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Cellular heterogeneity in the level of mtDNA heteroplasmy in mouse embryonic stem cells
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Assessment of nuclear transfer techniques to prevent the transmission of heritable mitochondrial disorders without compromising embryonic development competence in mice
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Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like syndrome carrier after blastocyst trophectoderm preimplantation genetic diagnosis
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Mutation-free baby born from a mitochondrial encephalopathy, lactic acidosis and stroke-like episodes carrier after trophectoderm pre-implantation genetic diagnosis
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A systematic analysis of the suitability of preimplantation genetic diagnosis for mitochondrial diseases in a heteroplasmic mitochondrial mouse model
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Heterogenity in the level of mitochondrial DNA heteroplasmy increases during progressive passaging of mouse embryonic stem cells
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Poor correlation between polar bodies and blastomere mutation load in a patient with m.3243A>G tRNALeu(UUR) point mutation
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Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutation
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Reduced amounts and abnormal forms of phospholipase C zeta (PLC zeta) in spermatozoa from infertile men
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INFLUENCE OF SPERM CRYOPRESERVATION ON THE OOCYTE ACTIVATING FACTOR PLCAE