Rocchi M - Search Results

1

Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22.

Montini E, Buchner G, Spalluto C, Andolfi G, Caruso A, den Dunnen JT, Trump D, Rocchi M, Ballabio A, Franco B. Montini E, et al. Among authors: rocchi m. Genomics. 1999 May 15;58(1):65-72. doi: 10.1006/geno.1999.5755. Genomics. 1999. PMID: 10331946

2

Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region.

Meroni G, Franco B, Archidiacono N, Messali S, Andolfi G, Rocchi M, Ballabio A. Meroni G, et al. Among authors: rocchi m. Hum Mol Genet. 1996 Apr;5(4):423-31. doi: 10.1093/hmg/5.4.423. Hum Mol Genet. 1996. PMID: 8845834

3

Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region.

Vacca M, Matarazzo MR, Jones J, Spalluto C, Archidiacono N, Ma P, Rocchi M, D'Urso M, Chen EY, D'Esposito M, Mumm S. Vacca M, et al. Among authors: rocchi m. Genomics. 1999 Dec 1;62(2):293-6. doi: 10.1006/geno.1999.5996. Genomics. 1999. PMID: 10610725

4

A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expression.

Marino M, Archidiacono N, Franzé A, Rosati M, Rocchi M, Ballabio A, Grimaldi G. Marino M, et al. Among authors: rocchi m. Mamm Genome. 1993;4(5):252-7. doi: 10.1007/BF00417431. Mamm Genome. 1993. PMID: 8507979

5

Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21-->q22.

D'Esposito M, Strazzullo M, Cuccurese M, Spalluto C, Rocchi M, D'Urso M, Ciccodicola A. D'Esposito M, et al. Among authors: rocchi m. Cytogenet Cell Genet. 1998;83(1-2):46-7. doi: 10.1159/000015165. Cytogenet Cell Genet. 1998. PMID: 9925922 No abstract available.

6

Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and Yq.

Ballabio A, Carrozzo R, Gil A, Gillard B, Affara N, Ferguson-Smith MA, Fraser N, Craig I, Rocchi M, Romeo G. Ballabio A, et al. Among authors: rocchi m. Ann Hum Genet. 1989 Jan;53(1):9-14. doi: 10.1111/j.1469-1809.1989.tb01117.x. Ann Hum Genet. 1989. PMID: 2729897

7

PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/C.

Berthelsen J, Viggiano L, Schulz H, Ferretti E, Consalez GG, Rocchi M, Blasi F. Berthelsen J, et al. Among authors: rocchi m. Genomics. 1998 Jan 15;47(2):323-4. doi: 10.1006/geno.1997.5086. Genomics. 1998. PMID: 9479508 No abstract available.

8

A high resolution deletion map of human chromosome Xp22.

Schaefer L, Ferrero GB, Grillo A, Bassi MT, Roth EJ, Wapenaar MC, van Ommen GJ, Mohandas TK, Rocchi M, Zoghbi HY, Ballabio A. Schaefer L, et al. Among authors: rocchi m. Nat Genet. 1993 Jul;4(3):272-9. doi: 10.1038/ng0793-272. Nat Genet. 1993. PMID: 8358436

9

Evolution of chromosome Y in primates.

Archidiacono N, Storlazzi CT, Spalluto C, Ricco AS, Marzella R, Rocchi M. Archidiacono N, et al. Among authors: rocchi m. Chromosoma. 1998 Sep;107(4):241-6. doi: 10.1007/s004120050303. Chromosoma. 1998. PMID: 9745049

10

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: rocchi m. Genomics. 1995 Jun 10;27(3):555-7. doi: 10.1006/geno.1995.1094. Genomics. 1995. PMID: 7558044 No abstract available.

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