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Results: 1-10 |
Results: 10
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria
Authors: Cagliani, R Comi, GP Tancredi, L Sironi, M Fortunato, F Giorda, R Bardoni, A Moggio, M Prelle, A Bresolin, N Scarlato, G
Citation: R. Cagliani et al., Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria, NEUROMUSC D, 11(4), 2001, pp. 389-394
CNGA3 mutations in hereditary cone photoreceptor disorders
Authors: Wissinger, B Gamer, D Jagle, H Giorda, R Marx, T Mayer, S Tippmann, S Broghammer, M Jurklies, B Rosenberg, T Jacobson, SG Sener, EC Tatlipinar, S Hoyng, CB Castellan, C Bitoun, P Andreasson, S Rudolph, G Kellner, U Lorenz, B Wolff, G Verellen-Dumoulin, C Schwartz, M Cremers, FPM Apfelstedt-ylla, E Zrenner, E Salati, R Sharpe, LT Kohl, S
Citation: B. Wissinger et al., CNGA3 mutations in hereditary cone photoreceptor disorders, AM J HU GEN, 69(4), 2001, pp. 722-737
Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome
Authors: Bonglia, MC Giorda, R Borgatti, R Felisari, G Gagliardi, C Selicorni, A Zuffardi, O
Citation: Mc. Bonglia et al., Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome, AM J HU GEN, 69(2), 2001, pp. 261-268
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements
Authors: Giglio, S Broman, KW Matsumoto, N Calvari, V Gimelli, G Neumann, T Ohashi, H Voullaire, L Larizza, D Giorda, R Weber, JL Ledbetter, DH Zuffardi, O
Citation: S. Giglio et al., Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements, AM J HU GEN, 68(4), 2001, pp. 874-883
Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q
Authors: Bonaglia, MC Giorda, R Poggi, G Raggi, ME Rossi, E Baroncini, A Giglio, S Borgatti, R Zuffardi, O
Citation: Mc. Bonaglia et al., Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q, EUR J HUM G, 8(8), 2000, pp. 597-603
Cell type specificity and mechanism of control of a gene may be reverted in different strains of Dictyostelium discoideum
Authors: Mangiarotti, G Giorda, R
Citation: G. Mangiarotti et R. Giorda, Cell type specificity and mechanism of control of a gene may be reverted in different strains of Dictyostelium discoideum, BBA-GENE ST, 1492(1), 2000, pp. 23-30
Effects of serotonin transporter promoter genotype on platelet serotonin transporter functionality in depressed children and adolescents
Authors: Nobile, M Begni, B Giorda, R Frigerio, A Marino, C Molteni, M Ferrarese, C Battaglia, M
Citation: M. Nobile et al., Effects of serotonin transporter promoter genotype on platelet serotonin transporter functionality in depressed children and adolescents, J AM A CHIL, 38(11), 1999, pp. 1396-1402
Constitutive expression and role of the TNF family ligands in apoptotic killing of tumor cells by human NK cells
Authors: Kashii, Y Giorda, R Herberman, RB Whiteside, TL Vujanovic, NL
Citation: Y. Kashii et al., Constitutive expression and role of the TNF family ligands in apoptotic killing of tumor cells by human NK cells, J IMMUNOL, 163(10), 1999, pp. 5358-5366
Rat natural killer cell antigen, NKR-PI, related to C-type animal lectins is a carbohydrate-binding protein (vol 269, pg 16945, 1994)
Authors: Bezouska, K Vlahas, G Horvath, O Jinochova, G Fiserova, A Giorda, R Chambers, WH Feizi, T Pospisil, M
Citation: K. Bezouska et al., Rat natural killer cell antigen, NKR-PI, related to C-type animal lectins is a carbohydrate-binding protein (vol 269, pg 16945, 1994), J BIOL CHEM, 274(42), 1999, pp. 30335-30336
Case report: Essential iris atrophy in the Williams-Beuren syndrome
Authors: Salati, R Baraldi, E Giorda, R
Citation: R. Salati et al., Case report: Essential iris atrophy in the Williams-Beuren syndrome, J PEDIAT OP, 35(6), 1998, pp. 336-337
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