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Long-term retinal protection by MEK inhibition in Pax6 haploinsufficiency mice.
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Postnatal manipulation of Pax6 dosage reverses congenital tissue malformation defects.
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Xenopus pax6 mutants affect eye development and other organ systems, and have phenotypic similarities to human aniridia patients.
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The Triple Procedure in Patients with Congenital Aniridia.
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Breaking genetic shackles: The advance of base editing in genetic disorder treatment.
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Characterization of neural damage and neuroinflammation in Pax6 small-eye mice.
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ABE8e Corrects Pax6-Aniridic Variant in Humanized Mouse ESCs and via LNPs in Ex Vivo Cortical Neurons.
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MAPK Pathways in Ocular Pathophysiology: Potential Therapeutic Drugs and Challenges.
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Differential effects of experimental glaucoma on intrinsically photosensitive retinal ganglion cells in mice.
J Comp Neurol. 2022 Jun;530(9):1494-1506. doi: 10.1002/cne.25293. Epub 2022 Jan 20.
4
Gene dosage manipulation alleviates manifestations of hereditary haploinsufficiency in mice.
Sci Transl Med. 2020 Dec 9;12(573). doi: 10.1126/scitranslmed.aaz4894.
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The Spectrum of Mutations and Genotype-Phenotype Correlations in the Eye.
Genes (Basel). 2019 Dec 17;10(12):1050. doi: 10.3390/genes10121050.
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Does Retinal Ganglion Cell Loss Precede Visual Field Loss in Glaucoma?
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A triple drug combination targeting components of the nutrient-sensing network maximizes longevity.
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10
Epistasis between Pax6 and genetic background reinforces the value of defined hybrid mouse models for therapeutic trials.
Gene Ther. 2018 Dec;25(8):524-537. doi: 10.1038/s41434-018-0043-6. Epub 2018 Sep 26.

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