Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Rossella Costantini"'
Autor:
Mattia Capulli, Rossella Costantini, Stephan Sonntag, Antonio Maurizi, Chiara Paganini, Luca Monti, Antonella Forlino, Doron Shmerling, Anna Teti, Antonio Rossi
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0213660 (2019)
The Cre-mediated genetic switch combines the ability of Cre recombinase to stably invert or excise a DNA fragment depending upon the orientation of flanking mutant loxP sites. In this work, we have tested this strategy in vivo with the aim to generat
Externí odkaz:
https://doaj.org/article/e2956b0ee85849c0bafe31a68df845d8
Autor:
Katarzyna A. Piróg, Valérie Cormier-Daire, Céline Huber, Silvia Lecci, Luca Monti, Jean-Marc Schwartz, Marco Biggiogera, Beth G Gibson, Rossella Costantini, Kun Tian, Chiara Paganini, Roberta Besio, Antonio Rossi, Antonella Forlino
Publikováno v:
Paganini, C, Monti, L, Costantini, R, Besio, R, Lecci, S, Biggiogera, M, Tian, K, Schwartz, J-M, Huber, C, Cormier-Daire, V, Gibson, B G, Pirog, K A, Forlino, A & Rossi, A 2019, ' Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification ', Matrix biology : journal of the International Society for Matrix Biology, vol. 81, pp. 70-90 . https://doi.org/10.1016/j.matbio.2018.11.002
Matrix Biology
Matrix Biology
Desbuquois dysplasia type 1 (DBQD1) is a chondrodysplasia caused by mutations in CANT1 gene encoding an ER/Golgi calcium activated nucleotidase 1 that hydrolyses UDP. Here, using Cant1 knock-in and knock-out mice recapitulating DBQD1 phenotype, we re
Publikováno v:
The FEBS Journal. 286:3008-3032
Glycosaminoglycans (GAGs) are a heterogeneous family of linear polysaccharides that constitute the carbohydrate moiety covalently attached to the protein core of proteoglycans, macromolecules present on the cell surface and in the extracellular matri
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1952
Experimental protocols for the synthesis and secretion of proteoglycans in cell culture models are important to study specific biosynthetic steps or disorders in which a defect in proteoglycans is expected. We describe a method using
Autor:
Luca Monti, Doron Shmerling, Stephan Sonntag, Anna Teti, Antonio Maurizi, Rossella Costantini, Antonio Rossi, Antonella Forlino, Chiara Paganini, Mattia Capulli
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 3, p e0213660 (2019)
PLoS ONE, 14 (3)
PLoS ONE, Vol 14, Iss 3, p e0213660 (2019)
PLoS ONE, 14 (3)
The Cre-mediated genetic switch combines the ability of Cre recombinase to stably invert or excise a DNA fragment depending upon the orientation of flanking mutant loxP sites. In this work, we have tested this strategy in vivo with the aim to generat
Publikováno v:
The Extracellular Matrix ISBN: 9781493991327
Experimental protocols for the synthesis and secretion of proteoglycans in cell culture models are important to study specific biosynthetic steps or disorders in which a defect in proteoglycans is expected. We describe a method using 35S-sulfate to m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26d4711eecd157fd6af0b16df86de3a7
https://doi.org/10.1007/978-1-4939-9133-4_6
https://doi.org/10.1007/978-1-4939-9133-4_6
Autor:
Shuhei Yamada, Antonio Rossi, Nikolaus Janocha, Ekkehart Lausch, Sheila Unger, Andrea Superti-Furga, Shiro Ikegawa, Andreas R. Janecke, Rainer Seidl, Rudolf Ganger, Shuji Mizumoto, Thomas Müller, Rossella Costantini, Julia Vodopiutz, Susanne Greber-Platzer, Bernd Jilma, Kazuyuki Sugahara
Publikováno v:
Human Mutation. 38:34-38
Mutations in genes encoding enzymes responsible for the biosynthesis and structural diversity of glycosaminoglycans (GAGs) cause a variety of disorders affecting bone and connective tissues, including Desbuquois dysplasia (DD). In an infant with pren
Autor:
Julia, Vodopiutz, Shuji, Mizumoto, Ekkehart, Lausch, Antonio, Rossi, Sheila, Unger, Nikolaus, Janocha, Rossella, Costantini, Rainer, Seidl, Susanne, Greber-Platzer, Shuhei, Yamada, Thomas, Müller, Bernd, Jilma, Rudolf, Ganger, Andrea, Superti-Furga, Shiro, Ikegawa, Kazuyuki, Sugahara, Andreas R, Janecke
Publikováno v:
Human mutation. 38(1)
Mutations in genes encoding enzymes responsible for the biosynthesis and structural diversity of glycosaminoglycans (GAGs) cause a variety of disorders affecting bone and connective tissues, including Desbuquois dysplasia (DD). In an infant with pren
Autor:
Silvia Lecci, Silvia Maruelli, Marco Biggiogera, Valérie Cormier-Daire, Luca Monti, Chiara Paganini, Antonio Rossi, Antonella Forlino, Rossella Costantini
Publikováno v:
Bone Abstracts.