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Year Number of Results
2012 2
2013 2
2015 1
2017 1
2018 2
2019 2
2020 3
2021 3
2022 1
2023 2
2024 0

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14 results

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Page 1
Axenfeld-Rieger syndrome: more than meets the eye.
Reis LM, Maheshwari M, Capasso J, Atilla H, Dudakova L, Thompson S, Zitano L, Lay-Son G, Lowry RB, Black J, Lee J, Shue A, Kremlikova Pourova R, Vaneckova M, Skalicka P, Jedlickova J, Trkova M, Williams B, Richard G, Bachman K, Seeley AH, Costakos D, Glaser TM, Levin AV, Liskova P, Murray JC, Semina EV. Reis LM, et al. J Med Genet. 2023 Apr;60(4):368-379. doi: 10.1136/jmg-2022-108646. Epub 2022 Jul 26. J Med Genet. 2023. PMID: 35882526 Free PMC article.
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.
Atoh7-independent specification of retinal ganglion cell identity.
Brodie-Kommit J, Clark BS, Shi Q, Shiau F, Kim DW, Langel J, Sheely C, Ruzycki PA, Fries M, Javed A, Cayouette M, Schmidt T, Badea T, Glaser T, Zhao H, Singer J, Blackshaw S, Hattar S. Brodie-Kommit J, et al. Sci Adv. 2021 Mar 12;7(11):eabe4983. doi: 10.1126/sciadv.abe4983. Print 2021 Mar. Sci Adv. 2021. PMID: 33712461 Free PMC article.
NAA10 polyadenylation signal variants cause syndromic microphthalmia.
Johnston JJ, Williamson KA, Chou CM, Sapp JC, Ansari M, Chapman HM, Cooper DN, Dabir T, Dudley JN, Holt RJ, Ragge NK, Schäffer AA, Sen SK, Slavotinek AM, FitzPatrick DR, Glaser TM, Stewart F, Black GC, Biesecker LG. Johnston JJ, et al. J Med Genet. 2019 Jul;56(7):444-452. doi: 10.1136/jmedgenet-2018-105836. Epub 2019 Mar 6. J Med Genet. 2019. PMID: 30842225 Free PMC article.
14 results