Full NCBI Bibliography can be found here

Cheung LYM, Menage L, Rizzoti K, Hamilton G, Dumontet T, Basham K, Daly AZ, Brinkmeier ML, Masser BE, Treier M, Cobb J, Delogu A, Lovell-Badge R, Hammer GD, Camper SA. Novel Candidate Regulators and Developmental Trajectory of Pituitary Thyrotropes. Endocrinology. 2023 Apr 17;164(6). doi: 10.1210/endocr/bqad076. PubMed PMID: 37183548; PubMed Central PMCID: PMC10227867.

Sena C, Iannello G, Skowronski AA, Dannheim K, Cheung L, Agrawal PB, Hirschhorn JN, Zeitler P, LeDuc CA, Stratigopoulos G, Thaker VV. Endocrine and behavioural features of Lowe syndrome and their potential molecular mechanisms. J Med Genet. 2022 Dec;59(12):1171-1178. doi: 10.1136/jmedgenet-2022-108490. Epub 2022 Jul 8. PubMed PMID: 35803701; PubMed Central PMCID: PMC10186212.

Cheung LYM, Rizzoti K. Cell population characterization and discovery using single-cell technologies in endocrine systems. J Mol Endocrinol. 2020 Aug;65(2):R35-R51. doi: 10.1530/JME-19-0276. Review. PubMed PMID: 32485670.

Cheung LYM, Camper SA. PROP1-Dependent Retinoic Acid Signaling Regulates Developmental Pituitary Morphogenesis and Hormone Expression. Endocrinology. 2020 Feb 1;161(2). doi: 10.1210/endocr/bqaa002. PubMed PMID: 31913463; PubMed Central PMCID: PMC7029777.

Cheung LYM, George AS, McGee SR, Daly AZ, Brinkmeier ML, Ellsworth BS, Camper SA. Single-Cell RNA Sequencing Reveals Novel Markers of Male Pituitary Stem Cells and Hormone-Producing Cell Types. Endocrinology. 2018 Dec 1;159(12):3910-3924. doi: 10.1210/en.2018-00750. PubMed PMID: 30335147; PubMed Central PMCID: PMC6240904.

Cheung L, Le Tissier P, Goldsmith SG, Treier M, Lovell-Badge R, Rizzoti K. NOTCH activity differentially affects alternative cell fate acquisition and maintenance. Elife. 2018 Mar 26;7. doi: 10.7554/eLife.33318. PubMed PMID: 29578405; PubMed Central PMCID: PMC5889214.

Cheung LY, Davis SW, Brinkmeier ML, Camper SA, Pérez-Millán MI. Regulation of pituitary stem cells by epithelial to mesenchymal transition events and signaling pathways. Mol Cell Endocrinol. 2017 Apr 15;445:14-26. doi: 10.1016/j.mce.2016.09.016. Epub 2016 Sep 17. Review. PubMed PMID: 27650955; PubMed Central PMCID: PMC5590650.

Cheung LYM, Okano H, Camper SA. Sox21 deletion in mice causes postnatal growth deficiency without physiological disruption of hypothalamic-pituitary endocrine axes. Mol Cell Endocrinol. 2017 Jan 5;439:213-223. doi: 10.1016/j.mce.2016.09.005. Epub 2016 Sep 8. PubMed PMID: 27616671; PubMed Central PMCID: PMC5123967.

Fang Q, George AS, Brinkmeier ML, Mortensen AH, Gergics P, Cheung LY, Daly AZ, Ajmal A, Pérez Millán MI, Ozel AB, Kitzman JO, Mills RE, Li JZ, Camper SA. Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era. Endocr Rev. 2016 Dec;37(6):636-675. doi: 10.1210/er.2016-1101. Epub 2016 Nov 9. Review. PubMed PMID: 27828722; PubMed Central PMCID: PMC5155665.

Cheung LY, Rizzoti K, Lovell-Badge R, Le Tissier PR. Pituitary phenotypes of mice lacking the notch signalling ligand delta-like 1 homologue. J Neuroendocrinol. 2013 Apr;25(4):391-401. doi: 10.1111/jne.12010. PubMed PMID: 23279263; PubMed Central PMCID: PMC3664429.