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Items: 1 to 20 of 171

1.
Endothelial glucocorticoid receptor is required for protection against sepsis
Julie E. Goodwin, Yan Feng, Heino Velazquez, William C. Sessa
Proc Natl Acad Sci U S A. 2013 Jan 2; 110(1): 306–311. Published online 2012 Dec 17. doi: 10.1073/pnas.1210200110
PMCID:
PMC3538225
AbstractArticlePDF–729K
2.
Glucocorticoids activate somatostatin gene transcription through co-operative interaction with the cyclic AMP signalling pathway.
J L Liu, D N Papachristou, Y C Patel
Biochem J. 1994 Aug 1; 301(Pt 3): 863–869. doi: 10.1042/bj3010863
PMCID:
PMC1137066
SummaryPage BrowsePDF–1.6M
3.
The mouse glucocorticoid receptor: mapping of functional domains by cloning, sequencing and expression of wild-type and mutant receptor proteins.
M Danielsen, J P Northrop, G M Ringold
EMBO J. 1986 Oct; 5(10): 2513–2522. doi: 10.1002/j.1460-2075.1986.tb04529.x
PMCID:
PMC1167147
SummaryPage BrowsePDF–2.2M
4.
Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population.
M Rämet, R Haataja, R Marttila, J Floros, M Hallman
Am J Hum Genet. 2000 May; 66(5): 1569–1579. Published online 2000 Apr 4. doi: 10.1086/302906
PMCID:
PMC1378016
SummaryPDF–273K
5.
Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency
Nicole Reisch, Jan Idkowiak, Beverly A. Hughes, Hannah E. Ivison, Omar A. Abdul-Rahman, Laura G. Hendon, Ann Haskins Olney, Shelly Nielsen, Rachel Harrison, Edward M. Blair, Vivek Dhir, Nils Krone, Cedric H. L. Shackleton, Wiebke Arlt
J Clin Endocrinol Metab. 2013 Mar; 98(3): E528–E536. Published online 2013 Jan 30. doi: 10.1210/jc.2012-3449
PMCID:
PMC3708032
AbstractArticle
6.
The Proton Pump Inhibitor Lansoprazole Improves the Skeletal Phenotype in Dystrophin Deficient mdx Mice
Arpana Sali, Gina M. Many, Heather Gordish-Dressman, Jack H. van der Meulen, Aditi Phadke, Christopher F. Spurney, Avital Cnaan, Eric P. Hoffman, Kanneboyina Nagaraju
PLoS One. 2013; 8(7): e66617. Published online 2013 Jul 2. doi: 10.1371/journal.pone.0066617
PMCID:
PMC3699610
AbstractArticlePDF–908K
7.
Wnt/β-Catenin Signaling Protects Mouse Liver against Oxidative Stress-induced Apoptosis through the Inhibition of Forkhead Transcription Factor FoxO3
Guo-Zhong Tao, Nadja Lehwald, Kyu Yun Jang, Joy Baek, Baohui Xu, M. Bishr Omary, Karl G. Sylvester
J Biol Chem. 2013 Jun 14; 288(24): 17214–17224. Published online 2013 Apr 25. doi: 10.1074/jbc.M112.445965
PMCID:
PMC3682526
AbstractArticlePDF–3.1M
8.
Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE) Cohort
Nils Krone, Ian T. Rose, Debbie S. Willis, James Hodson, Sarah H. Wild, Emma J. Doherty, Stefanie Hahner, Silvia Parajes, Roland H. Stimson, Thang S. Han, Paul V. Carroll, Gerry S. Conway, Brian R. Walker, Fiona MacDonald, Richard J. Ross, Wiebke Arlt, for the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE)
J Clin Endocrinol Metab. 2013 Feb; 98(2): E346–E354. Published online 2013 Jan 21. doi: 10.1210/jc.2012-3343
PMCID:
PMC3651585
AbstractArticle
9.
Recommendations for Treatment of Nonclassic Congenital Adrenal Hyperplasia (NCCAH): an Update
Christine M. Trapp, Sharon E. Oberfield
Steroids. Author manuscript; available in PMC 2013 Apr 29.
Published in final edited form as: Steroids. 2012 Mar 10; 77(4): 342–346. Published online 2011 Dec 13. doi: 10.1016/j.steroids.2011.12.009
PMCID:
PMC3638754
AbstractArticlePDF–290K
10.
11β-Hydroxysteroid dehydrogenase type 1 contributes to the regulation of 7-oxysterol levels in the arterial wall through the inter-conversion of 7-ketocholesterol and 7β-hydroxycholesterol
Tijana Mitić, Ruth Andrew, Brian R. Walker, Patrick W.F. Hadoke
Biochimie. 2013 Mar; 95(3): 548–555. doi: 10.1016/j.biochi.2012.08.007
PMCID:
PMC3585959
AbstractArticlePDF–660K
11.
Regulation of cytosolic prostaglandin E synthase by phosphorylation
Tsuyoshi Kobayashi, Yoshihito Nakatani, Toshihiro Tanioka, Masafumi Tsujimoto, Shigeo Nakajo, Kazuyasu Nakaya, Makoto Murakami, Ichiro Kudo
Biochem J. 2004 Jul 1; 381(Pt 1): 59–69. Prepublished online 2004 Mar 25. Published online 2004 Jun 22. doi: 10.1042/BJ20040118
PMCID:
PMC1133762
AbstractArticlePDF–808K
12.
Adrenal function in Smith-Lemli-Opitz Syndrome
Simona E Bianconi, Sandra K Conley, Meg F Keil, Ninet Sinaii, Kristina I Rother, Forbes D Porter, Constantine A Stratakis
Am J Med Genet A. Author manuscript; available in PMC 2012 Nov 4.
Published in final edited form as: Am J Med Genet A. 2011 Nov; 155A(11): 2732–2738. Published online 2011 Oct 11. doi: 10.1002/ajmg.a.34271
PMCID:
PMC3488380
AbstractArticlePDF–183K
13.
KESTREL: a powerful method for identifying the physiological substrates of protein kinases
Philip Cohen, Axel Knebel
Biochem J. 2006 Jan 1; 393(Pt 1): 1–6. Published online 2005 Dec 12. doi: 10.1042/BJ20051545
PMCID:
PMC1383659
AbstractArticlePDF–203K
14.
CD73-generated adenosine facilitates Toxoplasma gondii differentiation to long-lived tissue cysts in the central nervous system
Deeqa A. Mahamed, Jeffrey H. Mills, Charlotte E. Egan, Eric Y. Denkers, Margaret S. Bynoe
Proc Natl Acad Sci U S A. 2012 Oct 2; 109(40): 16312–16317. Published online 2012 Sep 17. doi: 10.1073/pnas.1205589109
PMCID:
PMC3479617
AbstractArticlePDF–463K
15.
Impact of Glucocorticoid Receptor Gene Polymorphisms on the Metabolic Profile of Adult Patients with the Classical Form of 21-Hydroxylase Deficiency
Ricardo P. P. Moreira, Larissa G. Gomes, Berenice B. Mendonca, Tânia A. S. S. Bachega
PLoS One. 2012; 7(9): e44893. Published online 2012 Sep 18. doi: 10.1371/journal.pone.0044893
PMCID:
PMC3445550
AbstractArticlePDF–175K
16.
Biomarkers of hypothalamic–pituitary–adrenal axis activity in mice lacking 11β-HSD1 and H6PDH
Lianne Abrahams, Nina M Semjonous, Phil Guest, Agnieszka Zielinska, Beverly Hughes, Gareth G Lavery, Paul M Stewart
J Endocrinol. 2012 Sep; 214(3): 367–372. Prepublished online 2012 Jun 20. doi: 10.1530/JOE-12-0178
PMCID:
PMC3427643
AbstractArticlePDF–171K
17.
An Atypical Case of Familial Glucocorticoid Deficiency without Pigmentation Caused by Coexistent Homozygous Mutations in MC2R (T152K) and MC1R (R160W)
Serap Turan, Claire Hughes, Zeynep Atay, Tulay Guran, Belma Haliloglu, Adrian J. L. Clark, Abdullah Bereket, Louise A. Metherell
J Clin Endocrinol Metab. 2012 May; 97(5): E771–E774. Published online 2012 Feb 15. doi: 10.1210/jc.2011-2414
PMCID:
PMC3396854
AbstractArticle
18.
Loss of STAT1 in Bone Marrow-Derived Cells Accelerates Skeletal Muscle Regeneration
Yan Gao, Yanfeng Li, Xing Guo, Zhenguo Wu, Wei Zhang
PLoS One. 2012; 7(5): e37656. Published online 2012 May 23. doi: 10.1371/journal.pone.0037656
PMCID:
PMC3359303
AbstractArticlePDF–8.3M
19.
Haploinsufficiency of the E3 Ubiquitin Ligase C-Terminus of Heat Shock Cognate 70 Interacting Protein (CHIP) Produces Specific Behavioral Impairments
BethAnn McLaughlin, Matthew A. Buendia, Tommy P. Saborido, Amy M. Palubinsky, Jeannette N. Stankowski, Gregg D. Stanwood
PLoS One. 2012; 7(5): e36340. Published online 2012 May 11. doi: 10.1371/journal.pone.0036340
PMCID:
PMC3350526
AbstractArticlePDF–551K
20.
A Novel Point Mutation of the Human Glucocorticoid Receptor Gene Causes Primary Generalized Glucocorticoid Resistance Through Impaired Interaction With the LXXLL Motif of the p160 Coactivators: Dissociation of the Transactivating and Transreppressive Activities
Nicolas C. Nicolaides, Michael L. Roberts, Tomoshige Kino, Geoffrey Braatvedt, Darrell E. Hurt, Eleni Katsantoni, Amalia Sertedaki, George P. Chrousos, Evangelia Charmandari
J Clin Endocrinol Metab. 2014 May; 99(5): E902–E907. Published online 2014 Jan 31. doi: 10.1210/jc.2013-3005
PMCID:
PMC4010692
AbstractArticle

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