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Summary Literature (15)
Literature for DOID 10629: microphthalmia

Xenbase Articles :
( Denotes literature images)
Dystroglycan is required for proper retinal layering., Lunardi A,Cremisi F,Dente L, Dev Biol. February 15, 2006; 290(2):1095-564X.
Ocular malformations of Xenopus laevis exposed to nickel during embryogenesis., Hauptman O,Albert DM,Plowman MC,Hopfer SM,Sunderman FW, Ann Clin Lab Sci. November 1, 1993; 23(6):0091-7370.
Eye and neural defects associated with loss of GDF6., Hanel ML,Hensey C, BMC Dev Biol. September 29, 2006; 6:1471-213X.
Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination., Hilton EN,Manson FD,Urquhart JE,Johnston JJ,Slavotinek AM,Hedera P,Stattin EL,Nordgren A,Biesecker LG,Black GC, Hum Mol Genet. July 15, 2007; 16(14):1460-2083.
Over-expression of atf4 in Xenopus embryos interferes with neurogenesis and eye formation., Liu JT,Yang Y,Yang Y,Guo XG,Chen M,Ding HZ,Chen YL,Chen YL,Wang MR, Dongwuxue Yanjiu. October 1, 2011; 32(5):2095-8137.
Bcl6a function is required during optic cup formation to prevent p53-dependent apoptosis and colobomata., Lee J,Lee J,Lee J,Lee J,Lee J,Lee J,Lee J,Lee J,Lee BK,Gross JM, Hum Mol Genet. September 1, 2013; 22(17):1460-2083.
A potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome., Tanaka K,Kato A,Angelocci C,Watanabe M,Kato Y, Dev Biol. March 1, 2014; 387(1):1095-564X.
Xenopus mutant reveals necessity of rax for specifying the eye field which otherwise forms tissue with telencephalic and diencephalic character., Fish MB,Nakayama T,Fisher M,Hirsch N,Cox A,Reeder R,Carruthers S,Hall A,Stemple DL,Grainger RM, Dev Biol. November 15, 2014; 395(2):1095-564X.
Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome., Zhu X,Dai FR,Wang J,Zhang Y,Zhang Y,Tan ZP,Zhang Y,Zhang Y, Gene. October 15, 2015; 571(1):1879-0038.
Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy., Duncan AR,Khokha MK, Semin Cell Dev Biol. March 1, 2016; 51:1096-3634.
Nosip functions during vertebrate eye and cranial cartilage development., Flach H,Krieg J,Hoffmeister M,Dietmann P,Reusch A,Wischmann L,Kernl B,Riegger R,Oess S,Kühl SJ, Dev Dyn. September 1, 2018; 247(9):1058-8388.
CRISPR/Cas9 disease models in zebrafish and Xenopus: The genetic renaissance of fish and frogs., Naert T,Vleminckx K,Vleminckx K, Drug Discov Today Technol. August 1, 2018; 28:1740-6749.
Sprouty2 regulates positioning of retinal progenitors through suppressing the Ras/Raf/MAPK pathway., Sun J,Yoon J,Lee M,Hwang YS,Daar IO, Sci Rep. August 13, 2020; 10(1):2045-2322.
Retinol binding protein 1 affects Xenopus anterior neural development via all-trans retinoic acid signaling., Flach H,Basten T,Schreiner C,Dietmann P,Greco S,Nies L,Roßmanith N,Walter S,Kühl M,Kühl SJ, Dev Dyn. August 1, 2021; 250(8):1058-8388.
Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F,Liu H,Fechtner L,Neuhaus H,Ding J,Arlt D,Walentek P,Villavicencio-Lorini P,Gerhardt C,Hollemann T,Pfirrmann T, J Cell Sci. January 1, 2022; 135(9):1477-9137.