Rossi A - Search Results

1

Improved prolidase activity assay allowed enzyme kinetic characterization and faster prolidase deficiency diagnosis.

Besio R, Monzani E, Gioia R, Nicolis S, Rossi A, Casella L, Forlino A. Besio R, et al. Among authors: rossi a. Clin Chim Acta. 2011 Sep 18;412(19-20):1814-20. doi: 10.1016/j.cca.2011.06.011. Epub 2011 Jun 15. Clin Chim Acta. 2011. PMID: 21699887

2

Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chain.

Valli M, Sangalli A, Rossi A, Mottes M, Forlino A, Tenni R, Pignatti PF, Cetta G. Valli M, et al. Among authors: rossi a. Eur J Biochem. 1993 Feb 1;211(3):415-9. doi: 10.1111/j.1432-1033.1993.tb17565.x. Eur J Biochem. 1993. PMID: 7679635 Free article.

3

Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta.

Cetta G, Rossi A, Tenni R, Valli M, Forlino A, Zanaboni G, Dyne K, Burgio GR. Cetta G, et al. Among authors: rossi a. Connect Tissue Res. 1993;29(1):41-9. doi: 10.3109/03008209309061965. Connect Tissue Res. 1993. PMID: 8339545

4

Extracellular matrix deposition in cultured dermal fibroblasts from four probands affected by osteogenesis imperfecta.

Valli M, Rossi A, Forlino A, Tenni R, Cetta G. Valli M, et al. Among authors: rossi a. Matrix. 1993 Jul;13(4):275-80. doi: 10.1016/s0934-8832(11)80022-3. Matrix. 1993. PMID: 8412984

5

Type I collagen CNBr peptides: species and behavior in solution.

Rossi A, Zuccarello LV, Zanaboni G, Monzani E, Dyne KM, Cetta G, Tenni R. Rossi A, et al. Biochemistry. 1996 May 14;35(19):6048-57. doi: 10.1021/bi9518151. Biochemistry. 1996. PMID: 8634246

6

Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients.

Zanaboni G, Grimm R, Dyne KM, Rossi A, Cetta G, Iadarola P. Zanaboni G, et al. Among authors: rossi a. J Chromatogr B Biomed Appl. 1996 Aug 9;683(1):97-107. doi: 10.1016/0378-4347(95)00583-8. J Chromatogr B Biomed Appl. 1996. PMID: 8876444

7

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: rossi a. 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

8

Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship.

Lupi A, De Riso A, Torre SD, Rossi A, Campari E, Vilarinho L, Cetta G, Forlino A. Lupi A, et al. Among authors: rossi a. J Hum Genet. 2004;49(9):500-506. doi: 10.1007/s10038-004-0180-1. Epub 2004 Aug 11. J Hum Genet. 2004. PMID: 15309682

9

Prolidase deficiency: biochemical study of erythrocyte and skin fibroblast prolidase activity in Italian patients.

Zanaboni G, Dyne KM, Rossi A, Monafo V, Cetta G. Zanaboni G, et al. Among authors: rossi a. Haematologica. 1994 Jan-Feb;79(1):13-8. Haematologica. 1994. PMID: 15378943

10

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: rossi a. 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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

7,239 results

Search Page

Filters