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Retinal degeneration caused by mutations in TULP1.
Xi Q, Pauer GJ, West KA, Crabb JW, Hagstrom SA. Xi Q, et al. Among authors: pauer gj. Adv Exp Med Biol. 2003;533:303-8. doi: 10.1007/978-1-4615-0067-4_37. Adv Exp Med Biol. 2003. PMID: 15180277 No abstract available.
Early synaptic defects in tulp1-/- mice.
Grossman GH, Pauer GJ, Narendra U, Peachey NS, Hagstrom SA. Grossman GH, et al. Among authors: pauer gj. Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3074-83. doi: 10.1167/iovs.08-3190. Epub 2009 Feb 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19218615 Free PMC article.
Photoreceptor Compartment-Specific TULP1 Interactomes.
Ebke LA, Sinha S, Pauer GJT, Hagstrom SA. Ebke LA, et al. Among authors: pauer gjt. Int J Mol Sci. 2021 Jul 28;22(15):8066. doi: 10.3390/ijms22158066. Int J Mol Sci. 2021. PMID: 34360830 Free PMC article.
Histopathological comparison of eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations.
Bonilha VL, Rayborn ME, Bell BA, Marino MJ, Pauer GJ, Beight CD, Chiang J, Traboulsi EI, Hollyfield JG, Hagstrom SA. Bonilha VL, et al. Among authors: pauer gj. Graefes Arch Clin Exp Ophthalmol. 2015 Feb;253(2):295-305. doi: 10.1007/s00417-014-2868-z. Epub 2014 Dec 11. Graefes Arch Clin Exp Ophthalmol. 2015. PMID: 25491159 Free PMC article.
39 results