Found: 17
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Deletion of Emc1 in photoreceptor cells causes retinal degeneration in mice.
- Published in:
- FEBS Journal, 2023, v. 290, n. 17, p. 4356, doi. 10.1111/febs.16807
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- Publication type:
- Article
Three-Party Password Authentication and Key Exchange Protocol Based on MLWE.
- Published in:
- Symmetry (20738994), 2023, v. 15, n. 9, p. 1750, doi. 10.3390/sym15091750
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- Publication type:
- Article
Politeness in Professional Contexts.
- Published in:
- East Asian Pragmatics, 2022, v. 7, n. 2, p. 291, doi. 10.1558/eap.21751
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- Publication type:
- Article
Mettl14-mediated m6A modification is essential for visual function and retinal photoreceptor survival.
- Published in:
- BMC Biology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12915-022-01335-x
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- Publication type:
- Article
Specific ablation of Hippo signalling component Yap1 in retinal progenitors and Müller cells results in late onset retinal degeneration.
- Published in:
- Journal of Cellular Physiology, 2022, v. 237, n. 6, p. 2673, doi. 10.1002/jcp.30757
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- Publication type:
- Article
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis.
- Published in:
- Cell Death & Disease, 2021, v. 12, n. 11, p. 1, doi. 10.1038/s41419-021-04331-1
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- Publication type:
- Article
The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis.
- Published in:
- SCIENCE CHINA Life Sciences, 2021, v. 64, n. 11, p. 1868, doi. 10.1007/s11427-021-1941-7
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- Publication type:
- Article
Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling.
- Published in:
- 2021
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- Publication type:
- journal article
Loss of the ER membrane protein complex subunit Emc3 leads to retinal bipolar cell degeneration in aged mice.
- Published in:
- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0238435
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- Publication type:
- Article
Identification of novel USH2A mutations in patients with autosomal recessive retinitis pigmentosa via targeted next-generation sequencing.
- Published in:
- Molecular Medicine Reports, 2020, v. 22, n. 1, p. 193, doi. 10.3892/mmr.2020.11087
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- Publication type:
- Article
Disease Mutation Study Identifies Critical Residues for Phosphatidylserine Flippase ATP11A.
- Published in:
- BioMed Research International, 2020, p. 1, doi. 10.1155/2020/7342817
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- Publication type:
- Article
Deletion of the Impg2 gene causes the degeneration of rod and cone cells in mice.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 10, p. 1624, doi. 10.1093/hmg/ddaa062
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- Publication type:
- Article
Tmem30a deficiency leads to retinal rod bipolar cell degeneration.
- Published in:
- Journal of Neurochemistry, 2019, v. 148, n. 3, p. 400, doi. 10.1111/jnc.14643
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- Publication type:
- Article
Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 23, p. 4157, doi. 10.1093/hmg/ddy281
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- Publication type:
- Article
Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells.
- Published in:
- Cell Death & Disease, 2018, v. 9, n. 9, p. 1, doi. 10.1038/s41419-018-0938-6
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- Publication type:
- Article
A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 14, p. 2563, doi. 10.1093/hmg/ddy165
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- Publication type:
- Article
Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa.
- Published in:
- Scientific Reports, 2016, p. 33681, doi. 10.1038/srep33681
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- Publication type:
- Article