
Number of publications published per year by Rathkolb, Birgit. (Source : PubMed)

Distribution of publications types for Rathkolb, Birgit. (Source : PubMed)
(a publication can be of different types, so total may exceed publications count)
Phenotypic and pathomorphological characteristics of a novel mutant mouse model for maturity-onset diabetes of the young type 2 (MODY 2).
Am. J. Physiol. Endocrinol. Metab.
2010;298;3
Loss of the actin remodeler Eps8 causes intestinal defects and improved metabolic status in mice.
PLoS ONE
2010;5;3
Clinical chemistry of congenic mice with quantitative trait loci for predicted responses to Trypanosoma congolense infection.
Infect. Immun.
2009;77;9
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Cell
2009;137;5
The C-terminal cytoplasmic domain of human proEGF is a negative modulator of body and organ weights in transgenic mice.
FEBS Lett.
2009;583;8
Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models.
Exp. Physiol.
2009;94;4
Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes.
PLoS ONE
2009;4;6
Mechanisms controlling anaemia in Trypanosoma congolense infected mice.
PLoS ONE
2009;4;4
N-ethyl-N-nitrosourea mutagenesis produced a small number of mice with altered plasma electrolyte levels.
J. Biomed. Sci.
2009;16
ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta.
PLoS Genet.
2008;4;2
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Institute of Experimental Genetics, Helmholtz Zentrum Muenchen, German Research Center for Environmental Health, Neuherberg, Germany.
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