Colombi M - Search Results

1

Skeletal fragility: an emerging complication of Ehlers-Danlos syndrome.

Formenti AM, Doga M, Frara S, Ritelli M, Colombi M, Banfi G, Giustina A. Formenti AM, et al. Among authors: colombi m. Endocrine. 2019 Feb;63(2):225-230. doi: 10.1007/s12020-018-1822-y. Epub 2018 Dec 15. Endocrine. 2019. PMID: 30554346

2

Phenotypic correction of the defective fibronectin extracellular matrix of Ehlers-Danlos syndrome fibroblasts.

Barlati S, Moro L, Gardella R, Colombi M. Barlati S, et al. Among authors: colombi m. Cell Biol Int Rep. 1991 Dec;15(12):1183-94. doi: 10.1016/0309-1651(91)90090-6. Cell Biol Int Rep. 1991. PMID: 1802403

3

Altered fibronectin mRNA splicing in skin fibroblasts from Ehlers-Danlos syndrome patients: in situ hybridization analysis.

Colombi M, Moro L, Zoppi N, Ghinelli A, Barlati S. Colombi M, et al. Cell Biol Int Rep. 1991 Dec;15(12):1195-206. doi: 10.1016/0309-1651(91)90091-v. Cell Biol Int Rep. 1991. PMID: 1802404

4

Correction of the defective extracellular matrix of Ehlers-Danlos syndrome skin fibroblasts by dexamethasone.

Moro L, Colombi M, Zoppi N, Ghinelli A, Barlati S. Moro L, et al. Among authors: colombi m. Cell Biol Int. 1994 Jan;18(1):29-37. doi: 10.1006/cbir.1994.1004. Cell Biol Int. 1994. PMID: 8186768

5

Effect of dexamethasone on the assembly of the matrix of fibronectin and on its receptors organization in Ehlers-Danlos syndrome skin fibroblasts.

Zoppi N, Ghinelli A, Gardella R, Barlati S, Colombi M. Zoppi N, et al. Among authors: colombi m. Cell Biol Int. 1998;22(7-8):499-508. doi: 10.1006/cbir.1998.0283. Cell Biol Int. 1998. PMID: 10452818

6

The FN13 peptide inhibits human tumor cells invasion through the modulation of alpha v beta 3 integrins organization and the inactivation of ILK pathway.

Zoppi N, Ritelli M, Salvi A, Colombi M, Barlati S. Zoppi N, et al. Among authors: colombi m. Biochim Biophys Acta. 2007 Jun;1773(6):747-63. doi: 10.1016/j.bbamcr.2007.02.007. Epub 2007 Feb 24. Biochim Biophys Acta. 2007. PMID: 17383746 Free article.

7

Arterial tortuosity syndrome in two Italian paediatric patients.

Ritelli M, Drera B, Vicchio M, Puppini G, Biban P, Pilati M, Prioli MA, Barlati S, Colombi M. Ritelli M, et al. Among authors: colombi m. Orphanet J Rare Dis. 2009 Sep 25;4:20. doi: 10.1186/1750-1172-4-20. Orphanet J Rare Dis. 2009. PMID: 19781076 Free PMC article.

8

Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.

Drera B, Ritelli M, Zoppi N, Wischmeijer A, Gnoli M, Fattori R, Calzavara-Pinton PG, Barlati S, Colombi M. Drera B, et al. Among authors: colombi m. Orphanet J Rare Dis. 2009 Nov 2;4:24. doi: 10.1186/1750-1172-4-24. Orphanet J Rare Dis. 2009. PMID: 19883511 Free PMC article.

9

Palmoplantar keratoderma, pseudo-ainhum, and universal atrichia: A new patient and review of the palmoplantar keratoderma-congenital alopecia syndrome.

Castori M, Valiante M, Ritelli M, Preziosi N, Colombi M, Paradisi M, Grammatico P. Castori M, et al. Among authors: colombi m. Am J Med Genet A. 2010 Aug;152A(8):2043-7. doi: 10.1002/ajmg.a.33490. Am J Med Genet A. 2010. PMID: 20635335 Review.

10

Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio.

Chiarelli N, Ritelli M, Zoppi N, Benini A, Borsani G, Barlati S, Colombi M. Chiarelli N, et al. Among authors: colombi m. Int J Dev Biol. 2011;55(2):229-36. doi: 10.1387/ijdb.103179nc. Int J Dev Biol. 2011. PMID: 21553381 Free article.

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

290 results

Search Page

Filters