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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 5
2004 6
2005 2
2006 2
2008 2
2009 1
2010 1
2011 1
2013 1
2014 1
2015 2
2016 1
2019 3
2020 7
2021 6
2022 10
2023 9
2024 3

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61 results

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Page 1
Diverse clonal fates emerge upon drug treatment of homogeneous cancer cells.
Goyal Y, Busch GT, Pillai M, Li J, Boe RH, Grody EI, Chelvanambi M, Dardani IP, Emert B, Bodkin N, Braun J, Fingerman D, Kaur A, Jain N, Ravindran PT, Mellis IA, Kiani K, Alicea GM, Fane ME, Ahmed SS, Li H, Chen Y, Chai C, Kaster J, Witt RG, Lazcano R, Ingram DR, Johnson SB, Wani K, Dunagin MC, Lazar AJ, Weeraratna AT, Wargo JA, Herlyn M, Raj A. Goyal Y, et al. Among authors: jain n. Nature. 2023 Aug;620(7974):651-659. doi: 10.1038/s41586-023-06342-8. Epub 2023 Jul 19. Nature. 2023. PMID: 37468627 Free PMC article.
Infantile cortical hyperostosis.
Dutta S, Jain N, Bhattacharya A, Mukhopadhyay K. Dutta S, et al. Among authors: jain n. Indian Pediatr. 2005 Jan;42(1):64-6. Indian Pediatr. 2005. PMID: 15695863 Free article.
Follow-up studies - beyond survival.
Nair MK, Jain N. Nair MK, et al. Among authors: jain n. Indian Pediatr. 2013 Sep;50(9):830-1. Indian Pediatr. 2013. PMID: 24096842 Free article. No abstract available.
CODE Think! Rare Mutations of STX3 Causing Microvillus Inclusion Disease.
John EM, Sathyan S, Pournami F, Prithvi AK, Nandakumar A, Prabhakar J, Jain N. John EM, et al. Among authors: jain n. J Pediatr Genet. 2023 Aug 10;12(4):352. doi: 10.1055/s-0043-1772207. eCollection 2023 Dec. J Pediatr Genet. 2023. PMID: 38162158 No abstract available.
61 results