Found: 27
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Validation of specificity of antibodies for immunohistochemistry: the case of ROR2.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Erratum to: Validation of specificity of antibodies for immunohistochemistry: the case of ROR2.
- Published in:
- 2016
- By:
- Publication type:
- corrected article
Scarcity of Recurrent Regulatory Driver Mutations in Colorectal Cancer Revealed by Targeted Deep Sequencing.
- Published in:
- JNCI Cancer Spectrum, 2019, v. 3, n. 2, p. N.PAG, doi. 10.1093/jncics/pkz012
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- Publication type:
- Article
Lipid-Producing Ciliochoroidal Melanoma with Expression of HMG-CoA Reductase.
- Published in:
- Ocular Oncology & Pathology, 2020, v. 6, n. 6, p. 416, doi. 10.1159/000510393
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- Publication type:
- Article
The role of RASSF1A methylation in cancer.
- Published in:
- Disease Markers, 2007, v. 23, n. 1-2, p. 73, doi. 10.1155/2007/291538
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- Publication type:
- Article
CpG island promoter hypermethylation of a novel Ras-effector gene RASSF2A is an early event in colon carcinogenesis and correlates inversely with K-ras mutations.
- Published in:
- Oncogene, 2005, v. 24, n. 24, p. 3987, doi. 10.1038/sj.onc.1208566
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- Publication type:
- Article
Frequent epigenetic inactivation of RASSF1A and BLU genes located within the critical 3p21.3 region in gliomas.
- Published in:
- Oncogene, 2004, v. 23, n. 13, p. 2408, doi. 10.1038/sj.onc.1207407
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- Publication type:
- Article
Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma.
- Published in:
- Oncogene, 2003, v. 22, n. 43, p. 6794, doi. 10.1038/sj.onc.1206914
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- Publication type:
- Article
Frequent epigenetic inactivation of the SLIT2 gene in gliomas.
- Published in:
- Oncogene, 2003, v. 22, n. 29, p. 4611, doi. 10.1038/sj.onc.1206687
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- Publication type:
- Article
Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancers.
- Published in:
- Oncogene, 2003, v. 22, n. 10, p. 1580, doi. 10.1038/sj.onc.1206243
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- Publication type:
- Article
NORE1A, a homologue of RASSF1A tumour suppressor gene is inactivated in human cancers.
- Published in:
- Oncogene, 2003, v. 22, n. 6, p. 947, doi. 10.1038/sj.onc.1206191
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- Publication type:
- Article
Neuropathological Applications of Microscopy with Ultraviolet Surface Excitation (MUSE): A Concordance Study of Human Primary and Metastatic Brain Tumors.
- Published in:
- Brain Sciences (2076-3425), 2024, v. 14, n. 1, p. 108, doi. 10.3390/brainsci14010108
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- Publication type:
- Article
Defining the criteria for identifying constitutional epimutations.
- Published in:
- Clinical Epigenetics, 2016, v. 8, p. 1, doi. 10.1186/s13148-016-0207-4
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- Publication type:
- Article
Reassembly of Nucleosomes at the <i>MLH1</i> Promoter Initiates Resilencing Following Decitabine Exposure.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 7, p. 1, doi. 10.1371/journal.pgen.1003636
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- Publication type:
- Article
Poor mobilization of autologous CD34<sup>+</sup> peripheral blood stem cells in haematology patients undergoing autologous stem cell transplantation is associated with the presence of variants in genes implicated in clonal haematopoiesis of indeterminant potential
- Published in:
- British Journal of Haematology, 2021, v. 193, n. 4, p. 841, doi. 10.1111/bjh.17316
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- Publication type:
- Article
Biopsy for molecular risk stratification in uveal melanoma: Yields and molecular characteristics in 119 patients.
- Published in:
- Clinical & Experimental Ophthalmology, 2022, v. 50, n. 1, p. 50, doi. 10.1111/ceo.14022
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- Publication type:
- Article
The Microbiota and epigenetic Regulation of T Helper 17/Regulatory T Cells: in Search of a Balanced immune System.
- Published in:
- Frontiers in Immunology, 2017, v. 8, p. 1, doi. 10.3389/fimmu.2017.00417
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- Publication type:
- Article
ROR2 is epigenetically inactivated in the early stages of colorectal neoplasia and is associated with proliferation and migration.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Obesity‑induced sperm DNA methylation changes at satellite repeats are reprogrammed in rat offspring.
- Published in:
- Asian Journal of Andrology, 2016, v. 18, n. 6, p. 930, doi. 10.4103/1008-682X.163190
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- Publication type:
- Article
Single nucleotide polymorphism array profiling identifies distinct chromosomal aberration patterns across colorectal adenomas and carcinomas.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 5, p. 303, doi. 10.1002/gcc.22243
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- Publication type:
- Article
Understanding the Pathogenicity of Noncoding Mismatch Repair Gene Promoter Variants in Lynch Syndrome.
- Published in:
- Human Mutation, 2016, v. 37, n. 5, p. 417, doi. 10.1002/humu.22971
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- Publication type:
- Article
Lynch Syndrome Associated with Two MLH1 Promoter Variants and Allelic Imbalance of MLH1 Expression.
- Published in:
- Human Mutation, 2015, v. 36, n. 6, p. 622, doi. 10.1002/humu.22785
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- Publication type:
- Article
Identification of 5 novel genes methylated inbreast and other epithelial cancers.
- Published in:
- Molecular Cancer, 2010, v. 9, p. 51, doi. 10.1186/1476-4598-9-51
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- Publication type:
- Article
A Genome-wide screen identifies frequentlymethylated genes in haematological andepithelial cancers.
- Published in:
- Molecular Cancer, 2010, v. 9, p. 44, doi. 10.1186/1476-4598-9-44
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- Publication type:
- Article
A cluster of genes located in 1p36 are down-regulated in neuroblastomas with poor prognosis, but not due to CpG island methylation.
- Published in:
- Molecular Cancer, 2005, v. 4, p. 10, doi. 10.1186/1476-4598-4-10
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- Publication type:
- Article
Enhanced binding of TBK1 by an optineurin mutant that causes a familial form of primary open angle glaucoma
- Published in:
- FEBS Letters, 2008, v. 582, n. 6, p. 997, doi. 10.1016/j.febslet.2008.02.047
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- Publication type:
- Article
A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
- Published in:
- Carcinogenesis, 2016, v. 37, n. 1, p. 10, doi. 10.1093/carcin/bgv154
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- Publication type:
- Article