Pannain S - Search Results

1

Mutations of thyrotropin receptor isolated from thyroid autonomous functioning adenomas confer TSH-independent growth to thyroid cells.

Porcellini A, Ruggiano G, Pannain S, Ciullo I, Amabile G, Fenzi G, Avvedimento EV. Porcellini A, et al. Among authors: pannain s. Oncogene. 1997 Aug 14;15(7):781-9. doi: 10.1038/sj.onc.1201240. Oncogene. 1997. PMID: 9266964

2

Somatic mutations in the VI transmembrane segment of the thyrotropin receptor constitutively activate cAMP signalling in thyroid hyperfunctioning adenomas.

Porcellini A, Ciullo I, Pannain S, Fenzi G, Avvedimento E. Porcellini A, et al. Among authors: pannain s. Oncogene. 1995 Sep 21;11(6):1089-93. Oncogene. 1995. PMID: 7566968

3

Resistance to thyrotropin (TSH) in three families is not associated with mutations in the TSH receptor or TSH.

Xie J, Pannain S, Pohlenz J, Weiss RE, Moltz K, Morlot M, Asteria C, Persani L, Beck-Peccoz P, Parma J, Vassart G, Refetoff S. Xie J, et al. Among authors: pannain s. J Clin Endocrinol Metab. 1997 Dec;82(12):3933-40. doi: 10.1210/jcem.82.12.4418. J Clin Endocrinol Metab. 1997. PMID: 9398691

4

Role of oxidative metabolism on endothelium-dependent vascular relaxation of isolated vessels.

Cappelli-Bigazzi M, Battaglia C, Pannain S, Chiariello M, Ambrosio G. Cappelli-Bigazzi M, et al. Among authors: pannain s. J Mol Cell Cardiol. 1997 Mar;29(3):871-9. doi: 10.1006/jmcc.1996.0286. J Mol Cell Cardiol. 1997. PMID: 9152848

5

Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping.

Pannain S, Weiss RE, Jackson CE, Dian D, Beck JC, Sheffield VC, Cox N, Refetoff S. Pannain S, et al. J Clin Endocrinol Metab. 1999 Mar;84(3):1061-71. doi: 10.1210/jcem.84.3.5541. J Clin Endocrinol Metab. 1999. PMID: 10084596

6

Five new families with resistance to thyroid hormone not caused by mutations in the thyroid hormone receptor beta gene.

Pohlenz J, Weiss RE, Macchia PE, Pannain S, Lau IT, Ho H, Refetoff S. Pohlenz J, et al. Among authors: pannain s. J Clin Endocrinol Metab. 1999 Nov;84(11):3919-28. doi: 10.1210/jcem.84.11.6080. J Clin Endocrinol Metab. 1999. PMID: 10566629

7

Familial dysalbuminemic hyperthyroxinemia in a Swiss family caused by a mutant albumin (R218P) shows an apparent discrepancy between serum concentration and affinity for thyroxine.

Pannain S, Feldman M, Eiholzer U, Weiss RE, Scherberg NH, Refetoff S. Pannain S, et al. J Clin Endocrinol Metab. 2000 Aug;85(8):2786-92. doi: 10.1210/jcem.85.8.6746. J Clin Endocrinol Metab. 2000. PMID: 10946882 Review.

8

Search for abnormalities of nuclear corepressors, coactivators, and a coregulator in families with resistance to thyroid hormone without mutations in thyroid hormone receptor beta or alpha genes.

Reutrakul S, Sadow PM, Pannain S, Pohlenz J, Carvalho GA, Macchia PE, Weiss RE, Refetoff S. Reutrakul S, et al. Among authors: pannain s. J Clin Endocrinol Metab. 2000 Oct;85(10):3609-17. doi: 10.1210/jcem.85.10.6873. J Clin Endocrinol Metab. 2000. PMID: 11061510

9

Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1.

Grasberger H, Vaxillaire M, Pannain S, Beck JC, Mimouni-Bloch A, Vatin V, Vassart G, Froguel P, Refetoff S. Grasberger H, et al. Among authors: pannain s. Hum Genet. 2005 Dec;118(3-4):348-55. doi: 10.1007/s00439-005-0036-6. Epub 2005 Sep 28. Hum Genet. 2005. PMID: 16189712

10

A Novel Mutation in the TBG Gene Producing Partial Thyroxine-Binding Globulin Deficiency (Glencoe) Identified in 2 Families.

Pappa T, Moeller LC, Edidin DV, Pannain S, Refetoff S. Pappa T, et al. Among authors: pannain s. Eur Thyroid J. 2017 Jul;6(3):138-142. doi: 10.1159/000455097. Epub 2017 Feb 2. Eur Thyroid J. 2017. PMID: 28785540 Free PMC article.

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