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For instance, muscle and liver from PGC-1β KO mouse show a reduction of mitochondrial volume without changes in mitochondria number [20], [23].
The -1 exons identified in human and mouse show a high degree of homology (data not shown) and likewise the -2a exons share a region of high homology (Figure 4B).
Multiple lines of evidence from both human and mouse show a role for CYP1B1 in the development of PAH.
In addition, rat and mouse show a negative force-frequency relationship, while it has a positive slope in larger mammals, such as rabbits (16).
Muc1 knockout mice (Muc1-/; MUC1 is human; Muc1 is mouse) show a reduction in tumorigenic phenotype when crossed onto mice overexpressing the Wnt-1 [ 7] or polyomavirus middle T antigen [ 8] oncogenes in the mammary gland.
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Of note, cochlear tissues of Cmah-null mice showed extensive apoptosis, whereas control mouse showed a moderate apoptosis.
As you might expect from an Australian story, ancient often rubs up uncomfortably against modern, lending what could have been just another Hollywood-style hacktivism cat-and-mouse show a grander thematic scope, which manages to take in indigenous land rights.
Homozygote inositol transporter knockout mice show a lithium-like phenotype.
SIGN-R1-blocked mice show a significant decrease in meningeal neutrophil infiltration.
These mice show a reduction of oxidative stress in several organs, including heart.
These mice show a marked decrease in NMDA (N-methyl-d-aspartate) glutamate receptor (NMDAR) function.
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