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Mutation dependance of the mitochondrial DNA copy number in the first stages of human embryogenesis.
Monnot S, Samuels DC, Hesters L, Frydman N, Gigarel N, Burlet P, Kerbrat V, Lamazou F, Frydman R, Benachi A, Feingold J, Rotig A, Munnich A, Bonnefont JP, Steffann J
(2013) Hum Mol Genet 22: 1867-72
MeSH Terms: Acidosis, Lactic, DNA Copy Number Variations, DNA, Mitochondrial, Embryonic Development, Humans, MELAS Syndrome, MERRF Syndrome, Mutation, Oocytes, Oogenesis
Added December 12, 2013
0 Communities
1 Members
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10 MeSH Terms
Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.
Gigarel N, Hesters L, Samuels DC, Monnot S, Burlet P, Kerbrat V, Lamazou F, Benachi A, Frydman R, Feingold J, Rotig A, Munnich A, Bonnefont JP, Frydman N, Steffann J
(2011) Am J Hum Genet 88: 494-8
MeSH Terms: Blastomeres, DNA, Mitochondrial, Embryonic Development, Female, Humans, MELAS Syndrome, MERRF Syndrome, Male, Meiosis, Mutation, Oocytes, Oogenesis, Pregnancy, Preimplantation Diagnosis
Added December 12, 2013
0 Communities
1 Members
0 Resources
14 MeSH Terms