Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features.

(PDF) Lack of mutations in the gene coding for the hGR

Lack of mutations in the gene coding for the hGR ( NR3C1 ) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and …

Lack of mutations in the gene coding for the hGR ( NR3C1

Read «Lack of mutations in the gene coding for the hGR ( NR3C1 ) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features, Journal of Pediatric Endocrinology and Metabolism» on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.

Published in: Journal of Pediatric Endocrinology and Metabolism · 2012Authors: George Briassoulis · Anelia Horvath · Paola Christoforou · Maya Lodish · Paraskevi Xe…About: Cushing’s disease · Pituitary tumors

Lack of Mutations in the Gene Coding for the

Lack of Mutations in the Gene Coding for the Glucocorticoid Receptor (NR3C1) in a Pediatric Patient with an ACTH-Secreting Pituitary Adenoma, Absence of Stigmata of Cushing Syndrome, and Unusual Histologic Features.

Síndrome de Cushing: Artículos científicos

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. Journal of Pediatric Endocrinology and Metabolism, 25 (1–2), 213–219.

Cushing Syndrome: Scientific Articles | NICHD – Eunice

Dec 01, 2016 · Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. Journal of Pediatric Endocrinology and Metabolism, 25 (1–2), 213–219.

Medscape | J Pediatr Endocrinol – Publication Information

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. January 01, 2012

Pituitary Tumors: Scientific Articles | NICHD – Eunice

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. Journal of Pediatric Endocrinology and Metabolism, 25 (1–2),213–219.

Dr. Maya Lodish, Pediatric Endocrinologist in Bethesda, MD

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features.

Publications | The Horvath Lab

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. J Pediatr Endocrinol Metab. 2012;25:213-9.

Pediatric Cushing’s Disease and Pituitary Incidentaloma

Briassoulis et al. recently described a pediatric patient with a pituitary ACTH secreting adenoma confirmed by histology, with little clinical evidence of CD. However, in this case, no mutation in glucocorticoid receptor gene was detected .

Pediatric Cushing’s Disease and Pituitary Incidentaloma

G. Briassoulis, A. Horvath, P. Christoforou et al., “Lack of mutations in the gene coding for the hGR ( NR3C1 ) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features,” Journal of Pediatric Endocrinology and Metabolism, vol. 25, no. 1-2, pp. 213–219, 2012.

Tumores pituitarios: Artículos científicos – NICHD

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. Journal of Pediatric Endocrinology and Metabolism, 25 (1–2),213–219.

The New Molecular Landscape of Cushing’s Disease

New exciting insights in molecular driver mutations and the demonstration of targetable protein overexpression (e.g., HSP90) have greatly changed the molecular landscape of CD. Obviously, identification of mutated USP8 as a key event in the pathogenesis of ACTH-secreting pituitary adenomas indicates a major breakthrough.

The New Molecular Landscape of Cushing’s Disease: Trends

Lack of mutations in the gene coding for the hGR (NR3C1) in a pediatric patient with ACTH-secreting pituitary adenoma, absence of stigmata of Cushing’s syndrome and unusual histologic features. J. Pediatr.

NR3C1 gene – Genetics Home Reference – NIH

Nov 20, 2018 · From NCBI Gene:. This gene encodes glucocorticoid receptor, which can function both as a transcription factor that binds to glucocorticoid response elements in the promoters of glucocorticoid responsive genes to activate their transcription, and as a regulator of other transcription factors.