Peter H. Mathers

Affiliations: 
West Virginia University, Morgantown, WV, United States 
Area:
Biochemistry, Molecular Biology, Neuroscience Biology
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"Peter Mathers"
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Publications

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Moye AR, Bedoni N, Cunningham JG, et al. (2019) Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. Plos Genetics. 15: e1008315
Brachet C, Kozhemyakina EA, Boros E, et al. (2019) Truncating RAX Mutations: Anophthalmia, Hypopituitarism, Diabetes Insipidus, and Cleft Palate in Mice and Men. The Journal of Clinical Endocrinology and Metabolism. 104: 2925-2930
Rodgers HM, Huffman VJ, Voronina VA, et al. (2018) The role of the Rx homeobox gene in retinal progenitor proliferation and cell fate specification. Mechanisms of Development
Kolson DR, Wan J, Wu J, et al. (2015) Temporal Patterns of Gene Expression During Calyx of Held Development. Developmental Neurobiology
Marrs GS, Morgan WJ, Howell DM, et al. (2013) Embryonic origins of the mouse superior olivary complex. Developmental Neurobiology. 73: 384-98
Lu F, Kar D, Gruenig N, et al. (2013) Rax is a selector gene for mediobasal hypothalamic cell types. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 259-72
Hoffpauir BK, Marrs GS, Mathers PH, et al. (2009) Does the brain connect before the periphery can direct? A comparison of three sensory systems in mice. Brain Research. 1277: 115-29
Voronina VA, Kozlov S, Mathers PH, et al. (2005) Conditional alleles for activation and inactivation of the mouse Rx homeobox gene. Genesis (New York, N.Y. : 2000). 41: 160-4
Bailey TJ, El-Hodiri H, Zhang L, et al. (2004) Regulation of vertebrate eye development by Rx genes. The International Journal of Developmental Biology. 48: 761-70
Voronina VA, Kozhemyakina EA, O'Kernick CM, et al. (2004) Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea. Human Molecular Genetics. 13: 315-22
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