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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 255
2000 374
2001 279
2002 302
2003 301
2004 340
2005 327
2006 379
2007 376
2008 427
2009 487
2010 505
2011 523
2012 535
2013 576
2014 548
2015 514
2016 498
2017 518
2018 538
2019 385
2020 39
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10,188 results
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Page 1
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.
Kelly MA, Caleshu C, Morales A, Buchan J, Wolf Z, Harrison SM, Cook S, Dillon MW, Garcia J, Haverfield E, Jongbloed JDH, Macaya D, Manrai A, Orland K, Richard G, Spoonamore K, Thomas M, Thomson K, Vincent LM, Walsh R, Watkins H, Whiffin N, Ingles J, van Tintelen JP, Semsarian C, Ware JS, Hershberger R, Funke B. Kelly MA, et al. Version 2. Genet Med. 2018 Mar;20(3):351-359. doi: 10.1038/gim.2017.218. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300372 Free PMC article.
Regulation of molecular motor proteins.
Reilein AR, Rogers SL, Tuma MC, Gelfand VI. Reilein AR, et al. Int Rev Cytol. 2001;204:179-238. doi: 10.1016/s0074-7696(01)04005-0. Int Rev Cytol. 2001. PMID: 11243595 Review.
Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus.
Fassad MR, Shoemark A, Legendre M, Hirst RA, Koll F, le Borgne P, Louis B, Daudvohra F, Patel MP, Thomas L, Dixon M, Burgoyne T, Hayes J, Nicholson AG, Cullup T, Jenkins L, Carr SB, Aurora P, Lemullois M, Aubusson-Fleury A, Papon JF, O'Callaghan C, Amselem S, Hogg C, Escudier E, Tassin AM, Mitchison HM. Fassad MR, et al. Am J Hum Genet. 2018 Dec 6;103(6):984-994. doi: 10.1016/j.ajhg.2018.10.016. Epub 2018 Nov 21. Am J Hum Genet. 2018. PMID: 30471717 Free PMC article.
Motoring through: the role of kinesin superfamily proteins in female meiosis.
Camlin NJ, McLaughlin EA, Holt JE. Camlin NJ, et al. Hum Reprod Update. 2017 Jul 1;23(4):409-420. doi: 10.1093/humupd/dmx010. Hum Reprod Update. 2017. PMID: 28431155 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
Kinesin and Dynein Mechanics: Measurement Methods and Research Applications.
Abraham Z, Hawley E, Hayosh D, Webster-Wood VA, Akkus O. Abraham Z, et al. J Biomech Eng. 2018 Feb 1;140(2):0208051-02080511. doi: 10.1115/1.4037886. J Biomech Eng. 2018. PMID: 28901373 Free PMC article. Review.
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage.
Viswanathan SK, Sanders HK, McNamara JW, Jagadeesan A, Jahangir A, Tajik AJ, Sadayappan S. Viswanathan SK, et al. PLoS One. 2017 Nov 9;12(11):e0187948. doi: 10.1371/journal.pone.0187948. eCollection 2017. PLoS One. 2017. PMID: 29121657 Free PMC article.
Mutational analysis of motor proteins.
Sweeney HL, Holzbaur EL. Sweeney HL, et al. Annu Rev Physiol. 1996;58:751-92. doi: 10.1146/annurev.ph.58.030196.003535. Annu Rev Physiol. 1996. PMID: 8815819 Review.
Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects.
Loges NT, Antony D, Maver A, Deardorff MA, Güleç EY, Gezdirici A, Nöthe-Menchen T, Höben IM, Jelten L, Frank D, Werner C, Tebbe J, Wu K, Goldmuntz E, Čuturilo G, Krock B, Ritter A, Hjeij R, Bakey Z, Pennekamp P, Dworniczak B, Brunner H, Peterlin B, Tanidir C, Olbrich H, Omran H, Schmidts M. Loges NT, et al. Am J Hum Genet. 2018 Dec 6;103(6):995-1008. doi: 10.1016/j.ajhg.2018.10.020. Epub 2018 Nov 21. Am J Hum Genet. 2018. PMID: 30471718 Free PMC article.
Clinical and Genetic Analysis of Children with Kartagener Syndrome.
Pereira R, Barbosa T, Gales L, Oliveira E, Santos R, Oliveira J, Sousa M. Pereira R, et al. Cells. 2019 Aug 15;8(8):900. doi: 10.3390/cells8080900. Cells. 2019. PMID: 31443223 Free PMC article.
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