نتائج البحث - "Agnese Marrone"

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دورية أكاديمية

Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia

المؤلفون: Maria D’Apolito, Agnese Marrone, Veronica Servedio, Pietro Vajro, Luigia De Falco, Achille Iolascon

المصدر: Haematologica, Vol 92, Iss 1 (2007)

مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://haematologica.org/article/view/4292; https://doaj.org/toc/0390-6078; https://doaj.org/toc/1592-8721

URL الوصول: https://doaj.org/article/db1db9e57e3948118de49200015608fa

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Homozygosis for (12) CA repeats in the first intron of the human IFN-γ gene is significantly associated with the risk of aplastic anaemia in Caucasian population

المؤلفون: Marta Pillon, Carola Pongiglione, Lucia Giordani, Agnese Marrone, Anna Paola Iori, Riccardo Haupt, Achille Iolascon, Daniela Longoni, Marina Lanciotti, Andrea Bacigalupo, Carlo Dufour, Paola Di Michele, Mario Capasso, Angela Pistorio, Johanna Svahn

المساهمون: Dufour, C, Capasso, Mario, Svahn, J, Marrone, A, Haupt, R, Bacigalupo, A, Giordani, L, Longoni, D, Pillon, M, Pistorio, A, Di Michele, P, Iori, Ap, Pongiglione, C, Lanciotti, M, Iolascon, Achille, C., Dufour, J., Svahn, A., Marrone, R., Haupt, A., Bacigalupo, L., Giordani, D., Longoni, M., Pillon, A., Pistorio, P. D., Michele, A. P., Iori, C., Pongiglione, M., Lanciotti

المصدر: British Journal of Haematology. 126:682-685

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::062401033f5dcb7f2d7b3e24d6410252
https://doi.org/10.1111/j.1365-2141.2004.05102.x

View record at Wiley

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Plakoglobin is differentially expressed in alveolar and embryonal rhabdomyosarcoma and is regulated by DNA methylation and histone acetylation

المؤلفون: Agnese Marrone, F. Sartori, Paolo Bonvini, Tamara Gastaldi, Angelo Rosolen, Achille Iolascon

المساهمون: T., Gastaldi, P., Bonvini, F., Sartori, A., Marrone, Iolascon, Achille, A., Rosolen

المصدر: Carcinogenesis. 27(9)

مصطلحات موضوعية: Cancer Research, Cytoplasm, medicine.drug_class, Plakoglobin, Biology, Hydroxamic Acids, Methylation, BETA-CATENIN, Histones, LUNG-CANCER, RENAL-CELL CARCINOMA, Rhabdomyosarcoma, medicine, Rhabdomyosarcoma, Embryonal, DEACETYLASE, Promoter Regions, Genetic, Cytoskeleton, Rhabdomyosarcoma, Alveolar, Cell Proliferation, Cell Nucleus, Histone deacetylase inhibitor, Acetylation, General Medicine, IN-VITRO, DNA Methylation, Actin cytoskeleton, Molecular biology, GENE, GAMMA-CATENIN EXPRESSION, Gene Expression Regulation, Neoplastic, Trichostatin A, Histone, CpG site, CPG ISLANDS, DNA methylation, biology.protein, gamma Catenin, PAX3-FKHR FUSION PROTEIN, REDUCED EXPRESSION, medicine.drug

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe86f07be5f6ee11ef40ae32f9d6a84
https://pubmed.ncbi.nlm.nih.gov/16537559

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Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism

المؤلفون: Licia Lugli, Fabrizio Ferrari, Agnese Marrone, Maria D'Apolito, Alberto Berardi, Achille Iolascon, Giancarlo Gargano

المساهمون: Berardi, A, Lugli, L, Ferrari, F, Gargano, G, D'Apolito, M, Marrone, A, Iolascon, Achille

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef369472973ad28a7f39107da8c31598
http://hdl.handle.net/11588/472354

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The polymorphisms -318C>T in the promoter and 49A>G in exon 1 of CTLA4 and the risk of aplastic anemia in a Caucasian population

المساهمون: Svahn, J., Capasso, Mario, Lanciotti, M., Marrone, A., Haupt, R., Bacigalupo, A., Pongiglione, C., Boschetto, L., Longoni, D., Pillon, M., Pistorio, A., Michele, P. D., Iori, A. P., Calvillo, M., Locasciulli, A., Menna, G., Riccardi, R., Ramenghi, U., Dufour, C., Iolascon, Achille, Svahn, J, Lanciotti, M, Marrone, A, Haupt, R, Bacigalupo, A, Pongiglione, C, Boschetto, L, Longoni, D, Pillon, M, Pistorio, A, Di Michele, P, Iori, Ap, Calvillo, M, Locasciulli, A, Menna, G, Riccardi, R, Ramenghi, U, Dufour, C

مصطلحات موضوعية: Male, medicine.medical_treatment, SUSCEPTIBILITY, medicine.disease_cause, THERAPY, DISEASE, Autoimmunity, Immune tolerance, Exon, Risk Factors, CTLA-4 Antigen, SYSTEMIC-LUPUS-ERYTHEMATOSUS, Child, Promoter Regions, Genetic, GENE-EXPRESSION, education.field_of_study, Anemia, Aplastic, CTLA4 polymorphisms, Immunosuppression, MULTIPLE-SCLEROSIS, ASSOCIATION, Exons, Hematology, Middle Aged, Child, Preschool, Female, Adult, Adolescent, aplastic anemia, BONE-MARROW, Population, immunosuppressive therapy, chemical and pharmacologic phenomena, Polymorphism, Single Nucleotide, White People, Antigens, CD, medicine, Humans, Genetic Predisposition to Disease, Aplastic anemia, education, Transplantation, INTERFERON-GAMMA, business.industry, Case-control study, Infant, medicine.disease, Antigens, Differentiation, Gene Expression Regulation, Case-Control Studies, Immunology, business, Rare disease