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PMC 340383 Molecular cloning and characterization of the mouse Acdp gene family Abstract Background We have recently cloned and characterized a novel gene family named ancient conserved domain protein (ACDP) in 23.2 KB 2020-10-02 10 557
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PMC 341451 Late gestational lung hypoplasia in a mouse model of the Smith-Lemli-Opitz syndrome Abstract Background Normal post-squalene cholesterol biosynthesis is important for mammalian embryonic development. 49.1 KB 2020-10-02 9 1,312
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PMC 394351 A mouse model of sitosterolemia: absence of Abcg8/sterolin-2 results in failure to secrete biliary cholesterol Abstract Background Mutations in either of two genes comprising the STSL locus, ATP-bind 61.2 KB 2020-10-02 9 1,381
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PMC 400732 Dopamine D2 receptors mediate two-odor discrimination and reversal learning in C57BL/6 mice Abstract Background Dopamine modulation of neuronal signaling in the frontal cortex, midbrain, and striatum 30.2 KB 2020-10-02 9 510
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PMC 441373 Structure-function evolution of the Transforming acidic coiled coil genes revealed by analysis of phylogenetically diverse organisms Abstract Background Examination of ancient gene families can provi 50.5 KB 2020-10-02 9 1,248
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PMC 48141 Intraocular pressure in genetically distinct mice: an update and strain survey Abstract Background Little is known about genetic factors affecting intraocular pressure (IOP) in mice and other mammals 40.1 KB 2020-10-02 9 440
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PMC 509301 The Zebrafish moonshine Gene Encodes Transcriptional Intermediary Factor 1γ, an Essential Regulator of Hematopoiesis moonshine/tif1γ in Hematopoiesis Abstract Hematopoiesis is precisely orchestrated 40.8 KB 2020-10-02 9 1,009
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PMC 509305 Spontaneous Autoimmunity in 129 and C57BL/6 Mice—Implications for Autoimmunity Described in Gene-Targeted Mice Gene-Targeted Mice and Autoimmunity Abstract Systemic lupus erythematosus (SLE) is a mul 39.8 KB 2020-10-02 9 495
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PMC 509410 Regulation of Muscle Fiber Type and Running Endurance by PPARδ PPARδ Regulates Muscle Fiber and Endurance Abstract Endurance exercise training can promote an adaptive muscle fiber transformation and 25.3 KB 2020-10-02 6 535
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PMC 516044 Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model Abstract Background Pendred syndrome, a common autosomal-recessive disorder char 32.8 KB 2020-10-02 9 993
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