2017
DOI: 10.1002/dvdy.24511
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The occhiolino (occ) mutant Zebrafish, a model for development of the optical function in the biological lens

Abstract: The occ Zebrafish is a novel disease model for visual defects associated with abnormal lens development. Developmental Dynamics 246:915-924, 2017. © 2017 Wiley Periodicals, Inc.

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Cited by 8 publications
(12 citation statements)
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“…129 In zebrafish, the optical system is fully capable of OKR after 96 hours of development. 127 Among others, zebrafish OKR studies have revealed neuronal signaling pathways, [130][131][132][133] pharmacological and environmental impact, [134][135][136][137] and genetic players and mechanistic pathways 130,132,[138][139][140][141][142][143][144][145] involved in vertebrate vision.…”
Section: Functional Vision Testingmentioning
confidence: 99%
“…129 In zebrafish, the optical system is fully capable of OKR after 96 hours of development. 127 Among others, zebrafish OKR studies have revealed neuronal signaling pathways, [130][131][132][133] pharmacological and environmental impact, [134][135][136][137] and genetic players and mechanistic pathways 130,132,[138][139][140][141][142][143][144][145] involved in vertebrate vision.…”
Section: Functional Vision Testingmentioning
confidence: 99%
“…Secondly, the lens is transparent, and its transparency is due to the presence in it of special crystallin proteins with a complex structure characteristic of thermal chaperones (Jester, 2008;Aose et al, 2017). Some toxicants and penetrating radiation during chronic exposure can disrupt this structure, and then opacities will appear in the fiber part of the lens (Boswell et al, 2017).…”
Section: Introductionmentioning
confidence: 99%
“…20,21 The rapidly and externally developing transparent zebrafish embryos are amenable to easy genetic manipulation, allowing fast generation and identification of mutants modelling human ocular genetic disorders. [22][23][24][25][26][27][28] Such disease models can be concurrently investigated in large-scale genetics, drug screening, in vivo cell biology of early disease development as well as behavioral assays. [29][30][31][32] These potentials substantially aid fast progress in the validation of human genome association studies and in preclinical therapy development paths toward the early diagnosis and/or restoration of visual function.…”
Section: Introductionmentioning
confidence: 99%