| NF591 |
C. elegans |
mig-22(tk24) III. Show Description
DTC migration defect.
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| NF68 |
C. elegans |
mig-22(k141) III. Show Description
DTC migration defect.
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| BC10306 |
C. elegans |
dpy-5(e907) I; sEx10306. Show Description
sEx10306 [rCes PAR2.4::GFP + pCeh361]. Maintain by picking WT. WT animals are GFP+. Strain construction supported by Genome British Columbia and Genome Canada. Please acknowledge McKay et al, Cold Spring Harbor Symposia on Quantitative Biology 68: 159-169 2004 (WBPaper00006525).
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| NF1226 |
C. elegans |
mig-22(tk69) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). Show Description
mig-22(tk69): DTC migration defect and maternal effect embryonic lethal. Heterozygotes are WT with pharyngeal GFP signal. Homozygous hT2[bli-4 let-? qIs48] are inviable.
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| NF1796 |
C. elegans |
mig-22(k185) III. Show Description
Long lifespan and healthspan. mig-22(k185) is a gain-of-function allele that increase endogenous chondroitin and suppress the gonad migration defect of mig-17(k174). Reference: Shibata Y, et al. Sci Rep. 2024 Feb 27;14(1):4813. doi: 10.1038/s41598-024-55417-7. PMID: 38413743.
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