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Results:
1-21
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Results: 21
Authors:
Ferrante, MI
Ghiani, M
Bulfone, A
Franco, B
Citation: Mi. Ferrante et al., IL1RAPL2 maps to Xq22 and is specifically expressed in the central nervoussystem, GENE, 275(2), 2001, pp. 217-221
Authors:
Zannolli, R
Mostardini, R
Pucci, L
Sorrentino, L
Biagioli, M
Perotti, R
Guarna, M
Hadjistilianou, T
Zerega, G
Pierluigi, M
Franco, B
D'Ambrosio, A
Morgese, G
Citation: R. Zannolli et al., Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;14) (pter;q11.2)], AM J MED G, 102(1), 2001, pp. 29-35
Authors:
Ahmad, W
Noci, S
Haque, MFU
Sarno, T
Aridon, P
Ahmad, MM
Amin-ud-din, M
Rafiq, MA
Haque, SU
De Fusco, M
Ballabio, A
Franco, B
Casari, G
Citation: W. Ahmad et al., Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family, AM J MED G, 100(1), 2001, pp. 62-65
Authors:
Ferrante, MI
Giorgio, G
Feather, SA
Bulfone, A
Wright, V
Ghiani, M
Selicorni, A
Gammaro, L
Scolari, F
Woolf, AS
Sylvie, O
Bernard, LM
Malcolm, S
Winter, R
Ballabio, A
Franco, B
Citation: Mi. Ferrante et al., Identification of the gene for oral-facial-digital type I syndrome, AM J HU GEN, 68(3), 2001, pp. 569-576
Authors:
Buchner, G
Broccoli, V
Bulfone, A
Orfanelli, U
Gattuso, C
Ballabio, A
Franco, B
Citation: G. Buchner et al., MAEG, an EGF-repeat containing gene, is a new marker associated with dermatome specification and morphogenesis of its derivatives, MECH DEVEL, 98(1-2), 2000, pp. 179-182
Authors:
Buchner, G
Orfanelli, U
Quaderi, N
Bassi, MT
Andolfi, G
Ballabio, A
Franco, B
Citation: G. Buchner et al., Identification of a new EGF-repeat-containing gene from human Xp22: A candidate for developmental disorders, GENOMICS, 65(1), 2000, pp. 16-23
Authors:
Franco, B
Citation: B. Franco, A place to remember: Using history to build community, PUBLIC HIST, 22(4), 2000, pp. 46-48
Authors:
Franco, B
Citation: B. Franco, The novel in 18th century Europe, ESPRIT CR, 40(2), 2000, pp. 100-101
Authors:
Fukami, M
Kirsch, S
Schiller, S
Richter, A
Benes, V
Franco, B
Muroya, K
Rao, E
Merker, S
Niesler, B
Ballabio, A
Ansorge, W
Ogata, T
Rappold, GA
Citation: M. Fukami et al., A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation, AM J HU GEN, 67(3), 2000, pp. 563-573
Authors:
Ahmad, W
De Fusco, M
ul Haque, MF
Aridon, P
Sarno, T
Sohail, M
ul Haque, S
Ahmad, M
Ballabio, A
Franco, B
Casari, G
Citation: W. Ahmad et al., Linkage mapping of a new syndromic form of X-linked mental retardation, MRXS7, associated with obesity, EUR J HUM G, 7(7), 1999, pp. 828-832
Authors:
Buchner, G
Montini, E
Andolfi, G
Quaderi, N
Cainarca, S
Messali, S
Bassi, MT
Ballabio, A
Meroni, G
Franco, B
Citation: G. Buchner et al., MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during development, HUM MOL GEN, 8(8), 1999, pp. 1397-1407
Authors:
Buchner, G
Bassi, MT
Andolfi, G
Ballabio, A
Franco, B
Citation: G. Buchner et al., Identification of a novel homolog of the Drosophila staufen protein in thechromosome 8q13-q21.1 region, GENOMICS, 62(1), 1999, pp. 113-118
Authors:
Banfi, S
Bassi, MT
Andolfi, G
Marchitiello, A
Zanotta, S
Ballabio, A
Casari, G
Franco, B
Citation: S. Banfi et al., Identification and characterization of AFG3L2, a novel paraplegin-related gene, GENOMICS, 59(1), 1999, pp. 51-58
Authors:
Prakash, SK
Van den Veyver, IB
Franco, B
Volta, M
Ballabio, A
Zoghbi, HY
Citation: Sk. Prakash et al., Characterization of a novel chromo domain gene in Xp22.3 with homology to Drosophila msl-3, GENOMICS, 59(1), 1999, pp. 77-84
Authors:
Montini, E
Buchner, G
Spalluto, C
Andolfi, G
Caruso, A
den Dunnen, JT
Trump, D
Rocchi, M
Ballabio, A
Franco, B
Citation: E. Montini et al., Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22, GENOMICS, 58(1), 1999, pp. 65-72
Authors:
Vitelli, F
Piccini, M
Caroli, F
Franco, B
Malandrini, A
Pober, B
Jonsson, O
Sorrentino, V
Renieri, A
Citation: F. Vitelli et al., Identification and characterization of a highly conserved protein absent in the Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome (AMME), GENOMICS, 55(3), 1999, pp. 335-340
Authors:
Volta, M
Bulfone, A
Gattuso, C
Rossi, E
Mariani, M
Consalez, GG
Zuffardi, O
Ballabio, A
Banfi, S
Franco, B
Citation: M. Volta et al., Identification and characterization of CDS2, a mammalian homolog of the Drosophila CDP-diacylglycerol synthase gene, GENOMICS, 55(1), 1999, pp. 68-77
Authors:
Franco, B
Citation: B. Franco, The Enlightenment, from the West to the East, 1720-1778, REV HIST L, 99(6), 1999, pp. 1266-1267
Authors:
Franco, B
Citation: B. Franco, The poetics of the sublime from the end of the Enlightenment to Romanticism (Diderot, Schiller, Wordsworth, Shelley, Hugo, Michelet), REV HIST L, 99(6), 1999, pp. 1272-1273
Authors:
Franco, B
Citation: B. Franco, From popular genre to aesthetic model. The marionette theater according toKleist, ETUD GER, 54(3), 1999, pp. 391-413
Authors:
Tiranti, V
Hoertnagel, K
Carrozzo, R
Galimberti, C
Munaro, M
Granatiero, M
Zelante, L
Gasparini, P
Marzella, R
Rocchi, M
Bayona-Bafaluy, MP
Enriquez, JA
Uziel, G
Bertini, E
Dionisi-Vici, C
Franco, B
Meitinger, T
Zeviani, M
Citation: V. Tiranti et al., Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency, AM J HU GEN, 63(6), 1998, pp. 1609-1621
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1-21
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