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MS0621, a novel small-molecule modulator of Ewing sarcoma chromatin accessibility, interacts with an RNA-associated macromolecular complex and influences RNA splicing.
Vital T, Wali A, Butler KV, Xiong Y, Foster JP 2nd, Marcel SS, McFadden AW, Nguyen VU, Bailey BM, Lamb KN, James LI, Frye SV, Mosely AL, Jin J, Pattenden SG, Davis IJ. Vital T, et al. Among authors: foster jp 2nd. Front Oncol. 2023 Jan 30;13:1099550. doi: 10.3389/fonc.2023.1099550. eCollection 2023. Front Oncol. 2023. PMID: 36793594 Free PMC article.
KBG syndrome.
Morel Swols D, Foster J 2nd, Tekin M. Morel Swols D, et al. Among authors: foster j 2nd. Orphanet J Rare Dis. 2017 Dec 19;12(1):183. doi: 10.1186/s13023-017-0736-8. Orphanet J Rare Dis. 2017. PMID: 29258554 Free PMC article. Review.
Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.
Cengiz FB, Yilmazer R, Olgun L, Sennaroglu L, Kirazli T, Alper H, Olgun Y, Incesulu A, Atik T, Huesca-Hernandez F, Domínguez-Aburto J, González-Rosado G, Hernandez-Zamora E, Arenas-Sordo ML, Menendez I, Orhan KS, Avci H, Mahdieh N, Bonyadi M, Foster J 2nd, Duman D, Ozkinay F, Blanton SH, Bademci G, Tekin M. Cengiz FB, et al. Among authors: foster j 2nd. Int J Pediatr Otorhinolaryngol. 2017 Oct;101:167-171. doi: 10.1016/j.ijporl.2017.08.006. Epub 2017 Aug 8. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28964290 Free PMC article.
Novel EYA1 variants causing Branchio-oto-renal syndrome.
Klingbeil KD, Greenland CM, Arslan S, Llamos Paneque A, Gurkan H, Demir Ulusal S, Maroofian R, Carrera-Gonzalez A, Montufar-Armendariz S, Paredes R, Elcioglu N, Menendez I, Behnam M, Foster J 2nd, Guo S, Escarfuller S, Cengiz FB, Duman D, Bademci G, Tekin M. Klingbeil KD, et al. Among authors: foster j 2nd. Int J Pediatr Otorhinolaryngol. 2017 Jul;98:59-63. doi: 10.1016/j.ijporl.2017.04.037. Epub 2017 Apr 26. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28583505 Free PMC article.
Dominant deafness-onychodystrophy syndrome caused by an ATP6V1B2 mutation.
Menendez I, Carranza C, Herrera M, Marroquin N, Foster J 2nd, Cengiz FB, Bademci G, Tekin M. Menendez I, et al. Among authors: foster j 2nd. Clin Case Rep. 2017 Feb 8;5(4):376-379. doi: 10.1002/ccr3.761. eCollection 2017 Apr. Clin Case Rep. 2017. PMID: 28396750 Free PMC article.
Genetic screening revealed usher syndrome in a paediatric Chinese patient.
Qu C, Liang F, Long Q, Zhao M, Shang H, Fan L, Wang L, Foster J 2nd, Yan D, Liu X. Qu C, et al. Among authors: foster j 2nd. Hearing Balance Commun. 2017;15(2):98-106. doi: 10.1080/21695717.2017.1321217. Epub 2017 May 4. Hearing Balance Commun. 2017. PMID: 30800556 Free PMC article.
32 results