Additional file 2: Figure S2. of Progenitor potential of nkx6.1-expressing cells throughout zebrafish life and during beta cell regeneration
Authors: AurĂŠlie Ghaye; Bergemann, David; TarifeĂąo-Saldivia, Estefania; Flasse, Lydie; Berg, Virginie Von; Peers, Bernard; Voz, Marianne; +1 Authors
AurĂŠlie Ghaye; Bergemann, David; TarifeĂąo-Saldivia, Estefania; Flasse, Lydie; Berg, Virginie Von; Peers, Bernard; Voz, Marianne; Manfroid, Isabelle;
Additional file 2: Figure S2. of Progenitor potential of nkx6.1-expressing cells throughout zebrafish life and during beta cell regeneration
Abstract
The bacterial artificial chromosome (BAC) reporter line Tg (ascl1b:eGFP-creER T2 ) mirrors the expression of the endogenous ascl1b gene. A Schematic representation of the â 61 to +89 kb ascl1b:eGFP-2A-creER T2 BAC transgene. By BAC recombineering using galK selection, the eGFP-2A-creER T2 cassette is introduced into exon 1, replacing the beginning of the ascl1b open reading frame (aa 1 to 163). B Epifluorescence microscopy images of the immunodetection of GFP in 17-hpf Tg(ascl1b:eGFP-creER T2 ) embryos. C, D Visible WISH showing expression of endogenous ascl1b in a wild-type (WT) embryo (C) and of GFP in Tg(ascl1b:eGFP-creER T2 ) embryos (D) at 15 hpf. Lateral views with the anterior part to the left. P pancreas. (PNG 1068 kb)
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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