Niceta M - Search Results

1

De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy.

von Wintzingerode L, Ben-Zeev B, Cesario C, Chan KM, Depienne C, Elpeleg O, Iascone M, Kelley WV, Nassogne MC, Niceta M, Pezzani L, Rahner N, Revencu N, Bekheirnia MR, Santiago-Sim T, Tartaglia M, Thompson ML, Trivisano M, Hentschel J, Sticht H, Abou Jamra R, Oppermann H. von Wintzingerode L, et al. Among authors: niceta m. Genet Med. 2023 Jul;25(7):100859. doi: 10.1016/j.gim.2023.100859. Epub 2023 Apr 20. Genet Med. 2023. PMID: 37092538 Free article.

2

Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III.

Piccione M, Niceta M, Antona V, Di Fiore A, Cariola F, Gentile M, Corsello G. Piccione M, et al. Among authors: niceta m. Am J Med Genet A. 2009 Aug;149A(8):1837-41. doi: 10.1002/ajmg.a.32952. Am J Med Genet A. 2009. PMID: 19610100 No abstract available.

3

Development of S/MAR minicircles for enhanced and persistent transgene expression in the mouse liver.

Argyros O, Wong SP, Fedonidis C, Tolmachov O, Waddington SN, Howe SJ, Niceta M, Coutelle C, Harbottle RP. Argyros O, et al. Among authors: niceta m. J Mol Med (Berl). 2011 May;89(5):515-29. doi: 10.1007/s00109-010-0713-3. Epub 2011 Feb 8. J Mol Med (Berl). 2011. PMID: 21301798

4

Evaluation of serum CA 125 levels in patients with pelvic pain related to endometriosis.

Maiorana A, Cicerone C, Niceta M, Alio L. Maiorana A, et al. Among authors: niceta m. Int J Biol Markers. 2007 Jul-Sep;22(3):200-2. doi: 10.1177/172460080702200306. Int J Biol Markers. 2007. PMID: 17922463 Free article.

5

Vitiligo susceptibility and catalase gene polymorphisms in Sicilian population.

Caputo V, Niceta M, Fiorella S, La Vecchia M, Bastonini E, Bongiorno MR, Pistone G. Caputo V, et al. Among authors: niceta m. G Ital Dermatol Venereol. 2018 Oct;153(5):619-623. doi: 10.23736/S0392-0488.17.05488-8. Epub 2017 Feb 15. G Ital Dermatol Venereol. 2018. PMID: 28206724

6

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.

Orlando V, Alesi V, Di Giacomo G, Canestrelli M, Calacci C, Nardone AM, Calvieri G, Liambo MT, Sallicandro E, Di Tommaso S, Di Gregorio MG, Corrado F, Barrano G, Niceta M, Dallapiccola B, Novelli A. Orlando V, et al. Among authors: niceta m. Reprod Sci. 2021 Apr;28(4):1142-1149. doi: 10.1007/s43032-020-00419-9. Epub 2021 Jan 6. Reprod Sci. 2021. PMID: 33409881

7

Novel human pathological mutations. Gene symbol: F8. Disease: Haemophilia A.

Niceta M, Fabiano C, Sammarco P. Niceta M, et al. Hum Genet. 2010 Jan;127(1):115. Hum Genet. 2010. PMID: 20108391 No abstract available.

8

A large view of CYP21 locus among Sicilians and other populations: identification of a novel CYP21A2 variant in Sicily.

Niceta M, Bono M, Fabiano C, Pojero F, Niceta F, Sammarco P, Corsello G, Garofalo P. Niceta M, et al. Among authors: niceta f. J Endocrinol Invest. 2011 Dec;34(11):847-54. doi: 10.3275/7417. Epub 2010 Dec 15. J Endocrinol Invest. 2011. PMID: 21169732

9

Persistent episomal transgene expression in liver following delivery of a scaffold/matrix attachment region containing non-viral vector.

Argyros O, Wong SP, Niceta M, Waddington SN, Howe SJ, Coutelle C, Miller AD, Harbottle RP. Argyros O, et al. Among authors: niceta m. Gene Ther. 2008 Dec;15(24):1593-605. doi: 10.1038/gt.2008.113. Epub 2008 Jul 17. Gene Ther. 2008. PMID: 18633447

10

Refractory acne and 21-hydroxylase deficiency in a selected group of female patients.

Caputo V, Fiorella S, Curiale S, Caputo A, Niceta M. Caputo V, et al. Among authors: niceta m. Dermatology. 2010;220(2):121-7. doi: 10.1159/000277608. Epub 2010 Jan 29. Dermatology. 2010. PMID: 20110635

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