scholarly journals Evaluation of Developmental Competence of Vitrified-warmed Early Cleavage Stage Embryos and their Application for Chimeric Mouse Production.

2003 ◽  
Vol 52 (2) ◽  
pp. 179-183 ◽  
Author(s):  
Seiji KITO ◽  
Yoshiko NOGUCHI ◽  
Yuki OHTA ◽  
Tatsuya OHHATA ◽  
Masumi ABE ◽  
...  
2010 ◽  
Vol 20 (3) ◽  
pp. 371-379 ◽  
Author(s):  
Csaba Pribenszky ◽  
Eszter Losonczi ◽  
Miklós Molnár ◽  
Zsolt Lang ◽  
Szabolcs Mátyás ◽  
...  

1996 ◽  
Vol 45 (1) ◽  
pp. 180 ◽  
Author(s):  
H. Nagashima ◽  
M. Kuwayama ◽  
C.G. Grupen ◽  
R.J. Ashman ◽  
M.B. Nottle

1995 ◽  
Vol 43 (1) ◽  
pp. 285 ◽  
Author(s):  
H. Nagashima ◽  
N. Kashiwazaki ◽  
R.J. Ashman ◽  
M.B. Nottle

1971 ◽  
Vol 26 (8) ◽  
pp. 816-821 ◽  
Author(s):  
Larry E. Bockstahler

Incorporation of uridine in cleavage stage eggs of the sea urchin Paracentrotus lividus was investigated. It was shown by ion exchange and thin layer chromatography that most of the uridine taken up during the 16-cell stage was converted into UTP with some incorporation into UDP and UMP. Conversion of uridine to these phosphorylated nucleosides occurred throughout early cleavage stages. A very small amount of uridine taken up by cleavage stage eggs is incorporated into RNA heterogeneous in size. This RNA was examined by polyacrylamide gel electrophoresis.


2000 ◽  
Vol 8 (3) ◽  
pp. 241-287 ◽  
Author(s):  
GM Jones

The transfer of a blastocyst established the first human clinical pregnancy following in vitro fertilization (IVF). Nine years later Cohen et al. reported pregnancies resulting from the transfer of cryopreserved human blastocysts. However, it was another six years before the first report of births resulting from the transfer of human blastocysts produced in vitro appeared in the medical literature. In the intervening period clinics have opted to transfer embryos at the early cleavage stage to the uterus, despite the fact that in vivo the embryo does not enter the uterus until two to three days later at the morula to blastocyst stage of development. The viability and potential for implantation of blastocysts is high, as indicated by the finding that more than 60% of in-vivo-derived blastocysts, recovered by uterine lavage following artificial insemination of fertile donors, implant and develop into viable fetuses when transferred to recipients. This is in stark contrast to the 10–20% of in-vitro-produced embryos transferred at the early cleavage stage of development that result in a live-birth. This reduction in viability following transfer of in-vitro-derived early cleavage stage embryos may have several possible explanations: (1) a failure of implantation due to poor synchronization between the embryo and the uterine endometrium; (2) a hostile environment in the uterus for early cleavage stage embryos; (3) sub-optimal in vitro culture conditions which result in a reduction in embryo viability; (4) the assumption that all oocytes retrieved in an IVF cycle have an equal ability to develop into viable embryos; and (5) the failure to identify the most viable embryo in a cohort. Certainly, improving culture conditions and laboratory techniques for developing high quality blastocysts routinely in vitro will not only address many of the above questions but will also improve the quality and viability of earlier stages of embryo development.


2003 ◽  
Vol 80 ◽  
pp. 166 ◽  
Author(s):  
Alan Dudkiewicz ◽  
Erik Poole ◽  
Marilyn Novotny ◽  
Jian-Jun Zhu ◽  
Helen Kim ◽  
...  

Author(s):  
D.H Edgar ◽  
J Archer ◽  
D.A Gook ◽  
H Jericho ◽  
L Wilton ◽  
...  

2018 ◽  
Vol 110 (4) ◽  
pp. e218-e219
Author(s):  
S. Perez-Albala ◽  
B. Aparicio Ruiz ◽  
A. Galan Rivas ◽  
L. Alegre ◽  
M. Meseguer

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