Isolation and characterization of progenitor mesenchymal cells in human pituitary tumors

M Orciani, S Davis, G Appolloni, R Lazzarini… - Cancer gene …, 2015 - nature.com
Abstract The Cancer Stem Cells (CSCs) theory suggests that genetic alterations in stem
cells are the direct cause for cancer. The evidence for a CSC population that results in …

[HTML][HTML] The Neurod1/4-Ntrk3-Src pathway regulates gonadotrope cell adhesion and motility

C Le Ciclé, V Pacini, N Rama… - Cell Death …, 2023 - nature.com
Pituitary gonadotrope cells are essential for the endocrine regulation of reproduction in
vertebrates. These cells emerge early during embryogenesis, colonize the pituitary glands …

Pituitary cell turnover: from adult stem cell recruitment through differentiation to death

M Garcia-Lavandeira, E Diaz-Rodriguez, D Bahar… - …, 2015 - karger.com
The recent demonstration using genetic tracing that in the adult pituitary stem cells are
normally recruited from the niche in the marginal zone and differentiate into secretory cells in …

SOX2 is sequentially required for progenitor proliferation and lineage specification in the developing pituitary

S Goldsmith, R Lovell-Badge, K Rizzoti - Development, 2016 - journals.biologists.com
Sox2 mutations are associated with pituitary hormone deficiencies and the protein is
required for pituitary progenitor proliferation, but its function has not been well characterized …

[HTML][HTML] The proneural bHLH genes Mash1, Math3 and NeuroD are required for pituitary development

M Ando, M Goto, M Hojo, A Kita… - Journal of …, 2018 - jme.bioscientifica.com
Multiple signaling molecules and transcription factors are required for pituitary development.
Activator-type bHLH genes Mash1, Math, NeuroD (Neurod) and Neurogenin (Neurog) are …

Regulation of pituitary stem cells by epithelial to mesenchymal transition events and signaling pathways

LYM Cheung, SW Davis, ML Brinkmeier… - Molecular and cellular …, 2017 - Elsevier
The anterior pituitary gland is comprised of specialized cell-types that produce and secrete
polypeptide hormones in response to hypothalamic input and feedback from target organs …

Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD)

D Kelberman, JPG Turton, KS Woods… - Clinical …, 2009 - Wiley Online Library
Objective Homozygous mutations in the gene encoding the pituitary transcription factor
PROP1 are associated with combined pituitary hormone deficiency (CPHD) in both mice …

[HTML][HTML] Models of congenital adrenal hyperplasia for gene therapies testing

O Glazova, A Bastrich, A Deviatkin, N Onyanov… - International Journal of …, 2023 - mdpi.com
The adrenal glands are important endocrine organs that play a major role in the stress
response. Some adrenal glands abnormalities are treated with hormone replacement …

[HTML][HTML] Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other …

A Zygmunt-Górska, M Wójcik, A Gilis-Januszewska… - Hormones, 2024 - Springer
The most commonly identified genetic cause of combined pituitary hormone deficiency
(CPHD) is PROP1 gene mutations. The aim of the study was to compare selected clinical …

Pituitary stem cells drop their mask

H Vankelecom - Current stem cell research & therapy, 2012 - ingentaconnect.com
The pituitary gland represents the organism's endocrine hub, integrating central and
peripheral inputs to generate the appropriate hormonal signals that govern key …