Genetic Etiology of Congenital Hypopituitarism - Endotext - NCBI Bookshelf
Improving Disease Gene Prioritization by Comparing the Semantic Similarity of Phenotypes in Mice with Those of Human Diseases | PLOS ONE
Pituitary cell differentiation from stem cells and other cells: toward restorative therapy for hypopituitarism? | Regenerative Medicine
Frontiers | Mesencephalic Astrocyte-Derived Neurotrophic Factor (MANF) Is Highly Expressed in Mouse Tissues With Metabolic Function
Nestin-Cre Mice Are Affected by Hypopituitarism, Which Is Not Due to Significant Activity of the Transgene in the Pituitary Glan
Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans | Nature Communications
Evidence That the Etiology of Congenital Hypopituitarism Has a Major Genetic Component but Is Infrequently Monogenic - Frontiers
KCNQ1 is expressed in cells of the mouse hypothalamic–pituitary growth... | Download Scientific Diagram
Molecular Mechanisms Governing Embryonic Differentiation of Pituitary Somatotropes: Trends in Endocrinology & Metabolism
Cells | Free Full-Text | The Role of GH/IGF Axis in Dento-Alveolar Complex from Development to Aging and Therapeutics: A Narrative Review
The molecular basis of hypopituitarism: Trends in Endocrinology & Metabolism
A mouse model of autism implicates endosome pH in the regulation of presynaptic calcium entry | Nature Communications
Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans | Nature Communications
Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans | Nature Communications
Functional anterior pituitary generated in self-organizing culture of human embryonic stem cells | Nature Communications
SciELO - Brasil - Central adrenal insufficiency: who, when, and how? From the evidence to the controversies – an exploratory review Central adrenal insufficiency: who, when, and how? From the evidence to
Hesx1 Cre/+ ;Ctnnb1 +/lox(ex3) mice develop hypopituitarism and... | Download Scientific Diagram
Design and validation of the AOiGHD mouse model. ( A ) rGHp-Cre and... | Download Scientific Diagram
Frontiers | Traumatic Brain Injury as Frequent Cause of Hypopituitarism and Growth Hormone Deficiency: Epidemiology, Diagnosis, and Treatment
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency - ScienceDirect
ZBTB20 is required for anterior pituitary development and lactotrope specification | Nature Communications
![PDF] Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5e78def1664acddd99af83bcbb14ab2587ed32f7/7-Figure2-1.png "PDF] Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism | Semantic Scholar")
PDF] Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism | Semantic Scholar
Loss of growth hormone signaling in the mouse germline or in adulthood reduces islet mass and alters islet function with notable sex differences | American Journal of Physiology-Endocrinology and Metabolism
