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Structural analyses demonstrate that this configuration enhances stiffness in multiple directions.
Our longitudinal analyses demonstrate that PD and parkinsonism are modestly heritable.
The experimental results and security analyses demonstrate that the proposed method has a fine security performance.
Similarly, genetic analyses demonstrate that the p110α isoform is selectively required for angiogenesis [40].
Molecular analyses demonstrate that E74A protein shows diurnal changes in abundance, similar to LARK.
Results obtained by immunohistochemistry analyses demonstrate that CYP450 proteins such as CYP2J2 and CYP2Cs are expressed in human cardiomyocytes.
The GARD analyses demonstrate that phylogenetic breakpoints occur throughout the expression sites, consistent with frequent genetic exchange.
Collectively, these analyses demonstrate that TβRI inhibitors increase bone mass in mature mice via anabolic and anti-catabolic mechanisms.
Previous biochemical analyses demonstrate that these same amino acid positions are involved in G-protein binding function.
These analyses demonstrate that, overexpression of PKCζ, HOXB7, and ERBB3 diminished the reciprocal relationship between track length and solidity.
Further, biochemical analyses demonstrate that this helix replacement directs the distinct actin bundling and oligomerization properties of metavinculin.
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