Publications

Selected Publications

Brue T, Camper SA. Novel mechanism of pituitary hormone deficiency: genetic variants shift splicing to produce a dominant negative transcription factor isoform. Eur J Endocrinol. 2021 Nov 26;185(6):C19-C25. doi: 10.1530/EJE-21-0949. PMID: 34597272.

Nakaguma M, Ferreira NGBP, Benedetti AFF, Madi MC, Silva JM, Li JZ, Ma Q, Bilge Ozel A, Fang Q, Narcizo AM, Cardoso LC, Montenegro LR, Funari MFA, Nishi MY, Arnhold IJP, Jorge AAL, Mendonca BB, Camper SA, Carvalho LR. Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum. Genes (Basel). 2021 Jul 25;12(8):1128. doi: 10.3390/genes12081128. PMID: 34440302; PMCID: PMC8394260.

Cheung LYM, Camper SA.  PROP1-dependent retinoic acid signaling regulates developmental pituitary morphogenesis and hormone expression.  Endocrinology, Feb 1;161(2):bqaa002, 2020. PMC7029777

Bando H, Gergics P, Bohnsack BL, Toolan KP, Richter CE, Shavit JA, Camper SA. otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease.  Hum Mol Genet. 29:1648-1657, 2020. PMC7322578

Brinkmeier ML, Bando H, Camarano AC, Fujio S, Yoshimoto K, de Souza F, Camper SA.  Rathke’s cleft-like cysts arise from Isl1 deletion in pituitary progenitors.  J Clin Invest. 130:4501-4515, 2020.  PMC7410063.  (Editor's selection)

Daly AZ*, Mortensen AH*, Bando H, Camper SA.  Pituitary tumors and immortalized cell lines generated by cre-inducible expression of SV40 T-antigen.  Endocrinology, 2021.  doi:10.1210/endocr/bqab073. PMID: 33837405.  PMC in process.  *co-first authors

Daly AZ, Dudley LA, Peel MT, Liebhaber SA, Parker SCJ, Camper SA. Multi-omic profiling of pituitary thyrotropic cells and progenitors. BMC Biology, 19: 76, 2021. PMC8051135