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Items: 1 to 20 of 98

1.
Central Pars Plana Vitrectomy + Phacoemulsification + Intraocular Lens Implantation in Patients with Small Eyes, Cataract, and Narrow Anterior Chambers
Fermín Silva Cayatopa, Ana Luisa González Méndez, Robinson Barrientos Ortiz, Alejandro Silva Diaz, Fernando Godin Estrada
Clin Ophthalmol. 2021; 15: 4181–4187. Published online 2021 Oct 19. doi: 10.2147/OPTH.S336929
PMCID:
PMC8541767
AbstractArticlePDF–1.5M
2.
Spotting the “small eyes”: using photo-ID methodology to study a wild population of smalleye stingrays (Megatrygon microps) in southern Mozambique
Atlantine Boggio-Pasqua, Anna L. Flam, Andrea D. Marshall
PeerJ. 2019; 7: e7110. Published online 2019 Jun 11. doi: 10.7717/peerj.7110
PMCID:
PMC6568249
AbstractArticlePDF–25M
3.
Early Triassic marine reptile representing the oldest record of unusually small eyes in reptiles indicating non-visual prey detection
Long Cheng, Ryosuke Motani, Da-yong Jiang, Chun-bo Yan, Andrea Tintori, Olivier Rieppel
Sci Rep. 2019; 9: 152. Published online 2019 Jan 24. doi: 10.1038/s41598-018-37754-6
PMCID:
PMC6345829
AbstractArticlePDF–3.0M
4.
The remarkable visual capacities of nocturnal insects: vision at the limits with small eyes and tiny brains
Eric J. Warrant
Philos Trans R Soc Lond B Biol Sci. 2017 Apr 5; 372(1717): 20160063. doi: 10.1098/rstb.2016.0063
PMCID:
PMC5312013
AbstractArticlePDF–1.8M
5.
Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exon
Oliver Puk, Xiaohe Yan, Sibylle Sabrautzki, Helmut Fuchs, Valérie Gailus-Durner, Martin Hrabě de Angelis, Jochen Graw
Mol Vis. 2013; 19: 877–884. Published online 2013 Apr 12.
PMCID:
PMC3626302
AbstractArticlePDF–1.9M
6.
A dominant form of inherited retinal degeneration caused by a non-photoreceptor cell-specific mutation
Lei Li, John E. Dowling
Proc Natl Acad Sci U S A. 1997 Oct 14; 94(21): 11645–11650. doi: 10.1073/pnas.94.21.11645
PMCID:
PMC23565
AbstractArticlePDF–500K
7.
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice
Sarah J. Garnai, Michelle L. Brinkmeier, Ben Emery, Tomas S. Aleman, Louise C. Pyle, Biliana Veleva-Rotse, Robert A. Sisk, Frank W. Rozsa, Ayse Bilge Ozel, Jun Z. Li, Sayoko E. Moroi, Steven M. Archer, Cheng-mao Lin, Sarah Sheskey, Laurel Wiinikka-Buesser, James Eadie, Jill E. Urquhart, Graeme C.M. Black, Mohammad I. Othman, Michael Boehnke, Scot A. Sullivan, Gregory L. Skuta, Hemant S. Pawar, Alexander E. Katz, Laryssa A. Huryn, Robert B. Hufnagel, The Genomic Ascertainment Cohort, Sally A. Camper, Julia E. Richards, Lev Prasov
PLoS Genet. 2019 May; 15(5): e1008130. Published online 2019 May 2. doi: 10.1371/journal.pgen.1008130
PMCID:
PMC6527243
AbstractArticlePDF–6.4M
8.
A modifier screen in the eye reveals control genes for Krüppel activity in the Drosophila embryo
Pilar Carrera, Sarah Abrell, Birgit Kerber, Uwe Walldorf, Anette Preiss, Michael Hoch, Herbert Jäckle
Proc Natl Acad Sci U S A. 1998 Sep 1; 95(18): 10779–10784. doi: 10.1073/pnas.95.18.10779
PMCID:
PMC27972
AbstractArticlePDF–456K
9.
Ring chromosome 15 – cytogenetics and mapping arrays: a case report and review of the literature
César Paz-y-Miño, Jaime Guevara-Aguirre, Ariane Paz-y-Miño, Francesca Velarde, Isaac Armendáriz-Castillo, Verónica Yumiceba, Jesús María Hernández, Juan Luis García, Paola E. Leone
J Med Case Rep. 2018; 12: 340. Published online 2018 Nov 16. doi: 10.1186/s13256-018-1879-5
PMCID:
PMC6238305
AbstractArticlePDF–1.0M
10.
De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism
Yanjie Fan, Wu Yin, Bing Hu, Antonie D. Kline, Victor Wei Zhang, Desheng Liang, Yu Sun, Lili Wang, Sha Tang, Zöe Powis, Lei Li, Huifang Yan, Zhen Shi, Xiaoping Yang, Yinyin Chen, Jingmin Wang, Yuwu Jiang, Hu Tan, Xuefan Gu, Lingqian Wu, Yongguo Yu
Am J Hum Genet. 2018 Sep 6; 103(3): 448–455. Published online 2018 Aug 16. doi: 10.1016/j.ajhg.2018.07.019
PMCID:
PMC6128244
AbstractArticlePDF–1.9M
11.
NEAP/DUSP26 suppresses receptor tyrosine kinases and regulates neuronal development in zebrafish
Chi-Hwa Yang, Yu-Jung Yeh, Jiz-Yuh Wang, Ya-Wen Liu, Yen-Lin Chen, Hui-Wen Cheng, Chun-Mei Cheng, Yung-Jen Chuang, Chiou-Hwa Yuh, Yi-Rong Chen
Sci Rep. 2017; 7: 5241. Published online 2017 Jul 12. doi: 10.1038/s41598-017-05584-7
PMCID:
PMC5507855
AbstractArticlePDF–3.7M
12.
Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney
Maarit Rossi, Hiroyuki Morita, Raija Sormunen, Sari Airenne, Marjut Kreivi, Ling Wang, Naomi Fukai, Bjorn R. Olsen, Karl Tryggvason, Raija Soininen
EMBO J. 2003 Jan 15; 22(2): 236–245. doi: 10.1093/emboj/cdg019
PMCID:
PMC140094
AbstractArticlePDF–374K
13.
Requirement of Smad4 from Ocular Surface Ectoderm for Retinal Development
Jing Li, Shusheng Wang, Chastain Anderson, Fangkun Zhao, Yu Qin, Di Wu, Xinwei Wu, Jia Liu, Xuefei He, Jiangyue Zhao, Jinsong Zhang
PLoS One. 2016; 11(8): e0159639. Published online 2016 Aug 5. doi: 10.1371/journal.pone.0159639
PMCID:
PMC4975478
AbstractArticlePDF–12M
14.
Antagonism between Gdf6a and retinoic acid pathways controls timing of retinal neurogenesis and growth of the eye in zebrafish
Leonardo E. Valdivia, Dayna B. Lamb, Wilson Horner, Claudia Wierzbicki, Amanuel Tafessu, Audrey M. Williams, Gaia Gestri, Anna M. Krasnow, Terra S. Vleeshouwer-Neumann, McKenzie Givens, Rodrigo M. Young, Lisa M. Lawrence, Heather L. Stickney, Thomas A. Hawkins, Quenten P. Schwarz, Florencia Cavodeassi, Stephen W. Wilson, Kara L. Cerveny
Development. 2016 Apr 1; 143(7): 1087–1098. doi: 10.1242/dev.130922
PMCID:
PMC4852494
AbstractArticle
15.
Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish
Conghui Zhang, Qi Zhang, Fang Wang, Qin Liu
Biochem Biophys Res Commun. Author manuscript; available in PMC 2016 Oct 2.
Published in final edited form as: Biochem Biophys Res Commun. 2015 Oct 2; 465(4): 651–657. Published online 2015 Jul 15. doi: 10.1016/j.bbrc.2015.06.083
PMCID:
PMC4601574
AbstractArticlePDF–901K
16.
New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts
Sarah Kunze, Claudia Dalke, Helmut Fuchs, Matthias Klaften, Ute Rössler, Sabine Hornhardt, Maria Gomolka, Oliver Puk, Sibylle Sabrautzki, Ulrike Kulka, Martin Hrabě de Angelis, Jochen Graw
PLoS One. 2015; 10(5): e0125304. Published online 2015 May 7. doi: 10.1371/journal.pone.0125304
PMCID:
PMC4423972
AbstractArticlePDF–17M
17.
The Nuclear Pore Complex Function of Sec13 Protein Is Required for Cell Survival during Retinal Development
Xubo Niu, Jian Hong, Xiaofeng Zheng, David B. Melville, Ela W. Knapik, Anming Meng, Jinrong Peng
J Biol Chem. 2014 Apr 25; 289(17): 11971–11985. Published online 2014 Mar 13. doi: 10.1074/jbc.M114.547190
PMCID:
PMC4002104
AbstractArticlePDF–7.3M
18.
Novel role for carbamoyl phosphate synthetase 2 in cranial sensory circuit formation
Jane A. Cox, Angela LaMora, Stephen L. Johnson, Mark M. Voigt
Int J Dev Neurosci. Author manuscript; available in PMC 2015 Apr 1.
Published in final edited form as: Int J Dev Neurosci. 2014 Apr; 33: 41–48. Published online 2013 Nov 23. doi: 10.1016/j.ijdevneu.2013.11.003
PMCID:
PMC3944931
AbstractArticlePDF–2.5M
19.
Analysis of the Ush2a Gene in Medaka Fish (Oryzias latipes)
Elena Aller, Ana V. Sánchez-Sánchez, Javier U. Chicote, Gema García-García, Patricia Udaondo, Laura Cavallé, Marina Piquer-Gil, Antonio García-España, Manuel Díaz-Llopis, José M. Millán, José L. Mullor
PLoS One. 2013; 8(9): e74995. Published online 2013 Sep 23. doi: 10.1371/journal.pone.0074995
PMCID:
PMC3781144
AbstractArticlePDF–1.5M
20.
CERKL Knockdown Causes Retinal Degeneration in Zebrafish
Marina Riera, Demian Burguera, Jordi Garcia-Fernàndez, Roser Gonzàlez-Duarte
PLoS One. 2013; 8(5): e64048. Published online 2013 May 9. doi: 10.1371/journal.pone.0064048
PMCID:
PMC3650063
AbstractArticlePDF–1.5M

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