Collin GB - Search Results

1

Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model.

Weatherly SM, Collin GB, Charette JR, Stone L, Damkham N, Hyde LF, Peterson JG, Hicks W, Carter GW, Naggert JK, Krebs MP, Nishina PM. Weatherly SM, et al. Among authors: collin gb. PLoS Genet. 2022 Jun 8;18(6):e1009798. doi: 10.1371/journal.pgen.1009798. eCollection 2022 Jun. PLoS Genet. 2022. PMID: 35675330 Free PMC article.

2

Mouse models of human ocular disease for translational research.

Krebs MP, Collin GB, Hicks WL, Yu M, Charette JR, Shi LY, Wang J, Naggert JK, Peachey NS, Nishina PM. Krebs MP, et al. Among authors: collin gb. PLoS One. 2017 Aug 31;12(8):e0183837. doi: 10.1371/journal.pone.0183837. eCollection 2017. PLoS One. 2017. PMID: 28859131 Free PMC article.

3

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. Cells. 2020 Apr 10;9(4):931. doi: 10.3390/cells9040931. Cells. 2020. PMID: 32290105 Free PMC article. Review.

4

Genetic Interaction between Mfrp and Adipor1 Mutations Affect Retinal Disease Phenotypes.

Gogna N, Weatherly S, Zhao F, Collin GB, Pinkney J, Stone L, Naggert JK, Carter GW, Nishina PM. Gogna N, et al. Among authors: collin gb. Int J Mol Sci. 2022 Jan 30;23(3):1615. doi: 10.3390/ijms23031615. Int J Mol Sci. 2022. PMID: 35163536 Free PMC article.

5

Mutations in ALMS1 cause obesity, type 2 diabetes and neurosensory degeneration in Alström syndrome.

Collin GB, Marshall JD, Ikeda A, So WV, Russell-Eggitt I, Maffei P, Beck S, Boerkoel CF, Sicolo N, Martin M, Nishina PM, Naggert JK. Collin GB, et al. Nat Genet. 2002 May;31(1):74-8. doi: 10.1038/ng867. Epub 2002 Apr 8. Nat Genet. 2002. PMID: 11941369

6

A mouse model for Meckel syndrome type 3.

Cook SA, Collin GB, Bronson RT, Naggert JK, Liu DP, Akeson EC, Davisson MT. Cook SA, et al. Among authors: collin gb. J Am Soc Nephrol. 2009 Apr;20(4):753-64. doi: 10.1681/ASN.2008040412. Epub 2009 Feb 11. J Am Soc Nephrol. 2009. PMID: 19211713 Free PMC article.

7

Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesis.

Collin GB, Won J, Hicks WL, Cook SA, Nishina PM, Naggert JK. Collin GB, et al. Invest Ophthalmol Vis Sci. 2012 Feb 23;53(2):967-74. doi: 10.1167/iovs.11-8766. Print 2012 Feb. Invest Ophthalmol Vis Sci. 2012. PMID: 22247471 Free PMC article.

8

Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAs.

Soundararajan R, Won J, Stearns TM, Charette JR, Hicks WL, Collin GB, Naggert JK, Krebs MP, Nishina PM. Soundararajan R, et al. Among authors: collin gb. PLoS One. 2014 Oct 30;9(10):e110299. doi: 10.1371/journal.pone.0110299. eCollection 2014. PLoS One. 2014. PMID: 25357075 Free PMC article.

9

A Mutation in Syne2 Causes Early Retinal Defects in Photoreceptors, Secondary Neurons, and Müller Glia.

Maddox DM, Collin GB, Ikeda A, Pratt CH, Ikeda S, Johnson BA, Hurd RE, Shopland LS, Naggert JK, Chang B, Krebs MP, Nishina PM. Maddox DM, et al. Among authors: collin gb. Invest Ophthalmol Vis Sci. 2015 Jun;56(6):3776-87. doi: 10.1167/iovs.14-16047. Invest Ophthalmol Vis Sci. 2015. PMID: 26066746 Free PMC article.

10

Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation.

Collin GB, Hubmacher D, Charette JR, Hicks WL, Stone L, Yu M, Naggert JK, Krebs MP, Peachey NS, Apte SS, Nishina PM. Collin GB, et al. Hum Mol Genet. 2015 Dec 15;24(24):6958-74. doi: 10.1093/hmg/ddv399. Epub 2015 Sep 24. Hum Mol Genet. 2015. PMID: 26405179 Free PMC article.

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