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normalicata
(1 results)?
A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy.
Brain Sci. 2021 Jan 16;11(1):115. doi: 10.3390/brainsci11010115.
Brain Sci. 2021.
PMID: 33467104
Free PMC article.
Effect of exercise on telomere length and telomere proteins expression in mdx mice.
Vita GL, Aguennouz M, Sframeli M, Sanarica F, Mantuano P, Oteri R, Polito F, Licata N, Romeo S, Distefano MG, La Rosa M, Bonanno C, Nicocia G, Vita G, De Luca A, Messina S.
Vita GL, et al. Among authors: licata n.
Mol Cell Biochem. 2020 Jul;470(1-2):189-197. doi: 10.1007/s11010-020-03761-3. Epub 2020 May 23.
Mol Cell Biochem. 2020.
PMID: 32447718
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Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice.
Messina S, Bitto A, Vita GL, Aguennouz M, Irrera N, Licata N, Sframeli M, Bruschetta D, Minutoli L, Altavilla D, Vita G, Squadrito F.
Messina S, et al. Among authors: licata n.
Biofactors. 2015 Sep-Oct;41(5):324-9. doi: 10.1002/biof.1226. Epub 2015 Aug 31.
Biofactors. 2015.
PMID: 26332024
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Dysregulation of the Fas/FasL system in mononuclear cells recovered from peritoneal fluid of women with endometriosis.
Sturlese E, Salmeri FM, Retto G, Pizzo A, De Dominici R, Ardita FV, Borrielli I, Licata N, Laganà AS, Sofo V.
Sturlese E, et al. Among authors: licata n.
J Reprod Immunol. 2011 Dec;92(1-2):74-81. doi: 10.1016/j.jri.2011.08.005. Epub 2011 Oct 5.
J Reprod Immunol. 2011.
PMID: 21978769
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Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita.
Portaro S, Altamura C, Licata N, Camerino GM, Imbrici P, Musumeci O, Rodolico C, Conte Camerino D, Toscano A, Desaphy JF.
Portaro S, et al. Among authors: licata n.
Neuromolecular Med. 2015 Sep;17(3):285-96. doi: 10.1007/s12017-015-8356-8. Epub 2015 May 26.
Neuromolecular Med. 2015.
PMID: 26007199
Free PMC article.
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Skeletal phenotype of mandibuloacral dysplasia associated with mutations in ZMPSTE24.
Cunningham VJ, D'Apice MR, Licata N, Novelli G, Cundy T.
Cunningham VJ, et al. Among authors: licata n.
Bone. 2010 Sep;47(3):591-7. doi: 10.1016/j.bone.2010.06.004. Epub 2010 Jun 13.
Bone. 2010.
PMID: 20550970
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Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?
D'Apice MR, Novelli A, di Masi A, Biancolella M, Antoccia A, Gullotta F, Licata N, Minella D, Testa B, Nardone AM, Palmieri G, Calabrese E, Biancone L, Tanzarella C, Frontali M, Sangiuolo F, Novelli G, Pallone F.
D'Apice MR, et al. Among authors: licata n.
BMC Med Genet. 2015 Apr 2;16:20. doi: 10.1186/s12881-015-0164-3.
BMC Med Genet. 2015.
PMID: 25927938
Free PMC article.
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