Found: 16
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Clarin‐2 is essential for hearing by maintaining stereocilia integrity and function.
- Published in:
- EMBO Molecular Medicine, 2019, v. 11, n. 9, p. N.PAG, doi. 10.15252/emmm.201910288
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- Article
A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease.
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- BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-07109-5
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- Article
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants.
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- BMC Biology, 2018, v. 16, n. 1, p. 1, doi. 10.1186/s12915-018-0530-7
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- Article
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.
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- PLoS Genetics, 2017, v. 13, n. 8, p. 1, doi. 10.1371/journal.pgen.1006969
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- Article
Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout.
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- FASEB Journal, 2023, v. 37, n. 11, p. 1, doi. 10.1096/fj.202201918R
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- Article
Genic constraint against nonsynonymous variation across the mouse genome.
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- BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-023-09637-2
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- Article
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
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- Nature Communications, 2016, v. 7, n. 8, p. 12444, doi. 10.1038/ncomms12444
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- Article
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains.
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- Genome Biology, 2013, v. 14, n. 7, p. R82, doi. 10.1186/gb-2013-14-7-r82
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- Article
Mouse genomic and cellular annotations.
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- Mammalian Genome, 2022, v. 33, n. 1, p. 19, doi. 10.1007/s00335-021-09936-7
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- Article
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00595-4
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- Article
Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations.
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- PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003219
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- Article
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair.
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- Genome Medicine, 2016, v. 8, p. 1, doi. 10.1186/s13073-016-0273-4
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- Article
Making sense of the linear genome, gene function and TADs.
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- Epigenetics & Chromatin, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13072-022-00436-9
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- Article
Making sense of the linear genome, gene function and TADs.
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- Epigenetics & Chromatin, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13072-022-00436-9
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- Article
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
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- Journal of Bone & Mineral Research, 2019, v. 34, n. 7, p. 1324, doi. 10.1002/jbmr.3695
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- Article
An N‐Ethyl‐N‐Nitrosourea (ENU)‐Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in Mice.
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- Journal of Bone & Mineral Research, 2019, v. 34, n. 3, p. 497, doi. 10.1002/jbmr.3624
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- Article