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

Year Number of Results
1968 2
1970 1
1972 4
1973 3
1974 1
1975 1
1976 4
1978 1
1979 1
1981 3
1983 1
1984 2
1985 2
1986 2
1987 6
1988 5
1989 2
1990 3
1991 5
1992 5
1993 4
1994 6
1995 5
1996 9
1997 3
1998 3
1999 7
2000 7
2001 10
2002 7
2003 6
2004 2
2005 8
2006 5
2007 6
2008 1
2009 1
2010 4
2011 1
2012 8
2013 8
2014 4
2015 4
2016 5
2017 1
2018 3
2019 1
2020 3
2021 2
2022 5
2023 4
2024 3
2025 1

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193 results

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Page 1
Muscle forces and fascicle behavior during three hamstring exercises.
Van Hooren B, Vanwanseele B, van Rossom S, Teratsias P, Willems P, Drost M, Meijer K. Van Hooren B, et al. Among authors: drost m. Scand J Med Sci Sports. 2022 Jun;32(6):997-1012. doi: 10.1111/sms.14158. Epub 2022 Mar 26. Scand J Med Sci Sports. 2022. PMID: 35307884 Free PMC article.
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome.
Drost M, Tiersma Y, Thompson BA, Frederiksen JH, Keijzers G, Glubb D, Kathe S, Osinga J, Westers H, Pappas L, Boucher KM, Molenkamp S, Zonneveld JB, van Asperen CJ, Goldgar DE, Wallace SS, Sijmons RH, Spurdle AB, Rasmussen LJ, Greenblatt MS, de Wind N, Tavtigian SV. Drost M, et al. Genet Med. 2019 Jul;21(7):1486-1496. doi: 10.1038/s41436-018-0372-2. Epub 2018 Dec 3. Genet Med. 2019. PMID: 30504929 Free PMC article.
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome.
Drost M, Tiersma Y, Glubb D, Kathe S, van Hees S, Calléja F, Zonneveld JBM, Boucher KM, Ramlal RPE, Thompson BA, Rasmussen LJ, Greenblatt MS, Lee A, Spurdle AB, Tavtigian SV, de Wind N. Drost M, et al. Genet Med. 2020 May;22(5):847-856. doi: 10.1038/s41436-019-0736-2. Epub 2020 Jan 22. Genet Med. 2020. PMID: 31965077 Free PMC article.
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
van der Klift HM, Mensenkamp AR, Drost M, Bik EC, Vos YJ, Gille HJ, Redeker BE, Tiersma Y, Zonneveld JB, García EG, Letteboer TG, Olderode-Berends MJ, van Hest LP, van Os TA, Verhoef S, Wagner A, van Asperen CJ, Ten Broeke SW, Hes FJ, de Wind N, Nielsen M, Devilee P, Ligtenberg MJ, Wijnen JT, Tops CM. van der Klift HM, et al. Among authors: drost m. Hum Mutat. 2016 Nov;37(11):1162-1179. doi: 10.1002/humu.23052. Epub 2016 Aug 21. Hum Mutat. 2016. PMID: 27435373
DNA mismatch repair: from biophysics to bedside.
Lebbink JH, Drost M, de Wind N. Lebbink JH, et al. Among authors: drost m. DNA Repair (Amst). 2016 Feb;38:1-2. doi: 10.1016/j.dnarep.2015.11.007. Epub 2015 Dec 8. DNA Repair (Amst). 2016. PMID: 26777339 No abstract available.
Complications during gestation in the cow.
Drost M. Drost M. Theriogenology. 2007 Aug;68(3):487-91. doi: 10.1016/j.theriogenology.2007.04.023. Epub 2007 May 24. Theriogenology. 2007. PMID: 17531308 Review.
Prognostic value of Mandard score and nodal status for recurrence patterns and survival after multimodal treatment of oesophageal adenocarcinoma.
Henckens SPG, Liu D, Gisbertz SS, Kalff MC, Anderegg MCJ, Crull D, Daams F, van Dalsen AD, Dekker JWT, van Det MJ, van Duijvendijk P, Eshuis WJ, Groenendijk RPR, Haveman JW, van Hillegersberg R, Luyer MDP, Olthof PB, Pierie JEN, Plat VD, Rosman C, Ruurda JP, van Sandick JW, Sosef MN, Voeten DM, Vijgen GHEJ, Bijlsma MF, Meijer SL, Hulshof MCCM, Oyarce C, Lagarde SM, van Laarhoven HWM, van Berge Henegouwen MI; IVORY study group. Henckens SPG, et al. Br J Surg. 2024 Jan 31;111(2):znae034. doi: 10.1093/bjs/znae034. Br J Surg. 2024. PMID: 38387083 Free PMC article.
193 results