Zeviani M - Search Results

1

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

Spelbrink JN, Li FY, Tiranti V, Nikali K, Yuan QP, Tariq M, Wanrooij S, Garrido N, Comi G, Morandi L, Santoro L, Toscano A, Fabrizi GM, Somer H, Croxen R, Beeson D, Poulton J, Suomalainen A, Jacobs HT, Zeviani M, Larsson C. Spelbrink JN, et al. Among authors: zeviani m. Nat Genet. 2001 Jul;28(3):223-31. doi: 10.1038/90058. Nat Genet. 2001. PMID: 11431692

2

An autosomal locus predisposing to deletions of mitochondrial DNA.

Suomalainen A, Kaukonen J, Amati P, Timonen R, Haltia M, Weissenbach J, Zeviani M, Somer H, Peltonen L. Suomalainen A, et al. Among authors: zeviani m. Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146. Nat Genet. 1995. PMID: 7719341

3

Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals.

Rovio A, Tiranti V, Bednarz AL, Suomalainen A, Spelbrink JN, Lecrenier N, Melberg A, Zeviani M, Poulton J, Foury F, Jacobs HT. Rovio A, et al. Among authors: zeviani m. Eur J Hum Genet. 1999 Feb-Mar;7(2):140-6. doi: 10.1038/sj.ejhg.5200244. Eur J Hum Genet. 1999. PMID: 10196696

4

An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.

Kaukonen JA, Amati P, Suomalainen A, Rötig A, Piscaglia MG, Salvi F, Weissenbach J, Fratta G, Comi G, Peltonen L, Zeviani M. Kaukonen JA, et al. Among authors: zeviani m. Am J Hum Genet. 1996 Apr;58(4):763-9. Am J Hum Genet. 1996. PMID: 8644740 Free PMC article.

5

Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybrids.

Toompuu M, Tiranti V, Zeviani M, Jacobs HT. Toompuu M, et al. Among authors: zeviani m. Hum Mol Genet. 1999 Nov;8(12):2275-83. doi: 10.1093/hmg/8.12.2275. Hum Mol Genet. 1999. PMID: 10545608

6

Role of adenine nucleotide translocator 1 in mtDNA maintenance.

Kaukonen J, Juselius JK, Tiranti V, Kyttälä A, Zeviani M, Comi GP, Keränen S, Peltonen L, Suomalainen A. Kaukonen J, et al. Among authors: zeviani m. Science. 2000 Aug 4;289(5480):782-5. doi: 10.1126/science.289.5480.782. Science. 2000. PMID: 10926541

7

Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment.

Jacobs HT, Hutchin TP, Käppi T, Gillies G, Minkkinen K, Walker J, Thompson K, Rovio AT, Carella M, Melchionda S, Zelante L, Gasparini P, Pyykkö I, Shah ZH, Zeviani M, Mueller RF. Jacobs HT, et al. Among authors: zeviani m. Eur J Hum Genet. 2005 Jan;13(1):26-33. doi: 10.1038/sj.ejhg.5201250. Eur J Hum Genet. 2005. PMID: 15292920

8

Searching for genes affecting the structural integrity of the mitochondrial genome.

Zeviani M, Amati P, Comi G, Fratta G, Mariotti C, Tiranti V. Zeviani M, et al. Biochim Biophys Acta. 1995 May 24;1271(1):153-8. doi: 10.1016/0925-4439(95)00022-v. Biochim Biophys Acta. 1995. PMID: 7599202 Free article. Review.

9

Sequence analysis of mitochondrial DNA in a new maternally inherited encephalomyopathy.

Fabrizi GM, Tiranti V, Mariotti C, Guazzi GC, Malandrini A, DiDonato S, Zeviani M. Fabrizi GM, et al. Among authors: zeviani m. J Neurol. 1995 Aug;242(8):490-6. doi: 10.1007/BF00867418. J Neurol. 1995. PMID: 8530975

10

Mitochondrial disorders.

Zeviani M, Tiranti V, Piantadosi C. Zeviani M, et al. Medicine (Baltimore). 1998 Jan;77(1):59-72. doi: 10.1097/00005792-199801000-00006. Medicine (Baltimore). 1998. PMID: 9465864 Free article. Review.

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