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Results: 1-25 | 26-27
Results: 1-25/27
Genomic organisation of the mouse Ret proto-oncogene
Authors: Panetta, D Yin, L Barale, R Romeo, G Ravazzolo, R Ceccherini, I Puliti, A
Citation: D. Panetta et al., Genomic organisation of the mouse Ret proto-oncogene, DNA SEQ, 11(6), 2001, pp. 501-506
5,10-methylenetetrahydrofolate reductase polymorphism and early organ damage in primary hypertension
Authors: Ravera, M Viazzi, F Berruti, V Leoncini, G Zagami, P Bezante, GP Rosatto, N Ravazzolo, R Pontremoli, R Deferrari, G
Citation: M. Ravera et al., 5,10-methylenetetrahydrofolate reductase polymorphism and early organ damage in primary hypertension, AM J HYPERT, 14(4), 2001, pp. 371-376
Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization
Authors: Cinti, R Fava, M Sancandi, M Matera, I Ravazzolo, R Ceccherini, I
Citation: R. Cinti et al., Assignment of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4-A5 by in situ hybridization, CYTOG C GEN, 92(3-4), 2001, pp. 354-355
Fontaine-Farriaux craniosynostosis: Second report in the literature
Authors: Priolo, M De Toni, T Baffico, M Cama, A Seri, M Cusano, R Costabello, L Fondelli, P Capra, V Silengo, M Ravazzolo, R Lerone, M
Citation: M. Priolo et al., Fontaine-Farriaux craniosynostosis: Second report in the literature, AM J MED G, 100(3), 2001, pp. 214-218
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
Authors: Bertolini, S Pisciotta, L Seri, M Cusano, R Cantafora, A Calabresi, L Franceschini, G Ravazzolo, R Calandra, S
Citation: S. Bertolini et al., A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease, ATHEROSCLER, 154(3), 2001, pp. 599-605
Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction
Authors: De Giorgio, R Seri, M Cogliandro, RF Cusano, R Fava, M Caroli, F Panetta, D Forabosco, P Barbara, G Ravazzolo, R Ceccherini, R Corinaldesi, R Stanghellini, V
Citation: R. De Giorgio et al., Analysis of candidate genes for intrinsic neuropathy in a family with chronic idiopathic intestinal pseudo-obstruction, CLIN GENET, 59(2), 2001, pp. 131-133
A novel human homologue of the SH3BGR gene encodes a small protein similarto glutaredoxin 1 of Escherichia coli
Authors: Mazzocco, M Arrigo, P Egeo, A Maffei, M Vergano, A Di Lisi, R Ghiotto, F Ciccone, E Cinti, R Ravazzolo, R Scartezzini, P
Citation: M. Mazzocco et al., A novel human homologue of the SH3BGR gene encodes a small protein similarto glutaredoxin 1 of Escherichia coli, BIOC BIOP R, 285(2), 2001, pp. 540-545
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
Authors: Seri, M Cusano, R Gangarossa, S Caridi, G Bordo, D Lo Nigro, C Ghiggeri, GM Ravazzolo, R Savino, M Del Vecchio, M d'Apolito, M Iolascon, A Zelante, LL Savoia, A Balduini, CL Noris, P Magrini, U Belletti, S
Citation: M. Seri et al., Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes, NAT GENET, 26(1), 2000, pp. 103-105
cDNA sequence and genomic structure of the rat RET proto-oncogene
Authors: Matera, I Miguel-Rodriguez, MD Fernandez-Santos, JM Santamaria, G Puliti, A Ravazzolo, R Romeo, G Galera-Davidson, H Ceccherini, I
Citation: I. Matera et al., cDNA sequence and genomic structure of the rat RET proto-oncogene, DNA SEQ, 11(5), 2000, pp. 405-417
Total anonychia congenita in a woman with normal intelligence: Report of afurther case
Authors: Priolo, M Rosaia, L Seri, M Silengo, MC Ravazzolo, R Lerone, M
Citation: M. Priolo et al., Total anonychia congenita in a woman with normal intelligence: Report of afurther case, DERMATOLOGY, 200(1), 2000, pp. 84-85
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease
Authors: Griseri, P Sancandi, M Patrone, G Bocciardi, R Hofstra, R Ravazzolo, R Devoto, M Romeo, G Ceccherini, I
Citation: P. Griseri et al., A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease, EUR J HUM G, 8(9), 2000, pp. 721-724
Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13
Authors: Cusano, R Gangarossa, S Forabosco, P Caridi, G Ghiggeri, GM Russo, G Iolascon, A Ravazzolo, R Seri, M
Citation: R. Cusano et al., Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13, EUR J HUM G, 8(11), 2000, pp. 895-899
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2
Authors: Lo Nigro, C Cusano, R Scaranari, M Cinti, R Forabosco, P Morra, VB De Michele, G Santoro, L Davies, S Hurst, J Devoto, M Ravazzolo, R Seri, M
Citation: C. Lo Nigro et al., A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2, EUR J HUM G, 8(10), 2000, pp. 777-782
From developmental biology to dysmorphology
Authors: Ravazzolo, R Cossu, G Hennekam, RCM
Citation: R. Ravazzolo et al., From developmental biology to dysmorphology, EUR J HUM G, 8(10), 2000, pp. 813-813
Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?
Authors: Priolo, M Lerone, M Rosaia, L Calcagno, EP Sadeghi, AK Ghezzi, F Ravazzolo, R Silengo, M
Citation: M. Priolo et al., Question mark ears, temporo-mandibular joint malformation and hypotonia: auriculo-condylar syndrome or a distinct entity?, CLIN DYSMOR, 9(4), 2000, pp. 277-280
Characterization of a DNA binding site that mediates the stimulatory effect of cyclosporin-A on type III collagen expression in renal cells
Authors: Oleggini, R Musante, L Menoni, S Botti, G Di Duca, M Prudenziati, M Carrea, A Ravazzolo, R Ghiggeri, GM
Citation: R. Oleggini et al., Characterization of a DNA binding site that mediates the stimulatory effect of cyclosporin-A on type III collagen expression in renal cells, NEPH DIAL T, 15(6), 2000, pp. 778-785
Nuclear run-on assay using biotin labeling, magnetic bead capture and analysis by fluorescence-based RT-PCR
Authors: Patrone, G Puppo, F Cusano, R Scaranari, M Ceccherini, I Puliti, A Ravazzolo, R
Citation: G. Patrone et al., Nuclear run-on assay using biotin labeling, magnetic bead capture and analysis by fluorescence-based RT-PCR, BIOTECHNIQU, 29(5), 2000, pp. 1012
A DNA element in the alpha 1 type III collagen promoter mediates a stimulatory response by angiotensin II
Authors: Ghiggeri, GM Oleggini, R Musante, L Caridi, G Gusmano, R Ravazzolo, R
Citation: Gm. Ghiggeri et al., A DNA element in the alpha 1 type III collagen promoter mediates a stimulatory response by angiotensin II, KIDNEY INT, 58(2), 2000, pp. 537-548
Genetic polymorphism of the renin-angiotensin system and organ damage in essential hypertension
Authors: Pontremoli, R Ravera, M Viazzi, F Nicolella, C Berruti, V Leoncini, G Giacopelli, F Bezante, GP Sacchi, G Ravazzolo, R Deferrari, G
Citation: R. Pontremoli et al., Genetic polymorphism of the renin-angiotensin system and organ damage in essential hypertension, KIDNEY INT, 57(2), 2000, pp. 561-569
Lysyl oxidase activates the transcription activity of human collagene III promoter - Possible involvement of Ku antigen
Authors: Giampuzzi, M Botti, G Di Duca, M Arata, L Ghiggeri, G Gusmano, R Ravazzolo, R Di Donato, A
Citation: M. Giampuzzi et al., Lysyl oxidase activates the transcription activity of human collagene III promoter - Possible involvement of Ku antigen, J BIOL CHEM, 275(46), 2000, pp. 36341-36349
Adenovirus EIA down-regulates the EGF receptor via repression of its promoter
Authors: Prudenziati, M Sirito, M van Dam, H Ravazzolo, R
Citation: M. Prudenziati et al., Adenovirus EIA down-regulates the EGF receptor via repression of its promoter, INT J CANC, 88(6), 2000, pp. 943-948
Ectodermal dysplasias: not only 'skin' deep
Authors: Priolo, M Silengo, M Lerone, M Ravazzolo, R
Citation: M. Priolo et al., Ectodermal dysplasias: not only 'skin' deep, CLIN GENET, 58(6), 2000, pp. 415-430
Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene
Authors: Priolo, M Lerone, M Baffico, M Baldi, M Ravazzolo, R Cama, A Capra, V Silengo, M
Citation: M. Priolo et al., Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene, CLIN GENET, 58(1), 2000, pp. 81-83
Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome
Authors: Seri, M Melchionda, S Dreyer, S Marini, M Carella, M Cusano, R Piemontese, MR Caroli, F Silengo, M Zelante, L Romeo, G Ravazzolo, R Gasparini, P Lee, B
Citation: M. Seri et al., Identification of LMX1B gene point mutations in Italian patients affected with Nail-Patella syndrome, INT J MOL M, 4(3), 1999, pp. 285-290
Intron 16 insertion of the angiotensin converting enzyme gene and transcriptional regulation
Authors: Rosatto, N Pontremoli, R De Ferrari, G Ravazzolo, R
Citation: N. Rosatto et al., Intron 16 insertion of the angiotensin converting enzyme gene and transcriptional regulation, NEPH DIAL T, 14(4), 1999, pp. 868-871
Risultati: 1-25 | 26-27