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

Year Number of Results
1949 1
1959 1
1964 1
1965 1
1966 1
1967 1
1968 2
1969 1
1972 1
1973 2
1974 1
1975 5
1976 3
1977 7
1978 9
1979 10
1980 13
1981 8
1982 6
1983 5
1984 11
1985 8
1986 7
1987 6
1988 15
1989 11
1990 13
1991 14
1992 9
1993 15
1994 8
1995 14
1996 8
1997 19
1998 23
1999 19
2000 29
2001 37
2002 43
2003 43
2004 43
2005 42
2006 65
2007 67
2008 89
2009 103
2010 103
2011 94
2012 100
2013 103
2014 98
2015 107
2016 93
2017 127
2018 89
2019 108
2020 100
2021 114
2022 114
2023 92
2024 88
2025 91

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2,226 results

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Page 1
RUNX2 promotes fibrosis via an alveolar-to-pathological fibroblast transition.
Fang Y, Chung SSW, Xu L, Xue C, Liu X, Jiang D, Li R, Korogi Y, Yuan K, Saqi A, Hibshoosh H, Huang Y, Lin CS, Takarada T, Tsukui T, Sheppard D, Sun X, Que J. Fang Y, et al. Among authors: lin cs. Nature. 2025 Apr;640(8057):221-230. doi: 10.1038/s41586-024-08542-2. Epub 2025 Feb 5. Nature. 2025. PMID: 39910313 Free article.
Guideline for the diagnosis, treatment and long-term management of cutaneous lupus erythematosus.
Lu Q, Long H, Chow S, Hidayat S, Danarti R, Listiawan Y, Deng D, Guo Q, Fang H, Tao J, Zhao M, Xiang L, Che N, Li F, Zhao H, Lau CS, Ip FC, Ho KM, Paliza AC, Vicheth C, Godse K, Cho S, Seow CS, Miyachi Y, Khang TH, Ungpakorn R, Galadari H, Shah R, Yang K, Zhou Y, Selmi C, Sawalha AH, Zhang X, Chen Y, Lin CS. Lu Q, et al. Among authors: lin cs. J Autoimmun. 2021 Sep;123:102707. doi: 10.1016/j.jaut.2021.102707. Epub 2021 Aug 5. J Autoimmun. 2021. PMID: 34364171
Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction-associated steatohepatitis.
Shi H, Wang X, Sloas C, Gerlach B, Yurdagul A Jr, Moore MP, Jung EJ, Mirshahi F, Ronzoni L, Sanyal AJ, Valenti L, Lin CS, Montgomery J, Zinker B, Klichinsky M, Tabas I. Shi H, et al. Among authors: lin cs. Sci Transl Med. 2025 Sep 10;17(815):eadv2106. doi: 10.1126/scitranslmed.adv2106. Epub 2025 Sep 10. Sci Transl Med. 2025. PMID: 40929246
Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis.
Bisikirska B, Labella R, Cuesta-Dominguez A, Luo N, De Angelis J, Mosialou I, Lin CS, Beck D, Lata S, Shyu PT, McMahon DJ, Guo E, Hagen J, Chung WK, Shane E, Cohen A, Kousteni S. Bisikirska B, et al. Among authors: lin cs. Sci Transl Med. 2024 Oct 16;16(769):eadj0085. doi: 10.1126/scitranslmed.adj0085. Epub 2024 Oct 16. Sci Transl Med. 2024. PMID: 39413162
2,226 results