Add to ORKGAll strains were grown using standard protocols for growth and maintenance of C. elegans [S1]. Worms were grown at 20ºC unless otherwise stated. A strain carrying a deletion in egg-1 designated as allele tm1071 was obtained from the Japanese Knock-out Con-sortium. This strain was back crossed to the wild-type strain Bristol (N2) three times before any phenotypic analysis was conducted. Ge-netic markers, mutations, or strains used in this work were: dpy-5(e61), let-23(sy1), him-5(e1490), glo-1(zu391), him-5(e1490), spe-9(eb19), fem-1(e1965), and strain DH1033 (carrying YP170:GFP) [S2]
<div><p>(A) The gonad/vulval region of wild-type worms is shown. In the left panel, black arrows ind...
The purpose of this study was to identify and clone the genes rescued by the cosmid T21G5 located i...
The DNA transposon Tc1 was the first transposable element to be characterized in Caenorhabditis eleg...
Wild-type strains were C. elegans variety Bristol, strain N2. Strains were maintained by standard me...
Methods for culturing C. elegans strains have been described previ-ously [S1]. All strains were grow...
All strains were maintained at 15°C using standard C. elegans techniques (Stiernagle, 2006). Double ...
C. elegans strains Animals were maintained on NG agar plates using standard methods. The following s...
General methods for culturing C. elegans strains were as described in [S1–S3]. Except where noted, a...
<p>(<b>A</b>) Larval growth of control worms (Vector), wild type β<sub>2</sub>-m expressing worms (W...
<p>Quantitative real-time PCR results of LWDH-EE treatment on the expression of the <i>amy1, sod3</i...
(e1489), (4) ego-1(om84)/; sDp3; dpy-17 sDf134 unc-32. The ccIs4251 unc-15 chromosome was used to ba...
Worms were cultured according to (Brenner, 1974). Alleles used in this study are as follows, in orde...
C. elegans Strains and Alleles Corrected cDNA and predicted protein structure have been submit-ted t...
<p>A population of wild-type worms was spiked the mutant <i>eat-4</i> (7 N2 wild-type plus 3 <i>eat-...
<p>(<b>A</b>) PCR genotyping of adult transgenic worms transfected with the empty vector (vector) or...
<div><p>(A) The gonad/vulval region of wild-type worms is shown. In the left panel, black arrows ind...
The purpose of this study was to identify and clone the genes rescued by the cosmid T21G5 located i...
The DNA transposon Tc1 was the first transposable element to be characterized in Caenorhabditis eleg...
Wild-type strains were C. elegans variety Bristol, strain N2. Strains were maintained by standard me...
Methods for culturing C. elegans strains have been described previ-ously [S1]. All strains were grow...
All strains were maintained at 15°C using standard C. elegans techniques (Stiernagle, 2006). Double ...
C. elegans strains Animals were maintained on NG agar plates using standard methods. The following s...
General methods for culturing C. elegans strains were as described in [S1–S3]. Except where noted, a...
<p>(<b>A</b>) Larval growth of control worms (Vector), wild type β<sub>2</sub>-m expressing worms (W...
<p>Quantitative real-time PCR results of LWDH-EE treatment on the expression of the <i>amy1, sod3</i...
(e1489), (4) ego-1(om84)/; sDp3; dpy-17 sDf134 unc-32. The ccIs4251 unc-15 chromosome was used to ba...
Worms were cultured according to (Brenner, 1974). Alleles used in this study are as follows, in orde...
C. elegans Strains and Alleles Corrected cDNA and predicted protein structure have been submit-ted t...
<p>A population of wild-type worms was spiked the mutant <i>eat-4</i> (7 N2 wild-type plus 3 <i>eat-...
<p>(<b>A</b>) PCR genotyping of adult transgenic worms transfected with the empty vector (vector) or...
<div><p>(A) The gonad/vulval region of wild-type worms is shown. In the left panel, black arrows ind...
The purpose of this study was to identify and clone the genes rescued by the cosmid T21G5 located i...
The DNA transposon Tc1 was the first transposable element to be characterized in Caenorhabditis eleg...