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The modulatory role of actin filaments in ENaC functioning has been described in A6 cells [10], Xenopus oocytes and planar lipid bilayers [23], [24].
Interestingly, for a number of these genes (indicated with §), intestinal expression and/or functioning has been described [ 55]-[ 59] but until now sexually dimorphic expression has not been reported.
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The relationships between children's sucking habits and the impact on the development of their oral anatomy and functioning have been described in the literature.
The principle of the pCAX-HA-2xXBP1deltaDBD9anATG -Luc-F function has been described by Iwawaki and Akai [ 24].
25 Furthermore, the functional impact of the SNP on protein function has been described as deleterious (disruptive) or non-deleterious (benign/neutral).
Duality in hand function has been described in terms of precision and power grips.
The population averaged input function has been described in neurological and some oncology studies using FDG and shows promise [15 18].
Notably, impairment of the protein targeting and function has been described also when Frazer's fraction of gliadin has been used, due to an interaction with the actin cytoskeleton [17, 18].
No function has been described for either collagen belonging to this clade.
The efficacy of the UAS-GBRi in diminishing GABABR2 levels and GBR function has been described previously [30].
Beside this enzymatic activity, a protein ubiquitin ligase (E3) function has been described for the RING domain of Not4p [6].
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