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Year Number of Results
2003 3
2006 2
2012 1
2016 1
2018 1
2019 3
2020 2
2021 4
2022 1
2023 5
2024 4

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Page 1
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Claus LR, Chen C, Stallworth J, Turner JL, Slaats GG, Hawks AL, Mabillard H, Senum SR, Srikanth S, Flanagan-Steet H, Louie RJ, Silver J, Lerner-Ellis J, Morel C, Mighton C, Sleutels F, van Slegtenhorst M, van Ham T, Brooks AS, Dorresteijn EM, Barakat TS, Dahan K, Demoulin N, Goffin EJ, Olinger E; Genomics England Research Consortium; Larsen M, Hertz JM, Lilien MR, Obeidová L, Seeman T, Stone HK, Kerecuk L, Gurgu M, Yousef Yengej FA, Ammerlaan CME, Rookmaaker MB, Hanna C, Rogers RC, Duran K, Peters E, Sayer JA, van Haaften G, Harris PC, Ling K, Mason JM, van Eerde AM, Steet R. Claus LR, et al. Among authors: srikanth s. Kidney Int. 2023 Nov;104(5):995-1007. doi: 10.1016/j.kint.2023.07.021. Epub 2023 Aug 19. Kidney Int. 2023. PMID: 37598857
Identification and diagnosis of long COVID-19: A scoping review.
Srikanth S, Boulos JR, Dover T, Boccuto L, Dean D. Srikanth S, et al. Prog Biophys Mol Biol. 2023 Sep;182:1-7. doi: 10.1016/j.pbiomolbio.2023.04.008. Epub 2023 May 12. Prog Biophys Mol Biol. 2023. PMID: 37182545 Free PMC article. Review.
A 96-Well Polyacrylamide Gel for Electrophoresis and Western Blotting.
Birtwistle MR, Huggins JR, Zadeh CO, Sarmah D, Srikanth S, Kelly Jones B, Cascio LN, Dean D. Birtwistle MR, et al. Among authors: srikanth s. bioRxiv [Preprint]. 2024 May 11:2024.05.10.593650. doi: 10.1101/2024.05.10.593650. bioRxiv. 2024. PMID: 38765957 Free PMC article. Preprint.
Sleep disturbances in Phelan-McDermid syndrome: Clinical and metabolic profiling of 56 individuals.
Moffitt BA, Oberman LM, Beamer L, Srikanth S, Jain L, Cascio L, Jones K, Pauly R, May M, Skinner C, Buchanan C, DuPont BR, Kaufmann WE, Valentine K, Ward LD, Ivankovic D, Rogers RC, Phelan K, Sarasua SM, Boccuto L. Moffitt BA, et al. Among authors: srikanth s. Clin Genet. 2023 Aug;104(2):198-209. doi: 10.1111/cge.14361. Epub 2023 May 18. Clin Genet. 2023. PMID: 37198960
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy.
Lee YR, Khan K, Armfield-Uhas K, Srikanth S, Thompson NA, Pardo M, Yu L, Norris JW, Peng Y, Gripp KW, Aleck KA, Li C, Spence E, Choi TI, Kwon SJ, Park HM, Yu D, Heo WD, Mooney MR, Baig SM, Wentzensen IM, Telegrafi A, McWalter K, Moreland T, Roadhouse C, Ramsey K, Lyons MJ, Skinner C, Alexov E, Katsanis N, Stevenson RE, Choudhary JS, Adams DJ, Kim CH, Davis EE, Schwartz CE. Lee YR, et al. Among authors: srikanth s. Nat Commun. 2020 Jul 23;11(1):3698. doi: 10.1038/s41467-020-17452-6. Nat Commun. 2020. PMID: 32703943 Free PMC article.
A new test for autism spectrum disorder: Metabolic data from different cell types.
Srikanth S, Cascio L, Pauly R, Jones K, Sorrow S, Cubillan R, Chen CF, Skinner CD, Champaigne K, Stevenson RE, Schwartz CE, Boccuto L. Srikanth S, et al. Data Brief. 2021 Nov 23;39:107598. doi: 10.1016/j.dib.2021.107598. eCollection 2021 Dec. Data Brief. 2021. PMID: 34877376 Free PMC article.
Mechanisms of Arg-Pro-Pro-Gly-Phe inhibition of thrombin.
Hasan AA, Warnock M, Nieman M, Srikanth S, Mahdi F, Krishnan R, Tulinsky A, Schmaier AH. Hasan AA, et al. Among authors: srikanth s. Am J Physiol Heart Circ Physiol. 2003 Jul;285(1):H183-93. doi: 10.1152/ajpheart.00490.2002. Epub 2003 Feb 21. Am J Physiol Heart Circ Physiol. 2003. PMID: 12598231 Free article.
25 results