Pages that link to "Q45096678"

The following pages link to PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis (Q45096678):

Displaying 50 items.

• United States multicenter study of factors predicting the persistence of GH deficiency during the transition period between childhood and adulthood (Q21245400) (← links)
• A GRFa2/Prop1/stem (GPS) cell niche in the pituitary (Q27350395) (← links)
• Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans (Q28586560) (← links)
• Combined pituitary hormone deficiency: current and future status (Q30848681) (← links)
• Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion. (Q31055358) (← links)
• Genetic regulation of pituitary gland development in human and mouse (Q33590141) (← links)
• Pituitary gland development and disease: from stem cell to hormone production (Q33687947) (← links)
• Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. (Q34017922) (← links)
• The use of neuroimaging for assessing disorders of pituitary development. (Q34033813) (← links)
• Aged PROP1 deficient dwarf mice maintain ACTH production (Q34092471) (← links)
• Model of pediatric pituitary hormone deficiency separates the endocrine and neural functions of the LHX3 transcription factor in vivo (Q34471926) (← links)
• A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency. (Q35970431) (← links)
• Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene (Q36021378) (← links)
• Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter? (Q36214845) (← links)
• All Hormone-Producing Cell Types of the Pituitary Intermediate and Anterior Lobes Derive From Prop1-Expressing Progenitors. (Q36753831) (← links)
• The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism (Q36793669) (← links)
• PROP1 overexpression in corticotrophinomas: evidence for the role of PROP1 in the maintenance of cells committed to corticotrophic differentiation (Q36906964) (← links)
• PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells (Q37083255) (← links)
• Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency (Q37131895) (← links)
• Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencing (Q37211277) (← links)
• Notch signaling in postnatal pituitary expansion: proliferation, progenitors, and cell specification (Q37732555) (← links)
• 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 (Q37830352) (← links)
• Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency (Q37852201) (← links)
• The role of homeodomain transcription factors in heritable pituitary disease (Q37905532) (← links)
• Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era. (Q38797075) (← links)
• Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes. (Q38868271) (← links)
• Regulation of pituitary stem cells by epithelial to mesenchymal transition events and signaling pathways. (Q42151609) (← links)
• Comparison of adrenal function tests in children--the glucagon stimulation test allows the simultaneous assessment of adrenal function and growth hormone response in children (Q46514351) (← links)
• Therapy-Induced Growth and Sexual Maturation in a Developmentally Infantile Adult Patient with a PROP1 Mutation (Q47152421) (← links)
• Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism? (Q47332580) (← links)
• MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarism (Q48099793) (← links)
• Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations (Q48362570) (← links)
• PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency (Q48418100) (← links)
• Sox21 deletion in mice causes postnatal growth deficiency without physiological disruption of hypothalamic-pituitary endocrine axes. (Q48519185) (← links)
• Waxing and waning of a pituitary mass in a young woman with combined pituitary hormone deficiency (CPHD) due to a PROP-1 mutation (Q48538094) (← links)
• Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD). (Q48849523) (← links)
• Case seminar: a young female with acute hyponatremia and a sellar mass (Q48935688) (← links)
• Correlation between adrenal function, growth hormone secretion, and insulin sensitivity in children with idiopathic growth hormone deficiency (Q51257234) (← links)
• Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency. (Q51627755) (← links)
• Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency (Q51968780) (← links)
• The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency. (Q53646077) (← links)
• Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes (Q58697169) (← links)
• Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary (Q64252302) (← links)
• High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency (Q80385487) (← links)
• The natural history of the R120C PROP1 mutation reveals a wide phenotypic variability in two untreated adult brothers with combined pituitary hormone deficiency (Q80385516) (← links)
• [Genetics of anterior hypopituitary diseases] (Q81909612) (← links)
• Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary (Q83324242) (← links)
• Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism (Q88605919) (← links)
• Sex-specific changes in postnatal GH and PRL secretion in somatotrope LEPR-null mice (Q89180788) (← links)
• Development of the Pituitary Gland (Q90260818) (← links)