(Q33735950)

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Familial glucocorticoid receptor haploinsufficiency by non-sense mediated mRNA decay, adrenal hyperplasia and apparent mineralocorticoid excess

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

Familial glucocorticoid receptor haploinsufficiency by non-sense mediated mRNA decay, adrenal hyperplasia and apparent mineralocorticoid excess (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

haploinsufficiency

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adrenal hyperplasia

1 reference

based on heuristic

inferred from title

Séverine Trabado

object named as

Séverine Trabado

7

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Say Viengchareun

object named as

Say Viengchareun

5

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author name string

Jérôme Bouligand

1

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Europe PubMed Central

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29 July 2017

Brigitte Delemer

2

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Europe PubMed Central

PubMed publication ID

29 July 2017

Annie-Claude Hecart

3

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29 July 2017

Geri Meduri

4

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Europe PubMed Central

PubMed publication ID

29 July 2017

Larbi Amazit

6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Bruno Fève

8

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Europe PubMed Central

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29 July 2017

Anne Guiochon-Mantel

9

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PubMed publication ID

29 July 2017

Jacques Young

10

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29 July 2017

Marc Lombès

11

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29 July 2017

language of work or name

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publication date

22 October 2010

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29 July 2017

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29 July 2017

5

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29 July 2017

10

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29 July 2017

e13563

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Europe PubMed Central

PubMed publication ID

29 July 2017

copyright license

Creative Commons Attribution 4.0 International

22 October 2010

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April 2022 Public Data File from Crossref

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A novel point mutation in helix 10 of the human glucocorticoid receptor causes generalized glucocorticoid resistance by disrupting the structure of the ligand-binding domain.

1 reference

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Molecular mechanisms regulating glucocorticoid sensitivity and resistance

1 reference

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Tissue-specific glucocorticoid action: a family affair

1 reference

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Glucocorticoid receptor haploinsufficiency causes hypertension and attenuates hypothalamic-pituitary-adrenal axis and blood pressure adaptions to high-fat diet

1 reference

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The meaning of nonsense

1 reference

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Generalized glucocorticoid resistance: clinical aspects, molecular mechanisms, and implications of a rare genetic disorder

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Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay

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Messenger RNA regulation: to translate or to degrade

1 reference

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The mineralocorticoid receptor: insights into its molecular and (patho)physiological biology

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Pivotal role of the mineralocorticoid receptor in corticosteroid-induced adipogenesis.

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International Union of Pharmacology. LXV. The pharmacology and classification of the nuclear receptor superfamily: glucocorticoid, mineralocorticoid, progesterone, and androgen receptors

1 reference

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Glucocorticoid signalling affects pancreatic development through both direct and indirect effects.

1 reference

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Mineralocorticoid receptors are indispensable for nongenomic modulation of hippocampal glutamate transmission by corticosterone.

1 reference

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Antiinflammatory action of glucocorticoids--new mechanisms for old drugs

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Reduction of hepatic and adipose tissue glucocorticoid receptor expression with antisense oligonucleotides improves hyperglycemia and hyperlipidemia in diabetic rodents without causing systemic glucocorticoid antagonism

1 reference

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The origin and functions of multiple human glucocorticoid receptor isoforms

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The clinically inapparent adrenal mass: update in diagnosis and management

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Eplerenone, a selective aldosterone blocker, in patients with left ventricular dysfunction after myocardial infarction

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Glucocorticoid-induced increase in lymphocytic FKBP51 messenger ribonucleic acid expression: a potential marker for glucocorticoid sensitivity, potency, and bioavailability

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11 beta-Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess

1 reference

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1 reference

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1 reference

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1 reference

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21 January 2018

Identifiers

10.1371/JOURNAL.PONE.0013563

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

2010PLoSO...513563B

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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