Zambruno G - Search Results

1

Human melanoma cells secrete and respond to placenta growth factor and vascular endothelial growth factor.

Lacal PM, Failla CM, Pagani E, Odorisio T, Schietroma C, Falcinelli S, Zambruno G, D'Atri S. Lacal PM, et al. Among authors: zambruno g. J Invest Dermatol. 2000 Dec;115(6):1000-7. doi: 10.1046/j.1523-1747.2000.00199.x. J Invest Dermatol. 2000. PMID: 11121133 Free article.

2

Expression of B7 costimulatory molecule in cultured human epidermal Langerhans cells is regulated at the mRNA level.

Girolomoni G, Zambruno G, Manfredini R, Zacchi V, Ferrari S, Cossarizza A, Giannetti A. Girolomoni G, et al. Among authors: zambruno g. J Invest Dermatol. 1994 Jul;103(1):54-9. doi: 10.1111/1523-1747.ep12389619. J Invest Dermatol. 1994. PMID: 7517982 Free article.

3

Functional intercellular adhesion molecule-3 is expressed by freshly isolated epidermal Langerhans cells and is not regulated during culture.

Zambruno G, Cossarizza A, Zacchi V, Ottani D, Luppi AM, Giannetti A, Girolomoni G. Zambruno G, et al. J Invest Dermatol. 1995 Aug;105(2):215-9. doi: 10.1111/1523-1747.ep12317494. J Invest Dermatol. 1995. PMID: 7636303 Free article.

4

Involvement of the mismatch repair system in temozolomide-induced apoptosis.

D'Atri S, Tentori L, Lacal PM, Graziani G, Pagani E, Benincasa E, Zambruno G, Bonmassar E, Jiricny J. D'Atri S, et al. Among authors: zambruno g. Mol Pharmacol. 1998 Aug;54(2):334-41. doi: 10.1124/mol.54.2.334. Mol Pharmacol. 1998. PMID: 9687575

5

Compound heterozygosity for a recessive glycine substitution and a splice site mutation in the COL7A1 gene causes an unusually mild form of localized recessive dystrophic epidermolysis bullosa.

Terracina M, Posteraro P, Schubert M, Sonego G, Atzori F, Zambruno G, Bruckner-Tuderman L, Castiglia D. Terracina M, et al. Among authors: zambruno g. J Invest Dermatol. 1998 Nov;111(5):744-50. doi: 10.1046/j.1523-1747.1998.00397.x. J Invest Dermatol. 1998. PMID: 9804332 Free article.

6

Genomic structure, promoter characterisation and mutational analysis of the S100A7 gene: exclusion of a candidate for familial psoriasis susceptibility.

Semprini S, Capon F, Bovolenta S, Bruscia E, Pizzuti A, Fabrizi G, Schietroma C, Zambruno G, Dallapiccola B, Novelli G. Semprini S, et al. Among authors: zambruno g. Hum Genet. 1999 Feb;104(2):130-4. doi: 10.1007/s004390050925. Hum Genet. 1999. PMID: 10190323

7

Autoimmunity of the dermal-epidermal junction.

Zambruno G, Failla CM. Zambruno G, et al. Eur J Dermatol. 1999 Sep;9(6):437-42. Eur J Dermatol. 1999. PMID: 10491497 Review. No abstract available.

8

A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus.

Terrinoni A, Candi E, Oddi S, Gobello T, Camaione DB, Mazzanti C, Zambruno G, Knight R, Melino G. Terrinoni A, et al. Among authors: zambruno g. J Invest Dermatol. 2000 Feb;114(2):388-91. doi: 10.1046/j.1523-1747.2000.00890.x. J Invest Dermatol. 2000. PMID: 10652003 Free article.

9

Placenta growth factor is induced in human keratinocytes during wound healing.

Failla CM, Odorisio T, Cianfarani F, Schietroma C, Puddu P, Zambruno G. Failla CM, et al. Among authors: zambruno g. J Invest Dermatol. 2000 Sep;115(3):388-95. doi: 10.1046/j.1523-1747.2000.00085.x. J Invest Dermatol. 2000. PMID: 10951273 Free article.

10

A homozygous nonsense mutation in type XVII collagen gene (COL17A1) uncovers an alternatively spliced mRNA accounting for an unusually mild form of non-Herlitz junctional epidermolysis bullosa.

Ruzzi L, Pas H, Posteraro P, Mazzanti C, Didona B, Owaribe K, Meneguzzi G, Zambruno G, Castiglia D, D'Alessio M. Ruzzi L, et al. Among authors: zambruno g. J Invest Dermatol. 2001 Jan;116(1):182-7. doi: 10.1046/j.1523-1747.2001.00229.x. J Invest Dermatol. 2001. PMID: 11168815 Free article.

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