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

Year Number of Results
1979 1
1991 1
1992 1
1995 1
1997 1
1998 2
2000 1
2002 1
2004 2
2006 1
2007 3
2008 2
2010 3
2011 7
2012 7
2013 5
2014 1
2015 5
2016 7
2017 3
2018 1
2019 3
2020 1
2021 1
2022 2
2024 1

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57 results

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Page 1
Myotonic dystrophy types 1 and 2.
Ashizawa T, Sarkar PS. Ashizawa T, et al. Among authors: sarkar ps. Handb Clin Neurol. 2011;101:193-237. doi: 10.1016/B978-0-08-045031-5.00015-3. Handb Clin Neurol. 2011. PMID: 21496635 Review.
Mucopolysaccharidoses.
Magotra ML, Sarkar PS. Magotra ML, et al. Among authors: sarkar ps. Indian Pediatr. 1979 Jul;16(7):607-9. Indian Pediatr. 1979. PMID: 120323 No abstract available.
Superior mesenteric artery syndrome: CT findings.
Biswas A, Babu AA, Neelakantan S, Sarkar PS. Biswas A, et al. Among authors: sarkar ps. BMJ Case Rep. 2016 Jun 28;2016:bcr2016215885. doi: 10.1136/bcr-2016-215885. BMJ Case Rep. 2016. PMID: 27353179 Free PMC article. No abstract available.
Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription.
Gao R, Chakraborty A, Geater C, Pradhan S, Gordon KL, Snowden J, Yuan S, Dickey AS, Choudhary S, Ashizawa T, Ellerby LM, La Spada AR, Thompson LM, Hazra TK, Sarkar PS. Gao R, et al. Among authors: sarkar ps. Elife. 2019 Apr 17;8:e42988. doi: 10.7554/eLife.42988. Elife. 2019. PMID: 30994454 Free PMC article.
PIAS1 modulates striatal transcription, DNA damage repair, and SUMOylation with relevance to Huntington's disease.
Morozko EL, Smith-Geater C, Monteys AM, Pradhan S, Lim RG, Langfelder P, Kachemov M, Kulkarni JA, Zaifman J, Hill A, Stocksdale JT, Cullis PR, Wu J, Ochaba J, Miramontes R, Chakraborty A, Hazra TK, Lau A, St-Cyr S, Orellana I, Kopan L, Wang KQ, Yeung S, Leavitt BR, Reidling JC, Yang XW, Steffan JS, Davidson BL, Sarkar PS, Thompson LM. Morozko EL, et al. Among authors: sarkar ps. Proc Natl Acad Sci U S A. 2021 Jan 26;118(4):e2021836118. doi: 10.1073/pnas.2021836118. Proc Natl Acad Sci U S A. 2021. PMID: 33468657 Free PMC article.
Deficiency in classical nonhomologous end-joining-mediated repair of transcribed genes is linked to SCA3 pathogenesis.
Chakraborty A, Tapryal N, Venkova T, Mitra J, Vasquez V, Sarker AH, Duarte-Silva S, Huai W, Ashizawa T, Ghosh G, Maciel P, Sarkar PS, Hegde ML, Chen X, Hazra TK. Chakraborty A, et al. Among authors: sarkar ps. Proc Natl Acad Sci U S A. 2020 Apr 7;117(14):8154-8165. doi: 10.1073/pnas.1917280117. Epub 2020 Mar 23. Proc Natl Acad Sci U S A. 2020. PMID: 32205441 Free PMC article.
57 results