Refetoff S - Search Results

1

An Essential Physiological Role for MCT8 in Bone in Male Mice.

Leitch VD, Di Cosmo C, Liao XH, O'Boy S, Galliford TM, Evans H, Croucher PI, Boyde A, Dumitrescu A, Weiss RE, Refetoff S, Williams GR, Bassett JHD. Leitch VD, et al. Among authors: refetoff s. Endocrinology. 2017 Sep 1;158(9):3055-3066. doi: 10.1210/en.2017-00399. Endocrinology. 2017. PMID: 28637283 Free PMC article.

2

Thyroid function and effect of aging in combined hetero/homozygous mice deficient in thyroid hormone receptors alpha and beta genes.

Weiss RE, Chassande O, Koo EK, Macchia PE, Cua K, Samarut J, Refetoff S, Refetoff S. Weiss RE, et al. Among authors: refetoff s. J Endocrinol. 2002 Jan;172(1):177-85. doi: 10.1677/joe.0.1720177. J Endocrinol. 2002. PMID: 11786385

3

Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene.

Pohlenz J, Dumitrescu A, Aumann U, Koch G, Melchior R, Prawitt D, Refetoff S. Pohlenz J, et al. Among authors: refetoff s. J Clin Endocrinol Metab. 2002 Jan;87(1):336-9. doi: 10.1210/jcem.87.1.8154. J Clin Endocrinol Metab. 2002. PMID: 11788671

4

Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice.

Pohlenz J, Dumitrescu A, Zundel D, Martiné U, Schönberger W, Koo E, Weiss RE, Cohen RN, Kimura S, Refetoff S. Pohlenz J, et al. Among authors: refetoff s. J Clin Invest. 2002 Feb;109(4):469-73. doi: 10.1172/JCI14192. J Clin Invest. 2002. PMID: 11854318 Free PMC article.

5

Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping.

Reutrakul S, Dumitrescu A, Macchia PE, Moll GW Jr, Vierhapper H, Refetoff S. Reutrakul S, et al. Among authors: refetoff s. J Clin Endocrinol Metab. 2002 Mar;87(3):1045-51. doi: 10.1210/jcem.87.3.8275. J Clin Endocrinol Metab. 2002. PMID: 11889160

6

Steroid receptor coactivator-1 deficiency causes variable alterations in the modulation of T(3)-regulated transcription of genes in vivo.

Takeuchi Y, Murata Y, Sadow P, Hayashi Y, Seo H, Xu J, O'Malley BW, Weiss RE, Refetoff S. Takeuchi Y, et al. Among authors: refetoff s. Endocrinology. 2002 Apr;143(4):1346-52. doi: 10.1210/endo.143.4.8730. Endocrinology. 2002. PMID: 11897691

7

Thyroid function in mice with compound heterozygous and homozygous disruptions of SRC-1 and TIF-2 coactivators: evidence for haploinsufficiency.

Weiss RE, Gehin M, Xu J, Sadow PM, O'Malley BW, Chambon P, Refetoff S. Weiss RE, et al. Among authors: refetoff s. Endocrinology. 2002 Apr;143(4):1554-7. doi: 10.1210/endo.143.4.8828. Endocrinology. 2002. PMID: 11897715

8

RXR receptor agonist suppression of thyroid function: central effects in the absence of thyroid hormone receptor.

Macchia PE, Jiang P, Yuan YD, Chandarardna RA, Weiss RE, Chassande O, Samarut J, Refetoff S, Burant CF. Macchia PE, et al. Among authors: refetoff s. Am J Physiol Endocrinol Metab. 2002 Aug;283(2):E326-31. doi: 10.1152/ajpendo.00313.2001. Am J Physiol Endocrinol Metab. 2002. PMID: 12110538 Free article.

9

Effects of ligand and thyroid hormone receptor isoforms on hepatic gene expression profiles of thyroid hormone receptor knockout mice.

Yen PM, Feng X, Flamant F, Chen Y, Walker RL, Weiss RE, Chassande O, Samarut J, Refetoff S, Meltzer PS. Yen PM, et al. Among authors: refetoff s. EMBO Rep. 2003 Jun;4(6):581-7. doi: 10.1038/sj.embor.embor862. EMBO Rep. 2003. PMID: 12776178 Free PMC article.

10

Hypothyroidism in thyroid transcription factor 1 haploinsufficiency is caused by reduced expression of the thyroid-stimulating hormone receptor.

Moeller LC, Kimura S, Kusakabe T, Liao XH, Van Sande J, Refetoff S. Moeller LC, et al. Among authors: refetoff s. Mol Endocrinol. 2003 Nov;17(11):2295-302. doi: 10.1210/me.2003-0175. Epub 2003 Aug 7. Mol Endocrinol. 2003. PMID: 12907760

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