PubMed for id: 192159

Year	Number of Results
1996	1
1997	2
1999	1
2000	4
2001	2
2002	2
2003	1
2004	4
2005	3
2008	1
2010	1
2011	5
2012	1
2013	1
2014	3
2015	2
2017	1
2018	4
2019	2
2020	1
2023	1
2024	0

1

Retinitis pigmentosa-associated mutations in mouse Prpf8 cause misexpression of circRNAs and degeneration of cerebellar granule cells.

Krausová M, Kreplová M, Banik P, Cvačková Z, Kubovčiak J, Modrák M, Zudová D, Lindovský J, Kubik-Zahorodna A, Pálková M, Kolář M, Procházka J, Sedláček R, Staněk D. Krausová M, et al. Life Sci Alliance. 2023 Apr 5;6(6):e202201855. doi: 10.26508/lsa.202201855. Print 2023 Jun. Life Sci Alliance. 2023. PMID: 37019475 Free PMC article.

2

Proteomic analysis of interchromatin granule clusters.

Saitoh N, Spahr CS, Patterson SD, Bubulya P, Neuwald AF, Spector DL. Saitoh N, et al. Mol Biol Cell. 2004 Aug;15(8):3876-90. doi: 10.1091/mbc.e04-03-0253. Epub 2004 May 28. Mol Biol Cell. 2004. PMID: 15169873 Free PMC article.

3

A splicing factor, Prp8: preferential localization in the testis and ovary in adult mice.

Takahashi A, Muramatsu H, Takagi S, Fujisawa H, Miyake Y, Muramatsu T. Takahashi A, et al. J Biochem. 2001 Apr;129(4):599-606. doi: 10.1093/oxfordjournals.jbchem.a002896. J Biochem. 2001. PMID: 11275560 Free article.

4

Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epithelium.

Farkas MH, Lew DS, Sousa ME, Bujakowska K, Chatagnon J, Bhattacharya SS, Pierce EA, Nandrot EF. Farkas MH, et al. Am J Pathol. 2014 Oct;184(10):2641-52. doi: 10.1016/j.ajpath.2014.06.026. Epub 2014 Aug 8. Am J Pathol. 2014. PMID: 25111227 Free PMC article.

5

Three gene-targeted mouse models of RNA splicing factor RP show late-onset RPE and retinal degeneration.

Graziotto JJ, Farkas MH, Bujakowska K, Deramaudt BM, Zhang Q, Nandrot EF, Inglehearn CF, Bhattacharya SS, Pierce EA. Graziotto JJ, et al. Invest Ophthalmol Vis Sci. 2011 Jan 5;52(1):190-8. doi: 10.1167/iovs.10-5194. Print 2011 Jan. Invest Ophthalmol Vis Sci. 2011. PMID: 20811066 Free PMC article.

6

Autosomal dominant retinitis pigmentosa-associated gene PRPF8 is essential for hypoxia-induced mitophagy through regulating ULK1 mRNA splicing.

Xu G, Li T, Chen J, Li C, Zhao H, Yao C, Dong H, Wen K, Wang K, Zhao J, Xia Q, Zhou T, Zhang H, Gao P, Li A, Pan X. Xu G, et al. Autophagy. 2018;14(10):1818-1830. doi: 10.1080/15548627.2018.1501251. Epub 2018 Aug 13. Autophagy. 2018. PMID: 30103670 Free PMC article.

7

Temporal and tissue specific regulation of RP-associated splicing factor genes PRPF3, PRPF31 and PRPC8--implications in the pathogenesis of RP.

Cao H, Wu J, Lam S, Duan R, Newnham C, Molday RS, Graziotto JJ, Pierce EA, Hu J. Cao H, et al. PLoS One. 2011 Jan 19;6(1):e15860. doi: 10.1371/journal.pone.0015860. PLoS One. 2011. PMID: 21283520 Free PMC article.

8

Erbb2 is required for cardiac atrial electrical activity during development.

Tenin G, Clowes C, Wolton K, Krejci E, Wright JA, Lovell SC, Sedmera D, Hentges KE. Tenin G, et al. PLoS One. 2014 Sep 30;9(9):e107041. doi: 10.1371/journal.pone.0107041. eCollection 2014. PLoS One. 2014. PMID: 25269082 Free PMC article.

9

The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression.

Hamilton BA, Smith DJ, Mueller KL, Kerrebrock AW, Bronson RT, van Berkel V, Daly MJ, Kruglyak L, Reeve MP, Nemhauser JL, Hawkins TL, Rubin EM, Lander ES. Hamilton BA, et al. Neuron. 1997 May;18(5):711-22. doi: 10.1016/s0896-6273(00)80312-8. Neuron. 1997. PMID: 9182797 Free article.

10

Identification of phosphoproteins and their phosphorylation sites in the WEHI-231 B lymphoma cell line.

Shu H, Chen S, Bi Q, Mumby M, Brekken DL. Shu H, et al. Mol Cell Proteomics. 2004 Mar;3(3):279-86. doi: 10.1074/mcp.D300003-MCP200. Epub 2004 Jan 17. Mol Cell Proteomics. 2004. PMID: 14729942 Free article.

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