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Results: 1-12 |
Results: 12
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
Authors: Crisponi, L Deiana, M Loi, A Chiappe, F Uda, M Amati, P Bisceglia, L Zelante, L Nagaraja, R Porcu, S Ristaldi, MS Marzella, R Rocchi, M Nicolino, M Lienhardt-Roussie, A Nivelon, A Verloes, A Schlessinger, D Gasparini, P Bonneau, D Cao, A Pilia, G
Citation: L. Crisponi et al., The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome, NAT GENET, 27(2), 2001, pp. 159-166
RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISH
Authors: Cinti, R Yin, L Ilc, K Berger, N Basolo, F Cuccato, S Giannini, R Torre, G Miccoli, P Amati, P Romeo, G Corvi, R
Citation: R. Cinti et al., RET rearrangements in papillary thyroid carcinomas and adenomas detected by interphase FISH, CYTOG C GEN, 88(1-2), 2000, pp. 56-61
A mutation in the DE loop of the VP1 protein that prevents polyomavirus transcription and replication
Authors: Garcia, ML Perez, M Caruso, M Sthandier, O Ferreira, R Cermola, M Macchia, C Amati, P
Citation: Ml. Garcia et al., A mutation in the DE loop of the VP1 protein that prevents polyomavirus transcription and replication, VIROLOGY, 272(2), 2000, pp. 293-301
The polyomavirus major capsid protein VP1 interacts with the nuclear matrix regulatory protein YY1
Authors: Palkova, Z Spanielova, H Gottifredi, V Hollanderova, D Forstova, J Amati, P
Citation: Z. Palkova et al., The polyomavirus major capsid protein VP1 interacts with the nuclear matrix regulatory protein YY1, FEBS LETTER, 467(2-3), 2000, pp. 359-364
Anderson's disease - Exclusion of apolipoprotein and intracellular lipid transport genes
Authors: Dannoura, AH Berriot-Varoqueaux, N Amati, P Abadie, V Verthier, N Schmitz, J Wetterau, JR Samson-Bouma, ME Aggerbeck, LP
Citation: Ah. Dannoura et al., Anderson's disease - Exclusion of apolipoprotein and intracellular lipid transport genes, ART THROM V, 19(10), 1999, pp. 2494-2508
Medullary thyroid carcinomas in transgenic mice expressing a polyoma carboxyl-terminal truncated middle-T and wild type small-T antigens
Authors: Felici, A Giorgio, M Krauzewicz, N Della Rocca, C Santoro, M Rovere, P Manni, I Amati, P Pozzi, L
Citation: A. Felici et al., Medullary thyroid carcinomas in transgenic mice expressing a polyoma carboxyl-terminal truncated middle-T and wild type small-T antigens, ONCOGENE, 18(14), 1999, pp. 2387-2395
Splenogonadal fusion limb defect syndrome: Report of five new cases and review
Authors: Bonneau, D Roume, J Gonzalez, M Toutain, A Carles, D Marechaud, M Biran-Mucignat, V Amati, P Moraine, C
Citation: D. Bonneau et al., Splenogonadal fusion limb defect syndrome: Report of five new cases and review, AM J MED G, 86(4), 1999, pp. 347-358
Heterotaxy-neural tube defect and holoprosencephaly occurring independently in two sib fetuses
Authors: Bonneau, D Marechaud, M Odent, S Piegay, I Godard, A Amati, P
Citation: D. Bonneau et al., Heterotaxy-neural tube defect and holoprosencephaly occurring independently in two sib fetuses, AM J MED G, 84(4), 1999, pp. 373-376
Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene
Authors: Kraimps, JL Canzian, F Jost, C Menet, E Amati, P Levillian, P Harach, R Lesueur, F Barbier, J Romeo, G Bonneau, D
Citation: Jl. Kraimps et al., Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene, SURGERY, 126(6), 1999, pp. 1188-1194
Polyomavirus large T antigen induces alterations in cytoplasmic signallingpathways involving Shc activation
Authors: Gottifredi, V Pelicci, G Munarriz, E Maione, R Pelicci, PG Amati, P
Citation: V. Gottifredi et al., Polyomavirus large T antigen induces alterations in cytoplasmic signallingpathways involving Shc activation, J VIROLOGY, 73(2), 1999, pp. 1427-1437
Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2
Authors: Harach, HR Lesueur, F Amati, P Brown, A Canzian, F Kraimps, JL Levillain, P Menet, E Romeo, G Bonneau, D
Citation: Hr. Harach et al., Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2, J PATHOLOGY, 189(3), 1999, pp. 387-393
A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2
Authors: Canzian, F Amati, P Harach, HR Kraimps, JL Lesueur, F Barbier, J Levillain, P Romeo, G Bonneau, D
Citation: F. Canzian et al., A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2, AM J HU GEN, 63(6), 1998, pp. 1743-1748
Risultati: 1-12 |