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Clinical Cancer Research, ISSN 1078-0432, 04/2006, Volume 12, Issue 7, pp. 2109 - 2116
.... We hypothesized that combined methylation analysis of Wnt-antagonist genes could improve their use as a panel of biomarkers for diagnosing and staging of bladder cancers... 
secreted frizzled-related protein-1, 2, 4 and 5 | Wnt inhibitory factor-1 | Dickkopf family proteins-3 | bladder cancer | methylation | Life Sciences & Biomedicine | Oncology | Science & Technology | Intercellular Signaling Peptides and Proteins - analysis | Multivariate Analysis | Carrier Proteins - urine | Urinary Bladder Neoplasms - diagnosis | Carcinoma, Transitional Cell - urine | Humans | Proto-Oncogene Proteins - urine | Membrane Proteins - urine | Repressor Proteins - analysis | Membrane Proteins - analysis | DNA Methylation | Urinary Bladder Neoplasms - genetics | Biomarkers, Tumor - urine | Proto-Oncogene Proteins - analysis | Sensitivity and Specificity | Eye Proteins - genetics | Carrier Proteins - analysis | Carcinoma, Transitional Cell - genetics | Repressor Proteins - urine | Urinary Bladder Neoplasms - urine | Biomarkers, Tumor - analysis | Membrane Proteins - genetics | Carcinoma, Transitional Cell - diagnosis | RNA, Messenger - genetics | Intercellular Signaling Peptides and Proteins - genetics | Intercellular Signaling Peptides and Proteins - urine | Repressor Proteins - genetics | Proto-Oncogene Proteins - genetics | Eye Proteins - analysis | Reverse Transcriptase Polymerase Chain Reaction | Sequence Analysis, DNA | Carrier Proteins - genetics | Adaptor Proteins, Signal Transducing | Biomarkers, Tumor - genetics | Eye Proteins - urine | Urinary Bladder - physiology | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 02/2019, Volume 14, Issue 2, pp. e0212492 - e0212492
Background B-cell lymphoma/leukaemia 11A (BCL11A) is a C2H2-type zinc-finger transcription factor protein that is a critical modulator of haemoglobin switching and suppresses the production of foetal haemoglobin... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fetal Hemoglobin - biosynthesis | Humans | Repressor Proteins | Mutant Proteins - genetics | Mutant Proteins - metabolism | Nuclear Proteins - metabolism | Globins - metabolism | Nuclear Proteins - chemistry | Molecular Dynamics Simulation | Sequence Homology, Amino Acid | Carrier Proteins - genetics | Globins - genetics | Algorithms | Carrier Proteins - metabolism | Protein Interaction Domains and Motifs - genetics | Computer Simulation | Mutant Proteins - chemistry | Fetal Hemoglobin - genetics | Carrier Proteins - chemistry | Zinc Fingers - genetics | Polymorphism, Single Nucleotide | Nuclear Proteins - genetics | Databases, Nucleic Acid | Transcription factors | Sickle cell anemia | Analysis | Thalassemia | Research | Single nucleotide polymorphisms | Genetic regulation | Protein-protein interactions | Chromosome 19 | State of the art | Impact prediction | Ontology | Leukemia | Molecular dynamics | Amino acids | Homology | Single-nucleotide polymorphism | Proteins | Databases | Hemoglobin | Sickle cell disease | Computer simulation | Lymphoma | Zinc | Switching | Lymphocytes B | 3' Untranslated regions | Genetic research | Software | Disruption | Protein interaction | Methods | Polymorphism | Structure-function relationships | B-cell lymphoma | Index Medicus
Journal Article
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 (London), ISSN 1476-4687, 01/2017, 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... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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 | Index Medicus | 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
Molecular & cellular proteomics, ISSN 1535-9484, 04/2011, Volume 10, Issue 4, pp. M110.002642 - M110.002642
Journal Article
Nature (London), ISSN 1476-4687, 05/2012, Volume 485, Issue 7399, pp. 507 - 511
.... Many of these disorders, including Alzheimer's, Parkinson's and prion diseases, are associated with the accumulation of misfolded disease-specific proteins... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neurons - pathology | Neuroprotective Agents | Phosphorylation | Prions - genetics | Eukaryotic Initiation Factor-2 - chemistry | Neurodegenerative Diseases - etiology | PrPSc Proteins - analysis | Synapses - pathology | Thiourea - pharmacology | Phosphoproteins - metabolism | Repressor Proteins - analysis | PrPSc Proteins - metabolism | Synapses - metabolism | Phosphoproteins - analysis | Protein Folding - drug effects | Protein Phosphatase 1 - genetics | Eukaryotic Initiation Factor-2 - metabolism | Synaptic Transmission - drug effects | Cell Death - drug effects | PrPSc Proteins - toxicity | Neurons - drug effects | Repressor Proteins - metabolism | Prions - metabolism | Synapses - drug effects | Repressor Proteins - chemistry | Neurodegenerative Diseases - pathology | Mice, Inbred C57BL | Kaplan-Meier Estimate | Hippocampus - pathology | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Hippocampus - cytology | Cinnamates - pharmacology | Eukaryotic Initiation Factor-2 - analysis | Hippocampus - metabolism | Protein Phosphatase 1 - metabolism | Animals | Prions - biosynthesis | Protein Biosynthesis - drug effects | Mice | Unfolded Protein Response - physiology | Thiourea - analogs & derivatives | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 03/2016, Volume 11, Issue 3, pp. e0150239 - e0150239
...*) allows stringent streptavidin affinity purification of proximal proteins. This socalled BioID method provides an alternative to the widely used co-immunoprecipitation (co-IP... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Recombinant Fusion Proteins - isolation & purification | Humans | Trans-Activators - isolation & purification | RNA, Messenger - metabolism | Carbon-Nitrogen Ligases - isolation & purification | Recombinant Fusion Proteins - metabolism | Carbon-Nitrogen Ligases - genetics | Protein Interaction Maps | Tandem Mass Spectrometry | Cloning, Molecular | Escherichia coli - metabolism | Trans-Activators - genetics | Chromatography, Liquid | Repressor Proteins - isolation & purification | Repressor Proteins - metabolism | Cell Line | Biotinylation | Carbon-Nitrogen Ligases - metabolism | Immunoprecipitation - methods | Repressor Proteins - genetics | Escherichia coli Proteins - metabolism | Transcription Factors - genetics | Escherichia coli Proteins - isolation & purification | Nonsense Mediated mRNA Decay | Transcription Factors - metabolism | Carrier Proteins - genetics | Protein Interaction Mapping - methods | Carrier Proteins - metabolism | Escherichia coli - genetics | Carrier Proteins - isolation & purification | Escherichia coli Proteins - genetics | Recombinant Fusion Proteins - genetics | Trans-Activators - metabolism | Transcription Factors - isolation & purification | HeLa Cells | Usage | Biotin | Liquid chromatography | Research | Protein-protein interactions | Post-transcription | Phosphorylation | Immunoprecipitation | Peptides | Protein purification | mRNA turnover | Mass spectroscopy | Biochemistry | Nonsense-mediated mRNA decay | Kinases | Machinery | Chromatography | Machinery and equipment | Proteins | Chemistry | E coli | Streptavidin | Scientific imaging | Protein interaction | Mass spectrometry | Index Medicus
Journal Article
Methods (San Diego, Calif.), ISSN 1046-2023, 12/2012, Volume 58, Issue 4, pp. 349 - 359
Journal Article