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10. A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development. Yu X; Hu L; Liu X; Zhan G; Mei M; Wang H; Zhang X; Qiu Z; Zhou W; Yang L Neurosci Bull; 2018 Oct; 34(5):854-858. PubMed ID: 29786759 [No Abstract] [Full Text] [Related]
11. SIRT1 regulates sphingolipid metabolism and neural differentiation of mouse embryonic stem cells through c-Myc-SMPDL3B. Fan W; Tang S; Fan X; Fang Y; Xu X; Li L; Xu J; Li JL; Wang Z; Li X Elife; 2021 May; 10():. PubMed ID: 34042046 [TBL] [Abstract][Full Text] [Related]
12. The N-Myc-DLL3 cascade is suppressed by the ubiquitin ligase Huwe1 to inhibit proliferation and promote neurogenesis in the developing brain. Zhao X; D' Arca D; Lim WK; Brahmachary M; Carro MS; Ludwig T; Cardo CC; Guillemot F; Aldape K; Califano A; Iavarone A; Lasorella A Dev Cell; 2009 Aug; 17(2):210-21. PubMed ID: 19686682 [TBL] [Abstract][Full Text] [Related]
13. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. Tedesco MG; Lonardo F; Ceccarini C; Cesarano C; Digilio MC; Magliozzi M; Rogaia D; Mencarelli A; Leoni C; Piscopo C; Imperatore V; Falco MT; Fontana P; Nardone AM; Novelli A; Troiani S; Seri M; Prontera P Am J Med Genet A; 2021 Apr; 185(4):1204-1210. PubMed ID: 33442900 [TBL] [Abstract][Full Text] [Related]
14. [Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?]. Shongo MY; Lubala TK; Mbuyi SM; Makinko PI; Ngwej DT; Kabange FN Pan Afr Med J; 2012; 13():85. PubMed ID: 23396887 [TBL] [Abstract][Full Text] [Related]
15. Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2. Fiori E; Babicola L; Andolina D; Coassin A; Pascucci T; Patella L; Han YC; Ventura A; Ventura R Behav Genet; 2015 Sep; 45(5):547-59. PubMed ID: 26026879 [TBL] [Abstract][Full Text] [Related]
16. A novel mutation in MYCN gene causing congenital absence of the flexor pollicis longus tendon as an unusual presentation of Feingold syndrome 1. Peleg A; Kurolap A; Sagi-Dain L; Larom-Khan G; Adir V; Mory A; Paperna T; Shuldiner AR; Gonzaga-Jauregui C; Adir N; Baris Feldman H; Wollstein R Clin Dysmorphol; 2021 Apr; 30(2):71-75. PubMed ID: 32925198 [TBL] [Abstract][Full Text] [Related]
18. Nestin is a potential mediator of malignancy in human neuroblastoma cells. Thomas SK; Messam CA; Spengler BA; Biedler JL; Ross RA J Biol Chem; 2004 Jul; 279(27):27994-9. PubMed ID: 15117961 [TBL] [Abstract][Full Text] [Related]
19. Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN. Burnside RD; Molinari S; Botti C; Brooks SS; Chung WK; Mehta L; Schwartz S; Papenhausen P Am J Med Genet A; 2018 Sep; 176(9):1956-1963. PubMed ID: 30088856 [TBL] [Abstract][Full Text] [Related]
20. Gene expression profiling of MYC-driven tumor signatures in porcine liver stem cells by transcriptome sequencing. Aravalli RN; Talbot NC; Steer CJ World J Gastroenterol; 2015 Feb; 21(7):2011-29. PubMed ID: 25717234 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]