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Improving the Identification of Phenotypic Abnormalities and Sexual Dimorphism in Mice When Studying Rare Event Categorical Characteristics.
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- Genetics, 2017, v. 205, n. 2, p. 491, doi. 10.1534/genetics.116.195388
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- Article
Leveraging genetic diversity in mice to inform individual differences in brain microstructure and memory.
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- Frontiers in Behavioral Neuroscience, 2023, v. 16, p. 1, doi. 10.3389/fnbeh.2022.1033975
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- Article
MacroH2A1 isoforms are associated with epigenetic markers for activation of lipogenic genes in fat-induced steatosis.
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- FASEB Journal, 2015, v. 29, n. 5, p. 1676, doi. 10.1096/fj.14-262717
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- Article
Optimising experimental design for high-throughput phenotyping in mice: a case study.
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- Mammalian Genome, 2010, v. 21, n. 9/10, p. 467, doi. 10.1007/s00335-010-9279-1
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- Article
Robust mouse tracking in complex environments using neural networks.
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- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0362-1
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- Article
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing.
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- EMBO Molecular Medicine, 2016, v. 8, n. 3, p. 191, doi. 10.15252/emmm.201505523
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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
Comparative Analysis of Two slc11 (Nramp) Loci in Takifugu rubripes.
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- DNA & Cell Biology, 2004, v. 23, n. 1, p. 45, doi. 10.1089/104454904322745925
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- Article
Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM).
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- Biomedicines, 2021, v. 9, n. 11, p. 1711, doi. 10.3390/biomedicines9111711
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- Article
SLC11A1 (formerly NRAMP1) and disease resistance.
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- Cellular Microbiology, 2001, v. 3, n. 12, p. 773, doi. 10.1046/j.1462-5822.2001.00150.x
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- Article
The venous system of E14.5 mouse embryos—reference data and examples for diagnosing malformations in embryos with gene deletions.
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- Journal of Anatomy, 2022, v. 240, n. 1, p. 11, doi. 10.1111/joa.13536
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- Article
The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities.
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- PLoS ONE, 2020, v. 15, n. 6, p. 1, doi. 10.1371/journal.pone.0230162
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- Article
Machine learning-based automated phenotyping of inflammatory nocifensive behavior in mice.
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- Molecular Pain, 2020, v. 16, p. 1, doi. 10.1177/1744806920958596
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- Article
Identification of Genes Important for Cutaneous Function Revealed by a Large Scale Reverse Genetic Screen in the Mouse.
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- PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004705
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- Article
Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss.
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- PLoS Genetics, 2014, v. 10, n. 10, p. 1, doi. 10.1371/journal.pgen.1004688
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- Article
Disruption of Mouse Cenpj, a Regulator of Centriole Biogenesis, Phenocopies Seckel Syndrome.
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- PLoS Genetics, 2012, v. 8, n. 11, p. 1, doi. 10.1371/journal.pgen.1003022
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- Article
Rapid-Throughput Skeletal Phenotyping of 100 Knockout Mice Identifies 9 New Genes That Determine Bone Strength.
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- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002858
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- Article
Publisher Correction: Accelerating functional gene discovery in osteoarthritis.
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- 2021
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- Correction Notice
Accelerating functional gene discovery in osteoarthritis.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20761-5
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- Article
The mouse genetics toolkit: revealing function and mechanism.
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- Genome Biology, 2011, v. 12, n. 6, p. 224, doi. 10.1186/gb-2011-12-6-224
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- Article
FBXO7 sensitivity of phenotypic traits elucidated by a hypomorphic allele.
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- PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0212481
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- Article
Into the Wild: A novel wild-derived inbred strain resource expands the genomic and phenotypic diversity of laboratory mouse models.
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- PLoS Genetics, 2024, v. 20, n. 4, p. 1, doi. 10.1371/journal.pgen.1011228
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- Article
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
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- PLoS Biology, 2019, v. 17, n. 4, p. 1, doi. 10.1371/journal.pbio.3000194
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- Article
Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
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- PLoS Biology, 2019, v. 17, n. 4, p. 1, doi. 10.1371/journal.pbio.3000194
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- Article
Targeting of NAT10 enhances healthspan in a mouse model of human accelerated aging syndrome.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03770-3
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- Article
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-01995-2
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- Article
Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen.
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- Nature Communications, 2014, v. 5, n. 4, p. 3540, doi. 10.1038/ncomms4540
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- Article
Impact of Temporal Variation on Design and Analysis of Mouse Knockout Phenotyping Studies.
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- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0111239
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- Article
Targeting of <i>Slc25a21</i> Is Associated with Orofacial Defects and Otitis Media Due to Disrupted Expression of a Neighbouring Gene.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0091807
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- Article
<i>Mcph1</i>-Deficient Mice Reveal a Role for MCPH1 in Otitis Media.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058156
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- Article
Modeling Partial Monosomy for Human Chromosome 21q11.2-q21.1 Reveals Haploinsufficient Genes Influencing Behavior and Fat Deposition.
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- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029681
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- Article
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in Hdh [sup Q92] and Hdh [sup Q111] knock-in mice.
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- Human Molecular Genetics, 2000, v. 9, n. 4, p. 503, doi. 10.1093/hmg/9.4.503
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- Article
Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse.
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- Human Molecular Genetics, 1999, v. 8, n. 1, p. 115, doi. 10.1093/hmg/8.1.115
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- Article
Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement.
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- Nature Genetics, 2012, v. 44, n. 12, p. 1375, doi. 10.1038/ng.2453
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- Article
Applying the ARRIVE Guidelines to an In Vivo Database.
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- PLoS Biology, 2015, v. 13, n. 5, p. 1, doi. 10.1371/journal.pbio.1002151
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- Article
The fallacy of ratio correction to address confounding factors.
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- Laboratory Animals, 2012, v. 46, n. 3, p. 245, doi. 10.1258/la.2012.012003
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- Article
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
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- BMC Biology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12915-022-01257-8
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- Article
Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme.
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- BMC Biology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12915-022-01257-8
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- Article
Discovery and validation of genes driving drug‐intake and related behavioral traits in mice.
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- Genes, Brain & Behavior, 2024, v. 23, n. 1, p. 1, doi. 10.1111/gbb.12875
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- Article
Whole genome analysis for 163 gRNAs in Cas9-edited mice reveals minimal off-target activity.
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- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-04974-0
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- Article
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse.
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- Scientific Reports, 2016, p. 28964, doi. 10.1038/srep28964
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- Article
Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11431-2
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- Article
Common and distinct transcriptional signatures of mammalian embryonic lethality.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10642-x
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- Article
Reporting phenotypes in mouse models when considering body size as a potential confounder.
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- Journal of Biomedical Semantics, 2016, v. 7, p. 1, doi. 10.1186/s13326-016-0050-8
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- Article
Mendelian gene identification through mouse embryo viability screening.
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- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01118-7
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- Article