(Q36621488)

15 August 2017

1 reference

title

PRKAR1A mutations in primary pigmented nodular adrenocortical disease (English)

1 reference

primary pigmented nodular adrenocortical disease

15 August 2017

0 references

4

Jérôme Bertherat

0 references

author name string

Laure Cazabat

series ordinal

1

1 reference

PubMed ID

17036196

15 August 2017

Bruno Ragazzon

series ordinal

2

1 reference

PubMed ID

17036196

15 August 2017

Lionel Groussin

series ordinal

3

1 reference

15 August 2017

1 January 2006

1 reference

15 August 2017

1 reference

15 August 2017

9

1 reference

15 August 2017

3

1 reference

15 August 2017

211-219

1 reference

https://scigraph.springernature.com/pub.10.1007/s11102-006-0266-1

15 August 2017

0 references

cites work

The complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11102-006-0266-1

A six month mitotane course induced sustained correction of hypercortisolism in a young woman with PPNAD and Carney complex

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11102-006-0266-1

Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine overactivity

21 January 2018

1 reference

12 December 2020

Carney complex (CNC).

1 reference

12 December 2020

Molecular and functional analysis of PRKAR1A and its locus (17q22-24) in sporadic adrenocortical tumors: 17q losses, somatic mutations, and protein kinase A expression and activity.

1 reference

12 December 2020

[Polymicroadenomatosis of the adrenal cortex in Cushing's syndrome. 15 cases]

1 reference

12 December 2020

Clinical and genetic analysis of primary bilateral adrenal diseases (micro- and macronodular disease) leading to Cushing syndrome.

1 reference

12 December 2020

PRKAR1A Mutations and protein kinase A interactions with other signaling pathways in the adrenal cortex.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Serial analysis of gene expression in adrenocortical hyperplasia caused by a germline PRKAR1A mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypodense nodularity on computed tomography: novel imaging and pathology of micronodular adrenocortical hyperplasia associated with myelolipomatous changes.

1 reference

12 December 2020

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.

1 reference

12 December 2020

Ectopic and abnormal hormone receptors in adrenal Cushing's syndrome

1 reference

12 December 2020

17q22-24 chromosomal losses and alterations of protein kinase a subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia.

1 reference

12 December 2020

Primary adrenocortical micronodular adenomatosis causing Cushing's syndrome. Effects of ketoconazole on steroid production and in vitro performance of adrenal cells

1 reference

12 December 2020

Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation

1 reference

12 December 2020

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

1 reference

12 December 2020

Localized effects of cAMP mediated by distinct routes of protein kinase A.

1 reference

12 December 2020

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

1 reference

12 December 2020

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Estradiol stimulates cortisol production by adrenal cells in estrogen-dependent primary adrenocortical nodular dysplasia

1 reference

12 December 2020

Adrenal pathophysiology: lessons from the Carney complex.

1 reference

12 December 2020

In vivo and in vitro screening for illegitimate receptors in adrenocorticotropin-independent macronodular adrenal hyperplasia causing Cushing's syndrome: identification of two cases of gonadotropin/gastric inhibitory polypeptide-dependent hypercorti

1 reference

12 December 2020

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

1 reference

12 December 2020

A mouse model for the Carney complex tumor syndrome develops neoplasia in cyclic AMP-responsive tissues

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

1 reference

12 December 2020

Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex).

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical, biological and histological study of a typical case of polymicroadenomatosis of the adrenal cortex

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Eyelid myxoma in Carney complex without PRKAR1A allelic loss

1 reference

12 December 2020

Minireview: PRKAR1A: normal and abnormal functions

1 reference

12 December 2020

New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.

1 reference

12 December 2020

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

1 reference

12 December 2020

10.1007/S11102-006-0266-1

Identifiers

DOI

1 reference

15 August 2017

1 reference

PubMed ID

17036196