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Somatic and germline mutations of the TSH receptor gene in thyroid diseases.
Van Sande J, Parma J, Tonacchera M, Swillens S, Dumont J, Vassart G. Van Sande J, et al. Among authors: parma j. J Clin Endocrinol Metab. 1995 Sep;80(9):2577-85. doi: 10.1210/jcem.80.9.7673398. J Clin Endocrinol Metab. 1995. PMID: 7673398 Review. No abstract available.
The G protein-coupled receptor family and one of its members, the TSH receptor.
Vassart G, Desarnaud F, Duprez L, Eggerickx D, Labbé O, Libert F, Mollereau C, Parma J, Paschke R, Tonacchera M, et al. Vassart G, et al. Among authors: parma j. Ann N Y Acad Sci. 1995 Sep 7;766:23-30. doi: 10.1111/j.1749-6632.1995.tb26645.x. Ann N Y Acad Sci. 1995. PMID: 7486665 Review. No abstract available.
Molecular genetics of thyroid diseases.
Ledent C, Parma J, Dumont J, Vassart G, Targovnik H. Ledent C, et al. Among authors: parma j. Eur J Endocrinol. 1994 Jan;130(1):8-14. doi: 10.1530/eje.0.1300008. Eur J Endocrinol. 1994. PMID: 8124482 Review.
Somatic mutations causing constitutive activity of the thyrotropin receptor are the major cause of hyperfunctioning thyroid adenomas: identification of additional mutations activating both the cyclic adenosine 3',5'-monophosphate and inositol phosphate-Ca2+ cascades.
Parma J, Van Sande J, Swillens S, Tonacchera M, Dumont J, Vassart G. Parma J, et al. Mol Endocrinol. 1995 Jun;9(6):725-33. doi: 10.1210/mend.9.6.8592518. Mol Endocrinol. 1995. PMID: 8592518
The TSH receptor and thyroid diseases.
Paschke R, Van Sande J, Parma J, Vassart G. Paschke R, et al. Among authors: parma j. Baillieres Clin Endocrinol Metab. 1996 Jan;10(1):9-27. doi: 10.1016/s0950-351x(96)80266-7. Baillieres Clin Endocrinol Metab. 1996. PMID: 8734449 Review.
91 results