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Role for DNA methylation in the control of cell type–specific maspin expression
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0215(20000315)85:6<805::aid-ijc12>3.0.co;2-5openalex-snapshot
Epigenetic silencing of maspin gene expression in human breast cancers
inferredcites →https://doi.org/10.1006/abbi.1999.1142openalex-snapshot
Transcription Factor AP-2 mRNA and DNA Binding Activity Are Constitutively Expressed in SV40-Immortalized but Not Normal Human Lung Fibroblasts
inferredcites →https://doi.org/10.1016/0022-2836(87)90689-9openalex-snapshot
CpG Islands in vertebrate genomes
inferredcites →https://doi.org/10.1016/0092-8674(80)90237-8openalex-snapshot
Cellular differentiation, cytidine analogs and DNA methylation
inferredcites →https://doi.org/10.1016/0092-8674(92)90611-fopenalex-snapshot
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
inferredcites →https://doi.org/10.1016/0168-9525(94)90228-3openalex-snapshot
Role for DNA methylation in genomic imprinting
inferredcites →https://doi.org/10.1016/0888-7543(92)90024-mopenalex-snapshot
CpG islands as gene markers in the human genome
inferredcites →https://doi.org/10.1016/s0009-9120(01)00220-xopenalex-snapshot
Down regulation of the tumor suppressor gene maspin in breast carcinoma is associated with a higher risk of distant metastasis
inferredcites →https://doi.org/10.1016/s0065-230x(08)60702-2openalex-snapshot
Alterations in DNA Methylation: A Fundamental Aspect of Neoplasia
inferredcites →https://doi.org/10.1016/s0168-9525(99)01971-xopenalex-snapshot
DNA hypermethylation in tumorigenesis: epigenetics joins genetics
inferredcites →https://doi.org/10.1016/s1368-8375(99)00026-3openalex-snapshot
Differential DNA methylation of the p16 INK4A/CDKN2A promoter in human oral cancer cells and normal human oral keratinocytes
inferredcites →https://doi.org/10.1038/366362a0openalex-snapshot
Role for DNA methylation in genomic imprinting
inferredcites →https://doi.org/10.1038/79189openalex-snapshot
Large-scale human promoter mapping using CpG islands
inferredcites →https://doi.org/10.1073/pnas.79.7.2352openalex-snapshot
Transformation with DNA from 5-azacytidine-reactivated X chromosomes.
inferredcites →https://doi.org/10.1073/pnas.90.24.11995openalex-snapshot
Number of CpG islands and genes in human and mouse.
inferredcites →https://doi.org/10.1073/pnas.94.11.5673openalex-snapshot
Expression of maspin in prostate cells is regulated by a positive Ets element and a negative hormonal responsive element site recognized by androgen receptor
inferredcites →https://doi.org/10.1074/jbc.275.9.6051openalex-snapshot
p53 Regulates the Expression of the Tumor Suppressor Gene Maspin
inferredcites →https://doi.org/10.1093/nar/22.15.2990openalex-snapshot
High sensitivity mapping of methylated cytosines
inferredcites →https://doi.org/10.1093/nar/28.17.3233openalex-snapshot
Transcriptional repression of BRCA1 by aberrant cytosine methylation, histone hypoacetylation and chromatin condensation of the BRCA1 promoter
inferredcites →https://doi.org/10.1101/gad.13.1.26openalex-snapshot
Cytosine methylation and mammalian development
inferredcites →https://doi.org/10.1101/gad.9.19.2325openalex-snapshot
Loss of methylation activates Xist in somatic but not in embryonic cells.
inferredcites →https://doi.org/10.1111/j.1600-0765.1997.tb00557.xopenalex-snapshot
Prostaglandin E2 and interleukin‐1 concentrations in nicotine‐exposed oral keratinocyte cultures
inferredcites →https://doi.org/10.1126/science.187.4173.226openalex-snapshot
DNA Modification Mechanisms and Gene Activity During Development
inferredcites →https://doi.org/10.1126/science.8290962openalex-snapshot
Maspin, a Serpin with Tumor-Suppressing Activity in Human Mammary Epithelial Cells
inferredcites →https://doi.org/10.1128/jvi.70.10.6994-7003.1996openalex-snapshot
Adenovirus-mediated gene transfer to ciliated airway epithelia requires prolonged incubation time
inferredcites →https://doi.org/10.1128/mcb.17.9.5612openalex-snapshot
Methylation of Discrete Regions of the O 6 -Methylguanine DNA Methyltransferase (MGMT) CpG Island Is Associated with Heterochromatinization of the MGMT Transcription Start Site and Silencing of the Gene
inferredcites →https://doi.org/10.1146/annurev.ge.17.120183.001103openalex-snapshot
MAMMALIAN X-CHROMOSOME INACTIVATION
inferredcites →https://doi.org/10.1152/ajpcell.1991.261.1.c106openalex-snapshot
Glucocorticoids increase Ca2+ uptake and [3H]dihydropyridine binding in A7r5 vascular smooth muscle cells
inferredcites →https://doi.org/10.1152/ajplung.1991.261.2.l106openalex-snapshot
Simple technique for culture of highly differentiated cells from dog tracheal epithelium
inferredcites →https://doi.org/10.1159/000130315openalex-snapshot
X inactivation, differentiation, and DNA methylation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9780470409770.ch2openalex-snapshot
Genomics Technologies as Tools in Drug Discovery
inferred← citeshttps://doi.org/10.1002/9781118005743.ch10openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781118349045.ch7openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajh.20178openalex-snapshot
5‐azacytidine supports the long‐term repopulating activity of cord blood CD34+ cells
inferred← citeshttps://doi.org/10.1002/ajmg.b.20142openalex-snapshot
Methylomics in psychiatry: Modulation of gene–environment interactions may be through DNA methylation
inferred← citeshttps://doi.org/10.1002/ange.202114600openalex-snapshot
A Nuclear‐Targeted AIE Photosensitizer for Enzyme Inhibition and Photosensitization in Cancer Cell Ablation
inferred← citeshttps://doi.org/10.1002/anie.202114600openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bies.10314openalex-snapshot
Cooperative interactions between epigenetic modifications and their function in the regulation of chromosome architecture
inferred← citeshttps://doi.org/10.1002/cm.20187openalex-snapshot
Maspin controls mammary tumor cell migration through inhibiting Rac1 and Cdc42, but not the RhoA GTPase
inferred← citeshttps://doi.org/10.1002/eji.200425469openalex-snapshot
Nuclear repositioning marks the selective exclusion of lineage‐inappropriate transcription factor loci during T helper cell differentiation
inferred← citeshttps://doi.org/10.1002/eji.200737357openalex-snapshot
Regulation of constitutive and microbial pathogen‐induced human macrophage migration inhibitory factor(MIF) gene expression
inferred← citeshttps://doi.org/10.1002/gene.10245openalex-snapshot
De novo DNA methylation at the CpG island of the zebrafish no tail gene
inferred← citeshttps://doi.org/10.1002/ijc.20766openalex-snapshot
TAp63γ can substitute for p53 in inducing expression of the maspin tumor suppressor
inferred← citeshttps://doi.org/10.1002/ijc.23893openalex-snapshot
Relationship of SNCG, S100A4, S100A9 and LCN2 gene expression and DNA methylation in bladder cancer
inferred← citeshttps://doi.org/10.1002/ijc.28494openalex-snapshot
Serpin B5 is a CEA‐interacting biomarker for colorectal cancer
inferred← citeshttps://doi.org/10.1002/iub.75openalex-snapshot
Gene expression and methylation status of 14‐3‐3σ in human renal carcinoma tissues
inferred← citeshttps://doi.org/10.1002/jcb.20721openalex-snapshot
Tumor suppressive maspin and epithelial homeostasis
inferred← citeshttps://doi.org/10.1002/jcp.20280openalex-snapshot
DNA methylation 40 years later: Its role in human health and disease
inferred← citeshttps://doi.org/10.1002/jcp.20786openalex-snapshot
A role of novel serpin maspin in tumor progression: The divergence revealed through efforts to converge
inferred← citeshttps://doi.org/10.1002/jcp.21224openalex-snapshot
DNA methylation: The nuts and bolts of repression
inferred← citeshttps://doi.org/10.1002/jcp.24141openalex-snapshot
On the role of retinoblastoma family proteins in the establishment and maintenance of the epigenetic landscape
inferred← citeshttps://doi.org/10.1002/jez.b.22695openalex-snapshot
Analysis of Genomewide DNA Methylation Reveals Differences in DNA Methylation Levels between Dormant and Naturally as well as Artificially Potentiated Pedicle Periosteum of Sika Deer (Cervus nippon)
inferred← citeshttps://doi.org/10.1002/jgm.644openalex-snapshot
Reversal of the silencing of tetracycline‐controlled genes requires the coordinate action of distinctly acting transcription factors
inferred← citeshttps://doi.org/10.1002/mc.23214openalex-snapshot
Role of class I histone deacetylases in the regulation of maspin expression in prostate cancer
inferred← citeshttps://doi.org/10.1002/mrd.21118openalex-snapshot
DNA methylation in early development
inferred← citeshttps://doi.org/10.1002/path.1732openalex-snapshot
Elevated nuclear maspin expression is associated with microsatellite instability and high tumour grade in colorectal cancer
inferred← citeshttps://doi.org/10.1007/1-4020-3414-8_24openalex-snapshot
Metastasis Suppressor Genes: A Brief Review of an Expanding Field
inferred← citeshttps://doi.org/10.1007/1-4020-3642-6_6openalex-snapshot
Epigenetic Dysregulation of Maspin (SerpinB5) in Cancer Invasion and Metastasis
inferred← citeshttps://doi.org/10.1007/4-431-27713-7_6openalex-snapshot
DNA Methylation and Gastric Carcinoma
inferred← citeshttps://doi.org/10.1007/978-0-387-40049-5_23openalex-snapshot
DNA Methylation Regulates Genomic Imprinting, X Inactivation, and Gene Expression during Mammalian Development
inferred← citeshttps://doi.org/10.1007/978-0-387-69805-2_17openalex-snapshot
Maspin and Suppression of Tumor Metastasis
inferred← citeshttps://doi.org/10.1007/978-1-4020-5129-6_7openalex-snapshot
EPIGENETIC REGULATION OF GENES THAT AFFECT TUMOR CELL ADHESION
inferred← citeshttps://doi.org/10.1007/978-1-4020-8533-8_20openalex-snapshot
CpG Island Hypermethylation, miRNAs, and Human Cancer
inferred← citeshttps://doi.org/10.1007/978-1-4020-9187-2_20openalex-snapshot
A Changing Epigenome in Health and Disease
inferred← citeshttps://doi.org/10.1007/978-1-4419-8216-2_1openalex-snapshot
An Introduction to Epigenetics
inferred← citeshttps://doi.org/10.1007/978-1-4419-9072-3_18openalex-snapshot
DNA Methylation and Human Diseases
inferred← citeshttps://doi.org/10.1007/978-1-4419-9072-3_23openalex-snapshot
Methods: DNA Methylation
inferred← citeshttps://doi.org/10.1007/978-1-4419-9967-2_5openalex-snapshot
Nucleosome Occupancy and Gene Regulation During Tumorigenesis
inferred← citeshttps://doi.org/10.1007/978-1-4939-0718-2_10openalex-snapshot
Methodological Approaches for Understanding the Epigenetic Landscape of the Human Breast and Its Implications in Cancer and Prevention
inferred← citeshttps://doi.org/10.1007/978-1-60327-367-1_2openalex-snapshot
Exploring the Landscape of the Genome
inferred← citeshttps://doi.org/10.1007/978-1-61779-358-5_9openalex-snapshot
The Role of Epigenetics in Cancer: From Molecular Function to High-Throughput Assays
inferred← citeshttps://doi.org/10.1007/978-1-61779-612-8_2openalex-snapshot
Epigenetics of Solid Cancer Stem Cells
inferred← citeshttps://doi.org/10.1007/978-1-62703-727-3_25openalex-snapshot
Epigenetic Markers of Prognosis in Melanoma
inferred← citeshttps://doi.org/10.1007/978-3-319-22711-5_9openalex-snapshot
Maspin Is a Multifunctional Tumor-Suppressing Serpin
inferred← citeshttps://doi.org/10.1007/978-3-642-38404-2_1openalex-snapshot
The Fundamental Role of Epigenetic Regulation in Normal and Disturbed Cell Growth, Differentiation, and Stemness
inferred← citeshttps://doi.org/10.1007/978-3-7643-8989-5_1openalex-snapshot
DNA Methylation and Cancer
inferred← citeshttps://doi.org/10.1007/978-90-481-9382-0_16openalex-snapshot
Circulating Fetal DNA/RNA in Maternal Plasma for Aneuploidy Detection
inferred← citeshttps://doi.org/10.1007/978-94-007-4525-4_27openalex-snapshot
Role of Epigenetics in Inflammation-Associated Diseases
inferred← citeshttps://doi.org/10.1007/s00018-003-3088-6openalex-snapshot
Structure, function and evolution of CpG island promoters
inferred← citeshttps://doi.org/10.1007/s00018-003-3240-3openalex-snapshot
Human clade B serpins (ov-serpins) belong to a cohort of evolutionarily dispersed intracellular proteinase inhibitor clades that protect cells from promiscuous proteolysis
inferred← citeshttps://doi.org/10.1007/s00018-005-5421-8openalex-snapshot
Endothelial nitric oxide synthase: insight into cell-specific gene regulation in the vascular endothelium
inferred← citeshttps://doi.org/10.1007/s00018-010-0600-7openalex-snapshot
Role of xenobiotic metabolism in cancer: involvement of transcriptional and miRNA regulation of P450s
inferred← citeshttps://doi.org/10.1007/s00428-002-0710-1openalex-snapshot
Maspin expression in normal skin and usual cutaneous carcinomas
inferred← citeshttps://doi.org/10.1007/s00438-003-0959-3openalex-snapshot
Non-methylated Genomic Sites Coincidence Cloning (NGSCC): an approach to large scale analysis of hypomethylated CpG patterns at predetermined genomic loci
inferred← citeshttps://doi.org/10.1007/s00438-006-0111-2openalex-snapshot
Methylation-free site patterns along a 1-Mb locus on Chr19 in cancerous and normal cells are similar. A new fast approach for analyzing unmethylated CCGG sites distribution
inferred← citeshttps://doi.org/10.1007/s00439-006-0192-3openalex-snapshot
Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation
inferred← citeshttps://doi.org/10.1007/s00441-007-0537-9openalex-snapshot
DNA methylation in mouse embryonic stem cells and development
inferred← citeshttps://doi.org/10.1007/s00534-005-1057-1openalex-snapshot
The role of epigenetic alterations in pancreatic cancer
inferred← citeshttps://doi.org/10.1007/s10126-019-09921-xopenalex-snapshot
Analysis on the Meiosis-Related Gene (Dmc1, Ph1) Expression in Autotriploid Carassius auratus
inferred← citeshttps://doi.org/10.1007/s10126-020-09963-6openalex-snapshot
Rapid Genomic and Epigenetic Alterations in Gynogenetic Carassius auratus Red Var. Derived from Distant Hybridization
inferred← citeshttps://doi.org/10.1007/s10541-005-0179-zopenalex-snapshot
DNA Demethylation and Carcinogenesis
inferred← citeshttps://doi.org/10.1007/s10555-010-9253-0openalex-snapshot
DNA methylation or histone modification status in metastasis and angiogenesis-related genes: a new hypothesis on usage of DNMT inhibitors and S-adenosylmethionine for genome stability
inferred← citeshttps://doi.org/10.1007/s10555-012-9361-0openalex-snapshot
Maspin: molecular mechanisms and therapeutic implications
inferred← citeshttps://doi.org/10.1007/s10571-015-0281-8openalex-snapshot
Maximal Expression of the Evolutionarily Conserved Slit2 Gene Promoter Requires Sp1
inferred← citeshttps://doi.org/10.1007/s10735-024-10212-6openalex-snapshot
Altered DNA methylation and Dnmt expression in obese uterus may cause implantation failure
inferred← citeshttps://doi.org/10.1007/s11033-013-2525-3openalex-snapshot
DNA methylation: the future of crime scene investigation?
inferred← citeshttps://doi.org/10.1007/s11670-008-0062-8openalex-snapshot
Expression of maspin, uPA and MMP-7 in human gastric carcinoma
inferred← citeshttps://doi.org/10.1007/s11670-011-0092-5openalex-snapshot
DNA methylation profiles of protease nexin 1 (SERPINE2) gene in human cell lines
inferred← citeshttps://doi.org/10.1007/s11814-022-1076-5openalex-snapshot
Epigenome editing and epigenetic gene regulation in disease phenotypes
inferred← citeshttps://doi.org/10.1007/s12265-010-9167-9openalex-snapshot
Human DNA Methyltransferase 3a does not Associate with MicroRNAs in the Regulation of DNA Methylation
inferred← citeshttps://doi.org/10.1007/s13277-011-0310-2openalex-snapshot
Hypermethylation in bladder cancer: biological pathways and translational applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-380866-0.60002-2openalex-snapshot
DNA Methylation and Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.00009-xopenalex-snapshot
Epigenomics – Understanding the Epigenetic Landscape of Cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-801899-6.00008-5openalex-snapshot
The Role of Methylation-Specific PCR and Associated Techniques in Clinical Diagnostics
inferred← citeshttps://doi.org/10.1016/bs.mcb.2025.02.021openalex-snapshot
Epigenetic analysis in cancer research
inferred← citeshttps://doi.org/10.1016/j.acthis.2008.10.006openalex-snapshot
Is maspin immunolocalization a tool to differentiate central low-grade mucoepidermoid carcinoma from glandular odontogenic cyst?
inferred← citeshttps://doi.org/10.1016/j.ajpath.2010.10.023openalex-snapshot
DNA Methylation Suppresses Expression of the Urea Cycle Enzyme Carbamoyl Phosphate Synthetase 1 (CPS1) in Human Hepatocellular Carcinoma
inferred← citeshttps://doi.org/10.1016/j.ajpath.2012.08.016openalex-snapshot
DNA Methylation Plasticity of Human Adipose-Derived Stem Cells in Lineage Commitment
inferred← citeshttps://doi.org/10.1016/j.ajpath.2024.07.015openalex-snapshot
Differential Abundance of DNA Damage Sensors and Innate Immune Signaling Proteins in Inositol Polyphosphate 4-Phosphatase Type II–Negative Triple-Negative Breast Cancer Classified by Immunotype
inferred← citeshttps://doi.org/10.1016/j.bbaexp.2007.06.004openalex-snapshot
Transcriptional and epigenetic regulation of the integrin collagen receptor locus ITGA1-PELO-ITGA2
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2011.01.022openalex-snapshot
DNA methylation restricts spontaneous multi-lineage differentiation of mesenchymal progenitor cells, but is stable during growth factor-induced terminal differentiation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2006.12.126openalex-snapshot
The role of CpG methylation in cell type-specific expression of the aquaporin-5 gene
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.11.137openalex-snapshot
Sequential changes in genome-wide DNA methylation status during adipocyte differentiation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2008.02.110openalex-snapshot
Methylation of a conserved intronic CpG island of mouse SF-1 is associated with cell-specific expression of SF-1 in a culture system but not with tissue-specific expression
inferred← citeshttps://doi.org/10.1016/j.bbrc.2009.04.023openalex-snapshot
CpG island methylation pattern in different human tissues and its correlation with gene expression
inferred← citeshttps://doi.org/10.1016/j.bbrc.2011.09.141openalex-snapshot
Expression of tyrosine hydroxylase is epigenetically regulated in neural stem cells
inferred← citeshttps://doi.org/10.1016/j.bbrc.2016.10.035openalex-snapshot
Histone deacetylase-mediated regulation of chondroitin 4-O-sulfotransferase-1 (Chst11) gene expression by Wnt/β-catenin signaling
inferred← citeshttps://doi.org/10.1016/j.biocel.2007.02.006openalex-snapshot
DNA methylation profiling of transcription factor genes in normal lymphocyte development and lymphomas
inferred← citeshttps://doi.org/10.1016/j.biocel.2008.07.021openalex-snapshot
Epigenomic profiling of cancer cells
inferred← citeshttps://doi.org/10.1016/j.bonr.2017.04.001openalex-snapshot
Systemic analysis of osteoblast-specific DNA methylation marks reveals novel epigenetic basis of osteoblast differentiation
inferred← citeshttps://doi.org/10.1016/j.canlet.2003.09.010openalex-snapshot
Expression and regulation of tumor suppressor gene maspin in human bladder cancer
inferred← citeshttps://doi.org/10.1016/j.cbi.2004.02.003openalex-snapshot
Regulation of cytochrome P450 gene expression in the olfactory mucosa
inferred← citeshttps://doi.org/10.1016/j.ceb.2007.04.011openalex-snapshot
Genomic patterns of DNA methylation: targets and function of an epigenetic mark
inferred← citeshttps://doi.org/10.1016/j.cellsig.2014.03.001openalex-snapshot
Re-expression and epigenetic modification of maspin induced apoptosis in MCF-7 cells mediated by myocardin
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2007.11.002openalex-snapshot
Identification and analysis of mammalian KLK6 orthologue genes for prediction of physiological substrates
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.10.005openalex-snapshot
Aberrant Epigenetic Landscape in Cancer: How Cellular Identity Goes Awry
inferred← citeshttps://doi.org/10.1016/j.diabres.2011.07.027openalex-snapshot
Abnormal DNA methylation in CD4+ T cells from people with latent autoimmune diabetes in adults
inferred← citeshttps://doi.org/10.1016/j.drup.2004.06.005openalex-snapshot
Epigenetic silencing mediated by CpG island methylation: potential as a therapeutic target and as a biomarker
inferred← citeshttps://doi.org/10.1016/j.exer.2008.01.003openalex-snapshot
Epigenetic silencing of maspin expression occurs early in the conversion of keratocytes to fibroblasts
inferred← citeshttps://doi.org/10.1016/j.exger.2013.02.008openalex-snapshot
Expression of the homeostasis-related markers, maspin, heat shock proteins 70 & 90, glutathione S-transferase, aquaporin 5 and NF-kB in young and old labial and palatal salivary glands
inferred← citeshttps://doi.org/10.1016/j.exger.2020.110951openalex-snapshot
DNA methylation of the RE-1 silencing transcription factor in peripheral blood mononuclear cells and gene expression of antioxidant enzyme in patients with late-onset Alzheimer disease
inferred← citeshttps://doi.org/10.1016/j.febslet.2009.04.012openalex-snapshot
CpG islands – ‘A rough guide’
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2007.06.027openalex-snapshot
An epigenetic perspective on the free radical theory of development
inferred← citeshttps://doi.org/10.1016/j.fsi.2014.06.033openalex-snapshot
CpG methylation in the 5′-flanking region of LGP2 gene lacks association with resistance/susceptibility to GCRV but contributes to the differential expression between muscle and spleen tissues in grass carp, Ctenopharyngodon idella
inferred← citeshttps://doi.org/10.1016/j.gene.2004.07.019openalex-snapshot
Identification of a genomic fragment that directs hematopoietic-specific expression of Rac2 and analysis of the DNA methylation profile of the gene locus
inferred← citeshttps://doi.org/10.1016/j.gene.2011.08.027openalex-snapshot
Identification of porcine polycystic kidney disease 1 (PKD1) gene: Molecular cloning, expression profile, and implication in disease model
inferred← citeshttps://doi.org/10.1016/j.gene.2012.08.050openalex-snapshot
Promoter CpG methylation status in porcine Lyn is associated with its expression levels
inferred← citeshttps://doi.org/10.1016/j.gene.2017.10.011openalex-snapshot
Insulin-like peptides and DNA/tRNA methyltransferases are involved in the nutritional regulation of female reproduction in Nilaparvata lugens (Stål)
inferred← citeshttps://doi.org/10.1016/j.gene.2017.12.032openalex-snapshot
Genome-wide analysis of DNA methylation in five tissues of sika deer (Cervus nippon)
inferred← citeshttps://doi.org/10.1016/j.gene.2023.147744openalex-snapshot
Genome-wide DNA methylation analysis reveals layer-specific methylation patterns in deer antler tissue
inferred← citeshttps://doi.org/10.1016/j.genrep.2016.07.012openalex-snapshot
Functional identification and evolutionary conservation of the yme1L1 mitochondrial integrity gene promoter
inferred← citeshttps://doi.org/10.1016/j.jaci.2008.02.031openalex-snapshot
Epigenetic mechanisms silence a disintegrin and metalloprotease 33 expression in bronchial epithelial cells
inferred← citeshttps://doi.org/10.1016/j.jaci.2019.06.006openalex-snapshot
Increased extracellular maspin levels after mechanical compression in vitro or allergen challenge in vivo
inferred← citeshttps://doi.org/10.1016/j.jelechem.2016.03.001openalex-snapshot
Methylation-specific electrochemical biosensing strategy for highly sensitive and quantitative analysis of promoter methylation of tumor-suppressor gene in real sample
inferred← citeshttps://doi.org/10.1016/j.jmb.2008.11.054openalex-snapshot
Effects of CpG Methylation on Recognition of DNA by the Tumour Suppressor p53
inferred← citeshttps://doi.org/10.1016/j.jmb.2018.05.014openalex-snapshot
S-adenosylhomocysteine Hydrolase Participates in DNA Methylation Inheritance
inferred← citeshttps://doi.org/10.1016/j.jnutbio.2011.08.001openalex-snapshot
BRCA-1 promoter hypermethylation and silencing induced by the aromatic hydrocarbon receptor-ligand TCDD are prevented by resveratrol in MCF-7 Cells
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2016.02.010openalex-snapshot
Association of gene expression and methylation of UQCRC1 to the predisposition of Alzheimer's disease in a Chinese population
inferred← citeshttps://doi.org/10.1016/j.lungcan.2005.10.017openalex-snapshot
Maspin gene expression is a significant prognostic factor in resected non-small cell lung cancer (NSCLC)
inferred← citeshttps://doi.org/10.1016/j.mce.2016.09.024openalex-snapshot
DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 and RARB genes in androgen-secreting cells of human adrenal cortex
inferred← citeshttps://doi.org/10.1016/j.mehy.2004.03.046openalex-snapshot
Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?
inferred← citeshttps://doi.org/10.1016/j.molbrainres.2005.06.009openalex-snapshot
Age-related changes in Usp9x protein expression and DNA methylation in mouse brain
inferred← citeshttps://doi.org/10.1016/j.molcel.2008.05.007openalex-snapshot
Lineage-Specific Polycomb Targets and De Novo DNA Methylation Define Restriction and Potential of Neuronal Progenitors
inferred← citeshttps://doi.org/10.1016/j.molimm.2011.09.022openalex-snapshot
DNA methylation signatures of the AIRE promoter in thymic epithelial cells, thymomas and normal tissues
inferred← citeshttps://doi.org/10.1016/j.molmed.2014.12.006openalex-snapshot
Noninvasive fetal genomic, methylomic, and transcriptomic analyses using maternal plasma and clinical implications
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2010.07.007openalex-snapshot
Epigenomics of human colon cancer
inferred← citeshttps://doi.org/10.1016/j.mrrev.2016.09.006openalex-snapshot
Human papillomaviruses in epigenetic regulations
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2010.09.019openalex-snapshot
5-Lipoxygenase in mouse cerebellar Purkinje cells
inferred← citeshttps://doi.org/10.1016/j.omtn.2021.03.011openalex-snapshot
Cell death pathways and viruses: Role of microRNAs
inferred← citeshttps://doi.org/10.1016/j.oraloncology.2003.12.008openalex-snapshot
Effects of demethylating agent 5-aza-2′-deoxycytidine and histone deacetylase inhibitor FR901228 on maspin gene expression in oral cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2014.09.005openalex-snapshot
Epigenetic therapy as a novel approach in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.semcancer.2012.06.007openalex-snapshot
Linking epithelial-to-mesenchymal-transition and epigenetic modifications
inferred← citeshttps://doi.org/10.1016/j.taap.2003.08.011openalex-snapshot
Nickel-induced down-regulation of serpin by hypoxic signaling
inferred← citeshttps://doi.org/10.1016/j.tig.2009.05.004openalex-snapshot
Non-invasive prenatal diagnosis by single molecule counting technologies
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.09.022openalex-snapshot
Correlation between Shh expression and DNA methylation status of the limb-specific Shh enhancer region during limb regeneration in amphibians
inferred← citeshttps://doi.org/10.1016/j.ydbio.2009.07.017openalex-snapshot
Loss of Dnmt1 catalytic activity reveals multiple roles for DNA methylation during pancreas development and regeneration
inferred← citeshttps://doi.org/10.1016/j.ygeno.2006.01.002openalex-snapshot
The length of CpG islands is associated with the distribution of Alu and L1 retroelements
inferred← citeshttps://doi.org/10.1016/j.ygeno.2006.11.006openalex-snapshot
Analysis of tissue-specific differentially methylated regions (TDMs) in humans
inferred← citeshttps://doi.org/10.1016/j.ygyno.2005.12.025openalex-snapshot
Epigenetic regulation of maspin expression in human ovarian carcinoma cells
inferred← citeshttps://doi.org/10.1016/j.ygyno.2011.08.003openalex-snapshot
The regulation of MASPIN expression in epithelial ovarian cancer: Association with p53 status, and MASPIN promoter methylation: A Gynecologic Oncology Group study
inferred← citeshttps://doi.org/10.1016/j.ymthe.2004.12.005openalex-snapshot
A novel knock-in prostate cancer model demonstrates biology similar to that of human prostate cancer and suitable for preclinical studies
inferred← citeshttps://doi.org/10.1016/s0002-9440(10)63549-3openalex-snapshot
Cell-Type-Specific Repression of the Maspin Gene Is Disrupted Frequently by Demethylation at the Promoter Region in Gastric Intestinal Metaplasia and Cancer Cells
inferred← citeshttps://doi.org/10.1016/s0002-9440(10)63748-0openalex-snapshot
Flipping the Epigenetic Switch
inferred← citeshttps://doi.org/10.1016/s0065-2423(10)52006-7openalex-snapshot
Methylation of DNA in Cancer
inferred← citeshttps://doi.org/10.1016/s0065-3101(23)00056-7openalex-snapshot
Cancer and Epigenesis: A Developmental Perspective
inferred← citeshttps://doi.org/10.1016/s0168-1702(02)00246-0openalex-snapshot
DNA from bovine papillomavirus type 2 induces warts in a xenograft model
inferred← citeshttps://doi.org/10.1016/s0304-3835(03)00304-5openalex-snapshot
Metastasis suppressor pathways—an evolving paradigm
inferred← citeshttps://doi.org/10.1016/s0304-3835(03)00390-2openalex-snapshot
Clinicopathological significance and molecular regulation of maspin expression in ductal adenocarcinoma of the pancreas
inferred← citeshttps://doi.org/10.1016/s1476-5586(03)80045-3openalex-snapshot
Human Pancreatic Carcinoma Cells Activate Maspin Expression Through Loss of Epigenetic Control
inferred← citeshttps://doi.org/10.1016/s1521-6616(03)00203-1openalex-snapshot
Age-related epigenetic changes and the immune system
inferred← citeshttps://doi.org/10.1016/s1672-0229(10)60009-5openalex-snapshot
The Most Redundant Sequences in Human CpG Island Library Are Derived from Mitochondrial Genome
inferred← citeshttps://doi.org/10.1017/cbo9780511976117.010openalex-snapshot
Metastasis Genes: Epigenetics
inferred← citeshttps://doi.org/10.1017/s0029665110004015openalex-snapshot
DNA methylation of genes in adipose tissue
inferred← citeshttps://doi.org/10.1034/j.1600-0560.2002.290902.xopenalex-snapshot
p63 expression in normal skin and usual cutaneous carcinomas
inferred← citeshttps://doi.org/10.1037/0033-2909.131.3.340openalex-snapshot
Epigenetic Inheritance and the Intergenerational Transfer of Experience.
inferred← citeshttps://doi.org/10.1038/cr.2011.23openalex-snapshot
Regulation and function of DNA methylation in plants and animals
inferred← citeshttps://doi.org/10.1038/emm.2007.10openalex-snapshot
Coordinated change of a ratio of methylated H3-Iysine 4 or acetylated H3 to acetylated H4 and DNA methylation is associated with tissue-specific gene expression in cloned pig
inferred← citeshttps://doi.org/10.1038/labinvest.3700214openalex-snapshot
Epigenetic status and aberrant expression of the maspin gene in human hepato-biliary tract carcinomas
inferred← citeshttps://doi.org/10.1038/nbt.1685openalex-snapshot
Epigenetic modifications and human disease
inferred← citeshttps://doi.org/10.1038/ng0602-123openalex-snapshot
Methylation matters: a new spin on maspin
inferred← citeshttps://doi.org/10.1038/ng1089openalex-snapshot
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals
inferred← citeshttps://doi.org/10.1038/ng1157openalex-snapshot
Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease
inferred← citeshttps://doi.org/10.1038/ng1563openalex-snapshot
Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3
inferred← citeshttps://doi.org/10.1038/ng1909openalex-snapshot
DNA methylation profiling of human chromosomes 6, 20 and 22
inferred← citeshttps://doi.org/10.1038/ng1990openalex-snapshot
Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome
inferred← citeshttps://doi.org/10.1038/nm.2305openalex-snapshot
Cancer epigenetics reaches mainstream oncology
inferred← citeshttps://doi.org/10.1038/nprot.2006.278openalex-snapshot
Methylation-specific digital karyotyping
inferred← citeshttps://doi.org/10.1038/nrc1045openalex-snapshot
The power and the promise of DNA methylation markers
inferred← citeshttps://doi.org/10.1038/nrc1571openalex-snapshot
Detection and interpretation of altered methylation patterns in cancer cells
inferred← citeshttps://doi.org/10.1038/nrc2620openalex-snapshot
Transitions between epithelial and mesenchymal states: acquisition of malignant and stem cell traits
inferred← citeshttps://doi.org/10.1038/nrg2005openalex-snapshot
Cancer epigenomics: DNA methylomes and histone-modification maps
inferred← citeshttps://doi.org/10.1038/onc.2010.223openalex-snapshot
Global analysis of CpG methylation reveals epigenetic control of the radiosensitivity in lung cancer cell lines
inferred← citeshttps://doi.org/10.1038/s41420-024-01935-2openalex-snapshot
Methylation in cornea and corneal diseases: a systematic review
inferred← citeshttps://doi.org/10.1038/s41467-021-25991-9openalex-snapshot
Unraveling the functional role of DNA demethylation at specific promoters by targeted steric blockage of DNA methyltransferase with CRISPR/dCas9
inferred← citeshttps://doi.org/10.1038/s41598-019-55051-8openalex-snapshot
DNA methylation of a NF-κB binding site in the aquaporin 5 promoter impacts on mortality in sepsis
inferred← citeshttps://doi.org/10.1038/sj.bjc.6602779openalex-snapshot
Overexpression of aurora B kinase (AURKB) in primary non-small cell lung carcinoma is frequent, generally driven from one allele, and correlates with the level of genetic instability
inferred← citeshttps://doi.org/10.1038/sj.mp.4001769openalex-snapshot
Mapping of hippocampal gene clusters regulated by the amygdala to nonlinkage sites for schizophrenia
inferred← citeshttps://doi.org/10.1038/sj.onc.1206095openalex-snapshot
Gene silencing in phenomena related to DNA repair
inferred← citeshttps://doi.org/10.1038/sj.onc.1206545openalex-snapshot
Mutant p53 and aberrant cytosine methylation cooperate to silence gene expression
inferred← citeshttps://doi.org/10.1038/sj.onc.1207211openalex-snapshot
Disruption of cell-type-specific methylation at the Maspin gene promoter is frequently involved in undifferentiated thyroid cancers
inferred← citeshttps://doi.org/10.1038/sj.onc.1207269openalex-snapshot
Identification of maspin and S100P as novel hypomethylation targets in pancreatic cancer using global gene expression profiling
inferred← citeshttps://doi.org/10.1038/sj.onc.1207557openalex-snapshot
Maspin expression in normal lung and non-small-cell lung cancers: cellular property-associated expression under the control of promoter DNA methylation
inferred← citeshttps://doi.org/10.1038/sj.onc.1208449openalex-snapshot
Targeted expression of maspin in tumor vasculatures induces endothelial cell apoptosis
inferred← citeshttps://doi.org/10.1038/sj.onc.1209319openalex-snapshot
Regulation of high molecular weight-melanoma associated antigen (HMW-MAA) gene expression by promoter DNA methylation in human melanoma cells
inferred← citeshttps://doi.org/10.1038/sj.onc.1209763openalex-snapshot
5-Aza-2′-deoxycytidine-mediated reductions in G9A histone methyltransferase and histone H3 K9 di-methylation levels are linked to tumor suppressor gene reactivation
inferred← citeshttps://doi.org/10.1038/sj.onc.1209805openalex-snapshot
Downregulation of RUNX3 and TES by hypermethylation in glioblastoma
inferred← citeshttps://doi.org/10.1038/sj.onc.1210072openalex-snapshot
Re-activation of a dormant tumor suppressor gene maspin by designed transcription factors
inferred← citeshttps://doi.org/10.1042/bj20040067openalex-snapshot
Epigenetic modifications affect Dnmt3L expression
inferred← citeshttps://doi.org/10.1042/bst0320913openalex-snapshot
Control of gene expression by CpG island methylation in normal cells
inferred← citeshttps://doi.org/10.1042/cs20060339openalex-snapshot
Role of the placenta in fetal programming: underlying mechanisms and potential interventional approaches
inferred← citeshttps://doi.org/10.1046/j.1095-8312.2003.00244.xopenalex-snapshot
Evolution of dioecy and sex chromosomes via methylation driving Muller's ratchet
inferred← citeshttps://doi.org/10.1073/pnas.0408436102openalex-snapshot
Association of tissue-specific differentially methylated regions (TDMs) with differential gene expression
inferred← citeshttps://doi.org/10.1073/pnas.0503335102openalex-snapshot
Detection of the placental epigenetic signature of the maspin gene in maternal plasma
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