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A single NGS-based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testing.
Nallamilli BRR, Chaubey A, Valencia CA, Stansberry L, Behlmann AM, Ma Z, Mathur A, Shenoy S, Ganapathy V, Jagannathan L, Ramachander V, Ferlini A, Bean L, Hegde M. Nallamilli BRR, et al. Among authors: stansberry l. Hum Mutat. 2021 May;42(5):626-638. doi: 10.1002/humu.24191. Epub 2021 Mar 19. Hum Mutat. 2021. PMID: 33644936
Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional Microarray.
Chaubey A, Shenoy S, Mathur A, Ma Z, Valencia CA, Reddy Nallamilli BR, Szekeres E Jr, Stansberry L, Liu R, Hegde MR. Chaubey A, et al. Among authors: stansberry l. J Mol Diagn. 2020 Jun;22(6):823-840. doi: 10.1016/j.jmoldx.2020.03.008. Epub 2020 Apr 25. J Mol Diagn. 2020. PMID: 32344035 Free article.
Hyperoxia inhibits oxidant-induced apoptosis in lung epithelial cells.
Franek WR, Horowitz S, Stansberry L, Kazzaz JA, Koo HC, Li Y, Arita Y, Davis JM, Mantell AS, Scott W, Mantell LL. Franek WR, et al. Among authors: stansberry l. J Biol Chem. 2001 Jan 5;276(1):569-75. doi: 10.1074/jbc.M004716200. J Biol Chem. 2001. PMID: 11034997 Free article.