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Academic Journal

LOX-1 and cancer: an indissoluble liaison

  • Source: Cancer Gene Therapy. November, 2021, Vol. 28 Issue 10-11, p1088, 11 p.

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Academic Journal

Expression analysis of miRNA hsa-let7b-5p in naso-oropharyngeal swabs of COVID-19 patients supports its role in regulating ACE2 and DPP4 receptors.

  • Authors : Latini A; Department of Biomedicine and Prevention, Genetics Unit, University of Rome 'Tor Vergata', Rome, Italy.; Vancheri C

  • Source: Journal of cellular and molecular medicine [J Cell Mol Med] 2022 Sep 08. Date of Electronic Publication: 2022 Sep 08.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101083777 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

MED13 mutation: A novel cause of developmental and epileptic encephalopathy with infantile spasms.

  • Authors : Trivisano M; Rare and Complex Epilepsy Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Full Member of European Reference Network EpiCARE, Rome, Italy. Electronic address: .; De Dominicis A

  • Source: Seizure [Seizure] 2022 Sep 03; Vol. 101, pp. 211-217. Date of Electronic Publication: 2022 Sep 03.Publisher: Elsevier Country of Publication: England NLM ID: 9306979 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2688

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Academic Journal

Characterization of full-length CNBP expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing.

  • Authors : Alfano M; Department of Biotechnology, University of Verona, Verona, Italy.; De Antoni L

Subjects: Myotonic Dystrophy*/Myotonic Dystrophy*/Myotonic Dystrophy*/genetics ; Nanopore Sequencing*; Alleles

  • Source: ELife [Elife] 2022 Aug 26; Vol. 11. Date of Electronic Publication: 2022 Aug 26.Publisher: eLife Sciences Publications, Ltd Country of Publication: England NLM ID: 101579614 Publication Model: Electronic Cited Medium: Internet

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Report

Decipher non-canonical SPAST splicing mutations with the help of functional assays in patients affected by spastic paraplegia 4 (SPG4).

Subjects: Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/genetics; Humans ; Mutation Spastic Paraplegia Type 4

  • Source: Clinical genetics [Clin Genet] 2022 Aug; Vol. 102 (2), pp. 155-156. Date of Electronic Publication: 2022 May 06.Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004

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Academic Journal

Peptide-Antibody Fusions Engineered by Phage Display Exhibit an Ultrapotent and Broad Neutralization of SARS-CoV-2 Variants.

  • Authors : Labriola JM; Department of Molecular Genetics, The Donnelly Centre, University of Toronto, 160 College St., M5S 3E1 Toronto, Ontario, Canada.; Miersch S

Subjects: Bacteriophages*/Bacteriophages*/Bacteriophages*/genetics ; COVID-19*/COVID-19*/COVID-19*/drug therapy; Antibodies, Neutralizing SARS-CoV-2 variants

  • Source: ACS chemical biology [ACS Chem Biol] 2022 Jul 15; Vol. 17 (7), pp. 1978-1988. Date of Electronic Publication: 2022 Jun 22.Publisher: American Chemical Society Country of Publication: United States NLM ID: 101282906 Publication Model: Print-Electronic Cited Medium: Internet

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Editorial & Opinion

Update on human genetic susceptibility to COVID-19: susceptibility to virus and response.

  • Authors : Colona VL; Department of Biomedicine and Prevention, 'Tor Vergata' University of Rome, 00133, Rome, Italy.; Vasiliou V

Subjects: Genetic Predisposition to Disease*; COVID-19/COVID-19/COVID-19/*genetics; Angiotensin-Converting Enzyme 2/Angiotensin-Converting Enzyme 2/Angiotensin-Converting Enzyme 2/genetics

  • Source: Human genomics [Hum Genomics] 2021 Aug 25; Vol. 15 (1), pp. 57. Date of Electronic Publication: 2021 Aug 25.Publisher: BioMed Central Country of Publication: England NLM ID: 101202210 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-7364

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Academic Journal

Hsa-miR223-3p circulating level is upregulated in Friedreich's ataxia and inversely associated with HCLS1 associated protein X-1, HAX-1.

  • Authors : Quatrana A; Department of Biomedicine and Prevention, Laboratory of Signal Transduction, University of Rome Tor Vergata, Rome 00133, Italy.; Morini E

Subjects: Adaptor Proteins, Signal Transducing*/Adaptor Proteins, Signal Transducing*/Adaptor Proteins, Signal Transducing*/genetics ; Friedreich Ataxia*/Friedreich Ataxia*/Friedreich Ataxia*/pathology ; MicroRNAs*/MicroRNAs*/MicroRNAs*/blood

  • Source: Human molecular genetics [Hum Mol Genet] 2022 Jun 22; Vol. 31 (12), pp. 2010-2022.Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN:

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  • 1-10 of  10,546 results for ""Novelli, G.""