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Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNA.
Falkenberg M, Gaspari M, Rantanen A, Trifunovic A, Larsson NG, Gustafsson CM. Falkenberg M, et al. Among authors: larsson ng. Nat Genet. 2002 Jul;31(3):289-94. doi: 10.1038/ng909. Epub 2002 Jun 17. Nat Genet. 2002. PMID: 12068295
Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.
Larsson NG, Tulinius MH, Holme E, Oldfors A, Andersen O, Wahlström J, Aasly J. Larsson NG, et al. Am J Hum Genet. 1992 Dec;51(6):1201-12. Am J Hum Genet. 1992. PMID: 1463006 Free PMC article.
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child.
Larsson NG, Eiken HG, Boman H, Holme E, Oldfors A, Tulinius MH. Larsson NG, et al. Am J Hum Genet. 1992 Feb;50(2):360-3. Am J Hum Genet. 1992. PMID: 1734716 Free PMC article.
De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring.
Tulinius MH, Houshmand M, Larsson NG, Holme E, Oldfors A, Holmberg E, Wahlström J. Tulinius MH, et al. Among authors: larsson ng. Hum Genet. 1995 Sep;96(3):290-4. doi: 10.1007/BF00210409. Hum Genet. 1995. PMID: 7649544
Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion.
Larsson NG, Oldfors A, Holme E, Clayton DA. Larsson NG, et al. Biochem Biophys Res Commun. 1994 May 16;200(3):1374-81. doi: 10.1006/bbrc.1994.1603. Biochem Biophys Res Commun. 1994. PMID: 8185589
Mitochondrial DNA deletions in inclusion body myositis.
Oldfors A, Larsson NG, Lindberg C, Holme E. Oldfors A, et al. Among authors: larsson ng. Brain. 1993 Apr;116 ( Pt 2):325-36. doi: 10.1093/brain/116.2.325. Brain. 1993. PMID: 8384916
Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.
Holme E, Larsson NG, Oldfors A, Tulinius M, Sahlin P, Stenman G. Holme E, et al. Among authors: larsson ng. Am J Hum Genet. 1993 Mar;52(3):551-6. Am J Hum Genet. 1993. PMID: 8447321 Free PMC article.
A single mouse gene encodes the mitochondrial transcription factor A and a testis-specific nuclear HMG-box protein.
Larsson NG, Garman JD, Oldfors A, Barsh GS, Clayton DA. Larsson NG, et al. Nat Genet. 1996 Jul;13(3):296-302. doi: 10.1038/ng0796-296. Nat Genet. 1996. PMID: 8673128
Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A --> G mutation at position 3251 in the mitochondrial tRNALeu(UUR) gne.
Houshmand M, Larsson NG, Oldfors A, Tulinius M, Holme E. Houshmand M, et al. Among authors: larsson ng. Hum Genet. 1996 Mar;97(3):269-73. doi: 10.1007/BF02185750. Hum Genet. 1996. PMID: 8786060
Molecular genetic aspects of human mitochondrial disorders.
Larsson NG, Clayton DA. Larsson NG, et al. Annu Rev Genet. 1995;29:151-78. doi: 10.1146/annurev.ge.29.120195.001055. Annu Rev Genet. 1995. PMID: 8825472 Review.
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