Megan G. Massa
Affiliations: | University of California, Los Angeles, Los Angeles, CA |
Area:
Neuroendocrinology, metabolismWebsite:
https://megangmassa.com/Google:
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Parents
Sign in to add mentorRichmond Thompson | research assistant | 2013-2014 | Bowdoin College |
Aiden Haghikia | research assistant | 2014-2016 | Ruhr-University Bochum/St. Josefs Hospital |
Stephanie Correa | grad student | 2016- | UCLA |
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Publications
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Massa MG, Scott RL, Cara AL, et al. (2023) Feeding neurons integrate metabolic and reproductive states in mice. Iscience. 26: 107918 |
Massa MG, Scott RL, Cara AL, et al. (2023) Feeding Neurons Integrate Metabolic and Reproductive States in Mice. Biorxiv : the Preprint Server For Biology |
Zhang Z, Reis FMCV, He Y, et al. (2020) Estrogen-sensitive medial preoptic area neurons coordinate torpor in mice. Nature Communications. 11: 6378 |
Massa MG, Correa SM. (2020) Sexes on the brain: Sex as multiple biological variables in the neuronal control of feeding. Biochimica Et Biophysica Acta. Molecular Basis of Disease. 165840 |
van Veen JE, Kammel LG, Bunda PC, et al. (2020) Hypothalamic estrogen receptor alpha establishes a sexually dimorphic regulatory node of energy expenditure. Nature Metabolism. 2: 351-363 |
Duscha A, Gisevius B, Hirschberg S, et al. (2020) Propionic Acid Shapes the Multiple Sclerosis Disease Course by an Immunomodulatory Mechanism. Cell |
Lee SD, Priest C, Bjursell M, et al. (2019) IDOL regulates systemic energy balance through control of neuronal VLDLR expression. Nature Metabolism. 1: 1089-1100 |
Massa MG, David C, Jörg S, et al. (2017) Testosterone Differentially Affects T Cells and Neurons in Murine and Human Models of Neuroinflammation and Neurodegeneration. The American Journal of Pathology. 187: 1613-1622 |
Berg J, Mahmoudjanlou Y, Duscha A, et al. (2016) The immunomodulatory effect of laquinimod in CNS autoimmunity is mediated by the aryl hydrocarbon receptor. Journal of Neuroimmunology. 298: 9-15 |
Massa MG, Gisevius B, Hirschberg S, et al. (2016) Multiple Sclerosis Patient-Specific Primary Neurons Differentiated from Urinary Renal Epithelial Cells via Induced Pluripotent Stem Cells. Plos One. 11: e0155274 |