Kay Elizabeth Davies - Related publications

Affiliations: 
University of Oxford, Oxford, United Kingdom 
Area:
Muscular Dystrophy, Ataxia
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50 most relevant papers in past 60 days:
Year Citation  Score
2021 Ding H, Lin Y, Zhang T, Chen L, Zhang G, Wang J, Xie K, Dai G. Transcriptome Analysis of Differentially Expressed mRNA Related to Pigeon Muscle Development. Animals : An Open Access Journal From Mdpi. 11. PMID 34438768 DOI: 10.3390/ani11082311   
2021 Singh AN, Sharma N. In-silico identification of frequently mutated genes and their co-enriched metabolic pathways associated with Prostate cancer progression. Andrologia. e14236. PMID 34468989 DOI: 10.1111/and.14236   
2021 Luo S, Li Z, Dai X, Zhang R, Liang Z, Li W, Zeng M, Su J, Wang J, Liang X, Wu Y, Liang D. CRISPR/Cas9-Mediated Genetic Correction in a Mouse Model of Hemophilia A. Frontiers in Cell and Developmental Biology. 9: 672564. PMID 34485274 DOI: 10.3389/fcell.2021.672564   
2021 Artigas-Jerónimo S, Villar M, Estrada-Peña A, Velázquez-Campoy A, Alberdi P, de la Fuente J. Function of cofactor Akirin2 in the regulation of gene expression in model human Caucasian neutrophil-like HL60 cells. Bioscience Reports. 41. PMID 34291801 DOI: 10.1042/BSR20211120   
2021 Artigas-Jerónimo S, Villar M, Estrada-Peña A, Velázquez-Campoy A, Alberdi P, de la Fuente J. Function of cofactor Akirin2 in the regulation of gene expression in model human Caucasian neutrophil-like HL60 cells. Bioscience Reports. PMID 34223621 DOI: 10.1042/BCJ20210294   
2021 Zou Q, Qi H. Deletion of ribosomal paralogs Rpl39 and Rpl39l compromises cell proliferation via protein synthesis and mitochondrial activity. The International Journal of Biochemistry & Cell Biology. 139: 106070. PMID 34428590 DOI: 10.1016/j.biocel.2021.106070   
2021 Qian L, Xia Z, Zhang M, Han Q, Hu D, Qi S, Xing D, Chen Y, Zhao X. Integrated Bioinformatics-Based Identification of Potential Diagnostic Biomarkers Associated with Diabetic Foot Ulcer Development. Journal of Diabetes Research. 2021: 5445349. PMID 34513999 DOI: 10.1155/2021/5445349   
2021 Lai X, Chen J. C-X-C motif chemokine ligand 12: a potential therapeutic target in Duchenne muscular dystrophy. Bioengineered. 12: 5428-5439. PMID 34424816 DOI: 10.1080/21655979.2021.1967029   
2021 Liang Y, Wang M, Liu Y, Wang C, Takahashi K, Naruse K. Meta-Analysis-Assisted Detection of Gravity-Sensitive Genes in Human Vascular Endothelial Cells. Frontiers in Cell and Developmental Biology. 9: 689662. PMID 34422812 DOI: 10.3389/fcell.2021.689662   
2021 Salemi M, Cannarella R, Marchese G, Salluzzo MG, Ravo M, Barone C, Giudice ML, Calogero AE, Romano C. Role of long non-coding RNAs in Down syndrome patients: a transcriptome analysis study. Human Cell. PMID 34510387 DOI: 10.1007/s13577-021-00602-3   
2021 Lopes FM, Woolf AS, Roberts NA. Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy. Journal of Pediatric Urology. PMID 34312114 DOI: 10.1016/j.jpurol.2021.07.002   
2021 Domm JM, Wootton SK, Medin JA, West ML. Gene therapy for Fabry disease: Progress, challenges, and outlooks on gene-editing. Molecular Genetics and Metabolism. PMID 34340879 DOI: 10.1016/j.ymgme.2021.07.006   
2021 Aviña-Padilla K, Ramírez-Rafael JA, Herrera-Oropeza GE, Muley VY, Valdivia DI, Díaz-Valenzuela E, García-García A, Varela-Echavarría A, Hernández-Rosales M. Evolutionary Perspective and Expression Analysis of Intronless Genes Highlight the Conservation of Their Regulatory Role. Frontiers in Genetics. 12: 654256. PMID 34306008 DOI: 10.3389/fgene.2021.654256   
2021 Monteys AM, Hundley AA, Ranum PT, Tecedor L, Muehlmatt A, Lim E, Lukashev D, Sivasankaran R, Davidson BL. Regulated control of gene therapies by drug-induced splicing. Nature. PMID 34321659 DOI: 10.1038/s41586-021-03770-2   
2021 Thomas AL, Marsman J, Antony J, Schierding W, O'Sullivan JM, Horsfield JA. Transcriptional Regulation of : An Informatics Analysis. Genes. 12. PMID 34440349 DOI: 10.3390/genes12081175   
2021 Duran BOS, Garcia de la Serrana D, Zanella BTT, Perez ES, Mareco EA, Santos VB, Carvalho RF, Dal-Pai-Silva M. An insight on the impact of teleost whole genome duplication on the regulation of the molecular networks controlling skeletal muscle growth. Plos One. 16: e0255006. PMID 34293047 DOI: 10.1371/journal.pone.0255006   
2021 Tooley JG, Catlin JP, Schaner Tooley CE. CREB-mediated transcriptional activation of NRMT1 drives muscle differentiation. Transcription. 1-17. PMID 34403304 DOI: 10.1080/21541264.2021.1963627   
2021 Laird DW, Lampe PD. Cellular mechanisms of connexin-based inherited diseases. Trends in Cell Biology. PMID 34429228 DOI: 10.1016/j.tcb.2021.07.007   
2021 Gandhi S, Li Y, Tang W, Christensen JB, Urrutia HA, Vieceli FM, Piacentino ML, Bronner ME. A single-plasmid approach for genome editing coupled with long-term lineage analysis in chick embryos. Development (Cambridge, England). 148. PMID 34437692 DOI: 10.1242/dev.193565   
2021 Pardo-Medina J, Gutiérrez G, Limón MC, Avalos J. The lncRNA Is a -Related Regulatory Element with Broad Effects on the Transcriptome. Non-Coding Rna. 7. PMID 34449676 DOI: 10.3390/ncrna7030046   
2021 Ramos ML, Park D, Lim J, Park J, Tran K, Garcia EJ, Green E. Adaptive local false discovery rate procedures for highly spiky data and their application RNA sequencing data of yeast SET4 deletion mutants. Biometrical Journal. Biometrische Zeitschrift. PMID 34320248 DOI: 10.1002/bimj.202000256   
2021 Ramos ML, Park D, Lim J, Park J, Tran K, Garcia EJ, Green E. Adaptive local false discovery rate procedures for highly spiky data and their application RNA sequencing data of yeast SET4 deletion mutants. Biometrical Journal. Biometrische Zeitschrift. PMID 34320248 DOI: 10.1002/bimj.202000256   
2021 Decourty L, Malabat C, Frachon E, Jacquier A, Saveanu C. Investigation of RNA metabolism through large-scale genetic interaction profiling in yeast. Nucleic Acids Research. PMID 34358317 DOI: 10.1093/nar/gkab680   
2021 Wang B, Gong S, Shao W, Han L, Li Z, Zhang Z, Zheng Y, Ouyang F, Ma Y, Xu W, Feng Y. Comprehensive analysis of pivotal biomarkers, immune cell infiltration and therapeutic drugs for steroid-induced osteonecrosis of the femoral head. Bioengineered. 12: 5971-5984. PMID 34488536 DOI: 10.1080/21655979.2021.1972081   
2021 Zhang M, Dai R, Zhao Q, Zhou L, An Y, Tang X, Zhao X. Identification of Key Biomarkers and Immune Infiltration in Systemic Juvenile Idiopathic Arthritis by Integrated Bioinformatic Analysis. Frontiers in Molecular Biosciences. 8: 681526. PMID 34336925 DOI: 10.3389/fmolb.2021.681526   
2021 Goodwin LR, Zapata G, Timpano S, Marenger J, Picketts DJ. Impaired SNF2L Chromatin Remodeling Prolongs Accessibility at Promoters Enriched for Fos/Jun Binding Sites and Delays Granule Neuron Differentiation. Frontiers in Molecular Neuroscience. 14: 680280. PMID 34295220 DOI: 10.3389/fnmol.2021.680280   
2021 Liu X, Yue Y, Gu Z, Huang Q, Pan Z, Zhao Z, Zheng M, Zhang Z, Li C, Yi H, Yu T, Cao M. The characterization and candidate gene isolation for a novel male-sterile mutant ms40 in maize. Plant Cell Reports. PMID 34319484 DOI: 10.1007/s00299-021-02762-w   
2021 Abraham AA, Tisdale JF. Gene Therapy for Sickle Cell Disease - Moving from the Bench to the Bedside. Blood. PMID 34232993 DOI: 10.1182/blood.2019003776   
2021 Abraham AA, Tisdale JF. Gene Therapy for Sickle Cell Disease - Moving from the Bench to the Bedside. Blood. PMID 34232993 DOI: 10.1182/blood.2019003776   
2021 Wang L, Li J, Wang C, Tang R, Liang J, Gong Y, Dai Y, Ding N, Wu J, Dai N, Liu L, Zhao Y, Shao Y, Zhao W, Jiang P, et al. Mapping of de novo mutations in primary biliary cholangitis to a disease-specific co-expression network underlying homeostasis and metabolism. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 34433101 DOI: 10.1016/j.jgg.2021.07.019   
2021 Chau KK, Zhang P, Urresti J, Amar M, Pramod AB, Chen J, Thomas A, Corominas R, Lin GN, Iakoucheva LM. Full-length isoform transcriptome of the developing human brain provides further insights into autism. Cell Reports. 36: 109631. PMID 34469739 DOI: 10.1016/j.celrep.2021.109631   
2021 Wen J, Song J, Bai Y, Liu Y, Cai X, Mei L, Ma L, He C, Feng Y. A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Development. Frontiers in Cell and Developmental Biology. 9: 720858. PMID 34426786 DOI: 10.3389/fcell.2021.720858   
2021 Zhang K, Wang J, Ding F, Shi R, Wang W, Zhang G, Li L. Identification of Distant Regulatory Elements Using Expression Quantitative Trait Loci Mapping for Heat-Responsive Genes in Oysters. Genes. 12. PMID 34356056 DOI: 10.3390/genes12071040   
2021 Zinani OQH, Keseroğlu K, Özbudak EM. Regulatory mechanisms ensuring coordinated expression of functionally related genes. Trends in Genetics : Tig. PMID 34376301 DOI: 10.1016/j.tig.2021.07.008   
2021 Ren Y, Labinsky H, Palmowski A, Bäcker H, Müller M, Kienzle A. Altered molecular pathways and prognostic markers in active systemic juvenile idiopathic arthritis: integrated bioinformatic analysis. Bosnian Journal of Basic Medical Sciences. PMID 34480465 DOI: 10.17305/bjbms.2021.6016   
2021 Chen T, Peng X, Qin J, Qin X, Wu M, Huang J, Huang X, Wei D, Wang L, Jin G. [In silico cloning, expression and bioinformatics analysis of NtODB from common tobacco]. Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology. 37: 2836-2844. PMID 34472301 DOI: 10.13345/j.cjb.200669   
2021 Sharma T, Robinson DCL, Witwicka H, Dilworth FJ, Imbalzano AN. The Bromodomains of the mammalian SWI/SNF (mSWI/SNF) ATPases Brahma (BRM) and Brahma Related Gene 1 (BRG1) promote chromatin interaction and are critical for skeletal muscle differentiation. Nucleic Acids Research. PMID 34289068 DOI: 10.1093/nar/gkab617   
2021 Zhang X, Wang H, Lou L, Li Q, Zhang L, Ge Y. Transcript expression profiling of fibromelanosis-related genes in black-bone chickens. British Poultry Science. PMID 34402346 DOI: 10.1080/00071668.2021.1966750   
2021 Meng F, Du N, Xu D, Kuai L, Liu L, Xiu M. Bioinformatics Analysis of the Molecular Mechanism and Potential Treatment Target of Ankylosing Spondylitis. Computational and Mathematical Methods in Medicine. 2021: 7471291. PMID 34335866 DOI: 10.1155/2021/7471291   
2021 Xu L, Liu F, Li H, Li M, Xie Y, Li Z, Guo Y. Comprehensive characterization of pathological stage-related genes of papillary thyroid cancer along with survival prediction. Journal of Cellular and Molecular Medicine. PMID 34342109 DOI: 10.1111/jcmm.16799   
2021 Shi K, Zhu X, Wu J, Chen Y, Zhang J, Sun X. Centromere protein E as a novel biomarker and potential therapeutic target for retinoblastoma. Bioengineered. 12: 5950-5970. PMID 34482803 DOI: 10.1080/21655979.2021.1972080   
2021 Dai Z, Li R, Hou Y, Li Q, Zhao K, Li T, Li MJ, Wu X. Inducible CRISPRa screen identifies putative enhancers. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 34531148 DOI: 10.1016/j.jgg.2021.06.012   
2021 Luperchio TR, Boukas L, Zhang L, Pilarowski GO, Jiang J, Kalinousky A, Hansen KD, Bjornsson HT. Leveraging the mendelian disorders of the epigenetic machinery to systematically map functional epigenetic variation. Elife. 10. PMID 34463256 DOI: 10.7554/eLife.65884   
2021 Shi Q, Tang B, Li Y, Li Y, Lin T, He D, Wei G. Identification of CDC20 as a Novel Biomarker in Diagnosis and Treatment of Wilms Tumor. Frontiers in Pediatrics. 9: 663054. PMID 34513754 DOI: 10.3389/fped.2021.663054   
2021 Martinez NJ, Braisted JC, Dranchak PK, Moran JJ, Larson H, Queme B, Pak E, Dutra A, Rai G, Cheng KC, Svaren J, Inglese J. Genome-Edited Coincidence and PMP22-HiBiT Fusion Reporter Cell Lines Enable an Artifact-Suppressive Quantitative High-Throughput Screening Strategy for Gene-Dosage Disorder Drug Discovery. Acs Pharmacology & Translational Science. 4: 1422-1436. PMID 34423274 DOI: 10.1021/acsptsci.1c00110   
2021 Aleem MT, Shi J, Yu Z, Wen Z, Zhang Y, Liang M, Lakho SA, Haseeb M, Ali H, Hassan MW, Song X, Li X, Xu L, Yan R. Characterization of Membrane-Associated Progesterone Receptor Component-2 from and Its Interaction with Progesterone and Mifepristone. Vaccines. 9. PMID 34452060 DOI: 10.3390/vaccines9080934   
2021 Wang J, Chen Y, Liang J, Cao M, Shen J, Ke K. Study of the pathology and the underlying molecular mechanism of tissue injury around hematoma following intracerebral hemorrhage. Molecular Medicine Reports. 24. PMID 34368865 DOI: 10.3892/mmr.2021.12341   
2021 Gu H, Li L, Du M, Xu H, Gao M, Liu X, Wei X, Zhong X. Key Gene and Functional Pathways Identified in Unexplained Recurrent Spontaneous Abortion Using Targeted RNA Sequencing and Clinical Analysis. Frontiers in Immunology. 12: 717832. PMID 34421922 DOI: 10.3389/fimmu.2021.717832   
2021 Marion-Poll L, Forêt B, Zielinski D, Massip F, Attia M, Carter AC, Syx L, Chang HY, Gendrel AV, Heard E. Locus specific epigenetic modalities of random allelic expression imbalance. Nature Communications. 12: 5330. PMID 34504093 DOI: 10.1038/s41467-021-25630-3   
2021 Chun KH. Discovery of Cellular RhoA Functions by the Integrated Application of Gene Set Enrichment Analysis. Biomolecules & Therapeutics. PMID 34429388 DOI: 10.4062/biomolther.2021.075