[Pigmented micronodular dysplasia of the adrenal glands and Carney complex] (Q81909592)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15988379%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

review article

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title

[Pigmented micronodular dysplasia of the adrenal glands and Carney complex] (English)

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13 January 2020

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2

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13 January 2020

Jérome Bertherat

6

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13 January 2020

author name string

L Cazabat

1

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13 January 2020

F René-Corail

3

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13 January 2020

E Jullian

4

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13 January 2020

X Bertagna

5

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13 January 2020

publication date

1 June 2005

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13 January 2020

published in

Annales d'Endocrinologie

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13 January 2020

volume

66

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13 January 2020

issue

3

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13 January 2020

page(s)

187-193

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Increased basal cAMP-dependent protein kinase activity inhibits the formation of mesoderm-derived structures in the developing mouse embryo

13 January 2020

cites work

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Minireview: PRKAR1A: normal and abnormal functions

7 January 2021

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Primary pigmented nodular adrenocortical disease: paradoxical responses of cortisol secretion to dexamethasone occur in vitro and are associated with increased expression of the glucocorticoid receptor

7 January 2021

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The complex of myxomas, spotty pigmentation, and endocrine overactivity

7 January 2021

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Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

7 January 2021

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Down-regulation of regulatory subunit type 1A of protein kinase A leads to endocrine and other tumors

7 January 2021

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A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesions.

7 January 2021

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Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio

7 January 2021

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Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease

7 January 2021

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Cyclical Cushing syndrome presenting in infancy: an early form of primary pigmented nodular adrenocortical disease, or a new entity?

7 January 2021

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Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex

7 January 2021

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Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

7 January 2021

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Chromosome 2 (2p16) abnormalities in Carney complex tumours

7 January 2021

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Protein kinase-A activity in PRKAR1A-mutant cells, and regulation of mitogen-activated protein kinases ERK1/2.

7 January 2021

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Role of the PKA-regulated transcription factor CREB in development and tumorigenesis of endocrine tissues.

7 January 2021

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Severe osteopenia in young adults associated with Cushing's syndrome due to micronodular adrenal disease

7 January 2021

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Primary pigmented nodular adrenocortical disease: reevaluation of a patient with carney complex 27 years after unilateral adrenalectomy.

7 January 2021

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Bilateral primary pigmented nodular adrenocortical disease. Rare cause of the Cushing syndrome.

7 January 2021

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Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia.

7 January 2021

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Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

7 January 2021

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Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

7 January 2021

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Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice

7 January 2021

1 reference

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10.1016/S0003-4266(05)81750-0

7 January 2021

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15988379%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

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