Data from artificial models of mitochondrial DNA disorders are not always applicable to humans

Cell Reports

Volumn 7, Issue 4, 2014, Pages 933-934

  Steffann, Julie ^a   Gigarel, Nadine ^a   Samuels, David C ^b   Monnot, Sophie ^a   Borghese, Roxana ^a   Hesters, Laetitia ^c   Frydman, Nelly ^c   Burlet, Philippe ^a   Frydman, René ^a   Benachi, Alexandra ^d   Rotig, Agnes ^a   Munnich, Arnold ^a   Bonnefont, Jean Paul ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c Serv de Genet et Repro   (France)

^d INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

BLASTOMA; DISEASE MODEL; DNA POLYMORPHISM; EMBRYO (ANATOMY); GENE MUTATION; GENE SEGREGATION; GENETIC RISK; HETEROPLASMY; HUMAN; LETTER; MITOCHONDRIAL DNA DISORDER; NONHUMAN; PREDICTIVE VALUE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ARTIFICIAL MODEL; CHORION VILLUS SAMPLING; DEVELOPMENTAL STAGE; EMBRYO DEVELOPMENT; FETUS DEVELOPMENT; GENETIC SCREENING; HUMAN VERSUS ANIMAL COMPARISON; MOLECULAR PATHOLOGY; MUTATIONAL ANALYSIS; RISK ASSESSMENT; ANIMAL; BLASTOCYST; CELL DIVISION; CYTOLOGY; EMBRYOLOGY; FEMALE; GENETICS; HAPLOTYPE; OOCYTE; PREGNANCY; RHESUS MONKEY;

ANIMALS; BLASTOCYST; CELL DIVISION; DNA, MITOCHONDRIAL; EMBRYONIC DEVELOPMENT; FEMALE; HAPLOTYPES; MACACA MULATTA; OOCYTES; PREGNANCY;

EID: 84901202063     PISSN: None     EISSN: 22111247     Source Type: Journal    
DOI: 10.1016/j.celrep.2014.05.005     Document Type: Letter

References (10)

1. Craven L., Tuppen H.A., Greggains G.D., Harbottle S.J., Murphy J.L., Cree L.M., Murdoch A.P., Chinnery P.F., Taylor R.W., Lightowlers R.N., et al. Nature 2010, 465:82-85.
2. Dean N.L., Battersby B.J., Ao A., Gosden R.G., Tan S.L., Shoubridge E.A., Molnar M.J. Mol. Hum. Reprod. 2003, 9:631-638.
3. Lee H.S., Ma H., Juanes R.C., Tachibana M., Sparman M., Woodward J., Ramsey C., Xu J., Kang E.J., Amato P., et al. Cell Rep 2012, 1:506-515.
4. Meirelles F.V., Smith L.C. Genetics 1998, 148:877-883.
5. Monnot S., Gigarel N., Samuels D.C., Burlet P., Hesters L., Frydman N., Frydman R., Kerbrat V., Funalot B., Martinovic J., et al. Hum. Mutat. 2011, 32:116-125.
6. Sallevelt S.C., Dreesen J.C., Drüsedau M., Spierts S., Coonen E., van Tienen F.H., van Golde R.J., de Coo I.F., Geraedts J.P., de Die-Smulders C.E., Smeets H.J. J. Med. Genet. 2013, 50:125-132.
7. Steffann J., Frydman N., Gigarel N., Burlet P., Ray P.F., Fanchin R., Feyereisen E., Kerbrat V., Tachdjian G., Bonnefont J.P., et al. J. Med. Genet. 2006, 43:244-247.
8. Tachibana M., Sparman M., Sritanaudomchai H., Ma H., Clepper L., Woodward J., Li Y., Ramsey C., Kolotushkina O., Mitalipov S. Nature 2009, 461:367-372.
9. Treff N.R., Campos J., Tao X., Levy B., Ferry K.M., Scott R.T. Fertil. Steril. 2012, 98:1236-1240.
10. Vandewoestyne M., Heindryckx B., De Gheselle S., Lepez T., Neupane J., Gerris J., Van Coster R., De Sutter P., Deforce D. Mitochondrion 2012, 12:477-479.