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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2016 | 1 |
2017 | 1 |
2018 | 1 |
2019 | 1 |
2020 | 2 |
2024 | 0 |
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6 results
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Page 1
Whole-genome sequencing of patients with rare diseases in a national health system.
Nature. 2020 Jul;583(7814):96-102. doi: 10.1038/s41586-020-2434-2. Epub 2020 Jun 24.
Nature. 2020.
PMID: 32581362
Free PMC article.
Mavacamten rescues increased myofilament calcium sensitivity and dysregulation of Ca2+ flux caused by thin filament hypertrophic cardiomyopathy mutations.
Sparrow AJ, Watkins H, Daniels MJ, Redwood C, Robinson P.
Sparrow AJ, et al.
Am J Physiol Heart Circ Physiol. 2020 Mar 1;318(3):H715-H722. doi: 10.1152/ajpheart.00023.2020. Epub 2020 Feb 21.
Am J Physiol Heart Circ Physiol. 2020.
PMID: 32083971
Free PMC article.
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Antithrombotic Therapy and Device-Related Thrombosis Following Endovascular Left Atrial Appendage Closure.
Saw J, Nielsen-Kudsk JE, Bergmann M, Daniels MJ, Tzikas A, Reisman M, Rana BS.
Saw J, et al.
JACC Cardiovasc Interv. 2019 Jun 10;12(11):1067-1076. doi: 10.1016/j.jcin.2018.11.001. Epub 2019 May 15.
JACC Cardiovasc Interv. 2019.
PMID: 31103535
Free article.
Review.
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The American College of Cardiology 2018; a Starbuckian ODYSSEY and a Black Barbershop.
Daniels MJ.
Daniels MJ.
Cardiovasc Res. 2018 May 1;114(6):e44-e46. doi: 10.1093/cvr/cvy072.
Cardiovasc Res. 2018.
PMID: 29648584
Free PMC article.
No abstract available.
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Translation reprogramming is an evolutionarily conserved driver of phenotypic plasticity and therapeutic resistance in melanoma.
Falletta P, Sanchez-Del-Campo L, Chauhan J, Effern M, Kenyon A, Kershaw CJ, Siddaway R, Lisle R, Freter R, Daniels MJ, Lu X, Tüting T, Middleton M, Buffa FM, Willis AE, Pavitt G, Ronai ZA, Sauka-Spengler T, Hölzel M, Goding CR.
Falletta P, et al.
Genes Dev. 2017 Jan 1;31(1):18-33. doi: 10.1101/gad.290940.116. Epub 2017 Jan 17.
Genes Dev. 2017.
PMID: 28096186
Free PMC article.
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Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation.
Ng YS, Hardy SA, Shrier V, Quaghebeur G, Mole DR, Daniels MJ, Downes SM, Freebody J, Fratter C, Hofer M, Nemeth AH, Poulton J, Taylor RW.
Ng YS, et al.
Neuromuscul Disord. 2016 Oct;26(10):702-705. doi: 10.1016/j.nmd.2016.08.009. Epub 2016 Aug 17.
Neuromuscul Disord. 2016.
PMID: 27618137
Free PMC article.
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