<p>After siRNA injection into GV stage oocytes, the matured oocytes were subjected to PA, IVF and SCNT, and the morphologies of responding blastocysts (×40) were observed at 156 h after embryo culture.</p
The expression of TRP53 in blastocysts that had been cultured from the zygote stage in vitro for 90 ...
Therapeutic cloning has tremendous potential for cell therapy and tissue repair in some diseases. Ho...
<div><p>Establishment of totipotency after somatic cell nuclear transfer (NT) requires not only repr...
<p>Dnmt1 knockdown in cloned embryos at 6 h post activation improved the blastocyst rate.</p><p><sup...
<p><b>A.</b> Quantitative RT-PCR analysis of endogenous <i>Wdr74</i> mRNA during preimplantation dev...
Evidence indicates that failure of nuclear transfer (NT) embryos to develop normally can be attribut...
<p>Groups of embryos were either: non-injected, injected with negative control siRNA molecules or in...
<p>Failed-to-be-fertilized oocytes were vitrified and then thawed before evaluation for morphology a...
<p>A, the GSH content, and B, the mtDNA copy number per matured oocyte after Dnmt1 knockdown. After ...
<p>A, the cytoplasmic location of Dnmt1 in GV and MII stage oocytes (×400), and B, relative Dnmt1 tr...
3To whom correspondence should be addressed Primary oocytes recovered from small and growing follicl...
F development. MII = MII oocytes; 1 = 1-cell; 2 = 2-cell; 4 = 4-cell; 8 = 8-cell; Bl = blastocyst. S...
SummaryReprogramming somatic cells into pluripotent embryonic stem cells (ESCs) by somatic cell nucl...
<p><b>A–D</b>: GV oocytes injected with dsRNAs or control were cultured for 44 hours. Knockdown of J...
Development of blastocysts obtained from embryos cryopreserved at −80°C for up to three months and p...
The expression of TRP53 in blastocysts that had been cultured from the zygote stage in vitro for 90 ...
Therapeutic cloning has tremendous potential for cell therapy and tissue repair in some diseases. Ho...
<div><p>Establishment of totipotency after somatic cell nuclear transfer (NT) requires not only repr...
<p>Dnmt1 knockdown in cloned embryos at 6 h post activation improved the blastocyst rate.</p><p><sup...
<p><b>A.</b> Quantitative RT-PCR analysis of endogenous <i>Wdr74</i> mRNA during preimplantation dev...
Evidence indicates that failure of nuclear transfer (NT) embryos to develop normally can be attribut...
<p>Groups of embryos were either: non-injected, injected with negative control siRNA molecules or in...
<p>Failed-to-be-fertilized oocytes were vitrified and then thawed before evaluation for morphology a...
<p>A, the GSH content, and B, the mtDNA copy number per matured oocyte after Dnmt1 knockdown. After ...
<p>A, the cytoplasmic location of Dnmt1 in GV and MII stage oocytes (×400), and B, relative Dnmt1 tr...
3To whom correspondence should be addressed Primary oocytes recovered from small and growing follicl...
F development. MII = MII oocytes; 1 = 1-cell; 2 = 2-cell; 4 = 4-cell; 8 = 8-cell; Bl = blastocyst. S...
SummaryReprogramming somatic cells into pluripotent embryonic stem cells (ESCs) by somatic cell nucl...
<p><b>A–D</b>: GV oocytes injected with dsRNAs or control were cultured for 44 hours. Knockdown of J...
Development of blastocysts obtained from embryos cryopreserved at −80°C for up to three months and p...
The expression of TRP53 in blastocysts that had been cultured from the zygote stage in vitro for 90 ...
Therapeutic cloning has tremendous potential for cell therapy and tissue repair in some diseases. Ho...
<div><p>Establishment of totipotency after somatic cell nuclear transfer (NT) requires not only repr...
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