Found: 17
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ATM/ATR Phosphorylation of CtIP on Its Conserved Sae2-like Domain Is Required for Genotoxin-Induced DNA Resection but Dispensable for Animal Development.
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- Cells (2073-4409), 2023, v. 12, n. 23, p. 2762, doi. 10.3390/cells12232762
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- Article
An essential role of intestinal cell kinase in lung development is linked to the perinatal lethality of human ECO syndrome.
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- FEBS Letters, 2017, v. 591, n. 9, p. 1247, doi. 10.1002/1873-3468.12644
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- Article
Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype.
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- Human Molecular Genetics, 2015, v. 24, n. 8, p. 2163, doi. 10.1093/hmg/ddu736
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- Article
Mouse Models of Achromatopsia in Addressing Temporal "Point of No Return" in Gene-Therapy.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 15, p. 8069, doi. 10.3390/ijms22158069
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- Article
Effects on Murine Behavior and Lifespan of Selectively Decreasing Expression of Mutant Huntingtin Allele by Supt4h Knockdown.
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- PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005043
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- Article
Spatiotemporal control of genome engineering in cone photoreceptors.
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- Cell & Bioscience, 2023, v. 13, n. 1, p. 1, doi. 10.1186/s13578-023-01033-3
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- Article
Therapeutic Margins in a Novel Preclinical Model of Retinitis Pigmentosa.
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- Journal of Neuroscience, 2013, v. 33, n. 33, p. 13475, doi. 10.1523/JNEUROSCI.0419-13.2013
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- Article
Creation and characterization of BAC-transgenic mice with physiological overexpression of epitope-tagged RCAN1 ( DSCR1).
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- Mammalian Genome, 2013, v. 24, n. 1/2, p. 30, doi. 10.1007/s00335-012-9436-9
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- Article
Protective mucosal immunity mediated by epithelial CD1d and IL-10.
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- Nature, 2014, v. 509, n. 7501, p. 497, doi. 10.1038/nature13150
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- Article
Pparg signaling controls bladder cancer subtype and immune exclusion.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26421-6
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- Article
Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho<sup>D190N</sup> mutation.
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- Cellular & Molecular Life Sciences, 2019, v. 76, n. 18, p. 3657, doi. 10.1007/s00018-019-03090-9
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- Article
Increased expression of the distal, but not of the proximal, Gata1 transcripts during differentiation of primary erythroid cells.
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- Journal of Cellular Physiology, 1999, v. 180, n. 3, p. 390, doi. 10.1002/(SICI)1097-4652(199909)180:3<390::AID-JCP10>3.0.CO;2-K
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- Article
Transgenic mice carrying the H258N mutation in the gene encoding the β-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness.
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- Human Mutation, 2007, v. 28, n. 3, p. 243, doi. 10.1002/humu.20425
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- Article
Photoactivatable Cre recombinase 3.0 for in vivo mouse applications.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16030-0
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- Article
shRNA knockdown of guanylate cyclase 2e or cyclic nucleotide gated channel alpha 1 increases photoreceptor survival in a cGMP phosphodiesterase mouse model of retinitis pigmentosa.
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- Journal of Cellular & Molecular Medicine, 2011, v. 15, n. 8, p. 1778, doi. 10.1111/j.1582-4934.2010.01201.x
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- Article
Generation of mice encoding a conditional allele of Nkx2.2.
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- Transgenic Research, 2013, v. 22, n. 5, p. 965, doi. 10.1007/s11248-013-9700-0
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- Article
Long-term vitamin A supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa.
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- Human Molecular Genetics, 2022, v. 31, n. 14, p. 2438, doi. 10.1093/hmg/ddac032
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- Article