Crossref journal-article
Springer Science and Business Media LLC
Nature Genetics (297)
Bibliography

Suomalainen, A., Kaukonen, J., Amati, P., Timonen, R., Haltia, M., Weissenbach, J., Zeviani, M., Somer, H., & Peltonen, L. (1995). An autosomal locus predisposing to deletions of mitochondrial DNA. Nature Genetics, 9(2), 146–151.

Authors 9
  1. Anu Suomalainen (first)
  2. Jyrki Kaukonen (additional)
  3. Patrizia Amati (additional)
  4. Ritva Timonen (additional)
  5. Matti Haltia (additional)
  6. Jean Weissenbach (additional)
  7. Massimo Zeviani (additional)
  8. Hannu Somer (additional)
  9. Leena Peltonen (additional)
References 34 Referenced 174
  1. Wallace, D.C. Diseases of the mitochondrial DNA. Ann. Rev. Biochem. 61, 1175–1212 (1992). (10.1146/annurev.bi.61.070192.005523) / Ann. Rev. Biochem. by DC Wallace (1992)
  2. Clayton, D.A. Nuclear gadgets in mitochondrial DNA replication and transcription. Trends Biochem. 16, 107–111 (1991). (10.1016/0968-0004(91)90043-U) / Trends Biochem. by DA Clayton (1991)
  3. Virbasius, J.V. & Scarpulla, R.C. Activation of the human mitochondrial transcription factor A gene by nuclear respiratory factors: A potential regulatory link between nuclear and mitochondrial gene expression In organelle biogenesis. Proc. natn. Acad. Sci. U.S.A. 91, 1309–1313 (1994). (10.1073/pnas.91.4.1309) / Proc. natn. Acad. Sci. U.S.A. by JV Virbasius (1994)
  4. Liao, X. & Butow, R.A. RTG1 and RTG2: Two yeast genes required for a novel path of communication from mitochondria to the nucleus. Cell 72, 61–71 (1993). (10.1016/0092-8674(93)90050-Z) / Cell by X Liao (1993)
  5. Zeviani, M. et al. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region. Nature 339, 309–311 (1989). (10.1038/339309a0) / Nature by M Zeviani (1989)
  6. Servidei, S. et al. Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: Clinical, morphologic and biochemical studies. Neurology 41, 1053–1059 (1991). (10.1212/WNL.41.7.1053) / Neurology by S Servidei (1991)
  7. Yuzaki, M., Ohkoshi, N., Kanazawa, I., Kagawa, Y. & Ohta, S. Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy. Biochem. biophys. Res. Commun. 164, 1352–1357 (1989). (10.1016/0006-291X(89)91818-4) / Biochem. biophys. Res. Commun. by M Yuzaki (1989)
  8. Otsuka, M. et al. Marked decrease of mitochondrial DNA with multiple deletions in a patient with familial mitochondrial myopathy. Biochem. biophys. Res. Commun. 167, 680–685 (1990). (10.1016/0006-291X(90)92079-F) / Biochem. biophys. Res. Commun. by M Otsuka (1990)
  9. Suomalainen, A. et al. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. J. clin. Invest. 90, 61–66 (1992). (10.1172/JCI115856) / J. clin. Invest. by A Suomalainen (1992)
  10. Cormier, V. et al. Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy. Am. J. hum. Genet. 48, 643–648 (1991). / Am. J. hum. Genet. by V Cormier (1991)
  11. Suomalainen, A. et al. Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA. Lancet 340, 1319–1320 (1992). (10.1016/0140-6736(92)92496-3) / Lancet by A Suomalainen (1992)
  12. Ohno, K. et al. Mitochondrial DNA deletions in inherited recurrent myoglobinuria. Ann. Neurol. 29, 364–369 (1991). (10.1002/ana.410290406) / Ann. Neurol. by K Ohno (1991)
  13. Hirano, M. et al. Mitochondrial neurogastrolntestinal encephalomyopathy (MNGIE): Clinical, biochemical and genetic features of an autosomal recessive mitochondrial disorder. Neurology 44, 721–727 (1994). (10.1212/WNL.44.4.721) / Neurology by M Hirano (1994)
  14. Gyapay, G. et al. The 1993–94 Généthon human genetic linkage map. Nature Genet. 7, 246–339 (1994). (10.1038/ng0694supp-246) / Nature Genet. by G Gyapay (1994)
  15. Ott, J. Computer-simulation methods in human linkage analysis. Proc. natn. Acad. Sci. U.S.A. 86, 4175–4178 (1989). (10.1073/pnas.86.11.4175) / Proc. natn. Acad. Sci. U.S.A. by J Ott (1989)
  16. Weeks, D.E., Ott, J. & Lathrop, G.M. SLINK: a general simulation program for linkage analysis. Am. J. hum. Genet. (suppl.) 47, A204 (1990). / Am. J. hum. Genet. by DE Weeks (1990)
  17. Lathrop, G.M., Lalouel, J.M., Julier, C. & Ott, J. Strategies for multilocus linkage analysis in humans. Proc. natn. Acad. Sci. U.S.A. 81, 3443–3446 (1984). (10.1073/pnas.81.11.3443) / Proc. natn. Acad. Sci. U.S.A. by GM Lathrop (1984)
  18. Moir, D.T. et al. Toward a physical map of human chromosome 10: isolation of 183 YACs representing 80 loci and regional assignment of 94 YACs by fluorescence in situ hybridization. Genomics 22, 1–12 (1994). (10.1006/geno.1994.1338) / Genomics by DT Moir (1994)
  19. Zheng, C.-j. et al. Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10. Genomics 22, 55–67 (1994). (10.1006/geno.1994.1345) / Genomics by C-j Zheng (1994)
  20. Ott, J. Analysis of Human Genetic Linkage rev. edn. 203–216 (Johns Hopkins Univ. Press, Baltimore, 1991). / Analysis of Human Genetic Linkage by J Ott (1991)
  21. Tiranti, V. et al. Chromosomal localization of mitochondrial transcription factor A, single-stranded DNA binding protein and endonuclease G, three human housekeeping genes involved in mitochondrial biogenesis. Genomics, in the press. (10.1016/0888-7543(95)80058-T)
  22. Parisi, M.A. & Clayton, D.A. Similarity of human mitochondrial transcription factor 1 to high mobility group proteins. Science 252, 985–969 (1991). (10.1126/science.2035027) / Science by MA Parisi (1991)
  23. Mita, S. et al. Recombination via flanking direct repeats is a major cause of large–scale deletions of human mitochondrial DNA. Nucleic Acids Res. 18, 561–567 (1990). (10.1093/nar/18.3.561) / Nucleic Acids Res. by S Mita (1990)
  24. Zeviani, M. Nucleus-driven mutations of human mitochondrial DNA. J. inner. metab. Dis. 15, 456–471 (1992). (10.1007/BF01799604) / J. inner. metab. Dis. by M Zeviani (1992)
  25. Oldfors, A., Larsson, N.-G., Lindberg, C. & Holme, E. Mitochondrial DNA deletions in inclusion body myositis. Brain 116, 325–336 (1993). (10.1093/brain/116.2.325) / Brain by A Oldfors (1993)
  26. Cortopassi, G.A. & Amheim, N. Detection of a specific mitochondrial DNA deletion in tissues of older humans. Nucleic Acids Res. 18, 6927–6933 (1990). (10.1093/nar/18.23.6927) / Nucleic Acids Res. by GA Cortopassi (1990)
  27. Corral-Debrinski, M. et al. Mitochondrial DNA deletions In human brain: Regional variability and Increase with advanced age. Nature Genet. 2, 324–329 (1992). (10.1038/ng1292-324) / Nature Genet. by M Corral-Debrinski (1992)
  28. Fisher, R.P., Lisowsky, T., Parisi, M.A. & Clayton, D.A. DNA wrapping and bending by a mitochondrial high mobility group-like transcriptional activator protein. J. biol. Chem. 267, 3358–3367 (1992). (10.1016/S0021-9258(19)50739-6) / J. biol. Chem. by RP Fisher (1992)
  29. Megraw, T.L. & Chae, C.-B. Functional complementarity between the HMG1-like yeast mitochondrial histone HM and the bacterial histone-like protein HU. J. biol. Chem. 268, 12758–12763 (1993). (10.1016/S0021-9258(18)31453-4) / J. biol. Chem. by TL Megraw (1993)
  30. Anderson, S. et al. Sequence and organization of the human mitochondrial genome. Nature 290, 457–465 (1981). (10.1038/290457a0) / Nature by S Anderson (1981)
  31. Aaltonen, J., Björses, P., Sandkuijl, L., Perheentupa, J. & Peltonen, L. An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21. Nature Genet. 8, 83–87 (1994). (10.1038/ng0994-83) / Nature Genet. by J Aaltonen (1994)
  32. Suomalainen, A., Majander, A., Pihko, H., Peltonen, L. & Syvänen, A.-C. Quantification of tRNA3243Leu point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription. Hum. molec. Genet. 2, 525–534 (1993). (10.1093/hmg/2.5.525) / Hum. molec. Genet. by A Suomalainen (1993)
  33. Tominaga, K., Akiyama, S., Kagawa, Y. & Ohta, S. Upstream region of a genomic gene for human mitochondrial transcription factor 1. Biochim. Biophys. Acta 1131, 217–219 (1992). (10.1016/0167-4781(92)90082-B) / Biochim. Biophys. Acta by K Tominaga (1992)
  34. Syvänen, A.-C., Aalto-Setälä, K., Kontula, K. & Söderiund, H. Direct sequencing of affinity-captured amplified human DNA: application to the detection of apolipoprotein E polymorphism. FEBS Lett. 258, 71–74 (1989). (10.1016/0014-5793(89)81618-7) / FEBS Lett. by A-C Syvänen (1989)
Dates
Type When
Created 21 years ago (Aug. 18, 2004, 5:14 p.m.)
Deposited 2 years, 3 months ago (May 18, 2023, 4:21 p.m.)
Indexed 2 months, 1 week ago (June 27, 2025, 6:13 a.m.)
Issued 30 years, 7 months ago (Feb. 1, 1995)
Published 30 years, 7 months ago (Feb. 1, 1995)
Published Print 30 years, 7 months ago (Feb. 1, 1995)
Funders 0

None

@article{Suomalainen_1995, title={An autosomal locus predisposing to deletions of mitochondrial DNA}, volume={9}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/ng0295-146}, DOI={10.1038/ng0295-146}, number={2}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Suomalainen, Anu and Kaukonen, Jyrki and Amati, Patrizia and Timonen, Ritva and Haltia, Matti and Weissenbach, Jean and Zeviani, Massimo and Somer, Hannu and Peltonen, Leena}, year={1995}, month=feb, pages={146–151} }