Author:
Cock H.,Taanman J.-W.,Schapira A. H. V.
Reference138 articles.
1. Allsopp, R. C., Vaziri, H., Patterson, C., Goldstein, S., Younglai, E. V., Futcher, A. B., Greider, C. W., and Harley, C. B., 1992, Telomere length predicts replicative capacity of human fibroblasts, Proc. Natl. Acad. Sci. USA 89:10114–10118.
2. Anderson, S., Bankier, A. T., de Bruijin, M. H. L., Coulson, A. R., Drouin, J., Eperon, I. C., Nierlich, D. F., Roe, B. A., Sanger, F., Schreier, P. H., Smith, A. J. H., Staden, R., and Young, I. G., 1981, Sequence and organization of the human mitochondrial genome, Nature 290: 457–465.
3. Bakker, H. D., Scholte, H. R., Dingemans, K. P., Spelbrink, J. N., Wijburg, F. A., and Van den Bogert, C., 1996, Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease, J. Pediatr. 128:683–687.
4. Barrientes, A., Volpini, V., Casademont, J., Genís, D., Manzanares, J.-M, Ferrer, I., Corral, J., Cardellach, F., Urbano-Márquez, Estivili, X., and Nunes, V., 1996, A nuclear defect in the 4pl6 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome, J. Clin. Invest. 97:1570–1576.
5. Baumer, A., Zhang, C., Linnane, A. W., and Nagley, P., 1994, Age-related human mtDNA deletions: A heterogeneous set of deletions arising at a single pair of directly repeated sequences, Am. J. Hum. Genet. 54:618–630.