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1.5 Abstract in rivista: [250] Home page tipologia

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Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 21 a 40 di 250
Titolo Data di pubblicazione Autore(i) File
RARE-CUTTER RESTRICTION MAP OF YAC CONTIGS ACROSS XQ28 1-gen-1993 Romano, G; Palmieri, G; Ciccodicola, A; Cappa, V; Casamassimi, A; Campanile, C; Esposito, T; Johnson, S; Reinbold, R; Schlessinger, D; Durso, M
Incontinentia Pigmenti results from a common mutation in the NEMO gene and affects cellular signal transduction through the NF-kappa B pathway 1-gen-2000 Aradhya, S; Woffendin, H; Esposito, T; Smahl, A; Courtois, G; Jakins, T; Bardaro, T; Ciccodicola, A; Lewis, Ra; Nelson, Dl; Kenwrick, Sj; D'Urso, M; Israel, A; Munnich, A
Characterization of a new gene expressed in an undifferentiated teratocarcinoma cell line 1-gen-1987 Ciccodicola, A; Simeone, A; Zollo, M; D'Urso, M; Persico, Mg.
The complete genomic sequence of the human RPGR gene reveals new expressed sequences 1-gen-2000 Vervoort, R; Miano, Mg; Lennon, A; Meindl, A; Conte, I; D'Urso, M; Meitinger, T; Bird, Ac; Ciccodicola, A; Wright, Af
From sequence analysis to diseases identification in the distal human xq28 1-gen-1999 Ciccodicola, A; Esposito, T; Matarazzo, Mr; Gianfrancesco, F; Cocchia, M; Cuccerese, M; Bardaro, T; Manfellotto, M; Miano, Mg; Migliaccio, C; Vacca, M; Franze', A; Cocchia, S; Mercadante, G; Terracciano, A; Torino, A; Ventruto, V; D'Esposito, M; D'Urso, M
Clinical findings in an autosomal dominant Italian family with mutation in the RP1 gene 1-gen-2005 Simonelli, Ff; Ziviello, L; Testa, F; Nesti, A; Rinaldi, M; Rossi, S; Di Iorio, V; Banfi, S; Ciccodicola, A
Gene expression regulation in heart failure: from pathobiology to bioinformatics 1-gen-2016 Schiano, C; Grimaldi, V; Aprile, M; Esposito, R; Maiello, C; Soricelli, A; Colantuoni, V; Costa, V; Ciccodicola, A; Napoli, C.
ANALYSIS AND SEQUENCING OF THE GENOMIC DNA REGION SPANNING THE HUMAN DBL PROTOONCOGENE 1-gen-1993 Palmieri, G; Casamassimi, A; Ciccodicola, A; Arcucci, A; DE FRANCISCIS, V; Vecchio, G; Durso, M
Novel RP2 mutations in European families with X-linked retinitis pigmentosa (XLRP) 1-gen-2000 Vigo, L; Testa, F; Miano, Mg; Conte, I; Cennamo, G; D'Urso, M; Ayuso, C; Brancato, R; Simonelli, F; Ciccodicola, A
Systematic identification and characterization of eye-expressed transcripts: Novel candidate genes for eye diseases 1-gen-2000 Ciccodicola, A; den Hollander, A; Miano, Mg; D'Urso, M; Cremers, F; Ballabio, A; Banfi, S
CLONING OF THE FRAGILE-X LOCUS IN THE CONTEXT OF YEAST ARTIFICIAL CHROMOSOME-BASED MAPPING OF XQ24-28 1-gen-1991 Schlessinger, D; Zucchi, I; Nagaraja, R; Little, Rd; Abidi, F; Freije, D; Pilia, G; Porta, G; Yoon, Jy; Johnson, Sk; Palmieri, G; Montanaro, V; Romano, G; Casamassimi, A; Ciccodicola, A; Durso, M
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
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
ANALYSIS OF POLYMORPHISMS OF THE NUCLEAR RECEPTOR PPARG GENE IN OBESE INDIVIDUALS FROM SOUTHERN ITALY 1-gen-2008 Costa, V; Casamassimi, A; Villani, A; Santangelo, F; Ciccodicola, A
Characterization of Retinitis Pigmentosa GTPase (RPGR) regulator gene promoter and identification of a new allele in patients with Retinitis Pigmentosa X-linked 1-gen-2000 Miano, Mg; Conte, I; Strazzullo, M; Testa, F; Lanzara, C; Zullo, A; Simonelli, F; D'Urso, M; Wright, Af; Ciccodicola, A
SEQUENCING AND PRELIMINARY-ANALYSIS OF 220-KB OF DNA IN THE HIGH-GC RCP/GCP-G6PD INTERVAL OF XQ28 1-gen-1994 Zollo, M; Ciccodicola, A; Arcucci, A; Repetto, M; Zuo, L; Mazzarella, R; Schlessinger, D; D'Urso, M; Chen, E
Filamin a is mutated in chronic intestinal pseudoobstruction 1-gen-2007 Auricchio, R; Gargiulo, A; Ciccodicola, A; Barone, Mv; Reardon, W; Strisciuglio, C; Del Mastro, A; Auricchio, A
Association between the T239M missense variation in the FGF23 gene and renal phosphate leak 1-gen-2009 De Filippo, G; Rendina, D; Esposito, T; Gianfrancesco, F; Mossetti, G; Ciccodicola, A; Strazzullo, P
GENE EXPRESSION ALTERATIONS IN HUMAN HEART FAILURE BY RNA-SEQUENCING TECHNOLOGY 1-gen-2016 Schiano, C; Grimaldi, V; Aprile, M; Esposito, R; Maiello, C; Soricelli, A; Colantuoni, V; Costa, V; Ciccodicola, A; Napoli, C.
Clinical expression of X-linked retinitis pigmentosa in a family with a novel splice defect in the RPGR gene 1-gen-2001 Testa, F; Simonelli, F; Norcia, F; Milano, G; Olivieri, C; Danesino, C; Miano, Mg; Ciccodicola, A; Rinaldi, E; Ruberto, G
Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 21 a 40 di 250
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Scopri
Tipologia
  • 1 Contributo su Rivista250
Autore
  • VALERIO, GIULIANA65
  • CICCODICOLA, Alfredo49
  • Franzese A33
  • ORRU', Stefania32
  • BUONO, Pasqualina22
  • ARCONE, Rosaria19
  • Buono P18
  • SORRENTINO, Giuseppe17
  • Spagnuolo MI17
  • IMPERLINI, Esther16
Data di pubblicazione
  • 2020 - 20227
  • 2010 - 201990
  • 2000 - 2009105
  • 1990 - 199945
  • 1982 - 19893
Rivista
  • SPORT SCIENCES FOR HEALTH17
  • S.I.E.D.P. NEWS15
  • AMERICAN JOURNAL OF HUMAN GENETICS12
  • DIABETOLOGIA12
  • ITALIAN BIOCHEMICAL SOCIETY TRANS...12
  • RIVISTA ITALIANA DI PEDIATRIA12
  • THE FEBS JOURNAL11
  • INVESTIGATIVE OPHTHALMOLOGY & VIS...10
  • QUADERNI DI PEDIATRIA10
  • ITALIAN JOURNAL OF BIOCHEMISTRY8
Keyword
  • ERYTHROCYTES4
  • DHT3
  • IGF-13
  • MEMBRANE PROTEIN ERYTHROCYTES3
  • Rat cortical astrocytes3
  • Cognitive dysfunction2
  • differentiation2
  • human myoblast2
  • Interleukin-62
  • METHYL ESTERIFICATION2
Lingua
  • eng170
  • ita53
Accesso al fulltext
  • no fulltext247
  • reserved2
  • restricted1