Nishina PM - Search Results

1

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse.

Akhmedov NB, Piriev NI, Chang B, Rapoport AL, Hawes NL, Nishina PM, Nusinowitz S, Heckenlively JR, Roderick TH, Kozak CA, Danciger M, Davisson MT, Farber DB. Akhmedov NB, et al. Among authors: nishina pm. Proc Natl Acad Sci U S A. 2000 May 9;97(10):5551-6. doi: 10.1073/pnas.97.10.5551. Proc Natl Acad Sci U S A. 2000. PMID: 10805811 Free PMC article.

2

Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens.

Hawes NL, Chang B, Hageman GS, Nusinowitz S, Nishina PM, Schneider BS, Smith RS, Roderick TH, Davisson MT, Heckenlively JR. Hawes NL, et al. Among authors: nishina pm. Invest Ophthalmol Vis Sci. 2000 Sep;41(10):3149-57. Invest Ophthalmol Vis Sci. 2000. PMID: 10967077

3

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6.

Kameya S, Hawes NL, Chang B, Heckenlively JR, Naggert JK, Nishina PM. Kameya S, et al. Among authors: nishina pm. Hum Mol Genet. 2002 Aug 1;11(16):1879-86. doi: 10.1093/hmg/11.16.1879. Hum Mol Genet. 2002. PMID: 12140190

4

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.

Mehalow AK, Kameya S, Smith RS, Hawes NL, Denegre JM, Young JA, Bechtold L, Haider NB, Tepass U, Heckenlively JR, Chang B, Naggert JK, Nishina PM. Mehalow AK, et al. Among authors: nishina pm. Hum Mol Genet. 2003 Sep 1;12(17):2179-89. doi: 10.1093/hmg/ddg232. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915475

5

Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice.

Ikeda S, Hawes NL, Chang B, Avery CS, Smith RS, Nishina PM. Ikeda S, et al. Among authors: nishina pm. Invest Ophthalmol Vis Sci. 1999 Jul;40(8):1874-8. Invest Ophthalmol Vis Sci. 1999. PMID: 10393064

6

Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene.

Ikeda S, Shiva N, Ikeda A, Smith RS, Nusinowitz S, Yan G, Lin TR, Chu S, Heckenlively JR, North MA, Naggert JK, Nishina PM, Duyao MP. Ikeda S, et al. Among authors: nishina pm. Hum Mol Genet. 2000 Jan 22;9(2):155-63. doi: 10.1093/hmg/9.2.155. Hum Mol Genet. 2000. PMID: 10607826

7

Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.

Maddox DM, Vessey KA, Yarbrough GL, Invergo BM, Cantrell DR, Inayat S, Balannik V, Hicks WL, Hawes NL, Byers S, Smith RS, Hurd R, Howell D, Gregg RG, Chang B, Naggert JK, Troy JB, Pinto LH, Nishina PM, McCall MA. Maddox DM, et al. Among authors: nishina pm. J Physiol. 2008 Sep 15;586(18):4409-24. doi: 10.1113/jphysiol.2008.157289. Epub 2008 Aug 7. J Physiol. 2008. PMID: 18687716 Free PMC article.

8

Survey of common eye diseases in laboratory mouse strains.

Chang B, Hurd R, Wang J, Nishina P. Chang B, et al. Invest Ophthalmol Vis Sci. 2013 Jul 24;54(7):4974-81. doi: 10.1167/iovs.13-12289. Invest Ophthalmol Vis Sci. 2013. PMID: 23800770 Free PMC article.

9

Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss.

Collin GB, Gogna N, Chang B, Damkham N, Pinkney J, Hyde LF, Stone L, Naggert JK, Nishina PM, Krebs MP. Collin GB, et al. Among authors: nishina pm. Cells. 2020 Apr 10;9(4):931. doi: 10.3390/cells9040931. Cells. 2020. PMID: 32290105 Free PMC article. Review.

10

Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ.

Ji X, Liu Y, Hurd R, Wang J, Fitzmaurice B, Nishina PM, Chang B. Ji X, et al. Among authors: nishina pm. Invest Ophthalmol Vis Sci. 2016 Mar;57(3):877-88. doi: 10.1167/iovs.15-17495. Invest Ophthalmol Vis Sci. 2016. PMID: 26978024 Free PMC article.

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