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BMC Genomics|July 6, 2013
Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverageSandra Jansen, Bernhard Aigner, Hubert Pausch, et al.
Experimental Physiology|January 20, 2009
Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease modelsBernhard Aigner, Birgit Rathkolb, Matthias Klaften, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 10, 2011
Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parametersBernhard Aigner, Birgit Rathkolb, Martina Klempt, et al.
Human Molecular Genetics|June 11, 2013
Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in miceElisabeth Kemter, Petra Prueckl, Stefanie Sklenak, et al.
American Journal of Physiology. Renal Physiology|March 12, 2010
Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemiaElisabeth Kemter, Birgit Rathkolb, Lise Bankir, et al.
American Journal of Physiology. Renal Physiology|August 21, 2009
Novel missense mutation of uromodulin in mice causes renal dysfunction with alterations in urea handling, energy, and bone metabolismElisabeth Kemter, Birgit Rathkolb, Jan Rozman, et al.
Biometals : an International Journal on the Role of Metal Ions in Biology, Biochemistry, and Medicine|February 1, 2015
Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levelsBirgit Rathkolb, Martina Klempt, Sibylle Sabrautzki, et al.
Scientific Reports|November 17, 2022
New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetranceTanja Klein-Rodewald, Kateryna Micklich, Adrián Sanz-Moreno, et al.
Plos One|November 9, 2013
Standardized, systemic phenotypic analysis of Umod(C93F) and Umod(A227T) mutant miceElisabeth Kemter, Petra Prückl, Birgit Rathkolb, et al.
Journal of Biomedical Science|August 19, 2017
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant miceSudhir Kumar, Birgit Rathkolb, Sibylle Sabrautzki, et al.
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