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Diastrophic dysplasia sulfate transporter (DTDST) gene is not involved in pseudodiastrophic dysplasia 1-gen-1997 Cetta, Giuseppe; Rossi, Antonio; Beluffi, G.; Burgio, G. R.
Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2 1-gen-1997 Rossi, Antonio; Bonaventure, J.; Delezoide, A. L.; SUPERTI FURGA, A.; Cetta, Giuseppe
Stability of type I collagen peptide trimers. 1-gen-1997 Rossi, Antonio; Zanaboni, Giuseppe; Cetta, Giuseppe; Tenni, Ruggero
Lung injury and degradation of extracellular matrix components by Aspergillus fumigatus serine proteinase 1-gen-1998 Iadarola, Paolo; Lungarella, G.; Martorana, P. A.; Viglio, Simona; Guglielminetti, MARIA LIDIA; Korzus, E.; Gorrini, M.; Cavarra, E.; Rossi, Antonio; Travis, J.; Luisetti, Maurizio
Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production 1-gen-1998 Rossi, Antonio; Kaitila, I.; Wilcox, W. R.; Rimoin, D. L.; Steinmann, B.; Cetta, Giuseppe; SUPERTI FURGA, A.
EXT 1 gene mutation induces chondrocyte cytoskeletal abnormalities and collagen expression in the exostoses. 1-gen-2000 LEGEAI MALLET, L.; Rossi, Antonio; BENOIST LASSELIN, C.; Piazza, ROCCO GIOVANNI; Mallet, J. F.; Delezoide, A. L.; Munnich, A.; Bonaventure, J.; Zylberberg, L.
Stability and networks of hydrogen bonds of the collagen triple helical structure: influence of pH and chaotropic nature of three anions. 1-gen-2000 Zanaboni, Giuseppe; Rossi, Antonio; A. M., Tina Onana; Tenni, Ruggero
Mutations in the diastrophic dysplasia sulfate transporter (DTDST) gene (SLC26A2): 22 novel mutations, mutation review, associated skeletal phenotypes and diagnostic relevance. 1-gen-2001 Rossi, Antonio; SUPERTI FURGA, A.
New dysplasia or achondrogenesis type 1 B? The importance of histology and molecular biology in delineating skeletal dysplasias. 1-gen-2001 Unger, S; LE MERRER, M.; Meinecke, P.; Chitayat, D.; Rossi, Antonio; SUPERTI FURGA, A.
Infantile systemic hyalinosis in siblings: clinical report, biochemical and ultrastructural findings, and review of the literature. 1-gen-2001 Stucki, U.; Spycher, M. A.; Eich, G.; Rossi, Antonio; Sacher, P.; Steinmann, B.; SUPERTI FURGA, A.
A nucleotide insertion and frameshift cause albumin Kenitra, an extended and O-glycosylated mutant of human serum albumin with two additional disulfide bridges. 1-gen-2001 Minchiotti, Lorenzo; Campagnoli, Monica; Rossi, Antonio; Cosulich, MARIA ELISABETTA; Galliano, Monica; Monti, M; Pucci, P; Kragh Hansen, U.; Granel, B; Disdier, P; Weiller, P. j.
Interaction of decorin with CNBr peptides from collagens I and II. Evidence for multiple binding sites and essential lysyl residues in collagen 1-gen-2002 Tenni, Ruggero; Viola, Manuela; Welser, F.; Sini, P.; Giudici, Camilla; Rossi, Antonio; Tira, MARIA ENRICA
A novel splicing mutation causes an undescribed type of analbuminemia. 1-gen-2002 Campagnoli, Monica; Rossi, Antonio; Palmqvist, L; Flisberg, A; Niklasson, A; Minchiotti, Lorenzo; Galliano, Monica
Molecular diagnosis of analbuminemia: A novel mutation identified in two amerindian and two Turkish families 1-gen-2002 Galliano, Monica; Campagnoli, Monica; Rossi, Antonio; WIRSING VON KONIG, C. H.; Lyon, A. W.; Cefle, K.; Yildiz, A.; Palanduz, S.; Ozturk, S.; Minchiotti, Lorenzo
In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias 1-gen-2003 Rossi, Antonio; Cetta, Giuseppe; Piazza, ROCCO GIOVANNI; Bonaventure, J.; Steinmann, B.; SUPERTI FURGA, A.
Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts 1-gen-2003 Lupi, ANNA LISA; DELLA TORRE, Sara; Rossi, Antonio; Cetta, Giuseppe; Forlino, Antonella
Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship. 1-gen-2004 Lupi, ANNA LISA; De Riso, A; DELLA TORRE, Sara; Rossi, Antonio; Campari, Elena; Vilarinho, L; Cetta, Giuseppe; Forlino, Antonella
Novel nonsense mutation causes analbuminemia in a Moroccan family. 1-gen-2005 Campagnoli, Monica; Sala, Alberto; Romano, Assunta; Rossi, Antonio; Nauta, J.; Koot, B. G.; Minchiotti, Lorenzo; Galliano, Monica
A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype 1-gen-2005 Forlino, Antonella; Piazza, ROCCO GIOVANNI; Tiveron, C.; Torre, S. D.; Tatangelo, L.; Bonafe, L.; Gualeni, Benedetta; Romano, Assunta; Pecora, Fabio; SUPERTI FURGA, A.; Cetta, Giuseppe; Rossi, Antonio
N-benzyloxycarbonyl-L-proline: an in vitro inhibitor of prolidase. 1-gen-2005 Lupi, ANNA LISA; Rossi, Antonio; Vaghi, Patrizia; Gallanti, Angelo; Cetta, Giuseppe; Forlino, Antonella
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