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Genome Biology|June 26, 2026
Srr2-dependent SOX2 levels govern the chromatin and transcriptional landscape of adult neural stem cell fate decisions in mouseSara Cruces-Salguero, Antonio Jordán-Pla, Ana Domingo-Muelas, et al.Plos One|February 1, 2012
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic miceKristie Lee, Jacqueline Tan, Michael B Morris, et al.Cell Stem Cell|December 11, 2012
p27(Kip1) directly represses Sox2 during embryonic stem cell differentiationHan Li, Manuel Collado, Aranzazu Villasante, et al.The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.Endocrinology|May 16, 2026
NR3C1 is required for normal somatotrope differentiation and Foxo1 expression in pituitaryPratyusa Das, Ridwanullah A Abubakar, Nooshin Mojahed, et al.The Journal of Clinical Investigation|August 26, 2006
Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humansDaniel Kelberman, Karine Rizzoti, Ariel Avilion, et al.Endocrinology|May 15, 2023
Novel Candidate Regulators and Developmental Trajectory of Pituitary ThyrotropesLeonard Y M Cheung, Lucy Menage, Karine Rizzoti, et al.Science Signaling|November 4, 2025
The chordoid glioma <i>PRKCA</i> D463H mutation is a kinase inactive, gain-of-function allele that induces early-onset chondrosarcoma in miceVéronique Calleja, Jack C Henry, Mathias Cobbaut, et al.Endocrine Connections|January 22, 2020
Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidismKatie U Gaynor, Irina V Grigorieva, Samantha M Mirczuk, et al.The Journal of Clinical Investigation|December 25, 2010
Identification of SOX3 as an XX male sex reversal gene in mice and humansEdwina Sutton, James Hughes, Stefan White, et al.Pageof 5