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Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes.
Youssefian L, Vahidnezhad H, Saeidian AH, Sotoudeh S, Mahmoudi H, Daneshpazhooh M, Aghazadeh N, Adams R, Ghanadan A, Zeinali S, Fortina P, Uitto J. Youssefian L, et al. Among authors: adams r. Eur J Hum Genet. 2017 Nov;25(11):1282-1285. doi: 10.1038/ejhg.2017.137. Epub 2017 Sep 6. Eur J Hum Genet. 2017. PMID: 28875980 Free PMC article.
Epigenomic profiling of neuroblastoma cell lines.
Upton K, Modi A, Patel K, Kendsersky NM, Conkrite KL, Sussman RT, Way GP, Adams RN, Sacks GI, Fortina P, Diskin SJ, Maris JM, Rokita JL. Upton K, et al. Sci Data. 2020 Apr 14;7(1):116. doi: 10.1038/s41597-020-0458-y. Sci Data. 2020. PMID: 32286315 Free PMC article.
Adaptive clinical trial of AZD7442 and SARS-CoV-2 vaccination in immunosuppressed patients highly vulnerable to infection with SARS-CoV-2 virus (RAPID-PROTECTION): protocol for a multicentre, interventional open-label, randomised controlled trial.
Varley M, Euden J, Adams R, Barnes E, Bodman C, Choy E, Cicconi P, Dagley V, Ewer K, Griffin S, Harris D, Hill A, Hood K, Knapper S, Pringle S, Porter C, Ottensmeier CH, Raisanen L, Ray R, Tangney R, Wilson K, Nixon LS, Thomas-Jones E, Tuthill M. Varley M, et al. Among authors: adams r. BMJ Open. 2025 Jan 20;15(1):e084345. doi: 10.1136/bmjopen-2024-084345. BMJ Open. 2025. PMID: 39832967 Free PMC article. Clinical Trial.
A novel MXI1-NUTM2B fusion detected in an undifferentiated ovarian cancer.
Elshafey M, Ghandour M, Adams RM, Neill D, Gogoi R. Elshafey M, et al. Among authors: adams rm. Gynecol Oncol Rep. 2024 Dec 6;57:101653. doi: 10.1016/j.gore.2024.101653. eCollection 2025 Feb. Gynecol Oncol Rep. 2024. PMID: 39758708 Free PMC article. No abstract available.
4,411 results