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In this study, we further generated additional mouse models, including Trim37 ko2 , Trim37 ko3 , Trim37 RING , Trim37 MATH , Trim37 NLS , Trim37 NES , Blimp1-T2A-Cre , Trim28 flox , and Trim28 K774R+K779R

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FAK-paxillin signaling and F-actin cytoskeletal organization Molecular Modulation of the NO-system, VEGFR2 signaling, growth-hormone receptor expression in fibroblasts, and interactions with dopamine- and serotonin-related neurotransmitter pathways Systemic (Preclinical) Rodent models of gastrointestinal mucosal lesions, liver injury, tendon and ligament transection, and vascular occlusion syndromes References (BPC-157): Sikiric P, et al

Scrocchi LA, Brown TJ, MaClusky N et al (1996) Glucose intolerance but normal satiety in mice with a null mutation in the glucagon-like peptide 1 receptor gene