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Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness.
Tsang SH, Woodruff ML, Jun L, Mahajan V, Yamashita CK, Pedersen R, Lin CS, Goff SP, Rosenberg T, Larsen M, Farber DB, Nusinowitz S. Tsang SH, et al. Among authors: larsen m. Hum Mutat. 2007 Mar;28(3):243-54. doi: 10.1002/humu.20425. Hum Mutat. 2007. PMID: 17044014 Free PMC article.
[New treatments of hereditary blindness].
Bertelsen M, Rosenberg T, Larsen M. Bertelsen M, et al. Among authors: larsen m. Ugeskr Laeger. 2013 Sep 2;175(36):2038-42. Ugeskr Laeger. 2013. PMID: 23992912 Review. Danish.
Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia.
Grau T, Artemyev NO, Rosenberg T, Dollfus H, Haugen OH, Cumhur Sener E, Jurklies B, Andreasson S, Kernstock C, Larsen M, Zrenner E, Wissinger B, Kohl S. Grau T, et al. Among authors: larsen m. Hum Mol Genet. 2011 Feb 15;20(4):719-30. doi: 10.1093/hmg/ddq517. Epub 2010 Dec 1. Hum Mol Genet. 2011. PMID: 21127010 Free PMC article.
Oligocone trichromacy: clinical and molecular genetic investigations.
Andersen MK, Christoffersen NL, Sander B, Edmund C, Larsen M, Grau T, Wissinger B, Kohl S, Rosenberg T. Andersen MK, et al. Among authors: larsen m. Invest Ophthalmol Vis Sci. 2010 Jan;51(1):89-95. doi: 10.1167/iovs.09-3988. Epub 2009 Sep 24. Invest Ophthalmol Vis Sci. 2010. PMID: 19797231
Cadherin 5 is regulated by corticosteroids and associated with central serous chorioretinopathy.
Schubert C, Pryds A, Zeng S, Xie Y, Freund KB, Spaide RF, Merriam JC, Barbazetto I, Slakter JS, Chang S, Munch IC, Drack AV, Hernandez J, Yzer S, Merriam JE, Linneberg A, Larsen M, Yannuzzi LA, Mullins RF, Allikmets R. Schubert C, et al. Among authors: larsen m. Hum Mutat. 2014 Jul;35(7):859-67. doi: 10.1002/humu.22551. Hum Mutat. 2014. PMID: 24665005 Free PMC article.
2,986 results