Found: 33
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Combining DNA expression with positional information to detect functional silencing of chromosomal regions.
- Published in:
- Bioinformatics, 2003, v. 19, n. 18, p. 2335, doi. 10.1093/bioinformatics/btg314
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- Publication type:
- Article
Loss of heterozygosity of 1p in uveal melanomas with monosomy 3.
- Published in:
- International Journal of Cancer, 2005, v. 116, n. 6, p. 909, doi. 10.1002/ijc.21086
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- Publication type:
- Article
Massive parallel bisulfite sequencing of CG-rich DNA fragments reveals that methylation of many X-chromosomal CpG islands in female blood DNA is incomplete.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1439, doi. 10.1093/hmg/ddp054
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- Publication type:
- Article
Somatic mosaicism in patients with Angelman syndrome and an imprinting defect.
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- Human Molecular Genetics, 2004, v. 13, n. 21, p. 2547, doi. 10.1093/hmg/ddh296
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- Publication type:
- Article
Acquired IFNγ resistance impairs anti-tumor immunity and gives rise to T-cell-resistant melanoma lesions.
- Published in:
- Nature Communications, 2017, v. 8, n. 5, p. 15440, doi. 10.1038/ncomms15440
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- Publication type:
- Article
Evolutionary Origin and Methylation Status of Human Intronic CpG Islands that Are Not Present in Mouse.
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- Genome Biology & Evolution, 2014, v. 6, n. 7, p. 1579, doi. 10.1093/gbe/evu125
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- Publication type:
- Article
Next-Generation-Sequencing in der Epigenetik.
- Published in:
- Medizinische Genetik, 2019, v. 31, n. 2, p. 205, doi. 10.1007/s11825-019-0245-3
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- Publication type:
- Article
Low frequency of imprinting defects in ICSI children born small for gestational age.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 1, p. 22, doi. 10.1038/ejhg.2008.177
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- Publication type:
- Article
IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia.
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- European Journal of Human Genetics, 2008, v. 16, n. 3, p. 328, doi. 10.1038/sj.ejhg.5201974
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- Publication type:
- Article
Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15.
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- European Journal of Human Genetics, 2001, v. 9, n. 7, p. 519, doi. 10.1038/sj.ejhg.5200661
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- Publication type:
- Article
Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.
- Published in:
- Nature Genetics, 2013, v. 45, n. 8, p. 933, doi. 10.1038/ng.2674
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- Publication type:
- Article
eIF1A residues implicated in cancer stabilize translation preinitiation complexes and favor suboptimal initiation sites in yeast.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.31250.001
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- Publication type:
- Article
Analysis of uveal melanomas and paired constitutional DNA for exclusion of a BAP1-tumor predisposition syndrome.
- Published in:
- Familial Cancer, 2023, v. 22, n. 2, p. 193, doi. 10.1007/s10689-022-00310-3
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- Publication type:
- Article
Quantification of Regulatory T Cells in Septic Patients by Real-Time PCR--Based Methylation Assay and Flow.
- Published in:
- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0049962
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- Publication type:
- Article
Interdisziplinäre Diagnostik und Therapie von intraokularen Tumoren.
- Published in:
- Deutsches Ärzteblatt International, 2018, v. 115, n. 7, p. 1, doi. 10.3238/arztebl.2018.0106
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- Publication type:
- Article
Methylation analysis of the PWS/AS region does not support an enhancer-competition model.
- Published in:
- Nature Genetics, 1998, v. 19, n. 4, p. 324, doi. 10.1038/1211
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- Publication type:
- Article
Early detection of metastatic uveal melanoma by the analysis of tumor‐specific mutations in cell‐free plasma DNA.
- Published in:
- Cancer Medicine, 2021, v. 10, n. 17, p. 5974, doi. 10.1002/cam4.4153
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- Publication type:
- Article
Pancreatic cancer acquires resistance to MAPK pathway inhibition by clonal expansion and adaptive DNA hypermethylation.
- Published in:
- Clinical Epigenetics, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13148-024-01623-z
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- Publication type:
- Article
Relationships between DNA methylation and expression in erythrocyte membrane protein (band 3, protein 4.2, and beta-spectrin) genes during human erythroid development and differentiation.
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- 2005
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- Publication type:
- journal article
DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disorders.
- Published in:
- 2005
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- Publication type:
- journal article
Relevance of Foxp3<sup>+</sup> regulatory T cells for early and late phases of murine sepsis.
- Published in:
- Immunology, 2015, v. 146, n. 1, p. 144, doi. 10.1111/imm.12490
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- Publication type:
- Article
Impact of 5-aza-2′-deoxycytidine and epigallocatechin-3-gallate for induction of human regulatory T cells.
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- Immunology, 2014, v. 142, n. 3, p. 384, doi. 10.1111/imm.12261
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- Publication type:
- Article
EFS shows biallelic methylation in uveal melanoma with poor prognosis as well as tissue-specific methylation.
- Published in:
- 2011
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- Publication type:
- journal article
No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-22177-1
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- Publication type:
- Article
A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus.
- Published in:
- Nucleic Acids Research, 2004, v. 32, n. 16, p. e125, doi. 10.1093/nar/gnh122
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- Publication type:
- Article
Methylation mosaicism of 5′-(CGG)n-3′ repeats in fragile X, premutation and normal individuals.
- Published in:
- Nucleic Acids Research, 2000, v. 28, n. 10, p. 2141, doi. 10.1093/nar/28.10.2141
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- Publication type:
- Article
Detection of homozygous deletions in tumors by hybridization of representational difference analysis (RDA) products to chromosome-specific YAC clone arrays.
- Published in:
- Nucleic Acids Research, 1999, v. 27, n. 21, p. e30, doi. 10.1093/nar/27.21.e30
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- Publication type:
- Article
Secondary Somatic Mutations in G-Protein-Related Pathways and Mutation Signatures in Uveal Melanoma.
- Published in:
- Cancers, 2019, v. 11, n. 11, p. 1688, doi. 10.3390/cancers11111688
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- Publication type:
- Article
GNAQ Q209R Mutations Are Highly Specific for Circumscribed Choroidal Hemangioma.
- Published in:
- Cancers, 2019, v. 11, n. 7, p. 1031, doi. 10.3390/cancers11071031
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- Publication type:
- Article
FOXP3 Expression in GARP-Transduced Helper T Cells Is Not Associated with FOXP3 TSDR Demethylation.
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- Transfusion Medicine & Hemotherapy, 2011, v. 38, n. 5, p. 287, doi. 10.1159/000331499
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- Publication type:
- Article
Aberrant hypomethylation of the cancer–testis antigen PRAME correlates with PRAME expression in acute myeloid leukemia.
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- Annals of Hematology, 2008, v. 87, n. 10, p. 809, doi. 10.1007/s00277-008-0514-8
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- Publication type:
- Article
Imprinted Segments in the Human Genome: Different Dna Methylation Patterns in the Prader-Willi/Angelman Syndrome Region As Determined by the Genomic Sequencing Method.
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- Human Molecular Genetics, 1997, v. 6, n. 3, p. 387, doi. 10.1093/hmg/6.3.387
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- Publication type:
- Article
Lack of SF3B1 R625 mutations in cutaneous melanoma.
- Published in:
- Diagnostic Pathology, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1746-1596-8-87
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- Publication type:
- Article