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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1997 1
1999 1
2000 4
2001 1
2002 2
2004 2
2005 2
2011 3
2016 1
2018 1
2021 2
2022 3
2024 0

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PubMed for id: 66514

23 results

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Page 1
Deletion of Asrgl1 Leads to Photoreceptor Degeneration in Mice.
Zhou Y, Tian W, Jiang X, Yang H, Jiang Z, Li X, Jiang D, Sun K, Yang Y, Liu W, Zhu X. Zhou Y, et al. Front Cell Dev Biol. 2022 Jan 18;9:783547. doi: 10.3389/fcell.2021.783547. eCollection 2021. Front Cell Dev Biol. 2022. PMID: 35118070 Free PMC article.
A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.
Biswas P, Chavali VR, Agnello G, Stone E, Chakarova C, Duncan JL, Kannabiran C, Homsher M, Bhattacharya SS, Naeem MA, Kimchi A, Sharon D, Iwata T, Riazuddin S, Reddy GB, Hejtmancik JF, Georgiou G, Riazuddin SA, Ayyagari R. Biswas P, et al. Hum Mol Genet. 2016 Jun 15;25(12):2483-2497. doi: 10.1093/hmg/ddw113. Epub 2016 Apr 22. Hum Mol Genet. 2016. PMID: 27106100 Free PMC article.
Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies.
Murtaza N, Cheng AA, Brown CO, Meka DP, Hong S, Uy JA, El-Hajjar J, Pipko N, Unda BK, Schwanke B, Xing S, Thiruvahindrapuram B, Engchuan W, Trost B, Deneault E, Calderon de Anda F, Doble BW, Ellis J, Anagnostou E, Bader GD, Scherer SW, Lu Y, Singh KK. Murtaza N, et al. Cell Rep. 2022 Nov 22;41(8):111678. doi: 10.1016/j.celrep.2022.111678. Cell Rep. 2022. PMID: 36417873 Free article.
23 results