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

Year Number of Results
1959 1
1960 1
1962 1
1964 1
1965 1
1971 1
1978 1
1980 1
1994 1
1995 1
1997 1
1999 2
2000 1
2001 1
2002 1
2003 1
2004 2
2007 2
2009 2
2011 1
2013 1
2014 3
2015 1
2016 2
2019 1
2020 2
2024 0

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31 results

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Page 1
DJ-1 can form β-sheet structured aggregates that co-localize with pathological amyloid deposits.
Solti K, Kuan WL, Fórizs B, Kustos G, Mihály J, Varga Z, Herberth B, Moravcsik É, Kiss R, Kárpáti M, Mikes A, Zhao Y, Imre T, Rochet JC, Aigbirhio F, Williams-Gray CH, Barker RA, Tóth G. Solti K, et al. Among authors: karpati m. Neurobiol Dis. 2020 Feb;134:104629. doi: 10.1016/j.nbd.2019.104629. Epub 2019 Nov 11. Neurobiol Dis. 2020. PMID: 31669752 Free article.
Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay.
Kim M, Sandford E, Gatica D, Qiu Y, Liu X, Zheng Y, Schulman BA, Xu J, Semple I, Ro SH, Kim B, Mavioglu RN, Tolun A, Jipa A, Takats S, Karpati M, Li JZ, Yapici Z, Juhasz G, Lee JH, Klionsky DJ, Burmeister M. Kim M, et al. Among authors: karpati m. Elife. 2016 Jan 26;5:e12245. doi: 10.7554/eLife.12245. Elife. 2016. PMID: 26812546 Free PMC article.
Tay-Sachs disease and HEXA mutations among Moroccan Jews.
Kaufman M, Grinshpun-Cohen J, Karpati M, Peleg L, Goldman B, Akstein E, Adam A, Navon R. Kaufman M, et al. Among authors: karpati m. Hum Mutat. 1997;10(4):295-300. doi: 10.1002/(SICI)1098-1004(1997)10:4<295::AID-HUMU5>3.0.CO;2-G. Hum Mutat. 1997. PMID: 9338583
Novel mutations in two families with Darier's disease.
Amichai B, Karpati M, Goldman B, Peleg L. Amichai B, et al. Among authors: karpati m. Int J Dermatol. 2007 Jan;46(1):64-7. doi: 10.1111/j.1365-4632.2006.03049.x. Int J Dermatol. 2007. PMID: 17214724
31 results