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Similar articles for PubMed (Select 22577170)

1.

ZNF764 haploinsufficiency may explain partial glucocorticoid, androgen, and thyroid hormone resistance associated with 16p11.2 microdeletion.

Kino T, Pavlatou MG, Moraitis AG, Nemery RL, Raygada M, Stratakis CA.

J Clin Endocrinol Metab. 2012 Aug;97(8):E1557-66. doi: 10.1210/jc.2011-3493. Epub 2012 May 10.

2.

The atypical 16p11.2 deletion: a not so atypical microdeletion syndrome?

Barge-Schaapveld DQ, Maas SM, Polstra A, Knegt LC, Hennekam RC.

Am J Med Genet A. 2011 May;155A(5):1066-72. doi: 10.1002/ajmg.a.33991. Epub 2011 Apr 4.

PMID:
21465664
3.

Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterization.

Hempel M, Rivera Brugu├ęs N, Wagenstaller J, Lederer G, Weitensteiner A, Seidel H, Meitinger T, Strom TM.

Am J Med Genet A. 2009 Oct;149A(10):2106-12. doi: 10.1002/ajmg.a.33042.

PMID:
19676056
4.

Resistance to several steroids in two sisters.

New MI, Nimkarn S, Brandon DD, Cunningham-Rundles S, Wilson RC, Newfield RS, Vandermeulen J, Barron N, Russo C, Loriaux DL, O'Malley B.

J Clin Endocrinol Metab. 1999 Dec;84(12):4454-64.

PMID:
10599702
5.

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.

Shimojima K, Inoue T, Fujii Y, Ohno K, Yamamoto T.

Eur J Med Genet. 2009 Nov-Dec;52(6):433-5. doi: 10.1016/j.ejmg.2009.09.007. Epub 2009 Sep 19.

PMID:
19770079
7.

A natural transactivation mutation in the thyroid hormone beta receptor: impaired interaction with putative transcriptional mediators.

Collingwood TN, Rajanayagam O, Adams M, Wagner R, Cavaill├Ęs V, Kalkhoven E, Matthews C, Nystrom E, Stenlof K, Lindstedt G, Tisell L, Fletterick RJ, Parker MG, Chatterjee VK.

Proc Natl Acad Sci U S A. 1997 Jan 7;94(1):248-53.

9.

Glucocorticoids in malignant lymphoid cells: gene regulation and the minimum receptor fragment for lysis.

Thompson EB, Nazareth LV, Thulasi R, Ashraf J, Harbour D, Johnson BH.

J Steroid Biochem Mol Biol. 1992 Mar;41(3-8):273-82.

PMID:
1314075
10.

A novel 1297-1304delGCCTGCCA mutation in the exon 10 of the thyroid hormone receptor beta gene causes resistance to thyroid hormone.

Rivolta CM, Mallea Gil MS, Ballarino C, Ridruejo MC, Miguel CM, Gimenez SB, Bernacchi SS, Targovnik HM.

Mol Diagn. 2004;8(3):163-9.

PMID:
15771554
11.
12.

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
14.

Glucocorticosteroid resistance in humans. Elucidation of the molecular mechanisms and implications for pathophysiology.

Stratakis CA, Karl M, Schulte HM, Chrousos GP.

Ann N Y Acad Sci. 1994 Nov 30;746:362-74; discussion 374-6. Review.

PMID:
7825890
15.

The androgen-specific probasin response element 2 interacts differentially with androgen and glucocorticoid receptors.

Claessens F, Alen P, Devos A, Peeters B, Verhoeven G, Rombauts W.

J Biol Chem. 1996 Aug 9;271(32):19013-6.

17.

Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.

Willemsen MH, Fernandez BA, Bacino CA, Gerkes E, de Brouwer AP, Pfundt R, Sikkema-Raddatz B, Scherer SW, Marshall CR, Potocki L, van Bokhoven H, Kleefstra T.

Eur J Hum Genet. 2010 Apr;18(4):429-35. doi: 10.1038/ejhg.2009.192. Epub 2009 Nov 18.

18.
20.

A new function for the C-terminal zinc finger of the glucocorticoid receptor. Repression of RelA transactivation.

Liden J, Delaunay F, Rafter I, Gustafsson J, Okret S.

J Biol Chem. 1997 Aug 22;272(34):21467-72.

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