Sentence examples for mouse counterpart of from inspiring English sources

SAA, the mouse counterpart of human C-reactive protein, is an acute phase reactant known as a marker for systemic inflammation.

Actually, previous work on the mouse counterpart of cHES6-1, mHES6, containing a 8 amino acid loop, revealed that this protein is unable to bind DNA due to its short loop, acting mainly through heterodimerization with other HES proteins to inhibit their DNA binding-dependent transcriptional repressor activity [8] [11], [13].

In this regard, the mouse counterpart of this protease, mDESC1, forms stable inhibitory complexes with both plasminogen activator inhibitor-1 and protein C inhibitor (Hobson et al, 2004).

Nevertheless, with 73.6% of identity we cannot yet conclude that Np95 is the mouse counterpart of ICBP90 since the identity between the mouse and human NIRF is 90.3%, a percentage that is usually expected for interspecies homologies between transcription factors.

Furthermore, since trastuzumab does not recognize the mouse counterpart of human HER2 [ 16], non-target-mediated and FcRn-dependent clearance of PF-05280014, trastuzumab-US, and trastuzumab-EU can be compared in mice [ 17].

In our preliminary experiments on miRNA profiling for male and female mouse SMGs by microarray assay, mmu-miR-325*, which is the mouse counterpart of primate miR-325, was not expressed in high enough levels to estimate whether it was one of the miRNAs expressed in female SMGs rather than in male SMGs.

Next, they isolated the mouse counterparts of the human genes and investigated which taste cells in mice express them.

The mouse counterparts of human SIRT3, 4 and 5 (mSIRT3, 4, 5) also show mitochondrial localization [3], [4], [5].

Consistent with the clinical observations, heart-specific disruption of the mouse counterparts of these transcription factors results in cardiac dysfunction with reduced capacity in fatty acid oxidation (FAO) and mitochondrial ATP production (Huss et al., 2007; Smeets et al., 2008).

The pair showing the strongest correlation (r = 0.92) was human PCDH8 and its mouse counterpart, Pcdh8, both of which were found to be expressed in cerebrum, forebrain, hypothalamus, hippocampus, and whole brain (Fig. 3A).

The C-terminal region (C-ARF: residues 65 132), which is not conserved between human and mouse counterparts, is of uncertain function.