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Role of an Atypical Cadherin Gene, Cdh23 in Prepulse Inhibition, and Implication of CDH23 in Schizophrenia.
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- Schizophrenia Bulletin, 2021, v. 47, n. 4, p. 1190, doi. 10.1093/schbul/sbab007
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- Article
Alivin 1, a Novel Neuronal Activity-dependent Gene, Inhibits Apoptosis and Promotes Survival of Cerebellar Granule Neurons.
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- Journal of Neuroscience, 2003, v. 23, n. 13, p. 5887, doi. 10.1523/JNEUROSCI.23-13-05887.2003
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A Small Deletion Hotspot in the Type II Keratin Gene mK6irs1/Krt2-6g on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (Ca) Mutation.
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- Genetics, 2003, v. 165, n. 2, p. 721, doi. 10.1093/genetics/165.2.721
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Characterization of single nucleotide polymorphisms for a forward genetics approach using genetic crosses in C57BL/6 and BALB/c substrains of mice.
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- Experimental Animals, 2022, v. 71, n. 2, p. 240, doi. 10.1538/expanim.21-0181
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Characterization of SNPs for a forward genetics approach using genetic crosses in substrains of mice.
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- Experimental Animals, 2022, v. 71, p. 172
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Inspection of suppressive effect of ahl10 locus derived from MSM/Ms mice on age-related hearing loss.
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- Experimental Animals, 2022, v. 71, p. 131
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Anophthalmia of NAK rats with loss of neural retina is modified by genetic and maternal effects.
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- Experimental Animals, 2022, v. 71, p. 96
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Myosin VI Haploinsufficiency Reduced Hearing Ability in Mice.
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- Experimental Animals, 2022, v. 71, p. 110
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Expression of Truncated PITX3 in the Developing Lens Leads to Microphthalmia and Aphakia in Mice.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0111432
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Specific mtDNA Mutations in Mouse Carcinoma Cells Suppress Their Tumor Formation via Activation of the Host Innate Immune System.
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- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0075981
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Novel Basophil- or Eosinophil-Depleted Mouse Models for Functional Analyses of Allergic Inflammation.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060958
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Mitochondrial DNA Mutations in Mutator Mice Confer Respiration Defects and B-Cell Lymphoma Development.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055789
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- Article
A 5-bp Insertion in Mip Causes Recessive Congenital Cataract in KFRS4/Kyo Rats.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0050737
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- Article
Genetic Background Strongly Modifies the Severity of Symptoms of Hirschsprung Disease, but not Hearing Loss in Rats Carrying Ednrb<sup>sl</sup> Mutations.
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- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024086
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Gelsolin Plays a Role in the Actin Polymerization Complex of Hair Cell Stereocilia.
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- PLoS ONE, 2010, v. 5, n. 7, p. 1, doi. 10.1371/journal.pone.0011627
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Application of spatial transcriptomics analysis using the Visium system for the mouse nasal cavity after intranasal vaccination.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1209945
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Serum chemokine CC‐motif ligand 17 is a predictive marker of severe COVID‐19 in haemodialysis patients: A retrospective observational study.
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- Nephrology, 2023, v. 28, n. 4, p. 240, doi. 10.1111/nep.14151
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Phylogenetic Development of a Regulatory Gene for the Core 2 GlcNAc Transferase in Mus musculus.
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- Journal of Biochemistry, 2002, v. 132, n. 3, p. 387, doi. 10.1093/oxfordjournals.jbchem.a003234
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Expression analysis of the type I keratin protein keratin 33A in goat coat hair.
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- Animal Science Journal, 2011, v. 82, n. 6, p. 773, doi. 10.1111/j.1740-0929.2011.00912.x
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The complete mitochondrial genome of the domestic red deer ( Cervus elaphus) of New Zealand and its phylogenic position within the family Cervidae.
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- Animal Science Journal, 2010, v. 81, n. 5, p. 551, doi. 10.1111/j.1740-0929.2010.00799.x
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- Article
Heterozygous mutation of Ush1g/Sans in mice causes early-onset progressive hearing loss, which is recovered by reconstituting the strain-specific mutation in Cdh23.
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- Human Molecular Genetics, 2016, v. 25, n. 10, p. 2045, doi. 10.1093/hmg/ddw078
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A deletion in a cis element of Foxe3 causes cataracts and microphthalmia in rct mice.
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- Mammalian Genome, 2011, v. 22, n. 11/12, p. 693, doi. 10.1007/s00335-011-9358-y
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Origins of mouse inbred strains deduced from whole-genome scanning by polymorphic microsatellite loci.
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- Mammalian Genome, 2005, v. 16, n. 1, p. 11, doi. 10.1007/s00344-004-3013-9
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Microsatellite database for MSM/Ms and JF1/Ms, molossinus-derived inbred strains.
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- Mammalian Genome, 2001, v. 12, n. 9, p. 750, doi. 10.1007/s003350030008
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Two Loci Contribute to Age-Related Hearing Loss Resistance in the Japanese Wild-Derived Inbred MSM/Ms Mice.
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- Biomedicines, 2022, v. 10, n. 9, p. 2221, doi. 10.3390/biomedicines10092221
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Molecular architecture of the stria vascularis membrane transport system, which is essential for physiological functions of the mammalian cochlea.
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- European Journal of Neuroscience, 2015, v. 42, n. 3, p. 1984, doi. 10.1111/ejn.12973
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OHC-TRECK: A Novel System Using a Mouse Model for Investigation of the Molecular Mechanisms Associated with Outer Hair Cell Death in the Inner Ear.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-41711-2
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Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.
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- Human Molecular Genetics, 2005, v. 14, n. 3, p. 391, doi. 10.1093/hmg/ddi035
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Interactions in the network of Usher syndrome type 1 proteins.
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- Human Molecular Genetics, 2005, v. 14, n. 3, p. 347, doi. 10.1093/hmg/ddi031
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Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
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- Human Molecular Genetics, 2003, v. 12, n. 5, p. 463, doi. 10.1093/hmg/ddg051
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Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice.
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- Human Molecular Genetics, 2003, v. 12, n. 5, p. 453, doi. 10.1093/hmg/ddg042
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- Article
Comparative outcomes of hemodialysis patients facing pre‐Omicron and Omicron COVID‐19 epidemics.
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- Therapeutic Apheresis & Dialysis, 2024, v. 28, n. 1, p. 51, doi. 10.1111/1744-9987.14067
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Selective depletion of mouse kidney proximal straight tubule cells causes acute kidney injury.
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- Transgenic Research, 2012, v. 21, n. 1, p. 51, doi. 10.1007/s11248-011-9504-z
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A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells.
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- PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0183477
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