<p>Whole mount <i>in situ</i> hybridization of non-transgenic controls (A–F) and mutant animals (A′–F′) were performed for the indicated markers. G: Quantitation of the marker gene expression domains in control and mutant animals. * = p<0.01 ** = p<0.001 (Student's t-test). N refers to the number of measurements performed.</p
12hpf and 24hpf. (A, C, E, G, I) Results of in situ hybridization of candidate genes and standard co...
Fig 9A:unc-62(e644) mutant animals show a loss of RIC marker expression, including an eat-4 CRISPR r...
<div><p>(A) Percentage of late third-instar larvae with melanotic tumors (black bars) and fat body d...
<p>Whole mount <i>in situ</i> hybridization of non-transgenic controls (A–F) and mutant animals (A′–...
<p>Representative larvae of a crossing between heterozygous HSPCre13 males and heterozygous A263ins6...
<p>Representative larvae of crossings between heterozygous HSPCre13 males and heterozygous 328del4 f...
<p>Representative larvae of crossings between heterozygous HSPCre13 males and heterozygous 328del4 f...
<p>(A). Schematic diagram of genetic crosses for isolating mutations that derepress <i>br</i> expres...
<p>(A) Analyzed region for screening potential mutant within the upstream sequence of zebrafish <i>n...
<p>(a) Tadpoles were longitudinally sectioned (5 µm) at the frontal side (1), the ventral side (2), ...
<p>(A) The expression levels of ecdysteroidogenic genes in control and <i>ouib</i> mutant first inst...
(A) Confocal images of salivary glands from wild type and H3.3BK27R male third instar larvae stained...
<p>Transfectants were cultured with ATRA for 4 days under floating conditions, followed by cell harv...
<p>A) Box and Whisker plot showing non-synonymous to synonymous substitution ratios () for genes in ...
<p>A) Schematic of the fluorescent PCR strategy. Target region is shown as two black lines. Forward ...
12hpf and 24hpf. (A, C, E, G, I) Results of in situ hybridization of candidate genes and standard co...
Fig 9A:unc-62(e644) mutant animals show a loss of RIC marker expression, including an eat-4 CRISPR r...
<div><p>(A) Percentage of late third-instar larvae with melanotic tumors (black bars) and fat body d...
<p>Whole mount <i>in situ</i> hybridization of non-transgenic controls (A–F) and mutant animals (A′–...
<p>Representative larvae of a crossing between heterozygous HSPCre13 males and heterozygous A263ins6...
<p>Representative larvae of crossings between heterozygous HSPCre13 males and heterozygous 328del4 f...
<p>Representative larvae of crossings between heterozygous HSPCre13 males and heterozygous 328del4 f...
<p>(A). Schematic diagram of genetic crosses for isolating mutations that derepress <i>br</i> expres...
<p>(A) Analyzed region for screening potential mutant within the upstream sequence of zebrafish <i>n...
<p>(a) Tadpoles were longitudinally sectioned (5 µm) at the frontal side (1), the ventral side (2), ...
<p>(A) The expression levels of ecdysteroidogenic genes in control and <i>ouib</i> mutant first inst...
(A) Confocal images of salivary glands from wild type and H3.3BK27R male third instar larvae stained...
<p>Transfectants were cultured with ATRA for 4 days under floating conditions, followed by cell harv...
<p>A) Box and Whisker plot showing non-synonymous to synonymous substitution ratios () for genes in ...
<p>A) Schematic of the fluorescent PCR strategy. Target region is shown as two black lines. Forward ...
12hpf and 24hpf. (A, C, E, G, I) Results of in situ hybridization of candidate genes and standard co...
Fig 9A:unc-62(e644) mutant animals show a loss of RIC marker expression, including an eat-4 CRISPR r...
<div><p>(A) Percentage of late third-instar larvae with melanotic tumors (black bars) and fat body d...