Neitz M - Search Results

1

Toward an Indoor Lighting Solution for Social Jet Lag.

Neitz A, Rice A, Casiraghi L, Bussi IL, Buhr ED, Neitz M, Neitz J, de la Iglesia HO, Kuchenbecker JA. Neitz A, et al. Among authors: neitz m. J Biol Rhythms. 2024 Oct;39(5):502-507. doi: 10.1177/07487304241262918. Epub 2024 Jul 31. J Biol Rhythms. 2024. PMID: 39082441 Free PMC article.

2

Expression and Evolution of Short Wavelength Sensitive Opsins in Colugos: A Nocturnal Lineage That Informs Debate on Primate Origins.

Moritz GL, Lim NT, Neitz M, Peichl L, Dominy NJ. Moritz GL, et al. Among authors: neitz m. Evol Biol. 2013;40(4):542-553. doi: 10.1007/s11692-013-9230-y. Epub 2013 Apr 17. Evol Biol. 2013. PMID: 24293738 Free PMC article.

3

Protanomaly without darkened red is deuteranopia with rods.

Shevell SK, Sun Y, Neitz M. Shevell SK, et al. Among authors: neitz m. Vision Res. 2008 Nov;48(26):2599-603. doi: 10.1016/j.visres.2008.03.001. Epub 2008 Apr 18. Vision Res. 2008. PMID: 18423511 Free PMC article.

4

X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.

McClements M, Davies WI, Michaelides M, Carroll J, Rha J, Mollon JD, Neitz M, MacLaren RE, Moore AT, Hunt DM. McClements M, et al. Among authors: neitz m. Vision Res. 2013 Mar 22;80:41-50. doi: 10.1016/j.visres.2012.12.012. Epub 2013 Jan 18. Vision Res. 2013. PMID: 23337435 Free PMC article.

5

Adaptive optics retinal imaging reveals S-cone dystrophy in tritan color-vision deficiency.

Baraas RC, Carroll J, Gunther KL, Chung M, Williams DR, Foster DH, Neitz M. Baraas RC, et al. Among authors: neitz m. J Opt Soc Am A Opt Image Sci Vis. 2007 May;24(5):1438-47. doi: 10.1364/josaa.24.001438. J Opt Soc Am A Opt Image Sci Vis. 2007. PMID: 17429491 Free PMC article.

6

Substitution of isoleucine for threonine at position 190 of S-opsin causes S-cone-function abnormalities.

Baraas RC, Hagen LA, Dees EW, Neitz M. Baraas RC, et al. Among authors: neitz m. Vision Res. 2012 Nov 15;73:1-9. doi: 10.1016/j.visres.2012.09.007. Epub 2012 Sep 26. Vision Res. 2012. PMID: 23022137 Free PMC article.

7

Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.

McClements M, Davies WI, Michaelides M, Young T, Neitz M, MacLaren RE, Moore AT, Hunt DM. McClements M, et al. Among authors: neitz m. Invest Ophthalmol Vis Sci. 2013 Feb 15;54(2):1361-9. doi: 10.1167/iovs.12-11156. Invest Ophthalmol Vis Sci. 2013. PMID: 23322568 Free PMC article.

8

Identification of two novel mutations in families with X-linked ocular albinism.

Iannaccone A, Gallaher KT, Buchholz J, Jennings BJ, Neitz M, Sidjanin DJ. Iannaccone A, et al. Among authors: neitz m. Mol Vis. 2007 Oct 2;13:1856-61. Mol Vis. 2007. PMID: 17960122

9

Photoreceptor structure and function in patients with congenital achromatopsia.

Genead MA, Fishman GA, Rha J, Dubis AM, Bonci DM, Dubra A, Stone EM, Neitz M, Carroll J. Genead MA, et al. Among authors: neitz m. Invest Ophthalmol Vis Sci. 2011 Sep 21;52(10):7298-308. doi: 10.1167/iovs.11-7762. Invest Ophthalmol Vis Sci. 2011. PMID: 21778272 Free PMC article.

10

PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia.

Pedersen HR, Baraas RC, Landsend ECS, Utheim ØA, Utheim TP, Gilson SJ, Neitz M. Pedersen HR, et al. Among authors: neitz m. Invest Ophthalmol Vis Sci. 2020 May 11;61(5):14. doi: 10.1167/iovs.61.5.14. Invest Ophthalmol Vis Sci. 2020. PMID: 32396632 Free PMC article.

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