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Titolo Data di pubblicazione Autore(i) File
YAC CONTIG ORGANIZATION AND CPG ISLAND ANALYSIS IN XQ28 1-gen-1994 Palmieri, G; Romano, G; Ciccodicola, A; Casamassimi, A; Campanile, C; Esposito, T; Cappa, V; Lania, A; Johnson, S; Reinbold, R; Poustka, A; Schlessinger, D; Durso, M
HUMAN PROTEIN-KINASE-C LOTA GENE (PRKCI) IS CLOSELY LINKED TO THE BTK GENE IN XQ21.3 1-gen-1995 Mazzarella, R; Ciccodicola, A; Esposito, T; Arcucci, A; Migliaccio, C; Jones, C; Schlessinger, D; D'Urso, M; D'Esposito, M
SSCP DETECTION OF NOVEL MUTATIONS IN PATIENTS WITH EMERY-DREIFUSS MUSCULAR-DYSTROPHY - DEFINITION OF A SMALL C-TERMINAL REGION REQUIRED FOR EMERIN FUNCTION 1-gen-1995 Nigro, V; Bruni, P; Ciccodicola, A; Politano, L; Nigro, G; Piluso, G; Cappa, V; Covone, Ae; Romeo, G; D'Urso, M
IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE 1-gen-1995 Bione, S; Small, K; Aksmanovic, Vma; D'Urso, M; Ciccodicola, A; Merlini, L; Morandi, L; Kress, W; Yates, Jrw; Warren, St; Toniolo, D
A MUSCLE-SPECIFIC DNASE I-LIKE GENE IN HUMAN XQ28 1-gen-1995 Parrish, Je; Ciccodicola, A; Wehnert, M; Cox, Gf; Chen, E; Nelson, Dl
A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation 1-gen-1996 D'Esposito, M; Ciccodicola, A; Gianfrancesco, F; Esposito, T; Flagiello, L; Mazzarella, R; Schlessinger, D; D'Urso, M
A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3) 1-gen-1996 Meindl, A; Dry, K; Herrmann, K; Manson, F; Ciccodicola, A; Edgar, A; Carvalho, Mrs; Achatz, H; Hellebrand, H; Lennon, A; Migliaccio, C; Porter, K; Zrenner, E; Bird, A; Jay, M; Lorenz, B; Wittwer, B; D'Urso, M; Meitinger, T; Wright, A
Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2 1-gen-1996 D'Esposito, M; Quaderi, Na; Ciccodicola, A; Bruni, P; Esposito, T; D'Urso, M; Brown, Sdm
Long-range sequence analysis in Xq28: Thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and GGPD loci 1-gen-1996 Chen, Ey; Zollo, M; Mazzarella, R; Ciccodicola, A; Chen, Cn; Zuo, L; Heiner, C; Burough, F; Repetto, M; Schlessinger, D; D'Urso, M
Expressed STSs and transcription of human Xq28 1-gen-1997 Esposito, T; Ciccodicola, A; Flagiello, L; Matarazzo, Mr; Migliaccio, C; Cifarelli, Ra; Visone, R; Campanile, C; Mazzarella, R; Schlessinger, D; Durso, M; Desposito, M
An approach for testing gene dosage as a mechanism for cognitive dysfunction in Klinefelter's syndrome 1-gen-1997 Geschwind, Dh; Gregg, J; Karrim, J; Boone, K; Swerdloff, R; Rappold, G; Rao, E; D'Urso, M; Ciccodicola, A; Nelson, Sf
Mutation analysis of RPGR gene in patients with X-linked Retinitis Pigmentosa (RP3) 1-gen-1997 Ciccodicola, A; Miano, Mg; Testa, F; Simonelli, F; Baiget, M; Antinolo, G; Del Porto, G; Danesino, C; Rinaldi, E; Ventruto, V; D'Urso, M
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 1-gen-1997 D'Esposito, M; Matarazzo, Mr; Strazzullo, M; Curci, A; Cuccurese, M; Terracciano, A; D'Urso, M; Ciccodicola, A
A new gene encodes a putative GTP-binding protein, escapes X-inactivation and has related sequences on Y chromosome 1-gen-1997 Gianfrancesco, F; Esposito, T; Montanini, L; Ciccodicola, A; Forabosco, A
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp 1-gen-1997 Fisher, Se; Ciccodicola, A; Tanaka, K; Curci, A; Desicato, S; Durso, M; Craig, Iw
Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region 1-gen-1997 Desposito, M; Matarazzo, Mr; Ciccodicola, A; Strazzullo, M; Matzarella, R; Quaderi, Na; Fujiwara, H; Ko, Msh; Rowe, Lb; Ricco, A; Archidiacono, N; Rocchi, M; Schlessinger, D; Durso, M
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 1-gen-1997 Esposito, T; Gianfrancesco, F; Ciccodicola, A; Desposito, M; Nagaraja, R; Mazzarella, R; Durso, M; Forabosco, A
Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family 1-gen-1998 Flagiello, L; Cirigliano, V; Strazzullo, M; Cappa, V; Ciccodicola, A; D'Esposito, M; Torrente, I; Werner, R; Di Iorio, G; Rinaldi, M; Dallapiccola, A; Forabosco, A; Ventruto, V; D'Urso, M
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 1-gen-1998 D'Esposito, M; Strazzullo, M; Cuccurese, M; Spalluto, C; Rocchi, M; D'Urso, M; Ciccodicola, A
Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity 1-gen-1998 de Crecchio, G; Simonelli, F; Nunziata, G; Mazzeo, S; Greco, Gm; Rinaldi, E; Ventruto, V; Ciccodicola, A; Miano, Mg; Testa, F; Curci, A; D'Urso, M; Rinaldi, Mm; Cavaliere, Ml; Castelluccio, P
Mostrati risultati da 21 a 40 di 180
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