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Floxed Trsp mice [20] in a C57BL/6 background were intercrossed with K14-cre recombinase mice in a FVB background.
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To evaluate this possibility, Boc and Cdo mutant mice on a 129 background were intercrossed to construct double mutants.
For early-onset (germline) activation of Phox2b∆8 allele, Hprt- cre mice (JAX 004302 on C57/Bl6 background) were intercrossed to Phox2b∆8 heterozygotes.
Arf-/ mice on a C57BL/6 background [21] were intercrossed with transgenic mice expressing HTLV-1 Tax under the human granzyme B promoter on a C57BL/6 x FVB background (Tax+; previously described [14]).
NSE-tTA (line A) (40) promoter mice were maintained on a CD1 background and were intercrossed with transgenic tetop-LAG608G mice, line VF1-07, generandd and maintained on FVB/NCrl (36).
To generate Tsc1 c/c hGFAP2Cre conditional mice, mixed background (129S4/SvJae, C57BL/6) Tsc/cc/c mice (Jackson) of either sex were intercrossed with male or female hGFAP2Cre heterozygous mice (Zhuo et al., 2001).
For analyses of the p53-independence of the RIP-Tag2; Arf−/− phenotype, mice were intercrossed with Trp53−/− mice [46] in the C57BL/6 background.
Transgenic vascular endothelial-cadherin Cre recombinase or Tie-2 Cre mice were intercrossed with mTomato/mGreen fluorescent protein double-fluorescent Cre reporter mice to achieve endothelial genetic lineage marking with membrane-targeted green fluorescent protein.
Pdx1-Creearly mice ([10], [50]) were intercrossed with CLEG2 mice (A.
For this purpose TSLPR−/− mice [30] were intercrossed with N1N2K5 mice in order to generate triple mutants (N1N2K5 TSLPR−/−).
Founder mice were intercrossed with C57BL/6J mice to establish lines.
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