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by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
Emergency Medicine Journal, ISSN 1472-0205, 10/2017, Volume 34, Issue 10, pp. e8 - e8
BackgroundNational Institute for Health and Care Excellence guidelines on the recognition, diagnosis and early management of sepsis suggest that in all cases... 
Antibiotics | Sepsis | Ambulance services
Journal Article
Heart, ISSN 1355-6037, 06/2016, Volume 102, Issue Suppl 6, pp. A35 - A36
IntroductionAtrial fibrillation (AF) is one of the top ten reasons for hospital admissions. Failure to recognise this arrhythmia and risk stratify patients... 
Journal Article
European Radiology, ISSN 0938-7994, 06/2019, pp. 1 - 8
Objectives Fractional flow reserve computed tomography (FFRCT) depends upon nitroglycerin (NTG) inducing maximal hyperemia. However, the impact of NTG dosages... 
Rank tests | Image quality | Demographics | Demography | Computed tomography | Computation | Nitroglycerin | Stenosis | Hyperemia | Arteries | Vasodilation
Journal Article
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 2527 - 2527
Journal Article
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 2537 - 2537
Journal Article
Advances in Biological Regulation, ISSN 2212-4926, 01/2017, Volume 63, pp. 71 - 80
The gene encodes the Ikaros protein, a zinc finger transcriptional factor that acts as a master regulator of hematopoiesis and a tumor suppressor in leukemia.... 
PP1 | Phosphorylation | Casein Kinase II (CK2) | Ikaros | Leukemia | Protein phosphatase 1 | CX4945 | Cell Cycle - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - immunology | Humans | Jumonji Domain-Containing Histone Demethylases - immunology | Casein Kinase II - genetics | Chromatin Assembly and Disassembly - drug effects | Ikaros Transcription Factor - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy | T-Lymphocytes - drug effects | Chromatin - immunology | Antineoplastic Agents - pharmacology | Phosphorylation - drug effects | T-Lymphocytes - pathology | Nuclear Proteins - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology | Chromatin - drug effects | Chromatin - chemistry | Casein Kinase II - immunology | Signal Transduction | DNA Nucleotidylexotransferase - genetics | Casein Kinase II - antagonists & inhibitors | Gene Expression Regulation | Repressor Proteins - genetics | Nuclear Proteins - immunology | DNA Nucleotidylexotransferase - immunology | Jumonji Domain-Containing Histone Demethylases - genetics | Precursor Cell Lymphoblastic Leukemia-Lymphoma - genetics | Animals | Ikaros Transcription Factor - immunology | Repressor Proteins - immunology | T-Lymphocytes - immunology | Cell Proliferation - drug effects | Cell Cycle - drug effects | Naphthyridines - pharmacology | Medical colleges | Genetic transcription | Acute lymphocytic leukemia | DNA binding proteins | Casein | Analysis | Phosphatases | Genes | Ikaros protein | Acute lymphatic leukemia | Risk groups | Lymphatic leukemia | Gene expression | Casein kinase II | Zinc | Hemopoiesis | Studies | Molecular modelling | Hematopoiesis | Tumor suppressor genes | Zinc finger proteins | Deoxyribonucleic acid--DNA
Journal Article
Experimental Hematology, ISSN 0301-472X, 08/2018, Volume 64, pp. S62 - S63
Journal Article
Experimental Hematology, ISSN 0301-472X, 08/2018, Volume 64, pp. S62 - S63
Journal Article
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