Moeller LC - Search Results

1

A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.

Ferrara AM, Pappa T, Fu J, Brown CD, Peterson A, Moeller LC, Wyne K, White KP, Pluzhnikov A, Trubetskoy V, Nobrega M, Weiss RE, Dumitrescu AM, Refetoff S. Ferrara AM, et al. Among authors: moeller lc. J Clin Endocrinol Metab. 2015 Jan;100(1):E173-81. doi: 10.1210/jc.2014-3490. J Clin Endocrinol Metab. 2015. PMID: 25361180 Free PMC article.

2

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. Mol Endocrinol. 2003 Nov;17(11):2295-302. doi: 10.1210/me.2003-0175. Epub 2003 Aug 7. Mol Endocrinol. 2003. PMID: 12907760

3

Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene.

Narendran P, Lado-Abeal J, Moeller LC, Refetoff S. Narendran P, et al. Among authors: moeller lc. Clin Endocrinol (Oxf). 2003 Dec;59(6):824-5. doi: 10.1046/j.1365-2265.2003.01924.x. Clin Endocrinol (Oxf). 2003. PMID: 14974930 Review. No abstract available.

4

Partial deficiency of thyroxine-binding globulin-Allentown is due to a mutation in the signal peptide.

Fingerhut A, Reutrakul S, Knuedeler SD, Moeller LC, Greenlee C, Refetoff S, Janssen OE. Fingerhut A, et al. Among authors: moeller lc. J Clin Endocrinol Metab. 2004 May;89(5):2477-83. doi: 10.1210/jc.2003-031613. J Clin Endocrinol Metab. 2004. PMID: 15126580

5

A novel splice variant involving the 5' untranslated region of thyroid hormone receptor beta1 (TRbeta1).

Mannavola D, Moeller LC, Beck-Peccoz P, Persani L, Weiss RE, Refetoff S. Mannavola D, et al. Among authors: moeller lc. J Endocrinol Invest. 2004 Apr;27(4):318-22. doi: 10.1007/BF03351055. J Endocrinol Invest. 2004. PMID: 15233549

6

Thyroid hormone responsive genes in cultured human fibroblasts.

Moeller LC, Dumitrescu AM, Walker RL, Meltzer PS, Refetoff S. Moeller LC, et al. J Clin Endocrinol Metab. 2005 Feb;90(2):936-43. doi: 10.1210/jc.2004-1768. Epub 2004 Oct 26. J Clin Endocrinol Metab. 2005. PMID: 15507505

7

Cytosolic action of thyroid hormone leads to induction of hypoxia-inducible factor-1alpha and glycolytic genes.

Moeller LC, Dumitrescu AM, Refetoff S. Moeller LC, et al. Mol Endocrinol. 2005 Dec;19(12):2955-63. doi: 10.1210/me.2004-0542. Epub 2005 Jul 28. Mol Endocrinol. 2005. PMID: 16051672

8

Mutations in SECISBP2 result in abnormal thyroid hormone metabolism.

Dumitrescu AM, Liao XH, Abdullah MS, Lado-Abeal J, Majed FA, Moeller LC, Boran G, Schomburg L, Weiss RE, Refetoff S. Dumitrescu AM, et al. Among authors: moeller lc. Nat Genet. 2005 Nov;37(11):1247-52. doi: 10.1038/ng1654. Epub 2005 Oct 16. Nat Genet. 2005. PMID: 16228000

9

A case of Resistance to Thyroid Hormone without mutation in the thyroid hormone receptor beta.

McDermott JH, Agha A, McMahon M, Gasparro D, Moeller L, Dumitrescu AM, Refetoff S, Sreenan S. McDermott JH, et al. Ir J Med Sci. 2005 Oct-Dec;174(4):60-4. doi: 10.1007/BF03168985. Ir J Med Sci. 2005. PMID: 16445164

10

C-terminal amino acid alteration rather than late termination causes complete deficiency of thyroxine-binding globulin CD-NeuIsenburg.

Moeller LC, Fingerhut A, Lahner H, Grasberger H, Weimer B, Happ J, Mann K, Janssen OE. Moeller LC, et al. J Clin Endocrinol Metab. 2006 Aug;91(8):3215-8. doi: 10.1210/jc.2005-2261. Epub 2006 May 30. J Clin Endocrinol Metab. 2006. PMID: 16735497

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