Scott I. Kavanaugh, Ph.D.

Affiliations: 
2009 University of New Hampshire, Durham, NH, United States 
Area:
GnRH, GnRH receptors; neuroendocrinology
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"Scott Kavanaugh"
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Parents

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Stacia A. Sower grad student 2009 UNH
 (Gonadotropin releasing hormone in agnathans.)
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Publications

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Hausken KN, Tizo B, Shpilman M, et al. (2018) Cloning and Characterization of a Second Lamprey Pituitary Glycoprotein Hormone, Thyrostimulin (GpA2/GpB5). General and Comparative Endocrinology
Kavanaugh SI, Tsai PS. (2016) Functional Authentication of a Novel Gastropod Gonadotropin-Releasing Hormone Receptor Reveals Unusual Features and Evolutionary Insight. Plos One. 11: e0160292
Plachetzki DC, Tsai PS, Kavanaugh SI, et al. (2016) Ancient Origins of Metazoan Gonadotropin-Releasing Hormone and their Receptors Revealed by Phylogenomic Analyses. General and Comparative Endocrinology
Miller AV, Kavanaugh SI, Tsai PS. (2016) Disruption of the Suprachiasmatic Nucleus in Fibroblast Growth Factor Signaling-Deficient Mice. Frontiers in Endocrinology. 7: 11
Johnson JI, Kavanaugh SI, Nguyen C, et al. (2014) Localization and functional characterization of a novel adipokinetic hormone in the mollusk, Aplysia californica. Plos One. 9: e106014
Jung LH, Kavanaugh SI, Sun B, et al. (2014) Localization of a molluscan gonadotropin-releasing hormone in Aplysia californica by in situ hybridization and immunocytochemistry. General and Comparative Endocrinology. 195: 132-7
Joseph NT, Aquilina-Beck A, MacDonald C, et al. (2012) Molecular cloning and pharmacological characterization of two novel GnRH receptors in the lamprey (Petromyzon marinus). Endocrinology. 153: 3345-56
Tata BK, Chung WC, Brooks LR, et al. (2012) Fibroblast growth factor signaling deficiencies impact female reproduction and kisspeptin neurons in mice. Biology of Reproduction. 86: 119
Sun B, Kavanaugh SI, Tsai PS. (2012) Gonadotropin-releasing hormone in protostomes: insights from functional studies on Aplysia californica. General and Comparative Endocrinology. 176: 321-6
McCabe MJ, Gaston-Massuet C, Tziaferi V, et al. (2011) Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction. The Journal of Clinical Endocrinology and Metabolism. 96: E1709-18
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