Found: 21
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Prevention of autosomal dominant retinitis pigmentosa by systemic drug therapy targeting heat shock protein 90 (Hsp90).
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 22, p. 4421, doi. 10.1093/hmg/ddq369
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- Publication type:
- Article
Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10).
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 14, p. 2084, doi. 10.1093/hmg/ddn107
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- Publication type:
- Article
On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 6, p. 641, doi. 10.1093/hmg/ddh061
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- Article
RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD Models.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3847, doi. 10.3390/ijms24043847
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- Publication type:
- Article
Properties and Therapeutic Implications of an Enigmatic D477G RPE65 Variant Associated with Autosomal Dominant Retinitis Pigmentosa.
- Published in:
- Genes, 2020, v. 11, n. 12, p. 1420, doi. 10.3390/genes11121420
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- Publication type:
- Article
C1q enhances cone photoreceptor survival in a mouse model of autosomal recessive retinitis pigmentosa.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 1, p. 64, doi. 10.1038/ejhg.2011.151
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- Publication type:
- Article
A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 10, p. 1074, doi. 10.1038/ejhg.2011.86
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- Publication type:
- Article
A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.
- Published in:
- 2011
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- Correction notice
Improved Retinal Function in a Mouse Model of Dominant Retinitis Pigmentosa Following AAV-delivered Gene Therapy.
- Published in:
- Molecular Therapy, 2009, v. 17, n. 4, p. 593, doi. 10.1038/mt.2008.301
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- Publication type:
- Article
Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic background.
- Published in:
- Visual Neuroscience, 2001, v. 18, n. 3, p. 437, doi. 10.1017/s0952523801183100
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- Publication type:
- Article
AAV‐mediated gene therapy improving mitochondrial function provides benefit in age‐related macular degeneration models.
- Published in:
- Clinical & Translational Medicine, 2022, v. 12, n. 8, p. 1, doi. 10.1002/ctm2.952
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- Publication type:
- Article
Systemic low-molecular weight drug delivery to pre-selected neuronal regions.
- Published in:
- EMBO Molecular Medicine, 2011, v. 3, n. 4, p. 235, doi. 10.1002/emmm.201100126
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- Publication type:
- Article
Enhancement of Outflow Facility in the Murine Eye by Targeting Selected Tight-Junctions of Schlemm's Canal Endothelia.
- Published in:
- Scientific Reports, 2017, p. 40717, doi. 10.1038/srep40717
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- Publication type:
- Article
IL-18 Attenuates Experimental Choroidal Neovascularization as a Potential Therapy for Wet Age-Related Macular Degeneration.
- Published in:
- Science Translational Medicine, 2014, v. 6, n. 230, p. 1, doi. 10.1126/scitranslmed.3007616
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- Publication type:
- Article
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindness.
- Published in:
- Human Mutation, 1999, v. 13, n. 1, p. 75, doi. 10.1002/(SICI)1098-1004(1999)13:1<75::AID-HUMU9>3.0.CO;2-4
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- Publication type:
- Article
Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland.
- Published in:
- Human Mutation, 1996, v. 8, n. 1, p. 57, doi. 10.1002/(SICI)1098-1004(1996)8:1<57::AID-HUMU8>3.0.CO;2-M
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- Publication type:
- Article
A mutation (met→arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.
- Published in:
- Human Mutation, 1993, v. 2, n. 1, p. 37, doi. 10.1002/humu.1380020107
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- Publication type:
- Article
NLRP3 has a protective role in age-related macular degeneration through the induction of IL-18 by drusen components.
- Published in:
- Nature Medicine, 2012, v. 18, n. 5, p. 791, doi. 10.1038/nm.2717
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- Publication type:
- Article
Therapeutic potential of AAV-mediated MMP-3 secretion from corneal endothelium in treating glaucoma.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1230, doi. 10.1093/hmg/ddx028
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- Publication type:
- Article
Murine model of autosomal dominant retinitis pigmentosa generated by targeted deletion at codon 307 of the rds–peripherin gene.
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- Human Molecular Genetics, 2002, v. 11, n. 9, p. 1005, doi. 10.1093/hmg/11.9.1005
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- Article
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 7, p. 1309, doi. 10.1093/hmg/8.7.1309
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- Publication type:
- Article