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Cancer Genetics and Cytogenetics|June 1, 1993
Cytogenetic characterization of a new human papillary thyroid carcinoma permanent cell line (GLAG-66)P Antonini, G Linares, N Gaillard, et al.Oncogene|August 3, 1995
Pattern of ras and gsp oncogene mutations in radiation-associated human thyroid tumorsC Challeton, A Bounacer, J A Du Villard, et al.The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cellsJ M Bidart, L Lacroix, D Evain-Brion, et al.Human Genetics|April 1, 1995
Detection of a germline mutation at codon 918 of the RET proto-oncogene in French MEN 2B familiesM Rossel, I Schuffenecker, M Schlumberger, et al.Oncogene|June 15, 1995
RET mutations in exons 13 and 14 of FMTC patientsA Bolino, I Schuffenecker, Y Luo, et al.Stem Cell Research|September 20, 2017
Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) syndrome with "highest risk" RET mutationA Bennaceur-Griscelli, J Hadoux, O Féraud, et al.Journal of Endocrinological Investigation|February 12, 2021
Higher baseline TSH levels predict early hypothyroidism during cancer immunotherapyC Luongo, R Morra, C Gambale, et al.The Journal of Clinical Endocrinology and Metabolism|June 18, 1999
Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC ConsortiumF Lesueur, M Stark, T Tocco, et al.European Journal of Endocrinology|May 7, 1999
Catecholamine production in patients with gastroenteropancreatic neuroendocrine tumorsA Ciofu, E Baudin, P Chanson, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 5, 2002
Quality of life in patients at risk of medullary thyroid carcinoma and followed by a comprehensive medical network: trends for future evaluationsG Freyer, B Ligneau, M Schlumberger, et al.Pageof 30