Chrousos syndrome: a seminal report, a phylogenetic enigma and the clinical implications of glucocorticoid signalling changes

Chrousos syndrome: a seminal report, a phylogenetic enigma and the clinical implications of glucocorticoid signalling changes

Item
http://www.wikidata.org/entity/Q28288491
Diagnosis and Treatment of Primary Adrenal Insufficiency: An Endocrine Society Clinical Practice GuidelineMicroRNAs as tools to predict glucocorticoid response in inflammatory bowel diseasesA Natural Mutation in Helix 5 of the Ligand Binding Domain of Glucocorticoid Receptor Enhances Receptor-Ligand InteractionA 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 transreppressivPrimary generalized familial and sporadic glucocorticoid resistance (Chrousos syndrome) and hypersensitivityRecent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor.Non polycystic ovary syndrome-related endocrine disorders associated with hirsutism.Stress response and child health.A novel point mutation in the DNA-binding domain (DBD) of the human glucocorticoid receptor causes primary generalized glucocorticoid resistance by disrupting the hydrophobic structure of its DBD.Chrousos syndrome: from molecular pathogenesis to therapeutic management.A novel human glucocorticoid receptor SNP results in increased transactivation potential.Molecular mechanism of glucocorticoid resistance in inflammatory bowel disease.NR3C1 polymorphisms in Brazilians of Caucasian, African, and Asian ancestry: glucocorticoid sensitivity and genotype association.Primary generalized glucocorticoid resistance and hypersensitivity: the end-organ involvement in the stress response.Functional characterization of the hGRαT556I causing Chrousos syndrome.
P2860

Chrousos syndrome: a seminal report, a phylogenetic enigma and the clinical implications of glucocorticoid signalling changes

Item
http://www.wikidata.org/entity/Q28288491
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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type
label
Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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Chrousos syndrome: a seminal r ...... cocorticoid signalling changes
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P2093
P2860
P304
P31
P3181
P356
10.1111/J.1365-2362.2010.02336.X
P407
P433
P478
P50
P577
P5875
P698
P921
P932