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Molecular genetics of the early development of hindbrain serotonergic neurons.
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- Clinical Genetics, 2005, v. 68, n. 6, p. 487, doi. 10.1111/j.1399-0004.2005.00534.x
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- Article
Demented flies? usingDrosophilato model human neurodegenerative diseases.
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- Clinical Genetics, 2005, v. 67, n. 6, p. 468, doi. 10.1111/j.1399-0004.2005.00448.x
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- Article
Mechanisms regulating the development of the corpus callosum and its agenesis in mouse and human.
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- Clinical Genetics, 2004, v. 66, n. 4, p. 276, doi. 10.1111/j.1399-0004.2004.00354.x
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The beta-globin locus control region versus gene therapy vectors: a struggle for expression.
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- Clinical Genetics, 2001, v. 59, n. 1, p. 17, doi. 10.1034/j.1399-0004.2001.590103.x
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- Article
Recent advances in the molecular basis of inherited photoreceptor degeneration.
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- Clinical Genetics, 2000, v. 57, n. 5, p. 313, doi. 10.1034/j.1399-0004.2000.570501.x
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- Article
Developmental Biology: Frontiers for Clinical Genetics.
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- Clinical Genetics, 1998, v. 54, n. 1, p. 10, doi. 10.1111/j.1399-0004.1998.tb03684.x
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- Article
Developmental Biology: Frontiers for Clinical Genetics.
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- Clinical Genetics, 1998, v. 53, n. 3, p. 164, doi. 10.1111/j.1399-0004.1998.tb02667.x
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- Article
Endothelin-2 deficiency causes growth retardation, hypothermia, and emphysema in mice.
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- Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 2643, doi. 10.1172/JCI66735
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- Article
Maximizing Functional Photoreceptor Differentiation From Adult Human Retinal Stem Cells.
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- Stem Cells, 2010, v. 28, n. 3, p. 489, doi. 10.1002/stem.279
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Lifespan and mitochondrial control of neurodegeneration.
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- Nature Genetics, 2004, v. 36, n. 11, p. 1153, doi. 10.1038/ng1448
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Blinded by the light.
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- Nature Genetics, 2002, v. 32, n. 2, p. 215, doi. 10.1038/ng1002-215
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- Article
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
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- Nature Genetics, 2000, v. 25, n. 4, p. 397, doi. 10.1038/78071
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- Article
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis.
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- Nature Genetics, 2000, v. 25, n. 1, p. 67, doi. 10.1038/75621
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- Article
Endothelin-2-Mediated Protection of Mutant Photoreceptors in Inherited Photoreceptor Degeneration.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0058023
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- Article
Neto2 Interacts with the Scaffolding Protein GRIP and Regulates Synaptic Abundance of Kainate Receptors.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051433
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- Article
A Transgenic Mouse Line Expressing Cre Recombinase in Undifferentiated Postmitotic Mouse Retinal Bipolar Cell Precursors.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0027145
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- Article
Renal handling of phosphate in vivo and in vitro by the X- linked hypophosphatemic male mouse: Evidence for a defect in the brush border membrane.
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- Kidney International, 1978, v. 14, n. 3, p. 236, doi. 10.1038/ki.1978.115
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- Article
Genetic aspects of renal tubular transport: Diversity and topology of carriers.
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- Kidney International, 1976, v. 9, n. 2, p. 149, doi. 10.1038/ki.1976.18
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- Article
Neto2-null mice have impaired GABAergic inhibition and are susceptible to seizures.
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- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00368
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- Article
A one-hit model of cell death in inherited neuronal degenerations.
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- Nature, 2000, v. 406, n. 6792, p. 195, doi. 10.1038/35018098
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- Article
Neto1 Is a Novel CUB-Domain NMDA ReceptorInteracting Protein Required for Synaptic Plasticity and Learning.
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- PLoS Biology, 2009, v. 7, n. 2, p. e1000041, doi. 10.1371/journal.pbio.1000041
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- Article
Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X Chromosome short arm with respect to evolutionary breakpoints on the mouse X Chromosome.
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- Mammalian Genome, 2000, v. 11, n. 8, p. 710, doi. 10.1007/s003350010141
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- Article
Loss of retinal progenitor cells leads to an increase in the retinal stem cell population in vivo.
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- European Journal of Neuroscience, 2006, v. 23, n. 1, p. 75, doi. 10.1111/j.1460-9568.2005.04537.x
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- Article
Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase α sites.
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- Human Mutation, 2006, v. 27, n. 11, p. 1065, doi. 10.1002/humu.20352
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Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration.
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- Human Molecular Genetics, 2011, v. 20, n. 2, p. 322, doi. 10.1093/hmg/ddq467
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- Article
Natural antisense transcripts associated with genes involved in eye development.
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- Human Molecular Genetics, 2005, v. 14, n. 7, p. 913, doi. 10.1093/hmg/ddi084
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Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.
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- Human Molecular Genetics, 2004, v. 13, n. 17, p. 1893, doi. 10.1093/hmg/ddh198
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VSX1: A gene for posterior polymorphous dystrophy and keratoconus.
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- Human Molecular Genetics, 2002, v. 11, n. 9, p. 1029, doi. 10.1093/hmg/11.9.1029
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- Article
Blindness and the X.
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- Nature, 1996, v. 381, n. 6579, p. 194, doi. 10.1038/381194a0
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- Article
A Ubiquitin C-Terminal Hydrolase Gene on the Proximal Short Arm of the X Chromosome: Implications for X-Linked Retinal Disorders.
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- Human Molecular Genetics, 1996, v. 5, n. 4, p. 533, doi. 10.1093/hmg/5.4.533
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- Article
Mutation analysis of the ROM1 gene in retinitis pigmentosa.
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- Human Molecular Genetics, 1995, v. 4, n. 10, p. 1895
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Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine β-synthase using an improved bacterial expression system.
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- Human Molecular Genetics, 1994, v. 3, n. 7, p. 1103
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Polymorphisms and rare sequence variants at the ROM1 locus.
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- Human Molecular Genetics, 1993, v. 2, n. 11, p. 1975
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Neto Auxiliary Protein Interactions Regulate Kainate and NMDA Receptor Subunit Localization at Mossy Fiber-CA3 Pyramidal Cell Synapses.
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- Journal of Neuroscience, 2014, v. 34, n. 2, p. 622, doi. 10.1523/JNEUROSCI.3098-13.2014
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Neto1 Is an Auxiliary Subunit of Native Synaptic Kainate Receptors.
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- Journal of Neuroscience, 2011, v. 31, n. 27, p. 10009, doi. 10.1523/JNEUROSCI.6617-10.2011
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