Works matching AU Klaften, Matthias
Results: 12
Dominant-Negative Effects of a Novel Mutated Ins2 Allele Causes Early-Onset Diabetes and Severe β-Cell Loss in Munich Ins2<sup>C95S</sup> Mutant Mice.
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- Diabetes, 2007, v. 56, n. 5, p. 1268, doi. 10.2337/db06-0658
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- Article
New Mutation in the Mouse Xpd/Ercc2 Gene Leads to Recessive Cataracts.
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- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125304
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- Article
Generation of N-ethyl- N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models.
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- Experimental Physiology, 2009, v. 94, n. 4, p. 412, doi. 10.1113/expphysiol.2008.045864
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- Article
A Genetic Screen for Modifiers of the Deltal-Dependent Notch Signaling Function in the Mouse.
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- Genetics, 2007, v. 175, n. 3, p. 1451, doi. 10.1534/genetics.106.067298
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- Article
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels.
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- BioMetals, 2015, v. 28, n. 2, p. 293, doi. 10.1007/s10534-015-9824-1
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- Article
ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants.
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- Nucleic Acids Research, 2005, v. 33, n. suppl 2, p. w496, doi. 10.1093/nar/gki430
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- Article
Does enamelin have pleiotropic effects on organs other than the teeth? Lessons from a phenotyping screen of two enamelin-mutant mouse lines.
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- 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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Erratum to: New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
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- 2014
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- Erratum
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.
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- Mammalian Genome, 2012, v. 23, n. 7/8, p. 416, doi. 10.1007/s00335-012-9397-z
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Generation of N-ethyl- N-nitrosourea-induced mouse mutants with deviations in hematological parameters.
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- Mammalian Genome, 2011, v. 22, n. 9/10, p. 495, doi. 10.1007/s00335-011-9328-4
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Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice.
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- Mammalian Genome, 2009, v. 20, n. 3, p. 152, doi. 10.1007/s00335-009-9170-0
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- Article
Morphologic and molecular characterization of two novel Krt71 ( Krt2-6g) mutations: Krt71 <sup>rco12</sup> and Krt71 <sup>rco13</sup>.
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- Mammalian Genome, 2006, v. 17, n. 12, p. 1172, doi. 10.1007/s00335-006-0084-9
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- Article