(Q38785782)

6 September 2017

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease (English)

1 reference

6 September 2017

12

Nathan Pankratz

0 references

Amit Tirosh

object named as

Amit Tirosh

2

0 references

James L. Mills

object named as

James L Mills

15

0 references

Constantine A Stratakis

17

object named as

Constantine A Stratakis

1 reference

6 September 2017

11

Martha Quezado

1 reference

6 September 2017

9

Georgios Z Papadakis

1 reference

6 September 2017

Fabio R Faucz

1

1 reference

6 September 2017

Christina Tatsi

3

1 reference

6 September 2017

Annabel Berthon

4

1 reference

6 September 2017

Laura C Hernández-Ramírez

5

1 reference

6 September 2017

Nikolaos Settas

6

1 reference

6 September 2017

Anna Angelousi

7

1 reference

6 September 2017

Ricardo Correa

8

1 reference

6 September 2017

Prashant Chittiboina

10

1 reference

6 September 2017

John Lane

13

1 reference

6 September 2017

Aggeliki Dimopoulos

14

1 reference

6 September 2017

Maya Lodish

16

1 reference

6 September 2017

language of work or name

English

0 references

publication date

12 May 2017

1 reference

The Journal of Clinical Endocrinology and Metabolism

6 September 2017

1 reference

6 September 2017

102

1 reference

6 September 2017

8

1 reference

6 September 2017

2836-2843

1 reference

Corticotropinoma as a Component of Carney Complex.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Loss-of-function mutations in the CABLES1 gene are a novel cause of Cushing's disease

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Diagnosis and Clinical Genetics of Cushing Syndrome in Pediatrics

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

The New Molecular Landscape of Cushing's Disease.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Outcome of Transsphenoidal Surgery for Cushing Disease: A Single-Center Experience Over 32 Years

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Facial Plethora: Modern Technology for Quantifying an Ancient Clinical Sign and Its Use in Cushing Syndrome

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Decoding the genetic basis of Cushing's disease: USP8 in the spotlight

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

The Gene of the Ubiquitin-Specific Protease 8 Is Frequently Mutated in Adenomas Causing Cushing's Disease

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Pituitary adenoma with paraganglioma/pheochromocytoma (3PAs) and succinate dehydrogenase defects in humans and mice

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Recurrent gain-of-function USP8 mutations in Cushing's disease

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Mutations in the deubiquitinase gene USP8 cause Cushing's disease

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

USP8 is a novel target for overcoming gefitinib resistance in lung cancer

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Pediatric Cushing's disease: Management Issues

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Outcome of surgical treatment of 200 children with Cushing's disease

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

The Usp8 deubiquitination enzyme is post-translationally modified by tyrosine and serine phosphorylation

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

EGFR as a therapeutic target for human, canine, and mouse ACTH-secreting pituitary adenomas

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

A new medical therapy for Cushing disease?

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Effects of Cushing disease on bone mineral density in a pediatric population

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Regulation and cellular roles of ubiquitin-specific deubiquitinating enzymes

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Postoperative testing to predict recurrent Cushing disease in children

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Mechanisms of resistance to ErbB-targeted cancer therapeutics

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

14-3-3-dependent inhibition of the deubiquitinating activity of UBPY and its cancellation in the M phase.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Paediatric Cushing's syndrome: epidemiology, investigation and therapeutic advances.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

UBPY-mediated epidermal growth factor receptor (EGFR) de-ubiquitination promotes EGFR degradation

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

A genomic and functional inventory of deubiquitinating enzymes

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

Skin manifestations of Cushing disease in children and adolescents before and after the resolution of hypercortisolemia.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5546857

The USP8 mutational status may predict drug susceptibility in corticotroph adenomas of Cushing's disease

31 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28505279

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1210/JC.2017-00161

1 reference

6 September 2017

0 references

1 reference