Publications

• Controversies concerning the role of pendrin as an apical iodide transporter in thyroid follicular cells. Bizhanova A, Kopp P. Cell Physiol Biochem. 2011;28(3):485-90. Epub 2011 Nov 18. PMID: 22116361
• Analysis of cellular localization and function of carboxy-terminal mutants of pendrin. Bizhanova A, Chew TL, Khuon S, Kopp P. Cell Physiol Biochem. 2011;28(3):423-34. Epub 2011 Nov 16. PMID: 22116356
• TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells. Pesce L, Bizhanova A, Caraballo JC, Westphal W, Butti ML, Comellas A, Kopp P. Endocrinology. 2012 Jan;153(1):512-21. Epub 2011 Nov 22. PMID: 22109890
• Familial forms of diabetes insipidus: clinical and molecular characteristics. Babey M, Kopp P, Robertson GL. Nat Rev Endocrinol. 2011 Jul 5;7(12):701-14. doi: 10.1038/nrendo.2011.100. PMID: 21727914
• Clinical and molecular characteristics of Pendred syndrome. Kopp P, Bizhanova A. Ann Endocrinol (Paris). 2011 Apr;72(2):88-94. Epub 2011 Apr 20. PMID: 21511235
• [Molecular tests for (early) recognition of endocrine disorders - towards a sophisticated management of complex endocrine and metabolic diseases]. Kopp P. Ther Umsch. 2010 Jul;67(7):367-73. Review. German. PMID: 20577965
• Genetics and phenomics of Pendred syndrome. Bizhanova A, Kopp P. Mol Cell Endocrinol. 2010 Jun 30;322(1-2):83-90. Epub 2010 Mar 15. Review. PMID: 20298745
• Theodor kocher (1841-1917) Nobel prize centenary 2009. Kopp P. Arq Bras Endocrinol Metabol. 2009 Dec;53(9):1176-80. PMID: 20126876
• Association of endogenous sex hormones with diabetes and impaired fasting glucose in men: multi-ethnic study of atherosclerosis. Colangelo LA, Ouyang P, Liu K, Kopp P, Golden SH, Dobs AS, Szklo M, Vaidya D, Cushman M, Gapstur SM. Diabetes Care. 2009 Jun;32(6):1049-51. Epub 2009 Mar 16. PMID: 19289858
• Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. Bizhanova A, Kopp P. Endocrinology. 2009 Mar;150(3):1084-90. Epub 2009 Feb 5. Review. PMID: 19196800
• Serum IGF-I and C-reactive protein in healthy black and white young men: the CARDIA male hormone study. Colangelo LA, Chiu B, Kopp P, Liu K, Gapstur SM. Growth Horm IGF Res. 2009 Oct;19(5):420-5. Epub 2009 Jan 12. PMID: 19138871
• Primary CNS lymphoma with bilateral symmetric hypothalamic lesions presenting with panhypopituitarism and diabetes insipidus. Layden BT, Dubner S, Toft DJ, Kopp P, Grimm S, Molitch ME. Pituitary. 2011 Jun;14(2):194-7. PMID: 19123039
• Pendred syndrome and iodide transport in the thyroid. Kopp P, Pesce L, Solis-S JC. Trends Endocrinol Metab. 2008 Sep;19(7):260-8. Epub 2008 Aug 7. Review. PMID: 18692402
• Applications of molecular biology and genetics in endocrinology. Kopp P. Endocr Pract. 2007 Sep;13(5):534-41. Review. PMID: 17872356
• Total testosterone, androgen receptor polymorphism, and depressive symptoms in young black and white men: the CARDIA Male Hormone Study. Colangelo LA, Sharp L, Kopp P, Scholtens D, Chiu BC, Liu K, Gapstur SM. Psychoneuroendocrinology. 2007 Sep-Nov;32(8-10):951-8. Epub 2007 Jul 30. PMID: 17659846
• Changes in BMI modulate age-associated changes in sex hormone binding globulin and total testosterone, but not bioavailable testosterone in young adult men: the CARDIA Male Hormone Study. Gapstur SM, Kopp P, Gann PH, Chiu BC, Colangelo LA, Liu K. Int J Obes (Lond). 2007 Apr;31(4):685-91. Epub 2006 Sep 12. PMID: 16969359
• IGF-1, IGFBP-3, and nutritional factors in young black and white men: the CARDIA Male Hormone Study. Colangelo LA, Chiu BC, Liu K, Kopp PA, Gann PH, Gapstur SM. Nutr Cancer. 2005;53(1):57-64. PMID: 16351507
• Naturally occurring mutations in the thyroglobulin gene. Vono-Toniolo J, Rivolta CM, Targovnik HM, Medeiros-Neto G, Kopp P. Thyroid. 2005 Sep;15(9):1021-33. Review. PMID: 16187910
• Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome. Gillam MP, Bartolone L, Kopp P, Benvenga S. Thyroid. 2005 Jul;15(7):734-41. Erratum in: Thyroid. 2009 Nov;19(11):1294. Bevenga, S [corrected to Benvenga, S]. PMID: 16053392
• Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism. Vono-Toniolo J, Kopp P. Arq Bras Endocrinol Metabol. 2004 Feb;48(1):70-82. Epub 2004 Jun 1. Review. PMID: 15611820
• Longitudinal associations of age, anthropometric and lifestyle factors with serum total insulin-like growth factor-I and IGF binding protein-3 levels in Black and White men: the CARDIA Male Hormone Study.Gapstur SM, Kopp P, Chiu BC, Gann PH, Colangelo LA, Liu K.Cancer Epidemiol Biomarkers Prev. 2004 Dec;13(12):2208-16.PMID: 15598782
• Quantitative trait loci associated with elevated thyroid-stimulating hormone in the Wistar-Kyoto rat. Baum AE, Solberg LC, Kopp P, Ahmadiyeh N, Churchill G, Takahashi JS, Jameson JL, Redei EE. Endocrinology. 2005 Feb;146(2):870-8. Epub 2004 Oct 28. PMID: 15514085
• Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux. Gillam MP, Sidhaye AR, Lee EJ, Rutishauser J, Stephan CW, Kopp P. J Biol Chem. 2004 Mar 26;279(13):13004-10. Epub 2004 Jan 8. PMID: 14715652
• Men with acquired hypogonadotropic hypogonadism treated with testosterone may be fertile. Drincic A, Arseven OK, Sosa E, Mercado M, Kopp P, Molitch ME. Pituitary. 2003;6(1):5-10. PMID: 14674718
• Identification of thyroid hormone receptors in the human larynx. Altman KW, Haines GK 3rd, Vakkalanka SK, Keni SP, Kopp PA, Radosevich JA. Laryngoscope. 2003 Nov;113(11):1931-4. PMID: 14603050
• Serum androgen concentrations in young men: a longitudinal analysis of associations with age, obesity, and race. The CARDIA male hormone study. Gapstur SM, Gann PH, Kopp P, Colangelo L, Longcope C, Liu K. Cancer Epidemiol Biomarkers Prev. 2002 Oct;11(10 Pt 1):1041-7. PMID: 12376505
• Perspective: genetic defects in the etiology of congenital hypothyroidism. Kopp P. Endocrinology. 2002 Jun;143(6):2019-24. Review. PMID: 12021164
• Clinical and molecular analysis of three families with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel and recurrent mutations in the vasopressin-neurophysin II gene. Rutishauser J, Kopp P, Gaskill MB, Kotlar TJ, Robertson GL. Eur J Endocrinol. 2002 May;146(5):649-56. PMID: 11980620
• Cloning of the cat TSH receptor and evidence against an autoimmune etiology of feline hyperthyroidism. Nguyen LQ, Arseven OK, Gerber H, Stein BS, Jameson JL, Kopp P. Endocrinology. 2002 Feb;143(2):395-402. PMID: 11796491
• Genetic defects in thyroid hormone synthesis. Gillam MP, Kopp P. Curr Opin Pediatr. 2001 Aug;13(4):364-72. Review. PMID: 11717564
• Genetic regulation of thyroid development. Gillam MP, Kopp P. Curr Opin Pediatr. 2001 Aug;13(4):358-63. Review. PMID: 11717563
• Pendred's syndrome and genetic defects in thyroid hormone synthesis. Kopp P. Rev Endocr Metab Disord. 2000 Jan;1(1-2):109-21. Review. No abstract available. PMID: 11704986
• The TSH receptor and its role in thyroid disease. Kopp P. Cell Mol Life Sci. 2001 Aug;58(9):1301-22. Review. PMID: 11577986
• Postload plasma glucose concentration and 27-year prostate cancer mortality (United States). Gapstur SM, Gann PH, Colangelo LA, Barron-Simpson R, Kopp P, Dyer A, Liu K. Cancer Causes Control. 2001 Oct;12(8):763-72. PMID: 11562117
• A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child. Congdon T, Nguyen LQ, Nogueira CR, Habiby RL, Medeiros-Neto G, Kopp P. J Clin Endocrinol Metab. 2001 Aug;86(8):3962-7. PMID: 11502839
• A novel mutation (M310L) in the thyroid hormone receptor beta causing resistance to thyroid hormone in a Brazilian kindred and a neonate. Furlanetto TW, Kopp P, Peccin S, Gu WX, Jameson JL. Mol Genet Metab. 2000 Nov;71(3):520-6. PMID: 11073720
• A dominant negative CREB (cAMP response element-binding protein) isoform inhibits thyrocyte growth, thyroid-specific gene expression, differentiation, and function. Nguyen LQ, Kopp P, Martinson F, Stanfield K, Roth SI, Jameson JL. Mol Endocrinol. 2000 Sep;14(9):1448-61. PMID: 10976922
• Substitutions of tyrosine 601 in the human thyrotropin receptor result in increase or loss of basal activation of the cyclic adenosine monophosphate pathway and disrupt coupling to Gq/11. Arseven OK, Wilkes WP, Jameson JL, Kopp P. Thyroid. 2000 Jan;10(1):3-10. PMID: 10691307
• Rehabilitation of breast cancer. Kiel K, Kopp P. Cancer Treat Res. 1999;100:107-33. Review. PMID: 10645500
• A novel mutation (R97C) in the neurophysin moiety of prepro-vasopressin-neurophysin II associated with autosomal-dominant neurohypophyseal diabetes insipidus. Rutishauser J, Kopp P, Gaskill MB, Kotlar TJ, Robertson GL. Mol Genet Metab. 1999 May;67(1):89-92.
• Targeted disruption of the Ahch (Dax-1) gene: knockout of old concepts. Kopp P. Eur J Endocrinol. 1999 Apr;140(4):291-2. No abstract available. PMID: 10097246
• Aquaporin-2 water channel mutations and nephrogenic diabetes insipidus: new variations on a theme. Rutishauser J, Kopp P. Eur J Endocrinol. 1999 Feb;140(2):137-9. Review. No abstract available. PMID: 10069656
• Pendred's syndrome: identification of the genetic defect a century after its recognition. Kopp P. Thyroid. 1999 Jan;9(1):65-9. Review. PMID: 10037079
• Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene. Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavaliere H, Santos CL, Jameson JL, Medeiros-Neto G. J Clin Endocrinol Metab. 1999 Jan;84(1):336-41. PMID: 9920104
• A novel aminoterminal mutation in the KAL-1 gene in a large pedigree with X-linked Kallmann syndrome. Gu WX, Colquhoun-Kerr JS, Kopp P, Bode HH, Jameson JL. Mol Genet Metab. 1998 Sep;65(1):59-61. PMID: 9787096
• Surprising news: a putative sulfate transporter is defective in Pendred's syndrome. Rutishauser J, Kopp P. Eur J Endocrinol. 1998 Jun;138(6):623-4. No abstract available. PMID: 9678527
• Resveratrol, a phytoestrogen found in red wine. A possible explanation for the conundrum of the 'French paradox'? Kopp P. Eur J Endocrinol. 1998 Jun;138(6):619-20. No abstract available. PMID: 9678525
• The thyroid hormone receptor variant alpha2 is a weak antagonist because it is deficient in interactions with nuclear receptor corepressors. Tagami T, Kopp P, Johnson W, Arseven OK, Jameson JL. Endocrinology. 1998 May;139(5):2535-44. PMID: 9564869
• Congenital nonautoimmune hyperthyroidism in a nonidentical twin caused by a sporadic germline mutation in the thyrotropin receptor gene. Kopp P, Jameson JL, Roe TF. Thyroid. 1997 Oct;7(5):765-70. PMID: 9349581
• A long-sought needle in the haystack: the multiple endocrine neoplasia type 1 gene. Kopp P. Eur J Endocrinol. 1997 Sep;137(3):222-3. Review. PMID: 9330583
• Congenital hyperthyroidism caused by a solitary toxic adenoma harboring a novel somatic mutation (serine281-->isoleucine) in the extracellular domain of the thyrotropin receptor. Kopp P, Muirhead S, Jourdain N, Gu WX, Jameson JL, Rodd C. J Clin Invest. 1997 Sep 15;100(6):1634-9. PMID: 9294132
• Expression of nitric oxide synthase III in human thyroid follicular cells: evidence for increased expression in hyperthyroidism. Colin IM, Kopp P, Zbären J, Häberli A, Grizzle WE, Jameson JL. Eur J Endocrinol. 1997 Jun;136(6):649-55. PMID: 9225730
• Key elements involved in the negative regulation of the TSH receptor: G protein-coupled receptor kinases, arrestin and inducible cAMP early repressor. Kopp P. Eur J Endocrinol. 1997 Mar;136(3):269-70. PMID: 9100549
• X-linked adrenal hypoplasia and hypogonadotropic hypogonadism: multiple roles for the putative transcription factor DAX-1. Kopp P. Eur J Endocrinol. 1997 Feb;136(2):153-4. PMID: 9116909
• Sexually dimorphic transcriptional responses to gonadotropin-releasing hormone require chronic in vivo exposure to estradiol. Colin IM, Bauer-Dantoin AC, Sundaresan S, Kopp P, Jameson JL. Endocrinology. 1996 Jun;137(6):2300-7. PMID: 8641179
• Syndrome of resistance to thyroid hormone: insights into thyroid hormone action. Kopp P, Kitajima K, Jameson JL. Proc Soc Exp Biol Med. 1996 Jan;211(1):49-61. Review. PMID: 8594618
• Thyroid hormone (T3) inhibits ciprofibrate-induced transcription of genes encoding beta-oxidation enzymes: cross talk between peroxisome proliferator and T3 signaling pathways. Chu R, Madison LD, Lin Y, Kopp P, Rao MS, Jameson JL, Reddy JK. Proc Natl Acad Sci U S A. 1995 Dec 5;92(25):11593-7. PMID: 8524810
• The thyrotropin (TSH) receptor transmembrane domain mutation (Pro556-Leu) in the hypothyroid hyt/hyt mouse results in plasma membrane targeting but defective TSH binding. Gu WX, Du GG, Kopp P, Rentoumis A, Albanese C, Kohn LD, Madison LD, Jameson JL. Endocrinology. 1995 Jul;136(7):3146-53. PMID: 778934