D'Esposito M - Search Results

1

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.

Vacca M, Filippini F, Budillon A, Rossi V, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, MacDonald F, Kerr A, Dhanjal S, Hultén M. Vacca M, et al. J Mol Med (Berl). 2001;78(11):648-55. doi: 10.1007/s001090000155. J Mol Med (Berl). 2001. PMID: 11269512

2

Genetic mapping of a gene encoding an atypical protein kinase C, protein kinase C lambda, to the proximal region of mouse chromosome 3.

Quaderi NA, Gianfrancesco F, Brown SD, D'Urso M, D'Esposito M. Quaderi NA, et al. Genomics. 1995 Oct 10;29(3):815-6. doi: 10.1006/geno.1995.9923. Genomics. 1995. PMID: 8575788 No abstract available.

3

A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation.

D'Esposito M, Ciccodicola A, Gianfrancesco F, Esposito T, Flagiello L, Mazzarella R, Schlessinger D, D'Urso M. D'Esposito M, et al. Nat Genet. 1996 Jun;13(2):227-9. doi: 10.1038/ng0696-227. Nat Genet. 1996. PMID: 8640232

4

Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

D'Esposito M, Quaderi NA, Ciccodicola A, Bruni P, Esposito T, D'Urso M, Brown SD. D'Esposito M, et al. Mamm Genome. 1996 Jul;7(7):533-5. doi: 10.1007/s003359900157. Mamm Genome. 1996. PMID: 8672133 No abstract available.

5

Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome.

Gianfrancesco F, Esposito T, Ruini L, Houlgatte R, Nagaraja R, D'Esposito M, Rocchi M, Auffray C, Schlessinger D, D'Urso M, Forabosco A. Gianfrancesco F, et al. Gene. 1997 Mar 18;187(2):179-84. doi: 10.1016/s0378-1119(96)00743-3. Gene. 1997. PMID: 9099878

6

Expressed STSs and transcription of human Xq28.

Esposito T, Ciccodicola A, Flagiello L, Matarazzo MR, Migliaccio C, Cifarelli RA, Visone R, Campanile C, Mazzarella R, Schlessinger D, D'Urso M, D'Esposito M. Esposito T, et al. Gene. 1997 Mar 18;187(2):185-91. doi: 10.1016/s0378-1119(96)00772-x. Gene. 1997. PMID: 9099879

7

Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region.

D'Esposito M, Matarazzo MR, Ciccodicola A, Strazzullo M, Mazzarella R, Quaderi NA, Fujiwara H, Ko MS, Rowe LB, Ricco A, Archidiacono N, Rocchi M, Schlessinger D, D'Urso M. D'Esposito M, et al. Hum Mol Genet. 1997 Oct;6(11):1917-23. doi: 10.1093/hmg/6.11.1917. Hum Mol Genet. 1997. PMID: 9302271

8

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. Cytogenet Cell Genet. 1998;83(1-2):46-7. doi: 10.1159/000015165. Cytogenet Cell Genet. 1998. PMID: 9925922 No abstract available.

9

Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene.

Gianfrancesco F, Esposito T, Ciccodicola A, D'Esposito M, Mazzarella R, D'Urso M, Forabosco A. Gianfrancesco F, et al. Cytogenet Cell Genet. 1999;84(3-4):164-6. doi: 10.1159/000015247. Cytogenet Cell Genet. 1999. PMID: 10393420 No abstract available.

10

Human and mouse SYBL1 gene structure and expression.

Matarazzo MR, Cuccurese M, Strazzullo M, Vacca M, Curci A, Miano MG, Cocchia M, Mercadante G, Torino A, D'Urso M, Ciccodicola A, D'Esposito M. Matarazzo MR, et al. Gene. 1999 Nov 15;240(1):233-8. doi: 10.1016/s0378-1119(99)00375-3. Gene. 1999. PMID: 10564831

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