Similar articles for PMID: 24346171

Year	Number of Results
1999	1
2001	1
2003	1
2004	2
2005	2
2006	3
2007	5
2009	3
2010	1
2011	4
2012	7
2013	19
2014	12
2015	10
2016	7
2017	8
2018	6
2019	8
2020	10
2021	5
2022	5
2023	1
2024	0

1

Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repair.

Low BE, Krebs MP, Joung JK, Tsai SQ, Nishina PM, Wiles MV. Low BE, et al. Invest Ophthalmol Vis Sci. 2014 Jan 20;55(1):387-95. doi: 10.1167/iovs.13-13278. Invest Ophthalmol Vis Sci. 2014. PMID: 24346171 Free PMC article.

2

The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes.

Mattapallil MJ, Wawrousek EF, Chan CC, Zhao H, Roychoudhury J, Ferguson TA, Caspi RR. Mattapallil MJ, et al. Invest Ophthalmol Vis Sci. 2012 May 17;53(6):2921-7. doi: 10.1167/iovs.12-9662. Print 2012. Invest Ophthalmol Vis Sci. 2012. PMID: 22447858 Free PMC article.

3

Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele.

Chang B, FitzMaurice B, Wang J, Low BE, Wiles MV, Nishina PM. Chang B, et al. Invest Ophthalmol Vis Sci. 2018 Oct 1;59(12):5127-5139. doi: 10.1167/iovs.18-25046. Invest Ophthalmol Vis Sci. 2018. PMID: 30372741 Free PMC article.

4

Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse model.

Sahu B, Chavali VR, Alapati A, Suk J, Bartsch DU, Jablonski MM, Ayyagari R. Sahu B, et al. Mol Vis. 2015 Mar 13;21:273-84. eCollection 2015. Mol Vis. 2015. PMID: 25814825 Free PMC article.

5

Differences in the distribution, phenotype and gene expression of subretinal microglia/macrophages in C57BL/6N (Crb1 rd8/rd8) versus C57BL6/J (Crb1 wt/wt) mice.

Aredo B, Zhang K, Chen X, Wang CX, Li T, Ufret-Vincenty RL. Aredo B, et al. J Neuroinflammation. 2015 Jan 15;12:6. doi: 10.1186/s12974-014-0221-4. J Neuroinflammation. 2015. PMID: 25588310 Free PMC article.

6

Mthfr as a modifier of the retinal phenotype of Crb1(rd8/rd8) mice.

Markand S, Saul A, Tawfik A, Cui X, Rozen R, Smith SB. Markand S, et al. Exp Eye Res. 2016 Apr;145:164-172. doi: 10.1016/j.exer.2015.11.013. Epub 2015 Dec 2. Exp Eye Res. 2016. PMID: 26646559 Free PMC article.

7

Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice.

Kwon YS, Tham A, Lopez AJ, Edwards S, Woods S, Chen J, Wong-Fortunato J, Quiroz Alonso A, Javier S, Au I, Clarke M, Humpal D, Lloyd KCK, Thomasy S, Murphy C, Glaser TM, Moshiri A. Kwon YS, et al. Dev Biol. 2020 Feb 15;458(2):141-152. doi: 10.1016/j.ydbio.2019.10.013. Epub 2019 Oct 18. Dev Biol. 2020. PMID: 31634437 Free PMC article.

8

Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.

Aleman TS, Cideciyan AV, Aguirre GK, Huang WC, Mullins CL, Roman AJ, Sumaroka A, Olivares MB, Tsai FF, Schwartz SB, Vandenberghe LH, Limberis MP, Stone EM, Bell P, Wilson JM, Jacobson SG. Aleman TS, et al. Invest Ophthalmol Vis Sci. 2011 Aug 29;52(9):6898-910. doi: 10.1167/iovs.11-7701. Invest Ophthalmol Vis Sci. 2011. PMID: 21757580 Free PMC article.

9

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. 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.

10

The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors.

Luhmann UF, Carvalho LS, Holthaus SM, Cowing JA, Greenaway S, Chu CJ, Herrmann P, Smith AJ, Munro PM, Potter P, Bainbridge JW, Ali RR. Luhmann UF, et al. Hum Mol Genet. 2015 Jan 1;24(1):128-41. doi: 10.1093/hmg/ddu424. Epub 2014 Aug 21. Hum Mol Genet. 2015. PMID: 25147295 Free PMC article.

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