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101Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients
المؤلفون: Ciccarese, G., Dalmasso, B., Bruno, W., Queirolo, P., Pastorino, L., Andreotti, V., Spagnolo, F., Tanda, E., Ponti, G., Massone, C., Drago, F., Parodi, A., Ghigliotti, G., Pizzichetta, M. A., Ghiorzo, P.
المساهمون: Ciccarese, G., Dalmasso, B., Bruno, W., Queirolo, P., Pastorino, L., Andreotti, V., Spagnolo, F., Tanda, E., Ponti, G., Massone, C., Drago, F., Parodi, A., Ghigliotti, G., Pizzichetta, M. A., Ghiorzo, P.
المصدر: Journal of Translational Medicine
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-11 (2020)مصطلحات موضوعية: medicine.medical_specialty, Nevi and melanomas, Skin Neoplasms, lcsh:Medicine, Dermoscopy, Nodular melanoma, Melanocyte Inducing Transcription Factor, General Biochemistry, Genetics and Molecular Biology, 030207 dermatology & venereal diseases, 03 medical and health sciences, 0302 clinical medicine, CDKN2A, Dysplastic nevi, medicine, Humans, Genetic Predisposition to Disease, Melanoma, neoplasms, Cancer genetics, Retrospective Studies, E318K, Microphthalmia-Associated Transcription Factor, Germline variant, integumentary system, business.industry, Nevi, Research, lcsh:R, Cutaneous melanoma, Renal cell carcinoma, Susceptibility, General Medicine, medicine.disease, Microphthalmia-associated transcription factor, Penetrance, Dermatology, body regions, Phenotype, 030220 oncology & carcinogenesis, Dysplastic nevus, Cancer genetic, business
وصف الملف: ELETTRONICO
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cdbce6a7d062116beee14e6c68c07dTest
https://hdl.handle.net/11380/1201638Test -
102دورية أكاديمية
المؤلفون: Stefanaki, I., Stratigos, A.J., Kypreou, K.P., Evangelou, E., Gandini, S., Maisonneuve, P., Polsky, D., Lazovich, D., Newton-Bishop, J., Kanetsky, P.A., Puig, S., Gruis, N.A., Ghiorzo, P., Pellegrini, C., Nicolo, A. de, Ribas, G., Guida, G., Garcia-Borron, J.C., Fargnoli, M.C., Nan, H., Landi, M.T., Little, J., Sera, F., Raimondi, S., M-SKIP Study Grp
العلاقة: lumc-id: 172658073; https://hdl.handle.net/1887/3280198Test
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103دورية أكاديمية
المؤلفون: Cardinale, A, Cantalupo, S, Lasorsa, VA, Montella, A, Cimmino, F, Succoio, M, Vermeulen, M, Baltissen, MP, Esposito, M, Avitabile, M, Formicola, D, Testori, A, Bonfiglio, F, Ghiorzo, P, Scalvenzi, M, Ayla, F, Zambrano, N, Iles, MM, Xu, M, Law, MH, Brown, KM, Iolascon, A, Capasso, M
وصف الملف: text
العلاقة: https://eprints.whiterose.ac.uk/179071/8/OBFC1%20paper%20manuscript%2001072021%20v1.pdfTest; https://eprints.whiterose.ac.uk/179071/3/FIGURE%2001072021.pdfTest; Cardinale, A, Cantalupo, S, Lasorsa, VA et al. (20 more authors) (2021) Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation of OBFC1. Human Molecular Genetics. ISSN 0964-6906
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106دورية أكاديمية
المؤلفون: Casula M., Paliogiannis P., Ayala F., De Giorgi V., Stanganelli I., Mandala M., Colombino M., Manca A., Sini M. C., Caraco C., Ascierto P. A., Satta R. R., Dedola M. F., Denti S., Fedeli M. A., Montesu M. A., Profili S., Scotto T., Sini G., Tanda F., Lissia A., Cossu A., Palmieri G., Ghiorzo P., Queirolo P., Quaglino P., Botti G., Sileni V. C., Di Giacomo A. M.
المساهمون: Casula, M., Paliogiannis, P., Ayala, F., De Giorgi, V., Stanganelli, I., Mandala, M., Colombino, M., Manca, A., Sini, M. C., Caraco, C., Ascierto, P. A., Satta, R. R., Dedola, M. F., Denti, S., Fedeli, M. A., Montesu, M. A., Profili, S., Scotto, T., Sini, G., Tanda, F., Lissia, A., Cossu, A., Palmieri, G., Ghiorzo, P., Queirolo, P., Quaglino, P., Botti, G., Sileni, V. C., Di Giacomo, A. M.
مصطلحات موضوعية: BRAF, Cancer, CDKN2A, Melanoma, Mutation, NGS, Skin, Adult, Aged, Carcinogenesi, Cyclin-Dependent Kinase Inhibitor p16, Female, Follow-Up Studie, Gene Amplification, Gene Frequency, Genetic Loci, Genetic Predisposition to Disease, Germ-Line Mutation, Human, Italy, Male, Middle Aged, Neoplasms, Multiple Primary, Skin Neoplasm, Tumor Suppressor Protein, Ubiquitin Thiolesterase, High-Throughput Nucleotide Sequencing
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31382929; info:eu-repo/semantics/altIdentifier/wos/WOS:000479241800002; volume:19; issue:1; firstpage:772; journal:BMC CANCER; http://hdl.handle.net/11365/1119639Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85070388191
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107دورية أكاديمية
المؤلفون: Avitabile, M, Succoio, M, Testori, A, Cardinale, A, Vaksman, Z, Lasorsa, VA, Cantalupo, S, Esposito, M, Cimmino, F, Montella, A, Formicola, D, Koster, J, Andreotti, V, Ghiorzo, P, Romano, MF, Staibano, S, Scalvenzi, M, Ayala, F, Hakonarson, H, Corrias, MV, Devoto, M, Law, MH, Iles, MM, Brown, K, Diskin, S, Zambrano, N, Iolascon, A, Capasso, M
وصف الملف: text
العلاقة: https://eprints.whiterose.ac.uk/152744/8/1%20Chr1%20SLC16A1%20NB-MEL%20Manuscript%20only%20text%2028.8.19.pdfTest; Avitabile, M, Succoio, M, Testori, A et al. (25 more authors) (2020) Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene. Carcinogenesis, 41 (3). pp. 284-295. ISSN 0143-3334
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