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1 - 25 of 87 results for author:"Refetoff S." in Literature citations

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Generation of functional thyroid from embryonic stem cells.

Antonica F., Kasprzyk D.F., Opitz R., Iacovino M., Liao X.H., Dumitrescu A.M., Refetoff S., Peremans K., Manto M., Kyba M. et al.

Nature 491:66-71(2012) · Mapped (10)

Disruption of the melanin-concentrating hormone receptor 1 (MCH1R) affects thyroid function.

Chung S., Liao X.H., Di Cosmo C., Van Sande J., Wang Z., Refetoff S., Civelli O.

Endocrinology 153:6145-6154(2012) · Mapped (3)

Homozygous thyroid hormone receptor beta-gene mutations in resistance to thyroid hormone: three new cases and review of the literature.

Ferrara A.M., Onigata K., Ercan O., Woodhead H., Weiss R.E., Refetoff S.

J. Clin. Endocrinol. Metab. 97:1328-1336(2012) · Mapped (4)

Consecutive mutational events in a TSHR allele of Arab families with resistance to thyroid stimulating hormone.

Sriphrapradang C., German A., Dumitrescu A.M., Refetoff S.

Thyroid 22:252-257(2012) · Mapped (6)

Role of type 2 deiodinase in response to acute lung injury (ALI) in mice.

Barca-Mayo O., Liao X.H., DiCosmo C., Dumitrescu A., Moreno-Vinasco L., Wade M.S., Sammani S., Mirzapoiazova T., Garcia J.G., Refetoff S. et al.

Proc. Natl. Acad. Sci. U.S.A. 108:E1321-9(2011) · Mapped (8)

The coexistence of a novel inactivating mutant thyrotropin receptor allele with two thyroid peroxidase mutations: a genotype-phenotype correlation.

Sriphrapradang C., Tenenbaum-Rakover Y., Weiss M., Barkoff M.S., Admoni O., Kawthar D., Caltabiano G., Pardo L., Dumitrescu A.M., Refetoff S.

J. Clin. Endocrinol. Metab. 96:E1001-6(2011) · Mapped (6)

Thyroid hormone receptor alpha and regulation of type 3 deiodinase.

Barca-Mayo O., Liao X.H., Alonso M., Di Cosmo C., Hernandez A., Refetoff S., Weiss R.E.

Mol. Endocrinol. 25:575-583(2011) · Mapped (1)

Distinct roles of deiodinases on the phenotype of Mct8 defect: a comparison of eight different mouse genotypes.

Liao X.H., Di Cosmo C., Dumitrescu A.M., Hernandez A., Van Sande J., St Germain D.L., Weiss R.E., Galton V.A., Refetoff S.

Endocrinology 152:1180-1191(2011) · Mapped (12)

Thyrotrophin receptor signaling dependence of Braf-induced thyroid tumor initiation in mice.

Franco A.T., Malaguarnera R., Refetoff S., Liao X.H., Lundsmith E., Kimura S., Pritchard C., Marais R., Davies T.F., Weinstein L.S. et al.

Proc. Natl. Acad. Sci. U.S.A. 108:1615-1620(2011) · Mapped (22)

Stanniocalcin 1 induction by thyroid hormone depends on thyroid hormone receptor beta and phosphatidylinositol 3-kinase activation.

Moeller L.C., Haselhorst N.E., Dumitrescu A.M., Cao X., Seo H., Refetoff S., Mann K., Janssen O.E.

Exp. Clin. Endocrinol. Diabetes 119:81-85(2011) · Mapped (15)

Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion.

Di Cosmo C., Liao X.H., Dumitrescu A.M., Philp N.J., Weiss R.E., Refetoff S.

J. Clin. Invest. 120:3377-3388(2010) · Mapped (3)

Cross-talk between PI3K and estrogen in the mouse thyroid predisposes to the development of follicular carcinomas with a higher incidence in females.

Antico-Arciuch V.G., Dima M., Liao X.H., Refetoff S., Di Cristofano A.

Oncogene 29:5678-5686(2010) · Mapped (9)

Autoimmunity in patients with resistance to thyroid hormone.

Barkoff M.S., Kocherginsky M., Anselmo J., Weiss R.E., Refetoff S.

J. Clin. Endocrinol. Metab. 95:3189-3193(2010) · Mapped (4)

Distinct and histone-specific modifications mediate positive versus negative transcriptional regulation of TSHalpha promoter.

Wang D., Xia X., Weiss R.E., Refetoff S., Yen P.M.

PLoS ONE 5:e9853-e9853(2010) · Mapped (10)

Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter-8- and deiodinase-2-deficient mice.

Morte B., Ceballos A., Diez D., Grijota-Martinez C., Dumitrescu A.M., Di Cosmo C., Galton V.A., Refetoff S., Bernal J.

Endocrinology 151:2381-2387(2010) · Mapped (6)

White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene.

Gika A.D., Siddiqui A., Hulse A.J., Edward S., Fallon P., McEntagart M.E., Jan W., Josifova D., Lerman-Sagie T., Drummond J. et al.

Dev Med Child Neurol 52:475-482(2010) · Mapped (2)

Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X).

Di Cosmo C., McLellan N., Liao X.H., Khanna K.K., Weiss R.E., Papp L., Refetoff S.

J. Clin. Endocrinol. Metab. 94:4003-4009(2009) · Mapped (9)

A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport.

Di Cosmo C., Liao X.H., Dumitrescu A.M., Weiss R.E., Refetoff S.

Endocrinology 150:4450-4458(2009) · Mapped (3)

In vivo interaction of steroid receptor coactivator (SRC)-1 and the activation function-2 domain of the thyroid hormone receptor (TR) beta in TRbeta E457A knock-in and SRC-1 knockout mice.

Alonso M., Goodwin C., Liao X., Ortiga-Carvalho T., Machado D.S., Wondisford F.E., Refetoff S., Weiss R.E.

Endocrinology 150:3927-3934(2009) · Mapped (5)

Oncogenic Kras requires simultaneous PI3K signaling to induce ERK activation and transform thyroid epithelial cells in vivo.

Miller K.A., Yeager N., Baker K., Liao X.H., Refetoff S., Di Cristofano A.

Cancer Res. 69:3689-3694(2009) · Mapped (11)

Selenium supplementation fails to correct the selenoprotein synthesis defect in subjects with SBP2 gene mutations.

Schomburg L., Dumitrescu A.M., Liao X.H., Bin-Abbas B., Hoeflich J., Kohrle J., Refetoff S.

Thyroid 19:277-281(2009) · Mapped (9)

Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community.

Tenenbaum-Rakover Y., Grasberger H., Mamanasiri S., Ringkananont U., Montanelli L., Barkoff M.S., Dahood A.M., Refetoff S.

J. Clin. Endocrinol. Metab. 94:1706-1712(2009) · Mapped (6)

Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronine.

Ceballos A., Belinchon M.M., Sanchez-Mendoza E., Grijota-Martinez C., Dumitrescu A.M., Refetoff S., Morte B., Bernal J.

Endocrinology 150:2491-2496(2009) · Mapped (4)

Thyroid hormone receptor beta gene mutation (P453A) in a family producing resistance to thyroid hormone.

Bayraktaroglu T., Noel J., Alagol F., Colak N., Mukaddes N.M., Refetoff S.

Exp. Clin. Endocrinol. Diabetes 117:34-37(2009) · Mapped (4)

Molecular basis of inherited thyroxine-binding globulin defects.

Janssen O.E., Bertenshaw R., Takeda K., Weiss R., Refetoff S.

Trends Endocrinol. Metab. 3:49-53(1992) · UniProtKB (1)

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