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Assisted oocyte activation does not overcome recurrent embryo developmental problems
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Treatment options to overcome impaired fertilization and embryonic development caused by an oocyte-related deficiency in the Patl2-/- mouse model
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Assessment of molecular determinants underlying recurrent embryo developmental arrest and value of assisted oocyte activation as a treatment option
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Comparative study of preimplantation development following distinct assisted oocyte activation protocols in a PLC-zeta knockout mouse model
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Correcting PLCζ mutation in the germ line to overcome transmission of hereditary infertility in mice
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Vitrification negatively affects the Ca2+-releasing and activation potential of mouse oocytes, but vitrified oocytes are potentially useful for diagnostic purposes
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Comparative analysis of different nuclear transfer techniques to prevent the transmission of mitochondrial DNA variants
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Assisted oocyte activation significantly increases fertilization and pregnancy outcome in patients with low and total failed fertilization after intracytoplasmic sperm injection : a 17-year retrospective study
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The use of vitrified-thawed mouse oocytes and lysolecithin to determine the oocyte activation potential of human sperm by Ca2+ pattern analysis
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Using vitrified mouse oocytes and lysolecithin to evaluate the oocyte-activating potential of human sperm by Ca2+ pattern analysis
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PLCz knock-out sperm reveals the sole effect of altering calcium signals during assisted oocyte activation on later mouse embryogenesis
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Can vitrified-thawed mouse oocytes be efficiently used to determine the oocyte activation potential of human sperm?
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Vitrified-thawed mouse oocytes can be efficiently used to determine the oocyte activation potential of human sperm