Lucarini L - Search Results

1

Adenosine A₃ Receptor (A₃AR) Agonist for the Treatment of Bleomycin-Induced Lung Fibrosis in Mice.

Sgambellone S, Marri S, Catarinicchia S, Pini A, Tosh DK, Jacobson KA, Masini E, Salvemini D, Lucarini L. Sgambellone S, et al. Among authors: lucarini l. Int J Mol Sci. 2022 Nov 1;23(21):13300. doi: 10.3390/ijms232113300. Int J Mol Sci. 2022. PMID: 36362112 Free PMC article.

2

Fibroblast autofluorescence in connective tissue disorders: a future tool for clinical and differential diagnosis?

Monici M, Basile V, Romano G, Evangelisti L, Lucarini L, Attanasio M, Bertini E, Fusi F, Gensini GF, Pepe G. Monici M, et al. Among authors: lucarini l. J Biomed Opt. 2008 Sep-Oct;13(5):054025. doi: 10.1117/1.2982533. J Biomed Opt. 2008. PMID: 19021405 Free article.

3

PPARgamma promoter polymorphisms and acute coronary syndrome.

Evangelisti L, Attanasio M, Lucarini L, Sofi F, Marcucci R, Giglioli C, Valente S, Gensini G, Abbate R, Pepe G. Evangelisti L, et al. Among authors: lucarini l. Atherosclerosis. 2009 Jul;205(1):186-91. doi: 10.1016/j.atherosclerosis.2008.11.009. Epub 2008 Nov 18. Atherosclerosis. 2009. PMID: 19117570

4

May TGFBR1 act also as low penetrance allele in Marfan syndrome?

Lucarini L, Evangelisti L, Attanasio M, Lapini I, Chiarini F, Porciani MC, Abbate R, Gensini G, Pepe G. Lucarini L, et al. Int J Cardiol. 2009 Jan 9;131(2):281-4. doi: 10.1016/j.ijcard.2007.07.048. Epub 2007 Oct 22. Int J Cardiol. 2009. PMID: 17936924

5

A single heterozygous nucleotide substitution displays two different altered mechanisms in the FBN1 gene of five Italian Marfan patients.

Evangelisti L, Lucarini L, Attanasio M, Lapini I, Giusti B, Porciani C, Gensini GF, Abbate R, Pepe G. Evangelisti L, et al. Among authors: lucarini l. Eur J Med Genet. 2010 Sep-Oct;53(5):299-302. doi: 10.1016/j.ejmg.2010.06.002. Epub 2010 Jun 9. Eur J Med Genet. 2010. PMID: 20538085

6

Is ectopia lentis in some cases a mild phenotypic expression of Marfan syndrome? Need for a long-term follow-up.

Pepe G, Lapini I, Evangelisti L, Attanasio M, Giusti B, Lucarini L, Fattori R, Pellicanò G, Scrivanti M, Porciani MC, Abbate R, Gensini GF. Pepe G, et al. Among authors: lucarini l. Mol Vis. 2007 Nov 29;13:2242-7. Mol Vis. 2007. PMID: 18087243

7

Cytokine gene expression and production by human LPS-stimulated mononuclear cells are inhibited by sulfated heparin-like semi-synthetic derivatives.

Gori AM, Attanasio M, Gazzini A, Rossi L, Lucarini L, Miletti S, Chini J, Manoni M, Abbate R, Gensini GF. Gori AM, et al. Among authors: lucarini l. J Thromb Haemost. 2004 Sep;2(9):1657-62. doi: 10.1111/j.1538-7836.2004.00866.x. J Thromb Haemost. 2004. PMID: 15333044 Free article.

8

FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.

Attanasio M, Lapini I, Evangelisti L, Lucarini L, Giusti B, Porciani M, Fattori R, Anichini C, Abbate R, Gensini G, Pepe G. Attanasio M, et al. Among authors: lucarini l. Clin Genet. 2008 Jul;74(1):39-46. doi: 10.1111/j.1399-0004.2008.01007.x. Epub 2008 Apr 22. Clin Genet. 2008. PMID: 18435798

9

Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis.

Petrini S, D'Amico A, Sale P, Lucarini L, Sabatelli P, Tessa A, Giusti B, Verardo M, Carrozzo R, Mattioli E, Scarpelli M, Chu ML, Pepe G, Russo MA, Bertini E. Petrini S, et al. Among authors: lucarini l. Neuromuscul Disord. 2007 Aug;17(8):587-96. doi: 10.1016/j.nmd.2007.04.010. Epub 2007 Jun 27. Neuromuscul Disord. 2007. PMID: 17588753

10

ACE and TGFBR1 genes interact in influencing the susceptibility to abdominal aortic aneurysm.

Lucarini L, Sticchi E, Sofi F, Pratesi G, Pratesi C, Pulli R, Gensini GF, Abbate R, Pepe G, Fatini C. Lucarini L, et al. Atherosclerosis. 2009 Jan;202(1):205-10. doi: 10.1016/j.atherosclerosis.2008.04.038. Epub 2008 Apr 29. Atherosclerosis. 2009. PMID: 18550062

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