Cetta G - Search Results

1

Insights from a transgenic mouse model on the role of SLC26A2 in health and disease.

Forlino A, Gualeni B, Pecora F, Della Torre S, Piazza R, Tiveron C, Tatangelo L, Superti-Furga A, Cetta G, Rossi A. Forlino A, et al. Among authors: cetta g. Novartis Found Symp. 2006;273:193-206; discussion 206-12, 261-4. Novartis Found Symp. 2006. PMID: 17120769

2

A diastrophic dysplasia sulfate transporter (SLC26A2) mutant mouse: morphological and biochemical characterization of the resulting chondrodysplasia phenotype.

Forlino A, Piazza R, Tiveron C, Della Torre S, Tatangelo L, Bonafè L, Gualeni B, Romano A, Pecora F, Superti-Furga A, Cetta G, Rossi A. Forlino A, et al. Among authors: cetta g. Hum Mol Genet. 2005 Mar 15;14(6):859-71. doi: 10.1093/hmg/ddi079. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703192

3

In vivo contribution of amino acid sulfur to cartilage proteoglycan sulfation.

Pecora F, Gualeni B, Forlino A, Superti-Furga A, Tenni R, Cetta G, Rossi A. Pecora F, et al. Among authors: cetta g. Biochem J. 2006 Sep 15;398(3):509-14. doi: 10.1042/BJ20060566. Biochem J. 2006. PMID: 16719839 Free PMC article.

4

In vitro proteoglycan sulfation derived from sulfhydryl compounds in sulfate transporter chondrodysplasias.

Rossi A, Cetta G, Piazza R, Bonaventure J, Steinmann B, Supereti-Furga A. Rossi A, et al. Among authors: cetta g. Pediatr Pathol Mol Med. 2003 Jul-Aug;22(4):311-21. doi: 10.1080/pdp.22.4.311.321. Pediatr Pathol Mol Med. 2003. PMID: 14692227

5

A quantitative and qualitative method for direct 2-DE analysis of murine cartilage.

Pecora F, Forlino A, Gualeni B, Lupi A, Giorgetti S, Marchese L, Stoppini M, Tenni R, Cetta G, Rossi A. Pecora F, et al. Among authors: cetta g. Proteomics. 2007 Nov;7(21):4003-7. doi: 10.1002/pmic.200700276. Proteomics. 2007. PMID: 17960732

6

Defective proteoglycan sulfation of the growth plate zones causes reduced chondrocyte proliferation via an altered Indian hedgehog signalling.

Gualeni B, Facchini M, De Leonardis F, Tenni R, Cetta G, Viola M, Passi A, Superti-Furga A, Forlino A, Rossi A. Gualeni B, et al. Among authors: cetta g. Matrix Biol. 2010 Jul;29(6):453-60. doi: 10.1016/j.matbio.2010.05.001. Epub 2010 May 11. Matrix Biol. 2010. PMID: 20470884

7

Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for an L483P substitution in the diastrophic dysplasia sulfate transporter.

Rossi A, Bonaventure J, Delezoide AL, Cetta G, Superti-Furga A. Rossi A, et al. Among authors: cetta g. J Biol Chem. 1996 Aug 2;271(31):18456-64. doi: 10.1074/jbc.271.31.18456. J Biol Chem. 1996. PMID: 8702490 Free article.

8

Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2.

Rossi A, Bonaventure J, Delezoide AL, Superti-Furga A, Cetta G. Rossi A, et al. Among authors: cetta g. Eur J Biochem. 1997 Sep 15;248(3):741-7. doi: 10.1111/j.1432-1033.1997.t01-1-00741.x. Eur J Biochem. 1997. PMID: 9342225 Free article.

9

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.

Rossi A, Kaitila I, Wilcox WR, Rimoin DL, Steinmann B, Cetta G, Superti-Furga A. Rossi A, et al. Among authors: cetta g. Matrix Biol. 1998 Oct;17(5):361-9. doi: 10.1016/s0945-053x(98)90088-9. Matrix Biol. 1998. PMID: 9822202

10

Optimization of a capillary electrophoretic method to detect and quantify the Gly-Pro dipeptide in complex matrices from long term cultured prolidase deficiency fibroblasts.

Lupi A, Della Torre S, Rossi A, Cetta G, Forlino A. Lupi A, et al. Among authors: cetta g. J Chromatogr B Analyt Technol Biomed Life Sci. 2003 Sep 25;795(1):133-9. doi: 10.1016/s1570-0232(03)00547-6. J Chromatogr B Analyt Technol Biomed Life Sci. 2003. PMID: 12957177

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