2020
DOI: 10.1007/s00018-020-03630-8
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FGF primes angioblast formation by inducing ETV2 and LMO2 via FGFR1/BRAF/MEK/ERK

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Cited by 3 publications
(1 citation statement)
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“…The design of the short‐hairpin RNAs (shRNAs) targeting LMP1 (full sequences for cloning in Table ) was based on splashRNA and cloned into the donor vector below by Gibson assembly 23 . The forward and reverse oligos were cloned into an AAVS1 locus‐donor vector expressing GFP and the shRNA in tandem as described, 24 except that the Thy1.1 was replaced by GFP for staining‐free assessment of the induction. Five micrograms of the donor vector and 5 µg of the px459‐based AAVS1‐targeting vector were electroporated into the recipient cells with NEPA21 system.…”
Section: Methodsmentioning
confidence: 99%
“…The design of the short‐hairpin RNAs (shRNAs) targeting LMP1 (full sequences for cloning in Table ) was based on splashRNA and cloned into the donor vector below by Gibson assembly 23 . The forward and reverse oligos were cloned into an AAVS1 locus‐donor vector expressing GFP and the shRNA in tandem as described, 24 except that the Thy1.1 was replaced by GFP for staining‐free assessment of the induction. Five micrograms of the donor vector and 5 µg of the px459‐based AAVS1‐targeting vector were electroporated into the recipient cells with NEPA21 system.…”
Section: Methodsmentioning
confidence: 99%