E
Nature (London), ISSN 0028-0836, 2015, Volume 526, Issue 7574, pp. 519 - 524
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Alternative Splicing - genetics | Genomics | Humans | PAX5 Transcription Factor - genetics | 3' Untranslated Regions - genetics | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Receptor, Notch1 - metabolism | Transcription Factors - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Leukemia, Lymphocytic, Chronic, B-Cell - pathology | Carrier Proteins - genetics | Chromosomes, Human, Pair 9 - genetics | DNA Mutational Analysis | Leukemia, Lymphocytic, Chronic, B-Cell - metabolism | PAX5 Transcription Factor - biosynthesis | Enhancer Elements, Genetic - genetics | DNA, Neoplasm - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - genetics | Nuclear Proteins - genetics | Receptor, Notch1 - genetics | B-Lymphocytes - metabolism | Chronic lymphocytic leukemia | Relapse | Genetic aspects | Diseases | Studies | Immunoglobulins | Medical prognosis | Leukemia | Cell cycle | Genomes | Mutation | Multivariate analysis | Gene expression | Tumors | Index Medicus
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7. Full Text IgCaller for reconstructing immunoglobulin gene rearrangements and oncogenic translocations from whole-genome sequencing in lymphoid neoplasms
by Nadeu, Ferran and Mas-de-les-Valls, Rut and Navarro, Alba and Royo, Romina and Martin, Silvia and Villamor, Neus and Suarez-Cisneros, Helena and Mares, Roso and Lu, Junyan and Enjuanes, Anna and Rivas-Delgado, Alfredo and Aymerich, Marta and Baumann, Tycho and Colomer, Dolors and Delgado, Julio and Morin, Ryan D and Zenz, Thorsten and Puente, Xose S and Campbell, Peter J and Bea, Silvia and Maura, Francesco and Campo, Elias
Nature communications, ISSN 2041-1723, 07/2020, Volume 11, Issue 1, pp. 3390 - 3390
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Translocation | Immunoglobulins | Recombination | Fluorescence | Chains | Genomes | Hybridization | Loci | Neoplasms | Gene sequencing | Class switching | Next-generation sequencing | Algorithms | Fluorescence in situ hybridization | Tumors | Index Medicus
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8. Full Text Author Correction: A practical guide for mutational signature analysis in hematological malignancies
by Maura, Francesco and Degasperi, Andrea and Nadeu, Ferran and Leongamornlert, Daniel and Davies, Helen and Moore, Luiza and Royo, Romina and Ziccheddu, Bachisio and Puente, Xose S and Avet-Loiseau, Herve and Campbell, Peter J and Nik-Zainal, Serena and Campo, Elias and Munshi, Nikhil and Bolli, Niccolò
Nature communications, ISSN 2041-1723, 07/2019, Volume 10, Issue 1, pp. 3431 - 1
Hematology | Signature analysis | Index Medicus
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9. Full Text Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
by Puente, Xose S and Pinyol, Magda and Quesada, Victor and Conde, Laura and Ordóñez, Gonzalo R and Villamor, Neus and Escaramis, Georgia and Jares, Pedro and Beá, Sílvia and González-Díaz, Marcos and Bassaganyas, Laia and Baumann, Tycho and Juan, Manel and López-Guerra, Mónica and Colomer, Dolors and Tubío, José M. C and López, Cristina and Navarro, Alba and Tornador, Cristian and Aymerich, Marta and Rozman, Maria and Hernández, Jeśs M and Puente, Diana A and Freije, José M. P and Velasco, Gloria and Gutiérrez-Fernández, Ana and Costa, Dolors and Carrio, Anna and Guijarro, Sara and Enjuanes, Anna and Hernndez, Lluis and Yage, Jordi and Nicols, Pilar and Romeo-Casabona, Carlos M and Himmelbauer, Heinz and Castillo, Ester and Dohm, Juliane C and De Sanjos, Silvia and Piris, Miguel A and De Alava, Enrique and Miguel, Jesãs San and Royo, Romina and Gelpi, Josep L and Torrents, David and Orozco, Modesto and Pisano, David G and Valencia, Alfonso and Guigi, Roderic and Bayes, Mãnica and Heath, Simon and Gut, Marta and Klatt, Peter and Marshall, John and Raine, Keiran and Stebbings, Lucy A and Futreal, P. Andrew and Stratton, Michael R and Campbell, Peter J and Gut, Ivo and Lopez-Guillermo, Armando and Estivill, Xavier and Montserrat, Emili and López-Otín, Carlos and Campo, Elías
Nature (London), ISSN 0028-0836, 07/2011, Volume 475, Issue 7354, pp. 101 - 105
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Hematologic and hematopoietic diseases | Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis | Biological and medical sciences | Medical sciences | Amino Acid Sequence | Reproducibility of Results | Humans | Myeloid Differentiation Factor 88 - genetics | Molecular Sequence Data | Receptors, Cytoplasmic and Nuclear - genetics | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Mutation - genetics | Genome, Human - genetics | Carrier Proteins - genetics | Myeloid Differentiation Factor 88 - chemistry | Animals | DNA Mutational Analysis | Karyopherins - genetics | Receptor, Notch1 - genetics | Polymerase chain reaction | Chronic lymphocytic leukemia | Usage | Care and treatment | Nucleotide sequence | Gene mutations | Physiological aspects | Genetic aspects | Research | Cancer | Proteins | Studies | Flow cytometry | Phosphorylation | Genomes | Mutation | Index Medicus | Leucèmia limfocítica crònica | Mutagènesi | Genoma humà
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10. Full Text Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
by Quesada, Víctor and Conde, Laura and Villamor, Neus and Ordóñez, Gonzalo R and Jares, Pedro and Bassaganyas, Laia and Ramsay, Andrew J and Beà, Sílvia and Pinyol, Magda and Martínez-Trillos, Alejandra and López-Guerra, Mónica and Colomer, Dolors and Navarro, Alba and Baumann, Tycho and Aymerich, Marta and Rozman, María and Delgado, Julio and Giné, Eva and Hernández, Jesús M and González-Díaz, Marcos and Puente, Diana A and Velasco, Gloria and Freije, José M P and Tubío, José M C and Royo, Romina and Gelpí, Josep L and Orozco, Modesto and Pisano, David G and Zamora, Jorge and Vázquez, Miguel and Valencia, Alfonso and Himmelbauer, Heinz and Bayés, Mónica and Heath, Simon and Gut, Marta and Gut, Ivo and Estivill, Xavier and López-Guillermo, Armando and Puente, Xose S and Campo, Elías and López-Otín, Carlos
Nature genetics, ISSN 1061-4036, 01/2012, Volume 44, Issue 1, pp. 47 - 52
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Hematologic and hematopoietic diseases | Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Exome | Amino Acid Sequence | Sequence Alignment | Humans | RNA Splicing Factors | Ribonucleoprotein, U2 Small Nuclear - genetics | Leukemia, Lymphocytic, Chronic, B-Cell - mortality | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Mutation | Phosphoproteins - genetics | Disease Progression | Chronic lymphocytic leukemia | Usage | Gene mutations | Genetic aspects | Research | Nucleotide sequencing | Health aspects | Risk factors | DNA sequencing | Genetics | Genomes | Gene expression | Bioinformatics | Cancer | Tumors | Catalogs | Index Medicus
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