Covaciu C - Search Results

1

The increase in maternal expression of axin1 and axin2 contribute to the zebrafish mutant ichabod ventralized phenotype.

Valenti F, Ibetti J, Komiya Y, Baxter M, Lucchese AM, Derstine L, Covaciu C, Rizzo V, Vento R, Russo G, Macaluso M, Cotelli F, Castiglia D, Gottardi CJ, Habas R, Giordano A, Bellipanni G. Valenti F, et al. Among authors: covaciu c. J Cell Biochem. 2015 Mar;116(3):418-30. doi: 10.1002/jcb.24993. J Cell Biochem. 2015. PMID: 25335865

2

Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.

Covaciu C, Castori M, De Luca N, Ghirri P, Nannipieri A, Ragone G, Zambruno G, Castiglia D. Covaciu C, et al. Br J Dermatol. 2010 Jun;162(6):1384-7. doi: 10.1111/j.1365-2133.2010.09665.x. Epub 2010 Mar 10. Br J Dermatol. 2010. PMID: 20302579

3

A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicing.

Covaciu C, Grosso F, Pisaneschi E, Zambruno G, Gregersen PA, Sommerlund M, Hertz JM, Castiglia D. Covaciu C, et al. Br J Dermatol. 2011 Sep;165(3):678-82. doi: 10.1111/j.1365-2133.2011.10414.x. Epub 2011 Jul 28. Br J Dermatol. 2011. PMID: 21574979

4

MicroRNA-155 targets the SKI gene in human melanoma cell lines.

Levati L, Pagani E, Romani S, Castiglia D, Piccinni E, Covaciu C, Caporaso P, Bondanza S, Antonetti FR, Bonmassar E, Martelli F, Alvino E, D'Atri S. Levati L, et al. Among authors: covaciu c. Pigment Cell Melanoma Res. 2011 Jun;24(3):538-50. doi: 10.1111/j.1755-148X.2011.00857.x. Epub 2011 May 5. Pigment Cell Melanoma Res. 2011. PMID: 21466664

5

Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosis.

Castiglia D, Castori M, Pisaneschi E, Sommi M, Covaciu C, Zambruno G, Fischer J, Magnani C. Castiglia D, et al. Among authors: covaciu c. Clin Genet. 2009 Oct;76(4):392-7. doi: 10.1111/j.1399-0004.2009.01198.x. Epub 2009 Aug 3. Clin Genet. 2009. PMID: 19664001

6

Complete maternal isodisomy causing reduction to homozygosity for a novel LAMB3 mutation in Herlitz junctional epidermolysis bullosa.

Castori M, Floriddia G, Pisaneschi E, Covaciu C, Paradisi M, Torrente I, Castiglia D. Castori M, et al. Among authors: covaciu c. J Dermatol Sci. 2008 Jul;51(1):58-61. doi: 10.1016/j.jdermsci.2008.02.006. Epub 2008 Apr 1. J Dermatol Sci. 2008. PMID: 18387282 No abstract available.

7

The cyclin-dependent kinase inhibitor PHA-848125 suppresses the in vitro growth of human melanomas sensitive or resistant to temozolomide, and shows synergistic effects in combination with this triazene compound.

Caporali S, Alvino E, Starace G, Ciomei M, Brasca MG, Levati L, Garbin A, Castiglia D, Covaciu C, Bonmassar E, D'Atri S. Caporali S, et al. Among authors: covaciu c. Pharmacol Res. 2010 May;61(5):437-48. doi: 10.1016/j.phrs.2009.12.009. Epub 2009 Dec 21. Pharmacol Res. 2010. PMID: 20026273

8

A new SPINK5 donor splice site mutation in siblings with Netherton syndrome.

Tüysüz B, Ojalvo D, Mat C, Zambruno G, Covaciu C, Castiglia D, D'Alessio M. Tüysüz B, et al. Among authors: covaciu c. Acta Derm Venereol. 2010;90(1):95-6. doi: 10.2340/00015555-0769. Acta Derm Venereol. 2010. PMID: 20107740 Free article. No abstract available.

9

Clinical and genetic heterogeneity in keratosis follicularis spinulosa decalvans.

Castori M, Covaciu C, Paradisi M, Zambruno G. Castori M, et al. Among authors: covaciu c. Eur J Med Genet. 2009 Jan-Feb;52(1):53-8. doi: 10.1016/j.ejmg.2008.09.005. Epub 2008 Oct 17. Eur J Med Genet. 2009. PMID: 18984066

10

A rare cause of syndromic hypotrichosis: Nicolaides-Baraitser syndrome.

Castori M, Covaciu C, Rinaldi R, Grammatico P, Paradisi M. Castori M, et al. Among authors: covaciu c. J Am Acad Dermatol. 2008 Nov;59(5 Suppl):S92-8. doi: 10.1016/j.jaad.2008.05.016. J Am Acad Dermatol. 2008. PMID: 19119135

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