Zobrazeno 1 - 6
of 6
pro vyhledávání: '"N. A. Dathan"'
Autor:
F. Viparelli, F. Paturzo, N. Doti, A. Cassese, MARASCO, DANIELA, N. A. Dathan, S. M. Monti, M. Sabatella, C. Miele, M. Ruvo, BEGUINOT, FRANCESCO, FORMISANO, PIETRO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::1117575d5f141b1ecb6eee9855558ec2
http://hdl.handle.net/11588/468223
http://hdl.handle.net/11588/468223
Autor:
E. Truppo, A. Di Fiore, V. Alterio, N. A. Dathan, C. T. Supuran, C. Pedone, S. M. Monti, G. De Simone
Publikováno v:
info:cnr-pdr/source/autori:E. Truppo, A. Di Fiore, V. Alterio, N. A. Dathan, C. T. Supuran, C. Pedone, S. M. Monti, and G. De Simone/congresso_nome:/congresso_luogo:/congresso_data:2010/anno:2010/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::c83e214ee5b901aaaa5f23db70b74c12
http://www.cnr.it/prodotto/i/77341
http://www.cnr.it/prodotto/i/77341
Autor:
SANTORO, MASSIMO, CARLOMAGNO, Francesca, FUSCO, ALFREDO, VECCHIO, GIANCARLO, A. Romano, D. D. Bottaro, N. A. Dathan, M. Grieco, B. Matoskova, M. H. Kraus, P. P. Di Fiore
Multiple endocrine neoplasia types 2A and 2B (MEN2A and MEN2B) and familial medullary thyroid carcinoma are dominantly inherited cancer syndromes. All three syndromes are associated with mutations in RET, which encodes a receptor-like tyrosine kinase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::efdf02b1a35071452cf14245168c257f
http://hdl.handle.net/11588/340551
http://hdl.handle.net/11588/340551
Autor:
Vittorio de Franciscis, Carmen Monaco, Daniela Califano, Alfredo Fusco, Giancarlo Vecchio, G. Luca Colucci-D'Amato, Nina A. Dathan, Massimo Santoro, Gabriella De Vita, Giovanni Santelli, Claudia Rizzo, A D'Alessio
Publikováno v:
The Journal of biological chemistry
271 (1996): 29497–29501.
info:cnr-pdr/source/autori:Rizzo C, Califano D, Colucci-D'Amato GL, de Vita G, D'Alessio A, Dathan NA, Fusco A, Monaco C, Santelli G, Vecchio G, Santoro M, de Franciscis V/titolo:Ligand stimulation of a RET chimeric receptor carrying the activating mutation responsible for the multiple endocrine neoplasia type 2B/doi:/rivista:The Journal of biological chemistry (Print)/anno:1996/pagina_da:29497/pagina_a:29501/intervallo_pagine:29497–29501/volume:271
271 (1996): 29497–29501.
info:cnr-pdr/source/autori:Rizzo C, Califano D, Colucci-D'Amato GL, de Vita G, D'Alessio A, Dathan NA, Fusco A, Monaco C, Santelli G, Vecchio G, Santoro M, de Franciscis V/titolo:Ligand stimulation of a RET chimeric receptor carrying the activating mutation responsible for the multiple endocrine neoplasia type 2B/doi:/rivista:The Journal of biological chemistry (Print)/anno:1996/pagina_da:29497/pagina_a:29501/intervallo_pagine:29497–29501/volume:271
Inherited activating mutations of Ret, a receptor tyrosine kinase, predispose to multiple endocrine neoplasia (MEN) types 2A and 2B and familial medullary thyroid carcinoma. To investigate the effects induced by acute stimulation of Ret, we transfect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92e7f9181083e24c9226debb5fdda14a
http://hdl.handle.net/11588/463032
http://hdl.handle.net/11588/463032
Autor:
Avantaggiato, V., Dathan, N. A., Grieco, M., Fabien, N., Lazzaro, D., Alfredo Fusco, Simeone, A., Santoro, M.
Publikováno v:
Scopus-Elsevier
The RET protooncogene encodes a transmembrane protein of the receptor- type tyrosine kinase family whose ligand has not yet been identified. Its activation in vivo is restricted to human carcinomas of the thyroid. In order to learn more about the pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8848ae7cba679c38d5e869262e4a70fc
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027930997&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027930997&partnerID=MN8TOARS
Publikováno v:
Scopus-Elsevier
The RET proto-oncogene encodes a transmembrane receptor of the tyrosine kinase family, recently found to be the gene responsible for the multiple endocrine neoplasia type 2A and 2B syndromes. RET was found specifically activated, by gene rearrangemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b3a19127eef0d6747318abf38bed662a
http://www.scopus.com/inward/record.url?eid=2-s2.0-0029100756&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0029100756&partnerID=MN8TOARS