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luteal cells and CL tissues and the effect of PGF 2 α on the apoptosis of luteal cells is mediated by the Slit/Robo interaction. Materials and methods Reagents Rabbit IgG anti-Slit2 polyclonal antibodies and mouse IgM anti-Robo1 MABs were
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. 1998 , Saito et al . 2007 ). During the gestation period, I do was strongly expressed in the mouse concepti and placenta from days 8.5 to 12.5 of post-coitus ( Suzuki et al . 2001 , Minatogawa et al . 2003 ). Unexpectedly, tryptophan
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mouse ( Wharfe et al. 2016 ), and Wharfe and coworkers have also previously demonstrated that clock gene rhythms in the rat liver are altered by pregnancy ( Wharfe et al. 2011 ). Additionally, despite the high estradiol levels during pregnancy, the
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identification of extreme skeletal phenotypes in mutant mouse lines that carry single-gene knockouts representing all the known protein-coding genes. This approach has been made possible by the International Knockout Mouse Consortium (IKMC), whose aim is to
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per week using a Bayer Glucometer Elite. A mouse was deemed diabetic after two consecutive BG readings of >250 mg/dl. Mice were housed in accordance with the Ohio State University's requirements and regulations for animal care and use. Mice were
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Medizinische Klinik Innenstadt, Institute of Molecular Animal Breeding and Biotechnology, Division of Endocrinology, Institute for Molecular Medicine and Cell Research, Laboratory of Mouse Genetics, Ludwig-Maximilians University, Ziemssenstr. 1, 80336 Munich, Germany
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Medizinische Klinik Innenstadt, Institute of Molecular Animal Breeding and Biotechnology, Division of Endocrinology, Institute for Molecular Medicine and Cell Research, Laboratory of Mouse Genetics, Ludwig-Maximilians University, Ziemssenstr. 1, 80336 Munich, Germany
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. 2001 , Vinson 2003 , 2004 ). However, genetically altered animal models which are of increasing importance for intervention studies and to establish a genotype–phenotype relationship are restricted to the mouse ( Peters et al . 1999 , 2007
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effects that reduce their use in clinic. In this review, we discuss the cell-specific contribution of PPARγ in hepatic pathophysiology by using mechanistic mouse studies. PPARs were identified as orphan receptors and tested with reverse endocrinology
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Max Planck Institute of Psychiatry, Institut National de la Recherche Agronomique (INRA), University of Bordeaux, Research Group of Psychoneuroendocrinology, Kraepelinstrasse 2-10, 80804 Munich, Germany
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Max Planck Institute of Psychiatry, Institut National de la Recherche Agronomique (INRA), University of Bordeaux, Research Group of Psychoneuroendocrinology, Kraepelinstrasse 2-10, 80804 Munich, Germany
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Max Planck Institute of Psychiatry, Institut National de la Recherche Agronomique (INRA), University of Bordeaux, Research Group of Psychoneuroendocrinology, Kraepelinstrasse 2-10, 80804 Munich, Germany
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types of acute or chronic stressors, CBG expression was found to be downregulated, thereby increasing free GC levels ( Neufeld et al . 1994 , Fleshner et al . 1995 , Spencer et al . 1996 ). Recently, the analysis of a mouse model of targeted CBG
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context of the observed in vivo tissue distribution of PANDER. Therefore, to further elucidate the physiologic role of pancreas-secreted PANDER in vivo , our laboratory has created and phenotyped the only transgenic mouse model (PANDER transgenic, PANTG
The Third Xiangya Hospital of Central South University, Changsha, Hunan, China
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Animal Core Facility, Nanjing Medical University, Nanjing, Jiangsu, China
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). Therefore, investigating whether xenotransplanted rat BAT faces immunorejection remains important. In this study, we tested rat-to-mouse (RTM) BAT transplantation in 2-month-old pubescent mice. For comparison, we performed parallel mouse-to-mouse BAT