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Simon J. Rhodes

Affiliations: 
Biochemistry and Molecular Biology Indiana University, Bloomington, Bloomington, IN, United States 
Area:
Molecular Biology, Human Development, Endocrinology Biology
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"Simon Rhodes"
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Rachel D. Mullen grad student 2011 Indiana University
Raleigh E. Malik grad student 2013 Indiana University
Soyoung Park grad student 2013 Indiana University, Indianapolis

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Publications

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Gregory LC, Humayun KN, Turton JP, et al. (2015) Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation. The Journal of Clinical Endocrinology and Metabolism. 100: 2158-64
Gahete MD, Durán-Prado M, Delgado-Niebla E, et al. (2014) Porcine sst1 can physically interact with other somatostatin receptors, and its expression is regulated by metabolic/inflammatory sensors. American Journal of Physiology. Endocrinology and Metabolism. 306: E483-93
Malik RE, Rhodes SJ. (2014) The role of DNA methylation in regulation of the murine Lhx3 gene. Gene. 534: 272-81
Park S, Mullen RD, Rhodes SJ. (2013) Cell-specific actions of a human LHX3 gene enhancer during pituitary and spinal cord development. Molecular Endocrinology (Baltimore, Md.). 27: 2013-27
Hunter CS, Malik RE, Witzmann FA, et al. (2013) LHX3 interacts with inhibitor of histone acetyltransferase complex subunits LANP and TAF-1β to modulate pituitary gene regulation. Plos One. 8: e68898
Prince KL, Colvin SC, Park S, et al. (2013) Developmental analysis and influence of genetic background on the Lhx3 W227ter mouse model of combined pituitary hormone deficiency disease. Endocrinology. 154: 738-48
Dong Y, Zhang L, Zhang S, et al. (2012) Phosphatase of regenerating liver 2 (PRL2) is essential for placental development by down-regulating PTEN (Phosphatase and Tensin Homologue Deleted on Chromosome 10) and activating Akt protein. The Journal of Biological Chemistry. 287: 32172-9
Yusuf D, Butland SL, Swanson MI, et al. (2012) The transcription factor encyclopedia. Genome Biology. 13: R24
Bechtold-Dalla Pozza S, Hiedl S, Roeb J, et al. (2012) A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency. Hormone Research in Pã¦Diatrics. 77: 41-51
Mullen RD, Park S, Rhodes SJ. (2012) A distal modular enhancer complex acts to control pituitary- and nervous system-specific expression of the LHX3 regulatory gene. Molecular Endocrinology (Baltimore, Md.). 26: 308-19
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