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After generation of heterozygote mice (F1), we bred F1 mice and generated F2 mice.
Animal experiment results indicated that the skin equivalents could successfully repair full thickness skin defects in athymic mice and generated black skins by 6 weeks after grafting.
Immune responses were diverted from Th1 to Th2 in SJL/J mice and generated antibodies which did not cross-react with native MBP protein.
Next, we crossbred HSPB8 TG mice with R120G TG mice and generated tTA/HSPB8/R120G triple TG mice, which overexpress HSPB5 R120G and HSPB8 proteins in a cardiac-specific manner.
The yolk sac component grew in the mice and generated TGT44.
Cerebellar Granule Cells were derived from cerebellum of P7 C57Bl/6 mice and generated as already published [ 95].
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These purified FVIII fusion peptides were used individually or as a pool to immunize mice and generate antibodies.
These stimulate sensory neurons from mice and generate visceral hypersensitivity via activation of TRPV4.
Distinct strategies have been employed to circumvent the early embryonic lethality associated with the knockout of the single Smn gene in mice and generate mouse models of SMA [14] [17].
RPE cell line (B6-RPE07) was derived from a 12-week-old naïve female C57BL/6 mouse and generated as described previously 28.
To investigate the physiological role of Bcl-G, we have inactivated the gene in the mouse and generated monoclonal antibodies to determine its expression.
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