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Rapid and sensitive detection of SARS-CoV-2 variants in nasopharyngeal swabs and wastewaters.
Diagn Microbiol Infect Dis. 2022 Apr;102(4):115632. doi: 10.1016/j.diagmicrobio.2021.115632. Epub 2022 Jan 1.
Diagn Microbiol Infect Dis. 2022.
PMID: 35074623
Free PMC article.
Small Non-Coding RNA Profiling Identifies miR-181a-5p as a Mediator of Estrogen Receptor Beta-Induced Inhibition of Cholesterol Biosynthesis in Triple-Negative Breast Cancer.
Alexandrova E, Lamberti J, Saggese P, Pecoraro G, Memoli D, Cappa VM, Ravo M, Iorio R, Tarallo R, Rizzo F, Collina F, Cantile M, Bonito MD, Botti G, Nassa G, Weisz A, Giurato G.
Alexandrova E, et al. Among authors: cappa vm.
Cells. 2020 Apr 3;9(4):874. doi: 10.3390/cells9040874.
Cells. 2020.
PMID: 32260128
Free PMC article.
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Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online.
Flagiello L, Cirigliano V, Strazzullo M, Cappa V, Ciccodicola A, D'Esposito M, Torrente I, Werner R, Di Iorio G, Rinaldi M, Dallapiccola A, Forabosco A, Ventruto V, D'Urso M.
Flagiello L, et al.
Hum Mutat. 1998;12(5):361.
Hum Mutat. 1998.
PMID: 10671058
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A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease.
Di Iorio G, Cappa V, Ciccodicola A, Sampaolo S, Ammendola A, Sanges G, Giugliano R, D'Urso M.
Di Iorio G, et al.
Neurol Sci. 2000 Apr;21(2):109-12. doi: 10.1007/s100720070105.
Neurol Sci. 2000.
PMID: 10938190
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Lack of sodium channel mutation in an Italian family with paramyotonia congenita.
Sampaolo S, Puca AA, Nigro V, Cappa V, Sannino V, Sanges G, Bonavita V, Di Iorio G.
Sampaolo S, et al.
Neurology. 1999 Oct 22;53(7):1549-55. doi: 10.1212/wnl.53.7.1549.
Neurology. 1999.
PMID: 10534266
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YAC contig organization and CpG island analysis in Xq28.
Palmieri G, Romano G, Ciccodicola A, Casamassimi A, Campanile C, Esposito T, Cappa V, Lania A, Johnson S, Reinbold R, et al.
Palmieri G, et al.
Genomics. 1994 Nov 1;24(1):149-58. doi: 10.1006/geno.1994.1592.
Genomics. 1994.
PMID: 7896270
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SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function.
Nigro V, Bruni P, Ciccodicola A, Politano L, Nigro G, Piluso G, Cappa V, Covone AE, Romeo G, D'Urso M.
Nigro V, et al.
Hum Mol Genet. 1995 Oct;4(10):2003-4. doi: 10.1093/hmg/4.10.2003.
Hum Mol Genet. 1995.
PMID: 8595433
No abstract available.
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