Conteduca G - Search Results

1

Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome.

Cabrita Pinto RL, Viaggi S, Canale E, Martinez Popple M, Capra V, Conteduca G, Testa B, Coviello D, Covone AE. Cabrita Pinto RL, et al. Among authors: conteduca g. Genes (Basel). 2023 Mar 28;14(4):810. doi: 10.3390/genes14040810. Genes (Basel). 2023. PMID: 37107568 Free PMC article.

2

Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome.

Testa B, Conteduca G, Grasso M, Cecconi M, Lantieri F, Baldo C, Arado A, Andraghetti L, Malacarne M, Milani D, Coviello D, Sotos Collaborative Group. Testa B, et al. Among authors: conteduca g. Genes (Basel). 2023 Jan 22;14(2):295. doi: 10.3390/genes14020295. Genes (Basel). 2023. PMID: 36833222 Free PMC article.

3

Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects.

Conteduca G, Testa B, Baldo C, Arado A, Malacarne M, Candiano G, Garbarino A, Coviello DA, Cantoni C. Conteduca G, et al. Gene. 2023 Jan 30;851:146970. doi: 10.1016/j.gene.2022.146970. Epub 2022 Oct 17. Gene. 2023. PMID: 36261088 Free article.

4

NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint.

Conteduca G, Cangelosi D, Coco S, Malacarne M, Baldo C, Arado A, Pinto R, Testa B, Coviello DA. Conteduca G, et al. Life (Basel). 2022 Jul 2;12(7):988. doi: 10.3390/life12070988. Life (Basel). 2022. PMID: 35888078 Free PMC article.

5

Single-nucleotide polymorphisms in 3'-untranslated region inducible costimulator gene and the important roles of miRNA in alopecia areata.

Conteduca G, Rossi A, Megiorni F, Parodi A, Ferrera F, Tardito S, Altosole T, Fausti V, Occella C, Kalli F, Negrini S, Pizzuti A, Marchese C, Rizza E, Indiveri F, Coviello D, Fenoglio D, Filaci G. Conteduca G, et al. Skin Health Dis. 2021 May 6;1(2):e34. doi: 10.1002/ski2.34. eCollection 2021 Jun. Skin Health Dis. 2021. PMID: 35664973 Free PMC article.

6

The role of AIRE polymorphisms in melanoma.

Conteduca G, Ferrera F, Pastorino L, Fenoglio D, Negrini S, Sormani MP, Indiveri F, Scarrà GB, Filaci G. Conteduca G, et al. Clin Immunol. 2010 Jul;136(1):96-104. doi: 10.1016/j.clim.2010.03.002. Epub 2010 Apr 2. Clin Immunol. 2010. PMID: 20363194 Free article.

7

Cyclophosphamide inhibits the generation and function of CD8(+) regulatory T cells.

Traverso I, Fenoglio D, Negrini S, Parodi A, Battaglia F, Kalli F, Conteduca G, Tardito S, Traverso P, Indiveri F, Filaci G. Traverso I, et al. Among authors: conteduca g. Hum Immunol. 2012 Mar;73(3):207-13. doi: 10.1016/j.humimm.2011.12.020. Epub 2012 Jan 14. Hum Immunol. 2012. PMID: 22285846 Free article.

8

Single nucleotide polymorphisms in the promoter regions of Foxp3 and ICOSLG genes are associated with Alopecia areata.

Conteduca G, Rossi A, Megiorni F, Parodi A, Ferrera F, Tardito S, Battaglia F, Kalli F, Negrini S, Pizzuti A, Rizza E, Indiveri F, Fenoglio D, Filaci G. Conteduca G, et al. Clin Exp Med. 2014 Feb;14(1):91-7. doi: 10.1007/s10238-012-0224-3. Epub 2012 Nov 30. Clin Exp Med. 2014. PMID: 23196741 Free article.

9

Residual tumor micro-foci and overwhelming regulatory T lymphocyte infiltration are the causes of bladder cancer recurrence.

Parodi A, Traverso P, Kalli F, Conteduca G, Tardito S, Curto M, Grillo F, Mastracci L, Bernardi C, Nasi G, Minaglia F, Simonato A, Carmignani G, Ferrera F, Fenoglio D, Filaci G. Parodi A, et al. Among authors: conteduca g. Oncotarget. 2016 Feb 9;7(6):6424-35. doi: 10.18632/oncotarget.7024. Oncotarget. 2016. PMID: 26824503 Free PMC article.

10

Comparative analysis of cancer vaccine settings for the selection of an effective protocol in mice.

Kalli F, Machiorlatti R, Battaglia F, Parodi A, Conteduca G, Ferrera F, Proietti M, Tardito S, Sanguineti M, Millo E, Fenoglio D, De Palma R, Inghirami G, Filaci G. Kalli F, et al. Among authors: conteduca g. J Transl Med. 2013 May 12;11:120. doi: 10.1186/1479-5876-11-120. J Transl Med. 2013. PMID: 23663506 Free PMC article.

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