Sentence examples for mouse line where from inspiring English sources

In order to investigate the function of importin α7 in mice, we generated a knockout mouse line where importin α7 is completely deleted and a mouse line expressing a shortened form of importin α7 lacking the IBB domain.

The Sca1-GFP was generated as a mouse line where GFP was expressed in all hematopoietic cells [11]; recent studies demonstrated specific GFP expression in the vascular endothelium of skeletal muscle and retina [12], [13].The following primers were used for genotyping the Sca1-GFP transgene: forward-CTGGTCGAGCTGGACGGCGACG and reverse-CACGAACTCCAGCAGGACCATG.

In this study, we have utilized a MyoD-Cre mouse line, where the majority of early myogenic progenitors can be permanently labeled.

Utilizing a transgenic mouse line where GFP is expressed under the AHF-specific enhancer, labeling of CPCs was achieved with GFP.

To further strengthen this observation, we employed an inducible Col2a1-Cre ERT mouse line where the transgene expression is targeted to committed chondrocytes.

There is at least one other known example of a transgenic mouse line where transgenes have integrated as inverted repeats and are expressed at an unexpectedly low efficiency [ 26].

This construct first expresses enhance green fluorescent protein (EGFP), which enables rapid screen of transgenic mouse lines where the transgene is active in the desired tissue.

Therefore we made use of endothelioma mouse lines where VECad expression was permanently lost, to study the role of NCad at the junctions and the role of ICAM2 in regulating its function.

In order to address this question, we therefore took advantage of the Vwf-EGFP (Sanjuan-Pla et al, in preparation) and the miR-144/451-EGFP (Rasmussen and O'Carroll, 2011) reporter mouse lines, where platelets and erythrocytes, respectively, are labelled by EGFP.

To achieve this we used the Rx-cre transgenic mouse line [29], where the Cre recombinase is expressed under the control of an Rx promoter element.

We have confirmed these findings using brain sections from mouse line CRND8, where FSB visualized plaques when used at 0.1, 1, 10 and 100 μM.