Last Updated: 09/26/2026
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Found 13 publications
Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders.
Journal: Endocrine connections
Published: May 01, 2023
Murine SEC24D can substitute functionally for SEC24C during embryonic development.
Journal: Scientific reports
Published: May 12, 2021
High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency.
Journal: American journal of human genetics
Published: January 08, 2021
The phenotypic spectrum associated with OTX2 mutations in humans.
Journal: European journal of endocrinology
Published: December 19, 2020
Otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease.
Journal: Human molecular genetics
Published: January 09, 2020
Pituitary Transcription Factor Mutations Leading to Hypopituitarism.
Journal: Experientia supplementum (2012)
Published: October 08, 2019
Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency
Journal: Orvosi hetilap
Published: February 13, 2018
Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.
Journal: Endocrine reviews
Published: November 10, 2016
Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation.
Journal: Endocrinology
Published: September 02, 2016
ISL1-based LIM complexes control Slit2 transcription in developing cranial motor neurons.
Journal: Scientific reports
Published: July 21, 2016
ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism.
Journal: Molecular endocrinology (Baltimore, Md.)
Published: August 22, 2015
Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.
Journal: Molecular endocrinology (Baltimore, Md.)
Published: February 11, 2015
Last Updated: 09/26/2026