Amati P - Search Results

1

[Expression of a defect in the respiratory chain in cultured human cells].

Meola G, Rotondo G, Velicogna M, Toppi R, Sansone V, Bresolin N, Comi G, Bordoni A, Amati P, Ausenda C, et al. Meola G, et al. Among authors: amati p. Riv Neurol. 1991 Jul-Aug;61(4):122-34. Riv Neurol. 1991. PMID: 1667713 Italian.

2

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. Among authors: amati p. 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.

3

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.

Zeviani M, Bresolin N, Gellera C, Bordoni A, Pannacci M, Amati P, Moggio M, Servidei S, Scarlato G, DiDonato S. Zeviani M, et al. Among authors: amati p. Am J Hum Genet. 1990 Dec;47(6):904-14. Am J Hum Genet. 1990. PMID: 1978558 Free PMC article.

4

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

Zeviani M, Amati P, Bresolin N, Antozzi C, Piccolo G, Toscano A, DiDonato S. Zeviani M, et al. Among authors: amati p. Am J Hum Genet. 1991 Feb;48(2):203-11. Am J Hum Genet. 1991. PMID: 1899320 Free PMC article.

5

Expression of respiratory chain deficiencies in human cultured cells.

Bourgeron T, Chretien D, Amati P, Rötig A, Munnich A, Rustin P. Bourgeron T, et al. Among authors: amati p. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):605-8. doi: 10.1016/0960-8966(93)90124-3. Neuromuscul Disord. 1993. PMID: 8186720

6

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: amati p. Am J Hum Genet. 1996 Apr;58(4):763-9. Am J Hum Genet. 1996. PMID: 8644740 Free PMC article.

7

Mouse genes coding for "zinc-finger"-containing proteins: characterization and expression in differentiated cells.

Passananti C, Felsani A, Caruso M, Amati P. Passananti C, et al. Among authors: amati p. Proc Natl Acad Sci U S A. 1989 Dec;86(23):9417-21. doi: 10.1073/pnas.86.23.9417. Proc Natl Acad Sci U S A. 1989. PMID: 2512579 Free PMC article.

8

Mitochondrial myopathies.

Zeviani M, Amati P, Savoia A. Zeviani M, et al. Among authors: amati p. Curr Opin Rheumatol. 1994 Nov;6(6):559-67. doi: 10.1097/00002281-199411000-00003. Curr Opin Rheumatol. 1994. PMID: 7865374 Review.

9

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: amati p. Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146. Nat Genet. 1995. PMID: 7719341

10

Polyomavirus genome and polyomavirus enhancer-driven gene expression during myogenesis.

Maione R, Felsani A, Pozzi L, Caruso M, Amati P. Maione R, et al. Among authors: amati p. J Virol. 1989 Nov;63(11):4890-7. doi: 10.1128/JVI.63.11.4890-4897.1989. J Virol. 1989. PMID: 2552161 Free PMC article.

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