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The GhrR KO animals used in these studies were bred from a single founder mouse at the Charles River Laboratories (Wilmington, MA) [ 28].
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Mice used in this study were bred in the Experimental Animal Facility of the Leiden University Medical Center and kept in individually ventilated cages with 12 hours of light/dark cycles at 20.5 °C and had ad libitum access to standard RM3 chow (SDS, Essex, UK) and water.
All mouse models used in the study were bred on a C57B6/J background.
All mice used in this study were bred and housed under specific pathogen-free (SPF) conditions.
Mice used in this study were bred and maintained in the Department of Laboratory Animal Resources at SUNY Upstate Medical University in accordance with the specifications of the Association for Assessment and Accreditation of Laboratory Animal Care.
The animals used in this study were bred separately in glass jars (5 liter) in a greenhouse at 12 h:12 h day:night cycle and were fed Calliphora sp. once a week.
All mice used for this study were bred and housed in a specifi c pathogen-free colony at the animal facility of Johannes Gutenberg University using institutionally approved protocols (permission was obtained from the Landesuntersuchungsamt Koblenz, Germany).
The mice used in this study were bred and maintained under standard conditions in the research vivarium at the University of Nebraska Medical Center under protocol number 04 086 approved by the Animal Care and Use Committee at the University of Nebraska Medical Center.
All mice used in this study were bred and housed in the animal facility.
The degus used in this study were bred in our colony (Leibniz Institute for Neurobiology, Magdeburg).
Animals for the current study were bred and housed at the National Public Health Institute, Division of Environmental Health, in Kuopio, Finland.
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