Rustin P - Search Results

1

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice.

Larsson NG, Wang J, Wilhelmsson H, Oldfors A, Rustin P, Lewandoski M, Barsh GS, Clayton DA. Larsson NG, et al. Among authors: rustin p. Nat Genet. 1998 Mar;18(3):231-6. doi: 10.1038/ng0398-231. Nat Genet. 1998. PMID: 9500544

2

Mitochondrial transcription factor A regulates mtDNA copy number in mammals.

Ekstrand MI, Falkenberg M, Rantanen A, Park CB, Gaspari M, Hultenby K, Rustin P, Gustafsson CM, Larsson NG. Ekstrand MI, et al. Among authors: rustin p. Hum Mol Genet. 2004 May 1;13(9):935-44. doi: 10.1093/hmg/ddh109. Epub 2004 Mar 11. Hum Mol Genet. 2004. PMID: 15016765

3

Dilated cardiomyopathy and atrioventricular conduction blocks induced by heart-specific inactivation of mitochondrial DNA gene expression.

Wang J, Wilhelmsson H, Graff C, Li H, Oldfors A, Rustin P, Brüning JC, Kahn CR, Clayton DA, Barsh GS, Thorén P, Larsson NG. Wang J, et al. Among authors: rustin p. Nat Genet. 1999 Jan;21(1):133-7. doi: 10.1038/5089. Nat Genet. 1999. PMID: 9916807

4

Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy.

Li H, Wang J, Wilhelmsson H, Hansson A, Thoren P, Duffy J, Rustin P, Larsson NG. Li H, et al. Among authors: rustin p. Proc Natl Acad Sci U S A. 2000 Mar 28;97(7):3467-72. doi: 10.1073/pnas.97.7.3467. Proc Natl Acad Sci U S A. 2000. PMID: 10737799 Free PMC article.

5

Increased in vivo apoptosis in cells lacking mitochondrial DNA gene expression.

Wang J, Silva JP, Gustafsson CM, Rustin P, Larsson NG. Wang J, et al. Among authors: rustin p. Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):4038-43. doi: 10.1073/pnas.061038798. Epub 2001 Mar 20. Proc Natl Acad Sci U S A. 2001. PMID: 11259653 Free PMC article.

6

Animal models for respiratory chain disease.

Larsson NG, Rustin P. Larsson NG, et al. Among authors: rustin p. Trends Mol Med. 2001 Dec;7(12):578-81. doi: 10.1016/s1471-4914(01)02167-0. Trends Mol Med. 2001. PMID: 11733222

7

Late-onset corticohippocampal neurodepletion attributable to catastrophic failure of oxidative phosphorylation in MILON mice.

Sörensen L, Ekstrand M, Silva JP, Lindqvist E, Xu B, Rustin P, Olson L, Larsson NG. Sörensen L, et al. Among authors: rustin p. J Neurosci. 2001 Oct 15;21(20):8082-90. doi: 10.1523/JNEUROSCI.21-20-08082.2001. J Neurosci. 2001. PMID: 11588181 Free PMC article.

8

Genotypes and clinical phenotypes in children with cytochrome-c oxidase deficiency.

Darin N, Moslemi AR, Lebon S, Rustin P, Holme E, Oldfors A, Tulinius M. Darin N, et al. Among authors: rustin p. Neuropediatrics. 2003 Dec;34(6):311-7. doi: 10.1055/s-2003-44670. Neuropediatrics. 2003. PMID: 14681757 Review.

9

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.

Bourgeron T, Rustin P, Chretien D, Birch-Machin M, Bourgeois M, Viegas-Péquignot E, Munnich A, Rötig A. Bourgeron T, et al. Among authors: rustin p. Nat Genet. 1995 Oct;11(2):144-9. doi: 10.1038/ng1095-144. Nat Genet. 1995. PMID: 7550341

10

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits.

Puccio H, Simon D, Cossée M, Criqui-Filipe P, Tiziano F, Melki J, Hindelang C, Matyas R, Rustin P, Koenig M. Puccio H, et al. Among authors: rustin p. Nat Genet. 2001 Feb;27(2):181-6. doi: 10.1038/84818. Nat Genet. 2001. PMID: 11175786

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