Found: 6
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A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome.
- Published in:
- Molecular Vision, 2020, v. 26, p. 670
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- Article
Tulp1 deficiency causes early-onset retinal degeneration through affecting ciliogenesis and activating ferroptosis in zebrafish.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 11, p. 1, doi. 10.1038/s41419-022-05372-w
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- Publication type:
- Article
Knockout of mafba Causes Inner-Ear Developmental Defects in Zebrafish via the Impairment of Proliferation and Differentiation of Ionocyte Progenitor Cells.
- Published in:
- Biomedicines, 2021, v. 9, n. 11, p. 1699, doi. 10.3390/biomedicines9111699
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- Article
Prpf31 is essential for the survival and differentiation of retinal progenitor cells by modulating alternative splicing.
- Published in:
- Nucleic Acids Research, 2021, v. 49, n. 4, p. 2027, doi. 10.1093/nar/gkab003
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- Article
Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 3, p. 1, doi. 10.1371/journal.pgen.1009841
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- Publication type:
- Article
Cross-species single-cell landscapes identify the pathogenic gene characteristics of inherited retinal diseases.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1409016
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- Publication type:
- Article