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

Year Number of Results
1971 1
1977 2
1978 7
1979 3
1980 13
1981 8
1982 24
1983 29
1984 32
1985 48
1986 43
1987 54
1988 63
1989 101
1990 100
1991 126
1992 152
1993 179
1994 171
1995 207
1996 167
1997 222
1998 263
1999 256
2000 374
2001 279
2002 302
2003 301
2004 340
2005 327
2006 379
2007 376
2008 427
2009 487
2010 505
2011 524
2012 535
2013 576
2014 548
2015 514
2016 498
2017 518
2018 541
2019 491
2020 587
2021 552
2022 430
2023 380
2024 119

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12,070 results

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Page 1
MYH7 in cardiomyopathy and skeletal muscle myopathy.
Gao Y, Peng L, Zhao C. Gao Y, et al. Mol Cell Biochem. 2024 Feb;479(2):393-417. doi: 10.1007/s11010-023-04735-x. Epub 2023 Apr 20. Mol Cell Biochem. 2024. PMID: 37079208 Review.
Changes and Challenges.
Scharf RE. Scharf RE. Hamostaseologie. 2019 Feb;39(1):1-3. doi: 10.1055/s-0039-1678526. Epub 2019 Feb 18. Hamostaseologie. 2019. PMID: 30776836
Myosin-X recruits lamellipodin to filopodia tips.
Popović A, Miihkinen M, Ghimire S, Saup R, Grönloh MLB, Ball NJ, Goult BT, Ivaska J, Jacquemet G. Popović A, et al. J Cell Sci. 2023 Mar 1;136(5):jcs260574. doi: 10.1242/jcs.260574. Epub 2023 Mar 2. J Cell Sci. 2023. PMID: 36861887 Free PMC article.
Bacterial flagellar motor as a multimodal biosensor.
Krasnopeeva E, Barboza-Perez UE, Rosko J, Pilizota T, Lo CJ. Krasnopeeva E, et al. Methods. 2021 Sep;193:5-15. doi: 10.1016/j.ymeth.2020.06.012. Epub 2020 Jul 5. Methods. 2021. PMID: 32640316 Review.
Myosins and deafness.
Redowicz MJ. Redowicz MJ. J Muscle Res Cell Motil. 1999 Apr;20(3):241-8. doi: 10.1023/a:1005403725521. J Muscle Res Cell Motil. 1999. PMID: 10471988 Review.
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Holtz AM, VanCoillie R, Vansickle EA, Carere DA, Withrow K, Torti E, Juusola J, Millan F, Person R, Guillen Sacoto MJ, Si Y, Wentzensen IM, Pugh J, Vasileiou G, Rieger M, Reis A, Argilli E, Sherr EH, Aldinger KA, Dobyns WB, Brunet T, Hoefele J, Wagner M, Haber B, Kotzaeridou U, Keren B, Heron D, Mignot C, Heide S, Courtin T, Buratti J, Murugasen S, Donald KA, O'Heir E, Moody S, Kim KH, Burton BK, Yoon G, Campo MD, Masser-Frye D, Kozenko M, Parkinson C, Sell SL, Gordon PL, Prokop JW, Karaa A, Bupp C, Raby BA. Holtz AM, et al. Genet Med. 2022 Oct;24(10):2065-2078. doi: 10.1016/j.gim.2022.07.005. Epub 2022 Aug 18. Genet Med. 2022. PMID: 35980381 Free PMC article.
12,070 results
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