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Many characteristic features of vertebrate brains, from gross anatomy down to particular circuit motifs and cell-types, as well as conserved behaviors, can be found in zebrafish even just a few days post fertilization, and, at this early stage, the physical size of the brain makes it possible to analyze neural activity in a comprehensive fashion.
A small number of xanthophores can also be found in zebrafish larvae, but not in adults, which are homozygous for salz tl41a or pfeffer tm36b, two alleles that fail to complement fms j4blue (Maderspacher and Nusslein-Volhard 2003).
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Of the 455 known phosphosites on human 26S proteasome, 442 (97.1%) are conserved or semi-conserved (i.e. Ser/Thr substitutions) in mouse and rat proteasome subunits, and 391 sites (85.9% of total) are found in zebrafish.
A large number of highly conserved MS4A and TMEM176 genes was found in zebrafish (Danio rerio).
A first lineage was retrieved in all teleosts, while a second CXCL8 lineage was found in zebrafish and carp only.
In addition, raldh1 is expressed in the dorsal retina and mesencephalic flexure in mice [26], but has not been found in zebrafish.
It has recently been found in zebrafish that individual knockdown of genes implicated in junction stability such as Rap1b, Pak2a, β-Pix or ccm1/krit cause hemorrhagic phenotypes [43] [45].
Orthologs of the two genes were found in zebrafish, medaka, and threespine stickleback, but a single representative was observed in tetraodontidae species.
In this whole-genome survey, 6 distinct PMCAs and 7 distinct NCXs were found in zebrafish.
In particular, no equivalent of carp grn3 was found in zebrafish.
In general, most of the homologues of flounder miRNAs were found in zebrafish.
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