Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion
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The role of inbreeding in the extinction of a European royal dynastyPseudotumor of the pituitary due to PROP-1 deletionCombined pituitary hormone deficiency: current and future status.Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.Hypopituitarism oddities: congenital causes.Genetic regulation of pituitary gland development in human and mouseAged PROP1 deficient dwarf mice maintain ACTH production.Novel insights into the aetiology and pathogenesis of hypopituitarism.Model of pediatric pituitary hormone deficiency separates the endocrine and neural functions of the LHX3 transcription factor in vivoFacial metrics in children with corticotrophin-producing pituitary adenomas suggest abnormalities in midface development.Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene.Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?Pituitary changes in Prop1 transgenic mice: hormone producing tumors and signet-ring type gonadotropes.The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cellsIsolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencingNotch signaling in postnatal pituitary expansion: proliferation, progenitors, and cell specification.A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literature.The role of homeodomain transcription factors in heritable pituitary disease.Identification of SNPs within the sheep PROP1 gene and their effects on wool traits.PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).Case seminar: a young female with acute hyponatremia and a sellar mass.Long-term follow-up of combined pituitary hormone deficiency in two siblings with a Prophet of Pit-1 gene mutation.Bases Genéticas dos Distúrbios de Crescimento
P2860
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P2860
Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion
description
2000 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
artikull shkencor
@sq
artículu científicu espublizáu en 2000
@ast
im Dezember 2000 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: December 2000)
@en
vedecký článok (publikovaný 2000-12)
@sk
vědecký článek publikovaný v roce 2000
@cs
wetenschappelijk artikel (gepubliceerd in 2000-12)
@nl
наукова стаття, опублікована в грудні 2000
@uk
name
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@ast
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@en
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@nl
type
label
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@ast
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@en
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@nl
altLabel
Adrenocorticotropin Deficiency ...... ous for a Novel PROP1 Deletion
@ast
Adrenocorticotropin Deficiency ...... ous for a Novel PROP1 Deletion
@en
prefLabel
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@ast
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@en
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@nl
P2093
P3181
P1476
Adrenocorticotropin Deficiency ...... ous for a Novel PROP1 Deletion
@en
Adrenocorticotropin deficiency ...... ous for a novel PROP1 deletion
@en
P2093
P304
P3181
P356
10.1210/JC.85.12.4556
10.1210/JCEM.85.12.7013
P407
P577
2000-12-01T00:00:00Z