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Developmental Cell, ISSN 1534-5807, 04/2017, Volume 41, Issue 2, pp. 125 - 126
In a new report in , describe that T cell activation in tumors induces blood vessel normalization. Because abnormal vasculature in tumors is known to reduce... 
Journal Article
by Sifrim, Alejandro and Hitz, Marc-Phillip and Wilsdon, Anna and Breckpot, Jeroen and Turki, Saeed H. Al and Thienpont, Bernard and McRae, Jeremy and Fitzgerald, Tomas W and Singh, Tarjinder and Swaminathan, Ganesh Jawahar and Prigmore, Elena and Rajan, Diana and Abdul-Khaliq, Hashim and Banka, Siddharth and Bauer, Ulrike M.M and Bentham, Jamie and Berger, Felix and Bhattacharya, Shoumo and Bu'Lock, Frances and Canham, Natalie and Colgiu, Irina-Gabriela and Cosgrove, Catherine and Cox, Helen and Daehnert, Ingo and Daly, Allan and Danesh, John and Fryer, Alan and Gewillig, Marc and Hobson, Emma and Hoff, Kirstin and Homfray, Tessa and Kahlert, Anne-Karin and Ketley, Ami and Kramer, Hans-Heiner and Lachlan, Katherine and Lampe, Anne Katrin and Louw, Jacoba J and Manickara, Ashok Kumar and Manase, Dorin and McCarthy, Karen P and Metcalfe, Kay and Moore, Carmel and Newbury-Ecob, Ruth and Omer, Seham Osman and Ouwehand, Willem H and Park, Soo-Mi and Parker, Michael J and Pickardt, Thomas and Pollard, Martin O and Robert, Leema and Roberts, David J and Sambrook, Jennifer and Setchfield, Kerry and Stiller, Brigitte and Thornborough, Chris and Toka, Okan and Watkins, Hugh and Williams, Denise and Wright, Michael and Mital, Seema and Daubeney, Piers E.F and Keavney, Bernard and Goodship, Judith and Abu-Sulaiman, Riyadh Mahdi and Klaassen, Sabine and Wright, Caroline F and Firth, Helen V and Barrett, Jeffrey C and Devriendt, Koenraad and Fitzpatrick, David R and Brook, J David and Hurles, Matthew E and INTERVAL Study and Deciphering Dev Disorders Study and UK10K Consortium and the INTERVAL Study and the Deciphering Developmental Disorders Study and the UK10K Consortium
Nature Genetics, ISSN 1061-4036, 09/2016, Volume 48, Issue 9, pp. 1060 - 1065
Congenital heart defects (CHDs) have a neonatal incidence of 0.8-1% (refs. 1,2). Despite abundant examples of monogenic CHD in humans and mice, CHD has a low... 
DE-NOVO MUTATIONS | GENOTYPE | DISEASE | GENETICS & HEREDITY | FRAMEWORK | RECURRENCE | DISCOVERY | Genetic variation | Exome sequencing | Development and progression | Congenital heart disease | Genetic aspects | Identification and classification | Health aspects | Methods | Heart | Medical research | Biomedical research | Congenital diseases | Funding | Genes | Genomics | Genomes | RNA polymerase | Kinases | Defects | Autism | Mutation
Journal Article
Nature, ISSN 0028-0836, 08/2016, Volume 537, Issue 7618, pp. 63 - 68
Journal Article
NEW ENGLAND JOURNAL OF MEDICINE, ISSN 0028-4793, 08/2019, Volume 381, Issue 9, p. e16
Journal Article
Developmental Cell, ISSN 1534-5807, 04/2017, Volume 41, Issue 2, pp. 125 - 126
In a new report in Nature, Tian and colleagues (2017) describe that T cell activation in tumors induces blood vessel normalization. Because abnormal... 
HYPOXIA | DEVELOPMENTAL BIOLOGY | CELL BIOLOGY | Animals | Neoplasm Metastasis - immunology | T-Lymphocytes - cytology | Drug Therapy - methods | Neoplasm Metastasis - pathology | Humans | Immunotherapy | Neoplasms - blood supply | Neovascularization, Pathologic - physiopathology | T-Lymphocytes - immunology | T cells | Chemotherapy | Cancer
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2557 - 16
Preservation of bone mass is crucial for healthy ageing and largely depends on adequate responses of matrix-embedded osteocytes. These cells control bone... 
HYPOXIA-INDUCIBLE FACTOR | CELLS | MULTIDISCIPLINARY SCIENCES | IN-VIVO | BMP ANTAGONIST | SOST | POSTMENOPAUSAL WOMEN | TARGETED DELETION | EXPRESSION | SKELETAL DEVELOPMENT | MICE LACKING | Sirtuin 1 - metabolism | Coculture Techniques | Humans | Glycoproteins - metabolism | Wnt Signaling Pathway - physiology | Male | Bone Density - genetics | Osteoporosis - etiology | Heterocyclic Compounds, 4 or More Rings - pharmacology | Oxygen - metabolism | Epigenesis, Genetic - physiology | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Female | Osteoporosis - genetics | Acetylation | Osteogenesis - genetics | Disease Models, Animal | Glycoproteins - genetics | Cell Line | Promoter Regions, Genetic | Osteocytes - metabolism | Mice, Inbred C57BL | Hypoxia-Inducible Factor-Proline Dioxygenases - genetics | Mice, Transgenic | Sirtuin 1 - antagonists & inhibitors | Animals | Osteoporosis - pathology | Hypoxia-Inducible Factor-Proline Dioxygenases - metabolism | Primary Cell Culture | Carbazoles - pharmacology | Wnt protein | Osteocytes | SOST protein | Bone resorption | Osteoporosis | β-catenin | Bone growth | Control | Clonal deletion | Aging | Deletion | Oxygen probes | Biocompatibility | Prolyl hydroxylase | Bone loss | Phenotypes | Oxygen | Hydroxylase | Mechanical unloading | Unloading | Ablation | Signaling | Bone mass | Deacetylation | Epigenetics | Bone | Detection | Osteogenesis
Journal Article
Nature Genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 1061 - 1072
The mammalian TET enzymes catalyze DNA demethylation. While they have been intensely studied as major epigenetic regulators, little is known about their... 
PLURIPOTENT STEM-CELLS | TELOMERE ELONGATION | DNA METHYLATION | GROUND-STATE | MAMMALIAN DNA | BASE-RESOLUTION | GENETICS & HEREDITY | GENE-EXPRESSION | POSTNATAL-DEVELOPMENT | ES CELLS | GERM-CELL SPECIFICATION | Sequence Deletion | Brain - embryology | Gene Expression Regulation, Developmental - genetics | DNA-Binding Proteins - deficiency | Brain - metabolism | Ectoderm - metabolism | Catalysis | DNA Methylation - physiology | Telomere Homeostasis - physiology | DNA-Binding Proteins - physiology | Germ Layers - metabolism | Mice, Inbred C57BL | Embryonic Development - genetics | Proto-Oncogene Proteins - genetics | Gene Dosage | Proto-Oncogene Proteins - deficiency | DNA-Binding Proteins - genetics | Gene Knockout Techniques | Gestational Age | Jumonji Domain-Containing Histone Demethylases - genetics | Pluripotent Stem Cells - metabolism | Cell Lineage | Animals | Jumonji Domain-Containing Histone Demethylases - biosynthesis | Proto-Oncogene Proteins - physiology | Gastrula - metabolism | Mice | Crosses, Genetic | Translocation (Genetics) | Embryo | Research | Enzymes | Regulators | Ectoderm | Transcription | Redundancy | Genes | Implantation | Genomes | Roles | Gene expression | Embryos | Promoters | Defects | Demethylation | Stem cells | DNA methylation | Epigenetics | Inbreeding | Methylation | Differentiation | Bioinformatics | Deoxyribonucleic acid--DNA
Journal Article
Thorax, ISSN 0040-6376, 02/2019, Volume 74, Issue 2, pp. 132 - 140
BackgroundIdiopathic pulmonary fibrosis (IPF) is a severe lung disease characterised by extensive pathological changes. The objective for this study was to... 
idiopathic pulmonary fibrosis | ANALYSIS REVEALS | CELLS | LUNG | SIGNATURES | RESPIRATORY SYSTEM | DISEASE | EXPRESSION | Datasets | Studies | Thoracic surgery | Transcription factors | Pulmonary fibrosis | Lung diseases | Principal components analysis | Surfactants | Gene expression | Clustering | Cancer | Interstitial Lung Disease | 2313 | 1506
Journal Article
by Meyer, Kerstin B and O’Reilly, Martin and Michailidou, Kyriaki and Carlebur, Saskia and Edwards, Stacey L and French, Juliet D and Prathalingham, Radhika and Dennis, Joe and Bolla, Manjeet K and Wang, Xianshu and Wang, Qin and de Santiago, Ines and Hopper, John L and Tsimiklis, Helen and Apicella, Carmel and Southey, Melissa C and Schmidt, Marjanka K and Broeks, Annegien and Van ’t Veer, Laura J and Hogervorst, Frans B and Muir, Kenneth and Lophatananon, Artitaya and Stewart-Brown, Sarah and Siriwanarangsan, Pornthep and Fasching, Peter A and Lux, Michael P and Ekici, Arif B and Beckmann, Matthias W and Peto, Julian and dos Santos Silva, Isabel and Fletcher, Olivia and Johnson, Nichola and Sawyer, Elinor J and Tomlinson, Ian and Kerin, Michael J and Miller, Nicola and Marme, Federick and Schneeweiss, Andreas and Sohn, Christof and Burwinkel, Barbara and Guénel, Pascal and Truong, Thérèse and Laurent-Puig, Pierre and Menegaux, Florence and Bojesen, Stig E and Nordestgaard, Børge G and Nielsen, Sune F and Flyger, Henrik and Milne, Roger L and Zamora, M. Pilar and Arias, Jose I and Benitez, Javier and Neuhausen, Susan and Anton-Culver, Hoda and Ziogas, Argyrios and Dur, Christina C and Brenner, Hermann and Müller, Heiko and Arndt, Volker and Stegmaier, Christa and Meindl, Alfons and Schmutzler, Rita K and Engel, Christoph and Ditsch, Nina and Brauch, Hiltrud and Brüning, Thomas and Ko, Yon-Dschun and Nevanlinna, Heli and Muranen, Taru A and Aittomäki, Kristiina and Blomqvist, Carl and Matsuo, Keitaro and Ito, Hidemi and Iwata, Hiroji and Yatabe, Yasushi and Dörk, Thilo and Helbig, Sonja and Bogdanova, Natalia V and Lindblom, Annika and Margolin, Sara and Mannermaa, Arto and Kataja, Vesa and Kosma, Veli-Matti and Hartikainen, Jaana M and Chenevix-Trench, Georgia and Wu, Pei-Ei and Wu, Anna H and Tseng, Chiu-chen and Van Den Berg, David and Stram, Daniel O and Lambrechts, Diether and Thienpont, Bernard and Christiaens, Marie-Rose and Smeets, Ann and Chang-Claude, Jenny and Rudolph, Anja and Seibold, Petra and Flesch-Janys, Dieter and Radice, Paolo and Peterlongo, Paolo and ... and Network, G and Group, AOCS and Investigators, K and Australian Ovarian Cancer Study Group and kConFab Investigators and GENICA Network and Family Medicine and Clinical Epidemiology and EpiHealth: Epidemiology for Health and Lund University and Allmänmedicin och klinisk epidemiologi and Lunds universitet
The American Journal of Human Genetics, ISSN 0002-9297, 12/2013, Volume 93, Issue 6, pp. 1046 - 1060
Journal Article
Journal Article