(Q34810821)

English

Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma

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scholarly article

1 reference

Europe PubMed Central

4 August 2017

Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma (English)

1 reference

Europe PubMed Central

4 August 2017

adrenal hyperplasia

1 reference

based on heuristic

inferred from title

Cushing syndrome due to macronodular adrenal hyperplasia

1 reference

based on heuristic

inferred from title

object named as

Patrick May

13

0 references

Joachim Spranger

6

object named as

Joachim Spranger

1 reference

Europe PubMed Central

4 August 2017

11

object named as

Wiebke Arlt

1 reference

Europe PubMed Central

4 August 2017

14

object named as

Bruno Allolio

1 reference

Europe PubMed Central

4 August 2017

author name string

Ulf Elbelt

1

1 reference

Europe PubMed Central

4 August 2017

Alessia Trovato

2

1 reference

Europe PubMed Central

4 August 2017

Michael Kloth

3

1 reference

Europe PubMed Central

4 August 2017

Enno Gentz

4

1 reference

Europe PubMed Central

4 August 2017

Reinhard Finke

5

1 reference

Europe PubMed Central

4 August 2017

David Galas

7

1 reference

Europe PubMed Central

4 August 2017

Susanne Weber

8

1 reference

Europe PubMed Central

4 August 2017

Cristina Wolf

9

1 reference

Europe PubMed Central

4 August 2017

Katharina König

10

1 reference

Europe PubMed Central

4 August 2017

Reinhard Büttner

12

1 reference

Europe PubMed Central

4 August 2017

Jochen G Schneider

15

1 reference

Europe PubMed Central

4 August 2017

language of work or name

0 references

publication date

1 January 2015

1 reference

Europe PubMed Central

4 August 2017

The Journal of Clinical Endocrinology and Metabolism

1 reference

Europe PubMed Central

4 August 2017

100

1 reference

Europe PubMed Central

4 August 2017

1

1 reference

Europe PubMed Central

4 August 2017

E119-28

1 reference

Europe PubMed Central

4 August 2017

Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Intraadrenal corticotropin in bilateral macronodular adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

ARMC5 mutations in macronodular adrenal hyperplasia with Cushing's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

TOX3 mutations in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

TNRC9 downregulates BRCA1 expression and promotes breast cancer aggressiveness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Phosphodiesterase 11A (PDE11A) gene defects in patients with acth-independent macronodular adrenal hyperplasia (AIMAH): functional variants may contribute to genetic susceptibility of bilateral adrenal tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP-specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Wnt/β-catenin signalling in adrenal physiology and tumour development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Urine steroid metabolomics as a biomarker tool for detecting malignancy in adrenal tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

ACTH-independent macronodular adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

TOX3 regulates calcium-dependent transcription in neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Phosphodiesterase 11A (PDE11A) and genetic predisposition to adrenocortical tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Familial adrenocorticotropin-independent macronodular adrenal hyperplasia with aberrant serotonin and vasopressin adrenal receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Clinical and subclinical ACTH-independent macronodular adrenal hyperplasia and aberrant hormone receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Hereditary leiomyomatosis associated with bilateral, massive, macronodular adrenocortical disease and atypical cushing syndrome: a clinical and molecular genetic investigation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Overexpression of serotonin4 receptors in cisapride-responsive adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia causing Cushing's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Familial ACTH-independent Cushing's syndrome with bilateral macronodular adrenal hyperplasia clinically affecting only female family members

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Aberrant interleukin-1 receptors in a cortisol-secreting adrenal adenoma causing Cushing's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Adrenal masses in patients with familial adenomatous polyposis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Adrenocorticotropin-independent macronodular adrenocortical hyperplasia associated with multiple colon adenomas/carcinomas which showed a point mutation in the APC gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

The McCune-Albright syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

8 July 2018

Heredity and cortisol regulation in bilateral macronodular adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Whole exome sequencing identifies mutation of EDNRA involved in ACTH-independent macronodular adrenal hyperplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Intracranial meningiomas and neurofibromatosis type 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Ectopic expression of vasopressin V1b and V2 receptors in the adrenal glands of familial ACTH-independent macronodular adrenal hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Inherited adrenocorticotropin-independent macronodular adrenal hyperplasia with abnormal cortisol secretion by vasopressin and catecholamines: detection of the aberrant hormone receptors on adrenal gland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Corticotropin-independent macronodular adrenal hyperplasia: a clinicopathologic correlation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

Subclinical Cushing's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

26 October 2018

ARMC5Mutations Are a Frequent Cause of Primary Macronodular Adrenal Hyperplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

9 December 2018

Propranolol Therapy for Ectopic β-Adrenergic Receptors in Adrenal Cushing's Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283009

9 December 2018

Leuprolide acetate therapy in luteinizing hormone--dependent Cushing's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial adrenocorticotropin-independent Cushing's syndrome with bilateral macronodular adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysine vasopressin stimulation of cortisol secretion in patients with adrenocorticotropin-independent macronodular adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Food-dependent Cushing's syndrome: possible involvement of leptin in cortisol hypersecretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACTH independent Cushing's syndrome occurring in siblings

1 reference

https://pubmed.ncbi.nlm.nih.gov/25279498

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1210/JC.2014-2648

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

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