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Detection of Rare Mutations by Routine Analysis of KRAS, NRAS, and BRAF Oncogenes.
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- Bulletin of Experimental Biology & Medicine, 2017, v. 162, n. 3, p. 375, doi. 10.1007/s10517-017-3619-z
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- Article
Synthesis and Structural Properties of Hybrid Powder Materials Based on Colloidal Silica and Silver Iodide.
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- Inorganic Materials, 2020, v. 56, n. 8, p. 815, doi. 10.1134/S0020168520070018
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- Article
Synthesis, Structure, and Magnetic Characteristics of Mesoporous Fe<sub>2</sub>O<sub>3</sub>–SiO<sub>2</sub> Composites.
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- Inorganic Materials, 2019, v. 55, n. 7, p. 673, doi. 10.1134/S0020168519060062
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ESTABLISHING PATTERNS OF THE STRUCTURAL-PHASE TRANSFORMATIONS DURING THE REDUCTION OF TUNGSTEN-CONTAINING ORE CONCENTRATE WITH CARBON.
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- Eastern-European Journal of Enterprise Technologies, 2021, v. 109, n. 12, p. 16, doi. 10.15587/1729-4061.2021.225389
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DESIGNING A SYSTEM TO SYNCHRONIZE THE INPUT SIGNAL IN A TELECOMMUNICATION NETWORK UNDER THE CONDITION FOR REDUCING A TRANSITIONAL COMPONENT OF THE PHASE ERROR.
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- Eastern-European Journal of Enterprise Technologies, 2021, v. 109, n. 9, p. 66, doi. 10.15587/1729-4061.2021.225514
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Strategic planning in organizations of private retail food trade.
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- EurAsian Journal of Biosciences, 2020, v. 14, n. 2, p. 6997
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- Article
Increasing Sensitivity of Laser Interferometry Method Designed to Assess Residual Welding Stresses.
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- Russian Journal of Nondestructive Testing, 2022, v. 58, n. 7, p. 626, doi. 10.1134/S1061830922070038
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- Article
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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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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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
Epigenetic Regulation Disturbances on Gene Expression in Imprinting Diseases.
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- Molecular Biology, 2022, v. 56, n. 1, p. 1, doi. 10.1134/S0026893321050149
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- Article
Reduced representation bisulfite sequencing design for assessing the methylation of human CpG islands in large samples.
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- Molecular Biology, 2015, v. 49, n. 4, p. 618, doi. 10.1134/S0026893315040184
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- Article
DNA methylation in the promoter regions of the laminin family genes in normal and breast carcinoma tissues.
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- Molecular Biology, 2015, v. 49, n. 4, p. 598, doi. 10.1134/S0026893315040160
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Amplification of intermethylated sites experimental design and results analysis with AIMS in silico computer software.
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- Molecular Biology, 2010, v. 44, n. 2, p. 317, doi. 10.1134/S0026893310020172
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- Article
Inactivation and sensitization of tumor cells after transfection with geneBax.
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- Molecular Biology, 2005, v. 39, n. 1, p. 35, doi. 10.1007/s11008-005-0005-0
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Diagnostics of Epigenetic Alterations in Hereditary and Oncological Disorders.
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- Molecular Biology, 2004, v. 38, n. 2, p. 174, doi. 10.1023/B:MBIL.0000023731.25512.fa
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- Article
Methylation Profile of Several Tumor Suppressor Genes in Non-Small-Cell Lung Cancer.
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- Molecular Biology, 2003, v. 37, n. 6, p. 836, doi. 10.1023/B:MBIL.0000008351.36435.d6
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- Article
Abnormal Methylation of Several Tumor Suppressor Genes in Sporadic Breast Cancer.
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- Molecular Biology, 2003, v. 37, n. 4, p. 591, doi. 10.1023/A:1025195512841
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- Article
RB1 and CDKN2A Functional Defects Resulting in Retinoblastoma.
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- Molecular Biology, 2002, v. 36, n. 5, p. 625, doi. 10.1023/A:1020607010296
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- Article
Spectrum and Frequencies of RB1 Structural Defects in Retinoblastoma.
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- Molecular Biology, 2002, v. 36, n. 4, p. 487, doi. 10.1023/A:1019844125275
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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
Role of Molecular Genetic Factors in Formation of the Clinical Type of Neurofibromatosis Type 2.
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- Russian Journal of Genetics, 2024, v. 60, n. 2, p. 210, doi. 10.1134/S1022795424020054
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- Article
A Direct Digital Synthesizer of Complex Signals.
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- Instruments & Experimental Techniques, 2018, v. 61, n. 6, p. 788, doi. 10.1134/S0020441218050238
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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
Design of Marker Panels for Prediction of Neoadjuvant Chemotherapy Response of Triple-Negative Breast Tumors Based on the Results of Genome-Wide DNA Methylation Screening.
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- Russian Journal of Genetics, 2022, v. 58, n. 7, p. 835, doi. 10.1134/S1022795422070080
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- Article
Germline and Somatic Mutations of Genes Involved in Tumor Formation in Sporadic Renal Angiomyolipoma.
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- Russian Journal of Genetics, 2019, v. 55, n. 9, p. 1113, doi. 10.1134/S1022795419090023
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- Article
Diversity and Prevalence of Hereditary Diseases among Nogais of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2018, v. 54, n. 7, p. 858, doi. 10.1134/S1022795418070165
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Medical Genetic Study of Hereditary Diseases in Abazins of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2018, v. 54, n. 6, p. 703, doi. 10.1134/S1022795418060170
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Hereditary Disorders in Circassians of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2018, v. 54, n. 1, p. 83, doi. 10.1134/S1022795418010155
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- Article
Mutagen influence with different mechanisms of action on DNA global methylation in human whole-blood lymphocytes in vitro.
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- Russian Journal of Genetics, 2013, v. 49, n. 7, p. 765, doi. 10.1134/S1022795413060124
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Analysis of Polymorphic Variants of Gene GIPC1 CGG Repeats in Healthy Individuals and in Patients with Breast Cancer and Non-Small Cell Lung Cancer.
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- Russian Journal of Genetics, 2005, v. 41, n. 9, p. 1059, doi. 10.1007/s11177-005-0200-z
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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
High‐Purity Er<sub>3</sub>N@C<sub>80</sub> Films: Morphology, Spectroscopic Characterization, and Thermal Stability.
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- Physica Status Solidi (B), 2021, v. 258, n. 5, p. 1, doi. 10.1002/pssb.202000546
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Properties of ultra high molecular weight polyethylene fibers after ion beam treatment.
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- Journal of Applied Polymer Science, 2011, v. 122, n. 3, p. 1628, doi. 10.1002/app.33965
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- Article
A New Method to Identify Rubbers and Elastomers using Swelling in Various Solvents.
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- Polymer Science -- Series A, 2022, v. 64, n. 2, p. 115, doi. 10.1134/S0965545X22020109
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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
A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs.
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- Human Mutation, 1999, v. 13, n. 2, p. 166, doi. 10.1002/(SICI)1098-1004(1999)13:2<166::AID-HUMU10>3.0.CO;2-X
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- Article
Development of Technology for Soldering Small-Diameter Pipelines from Aluminum Alloys and Dissimilar Materials.
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- Solar System Research, 2020, v. 54, n. 7, p. 730, doi. 10.1134/S0038094620070187
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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