Works by Damante, Giuseppe
Results: 120
Enantioselective Cytotoxicity of Chiral Diphosphine Ruthenium(II) Complexes Against Cancer Cells.
- Published in:
- Chemistry - A European Journal, 2022, v. 28, n. 33, p. 1, doi. 10.1002/chem.202200200
- By:
- Publication type:
- Article
Frequency of factor V, prothrombin and methylenetetrahydrofolate reductase gene variants in preeclampsia.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Dihydrotanshinone I exhibits antitumor effects via β-catenin downregulation in papillary thyroid cancer cell lines.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-58495-9
- By:
- Publication type:
- Article
A Case Report on 13q12.3 Microdeletion Syndrome Caused by HMGB1 Haploinsufficiency.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
In thyroid cancer cell lines expression of periostin gene is controlled by p73 and is not related to epigenetic marks of active transcription.
- Published in:
- Cellular Oncology (2211-3428), 2011, v. 34, n. 2, p. 131, doi. 10.1007/s13402-011-0009-9
- By:
- Publication type:
- Article
Oral Administration of Oleuropein and Its Semisynthetic Peracetylated Derivative Prevents Hepatic Steatosis, Hyperinsulinemia, and Weight Gain in Mice Fed with High Fat Cafeteria Diet.
- Published in:
- International Journal of Endocrinology, 2015, p. 1, doi. 10.1155/2015/431453
- By:
- Publication type:
- Article
Synergy between HDAC and PARP Inhibitors on Proliferation of a Human Anaplastic Thyroid Cancer-Derived Cell Line.
- Published in:
- International Journal of Endocrinology, 2015, v. 2015, p. 1, doi. 10.1155/2015/978371
- By:
- Publication type:
- Article
Temperament and Character Inventory in Bipolar Disorder versus Healthy Controls and Modulatory Effects of 3 Key Functional Gene Variants.
- Published in:
- Neuropsychobiology, 2018, v. 76, n. 4, p. 209, doi. 10.1159/000490955
- By:
- Publication type:
- Article
Integrated multi-omics analyses on patient-derived CRC organoids highlight altered molecular pathways in colorectal cancer progression involving PTEN.
- Published in:
- Journal of Experimental & Clinical Cancer Research (17569966), 2021, v. 40, n. 1, p. 1, doi. 10.1186/s13046-021-01986-8
- By:
- Publication type:
- Article
Dihydrotanshinone exerts antitumor effects and improves the effects of cisplatin in anaplastic thyroid cancer cells.
- Published in:
- Oncology Reports, 2021, v. 46, n. 3, p. N.PAG, doi. 10.3892/or.2021.8155
- By:
- Publication type:
- Article
BET bromodomain inhibitor JQ1 modulates microRNA expression in thyroid cancer cells.
- Published in:
- Oncology Reports, 2018, v. 39, n. 2, p. 582, doi. 10.3892/or.2017.6152
- By:
- Publication type:
- Article
Effects of BP-14, a novel cyclin-dependent kinase inhibitor, on anaplastic thyroid cancer cells.
- Published in:
- Oncology Reports, 2016, v. 35, n. 4, p. 2413, doi. 10.3892/or.2016.4614
- By:
- Publication type:
- Article
Epigenetic bivalent marking is permissive to the synergy of HDAC and PARP inhibitors on TXNIP expression in breast cancer cells.
- Published in:
- Oncology Reports, 2015, v. 33, n. 5, p. 2199, doi. 10.3892/or.2015.3873
- By:
- Publication type:
- Article
JAK2 V617F-mutated polycythemia vera developing in a patient with a 20-year-long chronic myeloid leukemia at the time of first molecular response.
- Published in:
- Annals of Hematology, 2023, v. 102, n. 5, p. 1279, doi. 10.1007/s00277-023-05187-5
- By:
- Publication type:
- Article
A synonymous RET substitution enhances the oncogenic effect of an in-cis missense mutation by increasing constitutive splicing efficiency.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 10, p. 1, doi. 10.1371/journal.pgen.1007678
- By:
- Publication type:
- Article
Identification of Exosomal microRNAs and Their Targets in Papillary Thyroid Cancer Cells.
- Published in:
- Biomedicines, 2022, v. 10, n. 5, p. 961, doi. 10.3390/biomedicines10050961
- By:
- Publication type:
- Article
A novel de novo HDAC8 missense mutation causing Cornelia de Lange syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 9, p. 1, doi. 10.1002/mgg3.1612
- By:
- Publication type:
- Article
Missense NR2F1 variant in monozygotic twins affected with the Bosch–Boonstra–Schaaf optic atrophy syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1278
- By:
- Publication type:
- Article
The HuR CMLD-2 inhibitor exhibits antitumor effects via MAD2 downregulation in thyroid cancer cells.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-43894-0
- By:
- Publication type:
- Article
APE1 and NPM1 protect cancer cells from platinum compounds cytotoxicity and their expression pattern has a prognostic value in TNBC.
- Published in:
- Journal of Experimental & Clinical Cancer Research (17569966), 2019, v. 38, n. 1, p. N.PAG, doi. 10.1186/s13046-019-1294-9
- By:
- Publication type:
- Article
Nucleophosmin Delocalization in Thyroid Tumour Cells.
- Published in:
- Endocrine Pathology, 2011, v. 22, n. 1, p. 18, doi. 10.1007/s12022-011-9147-x
- By:
- Publication type:
- Article
Nucleotide receptors stimulation by extracellular ATP controls Hsp90 expression through APE1/Ref-1 in thyroid cancer cells: A novel tumorigenic pathway.
- Published in:
- Journal of Cellular Physiology, 2006, v. 209, n. 1, p. 44, doi. 10.1002/jcp.20704
- By:
- Publication type:
- Article
Missense mutations of human homeoboxes: A review.
- Published in:
- Human Mutation, 2002, v. 19, n. 4, p. 457, doi. 10.1002/humu.10070
- By:
- Publication type:
- Article
Missense mutations of human homeoboxes: A review.
- Published in:
- Human Mutation, 2001, v. 18, n. 5, p. 361, doi. 10.1002/humu.1207
- By:
- Publication type:
- Article
A Preliminary Study on Transcriptional Regulation of SNP Site C‐1888T in the Promoter Region of Human PLUNC Gene and Nasopharyngeal Carcinoma Susceptibility.
- Published in:
- Genetics Research, 2024, v. 2024, p. 1, doi. 10.1155/genr/5148918
- By:
- Publication type:
- Article
Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 12, p. 679, doi. 10.1007/s10038-005-0311-3
- By:
- Publication type:
- Article
Cyclic AMP-Response Element Modulator Inhibits the Promoter Activity of the Sodium Iodide Symporter Gene in Thyroid Cancer Cells.
- Published in:
- Thyroid, 2012, v. 22, n. 5, p. 487, doi. 10.1089/thy.2011.0360
- By:
- Publication type:
- Article
Prohibitin Is Overexpressed in Papillary Thyroid Carcinomas Bearing the BRAFV600EMutation.
- Published in:
- Thyroid, 2009, v. 19, n. 3, p. 247, doi. 10.1089/thy.2008.0235
- By:
- Publication type:
- Article
Expression of Differentiation Markers in Cultured Cells from Various Thyroid Diseases.
- Published in:
- Thyroid, 1997, v. 7, n. 6, p. 817, doi. 10.1089/thy.1997.7.817
- By:
- Publication type:
- Article
The Influence of 5-HTTLPR, BDNF Rs6265 and COMT Rs4680 Polymorphisms on Impulsivity in Bipolar Disorder: The Role of Gender.
- Published in:
- Genes, 2022, v. 13, n. 3, p. 482, doi. 10.3390/genes13030482
- By:
- Publication type:
- Article
Unexpected phenotype of a typical NPM1 mutant.
- Published in:
- 2009
- By:
- Publication type:
- Letter
Genome-wide analysis and proteomic studies reveal APE1/Ref-1 multifunctional role in mammalian cells.
- Published in:
- Proteomics, 2009, v. 9, n. 4, p. 1058, doi. 10.1002/pmic.200800638
- By:
- Publication type:
- Article
Mutations R67X and W303X of the protein Z-dependent protease inhibitor gene and venous thromboembolic disease: a case–control study in Italian subjects.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2007, v. 23, n. 1, p. 77, doi. 10.1007/s11239-006-9003-x
- By:
- Publication type:
- Article
Investigation of endothelin-1 type A receptor gene polymorphism (--231 G > A) in preeclampsia susceptibility.
- Published in:
- Journal of Maternal-Fetal & Neonatal Medicine, 2007, v. 20, n. 2, p. 145, doi. 10.1080/14767050601127797
- By:
- Publication type:
- Article
Balance between Cell Division and Cell Death as Predictor of Survival in Patients with Non-Small-Cell Lung Cancer.
- Published in:
- Oncology, 2002, v. 63, n. 1, p. 76, doi. 10.1159/000065724
- By:
- Publication type:
- Article
Precision oncology for RET-related tumors.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 01, doi. 10.3389/fonc.2022.992636
- By:
- Publication type:
- Article
Screening of PAX6 gene in Italian congenital aniridia patients revealed four novel mutations.
- Published in:
- Ophthalmic Genetics, 2016, v. 37, n. 3, p. 307, doi. 10.3109/13816810.2015.1059459
- By:
- Publication type:
- Article
Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Expression of PAX8 Target Genes in Papillary Thyroid Carcinoma.
- Published in:
- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0156658
- By:
- Publication type:
- Article
Evaluating the SERCA2 and VEGF mRNAs as Potential Molecular Biomarkers of the Onset and Progression in Huntington’s Disease.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0125259
- By:
- Publication type:
- Article
Concomitant ABCG2 overexpression and FLT3-ITD mutation identify a subset of acute myeloid leukemia patients at high risk of relapse.
- Published in:
- Cancer (0008543X), 2011, v. 117, n. 10, p. 2156, doi. 10.1002/cncr.25753
- By:
- Publication type:
- Article
Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study.
- Published in:
- Oncology Letters, 2020, v. 19, n. 6, p. 3743, doi. 10.3892/ol.2020.11494
- By:
- Publication type:
- Article
Longitudinal detection of somatic mutations in the saliva of head and neck squamous cell carcinoma–affected patients: a pilot study.
- Published in:
- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1480302
- By:
- Publication type:
- Article
How BRCA and homologous recombination deficiency change therapeutic strategies in ovarian cancer: a review of literature.
- Published in:
- Frontiers in Oncology, 2024, p. 1, doi. 10.3389/fonc.2024.1335196
- By:
- Publication type:
- Article
The impact of the European Society of Cardiology guidelines and whole exome sequencing on genetic testing in hereditary cardiac diseases.
- Published in:
- Clinical Genetics, 2024, v. 106, n. 4, p. 394, doi. 10.1111/cge.14569
- By:
- Publication type:
- Article
NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 1, p. 114, doi. 10.1111/cge.13961
- By:
- Publication type:
- Article
Molecular defects in thyroid dysgenesis.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 1, p. 222, doi. 10.1111/cge.13627
- By:
- Publication type:
- Article
Mesomelia‐synostoses syndrome: Description of a patient presenting a monoallelic expression of SULF1 without alterations in the SLCOA1 gene.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Molecular analysis of a human PAX6 homeobox mutant.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 6, p. 744, doi. 10.1038/sj.ejhg.5201579
- By:
- Publication type:
- Article
Blood-brain barrier dysfunction in disorders of the developing brain.
- Published in:
- Frontiers in Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fnins.2015.00040
- By:
- Publication type:
- Article