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Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2.
- Published in:
- 2010
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- Publication type:
- journal article
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation.
- Published in:
- Journal of Bone & Mineral Research, 2012, v. 27, n. 2, p. 413, doi. 10.1002/jbmr.547
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- Publication type:
- Article
Novel Mouse Model of Autosomal Semidominant Adult Hypophosphatasia Has a Splice Site Mutation in the Tissue Nonspecific Alkaline Phosphatase Gene Akp2.
- Published in:
- Journal of Bone & Mineral Research, 2007, v. 22, n. 9, p. 1397, doi. 10.1359/JBMR.070515
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- Publication type:
- Article
Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.
- Published in:
- Journal of Pathology, 2014, v. 233, n. 1, p. 18, doi. 10.1002/path.4308
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- Publication type:
- Article
A cis-acting control region is required exclusively for the tissue-specific imprinting of Gnas.
- Published in:
- Nature Genetics, 2004, v. 36, n. 8, p. 894, doi. 10.1038/ng1398
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- Publication type:
- Article
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
- Published in:
- Nature Genetics, 2000, v. 25, n. 4, p. 440, doi. 10.1038/78140
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- Publication type:
- Article
Pharmacological Inhibition of FTO.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0121829
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- Publication type:
- Article
Gene Dosage Effects at the Imprinted <i>Gnas</i> Cluster.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065639
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- Publication type:
- Article
Autosomal Dominant Hypercalciuria in a Mouse Model Due to a Mutation of the Epithelial Calcium Channel, TRPV5.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055412
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- Publication type:
- Article
A Mouse Model for Osseous Heteroplasia.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051835
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- Publication type:
- Article
A Mouse with an N-Ethyl- N-Nitrosourea (ENU) Induced Trp589Arg Galnt3Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043205
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- Publication type:
- Article
Chronically elevated branched chain amino acid levels are pro-arrhythmic.
- Published in:
- Cardiovascular Research, 2022, v. 118, n. 7, p. 1742, doi. 10.1093/cvr/cvab207
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- Publication type:
- Article
Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout.
- Published in:
- FASEB Journal, 2023, v. 37, n. 11, p. 1, doi. 10.1096/fj.202201918R
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- Publication type:
- Article
Exploring the Lean Phenotype of Glutathione-Depleted Mice: Thiol, Amino Acid and Fatty Acid Profiles.
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- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0163214
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- Publication type:
- Article
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Maternal inheritance of the Gnas cluster mutation Ex1A- T affects size, implicating NESP55 in growth.
- Published in:
- Mammalian Genome, 2013, v. 24, n. 7/8, p. 276, doi. 10.1007/s00335-013-9462-2
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- Publication type:
- Article
Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract.
- Published in:
- Mammalian Genome, 2009, v. 20, n. 3, p. 140, doi. 10.1007/s00335-008-9169-y
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- Publication type:
- Article
A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice.
- Published in:
- Mammalian Genome, 2006, v. 17, n. 2, p. 129, doi. 10.1007/s00335-005-0112-1
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- Publication type:
- Article
Novel phenotypes identified by plasma biochemical screening in the mouse.
- Published in:
- Mammalian Genome, 2002, v. 13, n. 10, p. 595, doi. 10.1007/s00335-002-2188-1
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- Publication type:
- Article
Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 7, p. 500, doi. 10.1007/s003350010096
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- Publication type:
- Article
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-01995-2
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- Publication type:
- Article
HIF--VEGF Pathways Are Critical for Chronic Otitis Media in Junbo and Jeff Mouse Mutants.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 10, p. 1, doi. 10.1371/journal.pgen.1002336
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- Publication type:
- Article
A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 6, p. 1, doi. 10.1371/journal.pgen.1001000
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- Publication type:
- Article
Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media.
- Published in:
- PLoS Genetics, 2006, v. 3, n. 4, p. 1556, doi. 10.1371/journal.pgen.0020149
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- Publication type:
- Article
Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 19, p. 3553, doi. 10.1093/hmg/ddp304
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- Publication type:
- Article
Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.
- Published in:
- Journal of Bone & Mineral Research, 2019, v. 34, n. 7, p. 1324, doi. 10.1002/jbmr.3695
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- Publication type:
- 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.
- Published in:
- Journal of Bone & Mineral Research, 2019, v. 34, n. 3, p. 497, doi. 10.1002/jbmr.3624
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- Publication type:
- Article
Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages.
- Published in:
- Laboratory Animals, 2010, v. 44, n. 3, p. 218, doi. 10.1258/la.2010.009128
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- Publication type:
- Article
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall‐Smith Syndrome.
- Published in:
- JBMR Plus, 2023, v. 7, n. 6, p. 1, doi. 10.1002/jbm4.10739
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- Publication type:
- Article
A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006033
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- Publication type:
- Article