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Interspecific Recombinant Congenic Strains Between C57BL/6 and Mice of the Mus spretus Species: A Powerful Tool to Dissect Genetic Control of Complex Traits.
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- Genetics, 2007, v. 177, n. 4, p. 2321, doi. 10.1534/genetics.107.078006
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- Article
Rat Gene Mapping Using PCR-Analyzed Microsatellites.
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- Genetics, 1992, v. 131, n. 3, p. 701
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- Article
Evidence for Mitotic Recombination in W<sup>ei</sup>/+ Heterozygous Mice.
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- Genetics, 1990, v. 125, n. 1, p. 175
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L'héritage de Mary F. Lyon (1925-2014).
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- Médecine Sciences, 2015, v. 31, n. 6/7, p. 687, doi. 10.1051/medsci/20153106024
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- Article
A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse.
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- Nature Genetics, 2005, v. 37, n. 8, p. 803, doi. 10.1038/ng1603
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A missense mutation in Tbce causes progressive motor neuronopathy in mice.
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- Nature Genetics, 2002, v. 32, n. 3, p. 443, doi. 10.1038/ng1016
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Animal models of human genetic diseases: do they need to be faithful to be useful?
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- Molecular Genetics & Genomics, 2011, v. 286, n. 1, p. 1, doi. 10.1007/s00438-011-0627-y
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Several Classical Mouse Inbred Strains, Including DBA/2, NOD/Lt, FVB/N, and SJL/J, Carry a Putative Loss-of-Function Allele of Gpr84.
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- Journal of Heredity, 2013, v. 104, n. 4, p. 565, doi. 10.1093/jhered/est023
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Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) Are Two New Mutations of Lmx1a Causing Severe Cochlear and Vestibular Defects.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0051065
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Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant.
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- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039203
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Investigation of genetic linkage between myosin and actin genes using an interspecific mouse back-cross.
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- Nature, 1985, v. 314, n. 6007, p. 181, doi. 10.1038/314181a0
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The Mitochondrial Protease AFG3L2 Is Essential for Axonal Development.
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- Journal of Neuroscience, 2008, v. 28, n. 11, p. 2827, doi. 10.1523/JNEUROSCI.4677-07.2008
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- Article
Progressive Motor Neuronopathy: A Critical Role of the Tubulin Chaperone TBCE in Axonal Tubulin Routing from the Golgi Apparatus.
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- Journal of Neuroscience, 2007, v. 27, n. 33, p. 8779, doi. 10.1523/JNEUROSCI.1599-07.2007
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Assessing the genetic component of the susceptibility of mice to viral infections.
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- Briefings in Functional Genomics & Proteomics, 2005, v. 4, n. 3, p. 225, doi. 10.1093/bfgp/4.3.225
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- Article
Hst-3: an X-linked hybrid sterility gene.
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- Genetics Research, 1990, v. 56, n. 2/3, p. 163, doi. 10.1017/S0016672300035254
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- Article
Recombination between two mouse t-haplotypes (tw12tf and tLub-1): segregation of lethal factors relative to centromere and tufted (tf) locus.
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- Genetics Research, 1983, v. 42, n. 3, p. 335, doi. 10.1017/S0016672300021819
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Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene.
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- Journal of Investigative Dermatology, 2015, v. 135, n. 12, p. 3133, doi. 10.1038/jid.2015.314
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Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (<em>bal</em>) Locus.
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- Journal of Investigative Dermatology, 1997, v. 109, n. 3, p. 324, doi. 10.1111/1523-1747.ep12335844
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Lanceolate Hair (<em>lah</em>): A Recessive Mouse Mutation with Alopecia and Abnormal Hair.
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- Journal of Investigative Dermatology, 1996, v. 107, n. 1, p. 20, doi. 10.1111/1523-1747.ep12297438
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- Article
Alopecia and male infertility in oligotriche mutant mice are caused by a deletion on distal chromosome 9.
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- Mammalian Genome, 2008, v. 19, n. 10-12, p. 691, doi. 10.1007/s00335-008-9150-9
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Two quantitative trait loci affecting progressive hearing loss in 101/H mice.
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- Mammalian Genome, 2006, v. 17, n. 8, p. 841, doi. 10.1007/s00335-004-2438-5
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A new mouse limb mutation identifies a Twist allele that requires interacting loci on Chromosome 4 for its phenotypic expression.
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- Mammalian Genome, 2003, v. 14, n. 12, p. 797, doi. 10.1007/s00335-003-2284-x
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The genes encoding mouse lysyl hydroxylase isoforms map to Chromosomes 4, 5, and 9.
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- Mammalian Genome, 2000, v. 11, n. 12, p. 1132, doi. 10.1007/s003350010214
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Genes encoding troponin I and troponin T are organized as three paralogous pairs in the mouse genome.
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- Mammalian Genome, 2000, v. 11, n. 10, p. 926, doi. 10.1007/s003350010171
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Genomic organization, chromosomal assignment, and expression analysis of the mouse Suppressor of fused gene (Sufu) coding a Gli protein partner.
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- Mammalian Genome, 2000, v. 11, n. 8, p. 614, doi. 10.1007/s003350010144
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A Mutation in the Gene Encoding Mitochondrial Mg<sup>2+</sup> Channel MRS2 Results in Demyelination in the Rat.
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- PLoS Genetics, 2011, v. 7, n. 1, p. 1, doi. 10.1371/journal.pgen.1001262
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Progressive Purkinje Cell Degeneration in tambaleante Mutant Mice Is a Consequence of a Missense Mutation in HERC1 E3 Ubiquitin Ligase.
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- PLoS Genetics, 2009, v. 5, n. 12, p. 1, doi. 10.1371/journal.pgen.1000784
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The CD4 T cell-deficient mouse mutation nackt (nkt) involves a deletion in the cathepsin L (Ctsl) gene.
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- Immunogenetics, 2001, v. 53, n. 3, p. 233, doi. 10.1007/s002510100320
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Infection of mouse neurones by West Nile virus is modulated by the interferon-inducible 2′-5′ oligoadenylate synthetase 1b protein.
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- Immunology & Cell Biology, 2003, v. 81, n. 3, p. 230, doi. 10.1046/j.1440-1711.2003.01166.x
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Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca<sup>2+</sup>-activated K<sup>+</sup> channels.
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- Neurogenetics, 2008, v. 9, n. 4, p. 237, doi. 10.1007/s10048-008-0136-2
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- Article