Found: 16
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The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.
- Published in:
- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 12, p. 4035, doi. 10.1534/g3.116.033670
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- Publication type:
- Article
Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over.
- Published in:
- 2015
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- Publication type:
- Bibliography
Viable Ednra mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.
- Published in:
- Mammalian Genome, 2016, v. 27, n. 11/12, p. 587, doi. 10.1007/s00335-016-9664-5
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- Publication type:
- Article
Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.
- Published in:
- Mammalian Genome, 2016, v. 27, n. 3/4, p. 111, doi. 10.1007/s00335-016-9619-x
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- Publication type:
- Article
Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
- Published in:
- 2014
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- Publication type:
- Erratum
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
- Published in:
- Mammalian Genome, 2012, v. 23, n. 7/8, p. 416, doi. 10.1007/s00335-012-9397-z
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- Publication type:
- Article
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 mutant mice.
- Published in:
- Journal of Biomedical Science, 2017, v. 24, n. 1, p. 1, doi. 10.1186/s12929-017-0365-5
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- Publication type:
- Article
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 mutant mice.
- Published in:
- Journal of Biomedical Science, 2017, v. 24, n. 1, p. 1, doi. 10.1186/s12929-017-0365-5
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- Publication type:
- Article
Combining fish and environmental PCR for diagnostics of diseased laboratory zebrafish in recirculating systems.
- Published in:
- PLoS ONE, 2019, v. 14, n. 9, p. 1, doi. 10.1371/journal.pone.0222360
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- Publication type:
- Article
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels.
- Published in:
- BioMetals, 2015, v. 28, n. 2, p. 293, doi. 10.1007/s10534-015-9824-1
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- Publication type:
- Article
Peroxidasin is essential for eye development in the mouse.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5597, doi. 10.1093/hmg/ddu274
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- Publication type:
- Article
New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125304
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- Publication type:
- Article
Cytoplasmic Mislocalization of POU3 F4 Due to Novel Mutations Leads to Deafness in Humans and Mice.
- Published in:
- Human Mutation, 2013, v. 34, n. 8, p. 1102, doi. 10.1002/humu.22339
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- Publication type:
- Article
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
- Published in:
- European Journal of Oral Sciences, 2012, v. 120, n. 4, p. 269, doi. 10.1111/j.1600-0722.2012.00966.x
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- Publication type:
- Article
Systemic Jak1 activation provokes hepatic inflammation and imbalanced FGF23 production and cleavage.
- Published in:
- FASEB Journal, 2021, v. 35, n. 2, p. 1, doi. 10.1096/fj.202002113R
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- Publication type:
- Article
Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3<sup>L423P</sup> Mutant Mice.
- Published in:
- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0150472
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- Publication type:
- Article