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Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure Closure.
Invest Ophthalmol Vis Sci. 2022 Nov 1;63(12):5. doi: 10.1167/iovs.63.12.5.
Invest Ophthalmol Vis Sci. 2022.
PMID: 36326727
Free PMC article.
Papillorenal syndrome-causing missense mutations in PAX2/Pax2 result in hypomorphic alleles in mouse and human.
Alur RP, Vijayasarathy C, Brown JD, Mehtani M, Onojafe IF, Sergeev YV, Boobalan E, Jones M, Tang K, Liu H, Xia CH, Gong X, Brooks BP.
Alur RP, et al. Among authors: boobalan e.
PLoS Genet. 2010 Mar 5;6(3):e1000870. doi: 10.1371/journal.pgen.1000870.
PLoS Genet. 2010.
PMID: 20221250
Free PMC article.
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nlz1 is required for cilia formation in zebrafish embryogenesis.
Dutta S, Sriskanda S, Boobalan E, Alur RP, Elkahloun A, Brooks BP.
Dutta S, et al. Among authors: boobalan e.
Dev Biol. 2015 Oct 15;406(2):203-11. doi: 10.1016/j.ydbio.2015.08.019. Epub 2015 Aug 29.
Dev Biol. 2015.
PMID: 26327644
Free PMC article.
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Nolz1 expression is required in dopaminergic axon guidance and striatal innervation.
Soleilhavoup C, Travaglio M, Patrick K, Garção P, Boobalan E, Adolfs Y, Spriggs RV, Moles-Garcia E, Dhiraj D, Oosterveen T, Ferri SL, Abel T, Brodkin ES, Pasterkamp RJ, Brooks BP, Panman L.
Soleilhavoup C, et al. Among authors: boobalan e.
Nat Commun. 2020 Jun 19;11(1):3111. doi: 10.1038/s41467-020-16947-6.
Nat Commun. 2020.
PMID: 32561725
Free PMC article.
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Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL.
Nichols LL 2nd, Alur RP, Boobalan E, Sergeev YV, Caruso RC, Stone EM, Swaroop A, Johnson MA, Brooks BP.
Nichols LL 2nd, et al. Among authors: boobalan e.
Hum Mutat. 2010 Jun;31(6):E1472-83. doi: 10.1002/humu.21268.
Hum Mutat. 2010.
PMID: 20513135
Free PMC article.
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