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DNA Methylation and Prospects for Predicting the Therapeutic Effect of Neoadjuvant Chemotherapy for Triple-Negative and Luminal B Breast Cancer.
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- Cancers, 2023, v. 15, n. 5, p. 1630, doi. 10.3390/cancers15051630
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- Article
Parental Origin of the RB1 Gene Mutations in Families with Low Penetrance Hereditary Retinoblastoma.
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- Cancers, 2021, v. 13, n. 20, p. 5068, doi. 10.3390/cancers13205068
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- Article
Mutations in Epigenetic Regulation Genes in Gastric Cancer.
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- Cancers, 2021, v. 13, n. 18, p. 4586, doi. 10.3390/cancers13184586
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- Article
DNA methylation markers panel can improve prediction of response to neoadjuvant chemotherapy in luminal B breast cancer.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66197-1
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- Article
Methylation of the BIN1 gene promoter CpG island associated with breast and prostate cancer.
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- Journal of Carcinogenesis, 2007, v. 6, n. 1, p. 1, doi. 10.1186/1477-3163-6-9
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- Article
Long noncoding RNA landscapes specific to benign and malignant thyroid neoplasms of distinct histological subtypes.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-96149-2
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- Article
Abnormal promoter DNA hypermethylation of the integrin, nidogen, and dystroglycan genes in breast cancer.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-81851-y
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- Article
Loss of heterozygosity and uniparental disomy of chromosome region 10q23.3-26.3 in glioblastoma.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 1, p. 42, doi. 10.1002/gcc.22506
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- Article
Abnormal Hypermethylation of CpG Dinucleotides in Promoter Regions of Matrix Metalloproteinases Genes in Breast Cancer and its Relation to Epigenomic Subtypes and HER2 Overexpression.
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- Biomedicines, 2020, v. 8, n. 5, p. 116, doi. 10.3390/biomedicines8050116
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- Article
Epigenomic Profiling Advises Therapeutic Potential of Leukotriene Receptor Inhibitors for a Subset of Triple-Negative Breast Tumors.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 24, p. 17343, doi. 10.3390/ijms242417343
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- Article
Major Contribution of c.[1622T>C;3113C>T] Complex Allele and c.5882G>A Variant in ABCA4 -Related Retinal Dystrophy in an Eastern European Population.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 22, p. 16231, doi. 10.3390/ijms242216231
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- Article
Case of Hereditary Papillary Renal Cell Carcinoma Type I in a Patient With a Germline MET Mutation in Russia.
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- Frontiers in Oncology, 2020, v. 9, p. 1, doi. 10.3389/fonc.2019.01566
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- Article