(Q36643559)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

review article

1 reference

title

Mechanisms of disease: adrenocortical tumors--molecular advances and clinical perspectives (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

1

1 reference

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21 December 2019

Lionel Groussin

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

author name string

Xavier Bertagna

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

publication date

1 November 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

Nature Clinical Practice Endocrinology and Metabolism

21 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

volume

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

issue

11

1 reference

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21 December 2019

page(s)

632-641

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

Management of the clinically inapparent adrenal mass ("incidentaloma")

21 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

Distinct transcriptional profiles of adrenocortical tumors uncovered by DNA microarray analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

The complex of myxomas, spotty pigmentation, and endocrine overactivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

Clinical features of adrenocortical carcinoma, prognostic factors, and the effect of mitotane therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Fetal adrenal development: insight gained from adrenal tumors

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Genetic analysis of adrenal absence: agenesis and aplasia

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Clonal analysis of human adrenocortical carcinomas and secreting adenomas

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Comparative genomic hybridization analysis of adrenocortical tumors

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Multiple primary cancers in families with Li-Fraumeni syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

An inherited mutation outside the highly conserved DNA-binding domain of the p53 tumor suppressor protein in children and adults with sporadic adrenocortical tumors

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

A novel mechanism of tumorigenesis involving pH-dependent destabilization of a mutant p53 tetramer

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Molecular genetics of adrenocortical tumours, from familial to sporadic diseases

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Gene expression profiling of human adrenocortical tumors using complementary deoxyribonucleic Acid microarrays identifies several candidate genes as markers of malignancy

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Impaired desensitization of a mutant adrenocorticotropin receptor associated with apparent constitutive activity

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Rare mutations of the Gs alpha subunit gene in human endocrine tumors. Mutation detection by polymerase chain reaction-primer-introduced restriction analysis

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Assessing the presence of abnormal regulation of cortisol secretion by membrane hormone receptors: in vivo and in vitro studies in patients with functioning and non-functioning adrenal adenoma

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Gastric inhibitory polypeptide-dependent cortisol hypersecretion--a new cause of Cushing's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Food-dependent Cushing's syndrome mediated by aberrant adrenal sensitivity to gastric inhibitory polypeptide

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Ectopic expression of the gastric inhibitory polypeptide receptor gene is a sufficient genetic event to induce benign adrenocortical tumor in a xenotransplantation model.

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Disruption of protein kinase a regulation causes immortalization and dysregulation of D-type cyclins.

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Tumor formation by genetic mutations in the components of the Wnt signaling pathway

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Adrenal adenomas in a patient with Gardner's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Analysis of somatic APC mutations in rare extracolonic tumors of patients with familial adenomatous polyposis coli

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Gene array analysis of macronodular adrenal hyperplasia confirms clinical heterogeneity and identifies several candidate genes as molecular mediators

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Mutations of beta-catenin in adrenocortical tumors: activation of the Wnt signaling pathway is a frequent event in both benign and malignant adrenocortical tumors

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Fine tuning of adrenocortical functions by locally produced growth factors

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

BRAF mutation predicts a poorer clinical prognosis for papillary thyroid cancer

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

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

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Emerging treatment strategies for adrenocortical carcinoma: a new hope.

1 reference

https://api.crossref.org/works/10.1038%2FNCPENDMET0321

7 January 2021

Identifiers

DOI

10.1038/NCPENDMET0321

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17082810%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

1 reference