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P4‐163: THE PATHOLOGICAL INTERACTOME OF TDP‐43 INCLUDES HUMAN WILDTYPE SOD1.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1336, doi. 10.1016/j.jalz.2019.06.3825
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Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 10, p. 2223, doi. 10.3390/ijms18102223
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- Article
Seizures are a druggable mechanistic link between TBI and subsequent tauopathy.
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- eLife, 2021, p. 1, doi. 10.7554/eLife.58744
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- Article
Spatio-temporal characterization of retinal opsin gene expression during thyroid hormone-induced and natural development of rainbow trout.
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- Visual Neuroscience, 2006, v. 23, n. 2, p. 169, doi. 10.1017/s0952523806232139
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- Article
Photic history modifies susceptibility to retinal damage in albino trout.
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- Visual Neuroscience, 2006, v. 23, n. 1, p. 25, doi. 10.1017/s0952523806231031
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- Article
Visual pigment composition in zebrafish: Evidence for a rhodopsin–porphyropsin interchange system.
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- Visual Neuroscience, 2005, v. 22, n. 2, p. 249, doi. 10.1017/s0952523805222113
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- Article
Zebrafish Prion Protein PrP2 Controls Collective Migration Process during Lateral Line Sensory System Development.
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- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113331
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- Article
<i>gdf6a</i> Is Required for Cone Photoreceptor Subtype Differentiation and for the Actions of <i>tbx2b</i> in Determining Rod Versus Cone Photoreceptor Fate.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092991
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- Article
Growth Differentiation Factor 6 As a Putative Risk Factor in Neuromuscular Degeneration.
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- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0089183
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Regeneration of Cone Photoreceptors when Cell Ablation Is Primarily Restricted to a Particular Cone Subtype.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055410
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- Article
Amyloid Beta Precursor Protein and Prion Protein Have a Conserved Interaction Affecting Cell Adhesion and CNS Development.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051305
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- Article
Toll‐like receptor 4 is activated by platinum and contributes to cisplatin‐induced ototoxicity.
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- EMBO Reports, 2021, v. 22, n. 5, p. 1, doi. 10.15252/embr.202051280
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- Article
Zebrafish Models of Photoreceptor Dysfunction and Degeneration.
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- Biomolecules (2218-273X), 2021, v. 11, n. 1, p. 78, doi. 10.3390/biom11010078
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- Article
Prion-Like Propagation Mechanisms in Tauopathies and Traumatic Brain Injury: Challenges and Prospects.
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- Biomolecules (2218-273X), 2020, v. 10, n. 11, p. 1487, doi. 10.3390/biom10111487
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- Article
Connectivity of cone photoreceptor telodendria in the zebrafish retina.
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- Journal of Comparative Neurology, 2018, v. 526, n. 4, p. 609, doi. 10.1002/cne.24354
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- Article
Functional and behavioral signatures of Kv7 activator drug subtypes.
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- Epilepsia (Series 4), 2020, v. 61, n. 8, p. 1678, doi. 10.1111/epi.16592
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- Article
Transmission from the dominant input shapes the stereotypic ratio of photoreceptor inputs onto horizontal cells.
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- Nature Communications, 2014, v. 5, n. 5, p. 3699, doi. 10.1038/ncomms4699
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- Article
Ontogeny of ultraviolet-sensitive cones in the retina of rainbow trout (Oncorhynchus mykiss).
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- Journal of Comparative Neurology, 2003, v. 461, n. 3, p. 294, doi. 10.1002/cne.10682
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- Article
Medium-throughput zebrafish optogenetic platform identifies deficits in subsequent neural activity following brief early exposure to cannabidiol and Δ9-tetrahydrocannabinol.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-90902-3
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- Article
Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies.
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- Human Molecular Genetics, 2013, v. 22, n. 7, p. 1432, doi. 10.1093/hmg/dds560
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Rapid Recovery of Visual Function Associated with Blue Cone Ablation in Zebrafish.
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- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0166932
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Progressive Photoreceptor Dysfunction and Age-Related Macular Degeneration-Like Features in rp1l1 Mutant Zebrafish.
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- Cells (2073-4409), 2020, v. 9, n. 10, p. 2214, doi. 10.3390/cells9102214
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Functional Domains and Evolutionary History of the PMEL and GPNMB Family Proteins.
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- Molecules, 2021, v. 26, n. 12, p. 3529, doi. 10.3390/molecules26123529
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A complex regulatory network of transcription factors critical for ocular development and disease.
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- Human Molecular Genetics, 2011, v. 20, n. 8, p. 1610, doi. 10.1093/hmg/ddr038
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Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.
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- Human Molecular Genetics, 2010, v. 19, n. 2, p. 287
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Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 19, p. 14423, doi. 10.3390/ijms241914423
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Salmonid Opsin Sequences Undergo Positive Selection and Indicate an Alternate Evolutionary Relationship in Oncorhynchus.
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- Journal of Molecular Evolution, 2004, v. 58, n. 4, p. 400, doi. 10.1007/s00239-003-2562-y
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Neurologic Complications in Hereditary Hemorrhagic Telangiectasia with Pulmonary Arteriovenous Malformations: A Systematic Review.
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- Canadian Journal of Neurological Sciences, 2023, v. 50, n. 4, p. 561, doi. 10.1017/cjn.2022.80
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