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Results: 1-25 | 26-36 |
Results: 26-36/36
Fluorescent in situ PCR allows sensitive three hours detection of human papilloma virus in cells and tissues
Authors: Marziliano, N Mancuso, T Comar, M Cernigoi, E Da Prato, L Garagna, S Boniotto, M Pirulli, D Puzzer, D Morgutti, M Amoroso, A Crovella, S
Citation: N. Marziliano et al., Fluorescent in situ PCR allows sensitive three hours detection of human papilloma virus in cells and tissues, EUR J HIST, 43(2), 1999, pp. 155-157
Patterning the ascidian nervous system: structure, expression and transgenic analysis of the CiHox3 gene
Authors: Locascio, A Aniello, F Amoroso, A Manzanares, M Krumlauf, R Branno, M
Citation: A. Locascio et al., Patterning the ascidian nervous system: structure, expression and transgenic analysis of the CiHox3 gene, DEVELOPMENT, 126(21), 1999, pp. 4737-4748
MFASAT: A new alphoid DNA sequence isolated from Macaca fascicularis (Cercopithecidae, Primates)
Authors: Crovella, S Del Pero, M Marziliano, N Garagna, S Pecile, V Morgutti, M Boniotto, M Amoroso, A Montagnon, D Campa, CC Lamberti, L Bigatti, MP Ardito, G
Citation: S. Crovella et al., MFASAT: A new alphoid DNA sequence isolated from Macaca fascicularis (Cercopithecidae, Primates), GENOME, 42(6), 1999, pp. 1066-1070
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene
Authors: Pirulli, D Puzzer, D Ferri, L Crovella, S Amoroso, A Ferrettini, C Marangella, M Mazzola, G Florian, F
Citation: D. Pirulli et al., Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene, HUM GENET, 104(6), 1999, pp. 523-525
Gene symbol: AGXT - Disease: Primary hyperoxaluria type I
Authors: Amoroso, A Pirulli, D Puzzer, D Ferri, L Crovella, S Ferrettini, C Marangella, M Mazzola, G Florian, F
Citation: A. Amoroso et al., Gene symbol: AGXT - Disease: Primary hyperoxaluria type I, HUM GENET, 104(5), 1999, pp. 441-441
Genetic mapping of the mouse homologue of the human angiopoitetin-1 gene (Agpt) to mouse chromosome 9E2 by in situ hybridization
Authors: Marziliano, N Crovella, S Audero, E Pecile, V Bussolino, F Amoroso, A Garagna, S
Citation: N. Marziliano et al., Genetic mapping of the mouse homologue of the human angiopoitetin-1 gene (Agpt) to mouse chromosome 9E2 by in situ hybridization, CYTOG C GEN, 87(3-4), 1999, pp. 199-200
Familial clustering of IgA nephropathy: Further evidence in an Italian population
Authors: Scolari, F Amoroso, A Savoldi, S Mazzola, G Prati, E Valzorio, B Viola, BF Nicola, B Movilli, E Sandrini, M Campanini, M Maiorca, R
Citation: F. Scolari et al., Familial clustering of IgA nephropathy: Further evidence in an Italian population, AM J KIDNEY, 33(5), 1999, pp. 857-865
Polymorphism at codon 54 of mannose-binding protein gene influences AIDS progression but not HIV infection in exposed children
Authors: Amoroso, A Berrino, M Boniotto, M Crovella, S Palomba, E Scarlatti, G Serra, C Tovo, PA Vatta, S
Citation: A. Amoroso et al., Polymorphism at codon 54 of mannose-binding protein gene influences AIDS progression but not HIV infection in exposed children, AIDS, 13(7), 1999, pp. 863-864
Primary antiphospholipid syndrome and cerebral atrophy: A rare association?
Authors: Amoroso, A del Porto, F Garzia, P Mariotti, A Addessi, MA Afeltra, A
Citation: A. Amoroso et al., Primary antiphospholipid syndrome and cerebral atrophy: A rare association?, AM J MED SC, 317(6), 1999, pp. 425-428
Identification of a new locus for medullary cystic disease, on chromosome 16p12
Authors: Scolari, F Puzzer, D Amoroso, A Caridi, G Ghiggeri, GM Maiorca, R Aridon, P De Fusco, M Ballabio, A Casari, G
Citation: F. Scolari et al., Identification of a new locus for medullary cystic disease, on chromosome 16p12, AM J HU GEN, 64(6), 1999, pp. 1655-1660
Polymorphisms in angiotensin-converting enzyme gene and severity of renal disease in Henoch-Schoenlein patients
Authors: Amoroso, A Danek, G Vatta, S Crovella, S Berrino, M Guarrera, S Fasano, ME Mazzola, G Amore, A Gianoglio, B Peruzzi, L Coppo, R
Citation: A. Amoroso et al., Polymorphisms in angiotensin-converting enzyme gene and severity of renal disease in Henoch-Schoenlein patients, NEPH DIAL T, 13(12), 1998, pp. 3184-3188
Risultati: 1-25 | 26-36 |