Zobrazeno 1 - 10
of 37
pro vyhledávání: '"R F, Gagel"'
Autor:
R. F. Gagel
Publikováno v:
Journal of Clinical Endocrinology & Metabolism. 76:809-814
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7633adc1b5fd2c8d73dc5d50edbc33b
https://doi.org/10.1210/jc.76.4.809
https://doi.org/10.1210/jc.76.4.809
Beyond RET: potential therapeutic approaches for advanced and metastatic medullary thyroid carcinoma
Publikováno v:
Journal of internal medicine. 266(1)
Medullary thyroid carcinoma (MTC) is a rare calcitonin-producing neuroendocrine tumour that originates from the parafollicular C-cells of the thyroid gland. The RET proto-oncogene encodes the RET receptor tyrosine kinase, which has essential roles in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2453e51cb54398a43c1809143fc5b7ea
https://pubmed.ncbi.nlm.nih.gov/19522829
https://pubmed.ncbi.nlm.nih.gov/19522829
Publikováno v:
Pituitary. 3(4)
This study reports a six year experience with quinagolide (CV205-502) in the treatment of 40 patients with hyperprolactinemia or prolactinoma.Forty patients with hyperprolactinemia were treated with quinagolide (CV 205-502, Norprolac) for 2-72 months
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0872fa26dedb3dcc7e499319814fc3dd
https://pubmed.ncbi.nlm.nih.gov/11788012
https://pubmed.ncbi.nlm.nih.gov/11788012
Publikováno v:
Revista medica de Chile. 129(7)
Medullary thyroid carcinoma (MTC) may occur either as a sporadic or familial disease. Multiple endocrine neoplasia (MEN) type 2, inherited as an autosomal dominant disease, is characterized by MTC only (FMTC) or coexistence of MTC with other endocrin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35e9841ab9e6b9b12d51a360cfc66b5a
https://pubmed.ncbi.nlm.nih.gov/11552438
https://pubmed.ncbi.nlm.nih.gov/11552438
Autor:
H, Lou, R F, Gagel
Publikováno v:
Frontiers of hormone research. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4b7b5b0c966f8bd575041bfbf422c1d
https://pubmed.ncbi.nlm.nih.gov/10941400
https://pubmed.ncbi.nlm.nih.gov/10941400
Autor:
G J, Cote, J E, Lee, D B, Evans, E, Huang, P N, Schultz, G T, Dang, H, Qiu, S, Shetelbine, R V, Sellin, R F, Gagel
Publikováno v:
Human mutation. 12(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8866c74d629ba17f9b5f6b27026c61af
https://pubmed.ncbi.nlm.nih.gov/10660339
https://pubmed.ncbi.nlm.nih.gov/10660339
Publikováno v:
Cancer research. 59(16)
Activating mutations of the RET proto-oncogene cause hereditary medullary thyroid carcinoma. To examine whether selective inactivation of mutant RET could prevent transformation, a hammerhead ribozyme was designed to cleave RET mRNA containing a tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::13d709e15e16d52e530c23e46269760f
https://pubmed.ncbi.nlm.nih.gov/10463581
https://pubmed.ncbi.nlm.nih.gov/10463581
Autor:
R F, Gagel, I E, McCutcheon
Publikováno v:
The New England journal of medicine. 340(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b43ce7ae61cd808c60a82a4f10a0cef4
https://pubmed.ncbi.nlm.nih.gov/10021473
https://pubmed.ncbi.nlm.nih.gov/10021473
Publikováno v:
Seminars in surgical oncology. 16(1)
Medullary thyroid carcinoma (MTC) is a unique disease in solid tumor oncology due to its ability to secrete calcitonin (iCT), a highly sensitive and specific serum marker of persistent or recurrent disease even at a microscopic level. The relatively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55825673ed1c482c430a4c68ea3a690a
https://pubmed.ncbi.nlm.nih.gov/9890740
https://pubmed.ncbi.nlm.nih.gov/9890740
Publikováno v:
Current therapy in endocrinology and metabolism. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5d1ea234ee2ef02097b3413af53e443
https://pubmed.ncbi.nlm.nih.gov/9174720
https://pubmed.ncbi.nlm.nih.gov/9174720