Colombi M - Search Results

1

GLUT10-Lacking in Arterial Tortuosity Syndrome-Is Localized to the Endoplasmic Reticulum of Human Fibroblasts.

Gamberucci A, Marcolongo P, Németh CE, Zoppi N, Szarka A, Chiarelli N, Hegedűs T, Ritelli M, Carini G, Willaert A, Callewaert BL, Coucke PJ, Benedetti A, Margittai É, Fulceri R, Bánhegyi G, Colombi M. Gamberucci A, et al. Among authors: colombi m. Int J Mol Sci. 2017 Aug 22;18(8):1820. doi: 10.3390/ijms18081820. Int J Mol Sci. 2017. PMID: 28829359 Free PMC article.

2

Exclusion of stromelysin-1, stromelysin-2, interstitial collagenase and fibronectin genes as the mutant loci in a family with recessive epidermolysis bullosa dystrophica and a form of cerebellar ataxia.

Colombi M, Gardella R, Zoppi N, Moro L, Marini D, Spurr NK, Barlati S. Colombi M, et al. Hum Genet. 1992 Jul;89(5):503-7. doi: 10.1007/BF00219174. Hum Genet. 1992. PMID: 1353052

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

Angiokeratoma corporis diffusum and arteriovenous fistulas with dominant transmission in the absence of metabolic disorders.

Calzavara-Pinton PG, Colombi M, Carlino A, Zane C, Gardella R, Clemente M, Facchetti F, Moro L, Zoppi N, Caimi L, et al. Calzavara-Pinton PG, et al. Among authors: colombi m. Arch Dermatol. 1995 Jan;131(1):57-62. Arch Dermatol. 1995. PMID: 7826098

5

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

6

Quantitative evaluation of mRNAs by in situ hybridization and image analysis: principles and applications.

Colombi M, Moro L, Zoppi N, Barlati S. Colombi M, et al. DNA Cell Biol. 1993 Sep;12(7):629-36. doi: 10.1089/dna.1993.12.629. DNA Cell Biol. 1993. PMID: 8397821

7

Identification of two splicing mutations in the collagen type VII gene (COL7A1) of a patient affected by the localisata variant of recessive dystrophic epidermolysis bullosa.

Gardella R, Belletti L, Zoppi N, Marini D, Barlati S, Colombi M. Gardella R, et al. Among authors: colombi m. Am J Hum Genet. 1996 Aug;59(2):292-300. Am J Hum Genet. 1996. PMID: 8755915 Free PMC article.

8

Three homozygous PTC mutations in the collagen type VII gene of patients affected by recessive dystrophic epidermolysis bullosa: analysis of transcript levels in dermal fibroblasts.

Gardella R, Zoppi N, Ferraboli S, Marini D, Tadini G, Barlati S, Colombi M. Gardella R, et al. Among authors: colombi m. Hum Mutat. 1999;13(6):439-52. doi: 10.1002/(SICI)1098-1004(1999)13:6<439::AID-HUMU3>3.0.CO;2-N. Hum Mutat. 1999. PMID: 10408773

9

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

10

Quantitative in situ hybridization for the evaluation of gene expression in asynchronous and synchronized cell cultures and in tissue sections.

Barlati S, Zoppi N, Copeta A, Tavian D, De Petro G, Colombi M. Barlati S, et al. Among authors: colombi m. Histol Histopathol. 1999 Oct;14(4):1231-40. doi: 10.14670/HH-14.1231. Histol Histopathol. 1999. PMID: 10506939 Review.

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