Zuffardi O - Search Results

1

Order of six loci at 2q24-q31 and orientation of the HOXD locus.

Rossi E, Faiella A, Zeviani M, Labeit S, Floridia G, Brunelli S, Cammarata M, Boncinelli E, Zuffardi O. Rossi E, et al. Among authors: zuffardi o. Genomics. 1994 Nov 1;24(1):34-40. doi: 10.1006/geno.1994.1579. Genomics. 1994. PMID: 7896287

2

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis.

Tiranti V, Rossi E, Ruiz-Carrillo A, Rossi G, Rocchi M, DiDonato S, Zuffardi O, Zeviani M. Tiranti V, et al. Among authors: zuffardi o. Genomics. 1995 Jan 20;25(2):559-64. doi: 10.1016/0888-7543(95)80058-t. Genomics. 1995. PMID: 7789991

3

Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1.

Corti O, Finocchiaro G, Rossi E, Zuffardi O, DiDonato S. Corti O, et al. Among authors: zuffardi o. Genomics. 1994 Sep 1;23(1):94-9. doi: 10.1006/geno.1994.1463. Genomics. 1994. PMID: 7829107

4

The gene (NFE2L1) for human NRF-1, an activator involved in nuclear-mitochondrial interactions, maps to 7q32.

Tiranti V, Rossi E, Rocchi M, DiDonato S, Zuffardi O, Zeviani M. Tiranti V, et al. Among authors: zuffardi o. Genomics. 1995 Jun 10;27(3):555-7. doi: 10.1006/geno.1995.1094. Genomics. 1995. PMID: 7558044 No abstract available.

5

Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32.

Gellera C, Verderio E, Floridia G, Finocchiaro G, Montermini L, Cavadini P, Zuffardi O, Taroni F. Gellera C, et al. Among authors: zuffardi o. Genomics. 1994 Nov 1;24(1):195-7. doi: 10.1006/geno.1994.1605. Genomics. 1994. PMID: 7896283 No abstract available.

6

Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3-q22.1.

Rossi E, Zarrilli R, Zuffardi O. Rossi E, et al. Among authors: zuffardi o. Hum Genet. 1993 Feb;90(6):653-4. doi: 10.1007/BF00202485. Hum Genet. 1993. PMID: 8444471

7

The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications.

Floridia G, Piantanida M, Minelli A, Dellavecchia C, Bonaglia C, Rossi E, Gimelli G, Croci G, Franchi F, Gilgenkrantz S, Grammatico P, Dalprá L, Wood S, Danesino C, Zuffardi O. Floridia G, et al. Among authors: zuffardi o. Am J Hum Genet. 1996 Apr;58(4):785-96. Am J Hum Genet. 1996. PMID: 8644743 Free PMC article.

8

Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivation.

Carrozzo R, Arrigo G, Rossi E, Bardoni B, Cammarata M, Gandullia P, Gatti R, Zuffardi O. Carrozzo R, et al. Among authors: zuffardi o. Am J Med Genet. 1997 Oct 31;72(3):329-34. Am J Med Genet. 1997. PMID: 9332664

9

Human FIGF: cloning, gene structure, and mapping to chromosome Xp22.1 between the PIGA and the GRPR genes.

Rocchigiani M, Lestingi M, Luddi A, Orlandini M, Franco B, Rossi E, Ballabio A, Zuffardi O, Oliviero S. Rocchigiani M, et al. Among authors: zuffardi o. Genomics. 1998 Jan 15;47(2):207-16. doi: 10.1006/geno.1997.5079. Genomics. 1998. PMID: 9479493

10

The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome.

Sperandeo MP, Borsani G, Incerti B, Zollo M, Rossi E, Zuffardi O, Castaldo P, Taglialatela M, Andria G, Sebastio G. Sperandeo MP, et al. Among authors: zuffardi o. Genomics. 1998 Apr 15;49(2):230-6. doi: 10.1006/geno.1998.5252. Genomics. 1998. PMID: 9598310

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