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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2016 | 3 |
2017 | 1 |
2020 | 1 |
2023 | 1 |
2024 | 0 |
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6 results
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Page 1
Discovery of dysregulated circular RNAs in whole blood transcriptomes from cystic fibrosis patients - implication of a role for cellular senescence in cystic fibrosis.
J Cyst Fibros. 2023 Jul;22(4):683-693. doi: 10.1016/j.jcf.2023.04.021. Epub 2023 May 2.
J Cyst Fibros. 2023.
PMID: 37142522
Free PMC article.
Nonsense Suppression as an Approach to Treat Lysosomal Storage Diseases.
Keeling KM.
Keeling KM.
Diseases. 2016 Dec;4(4):32. doi: 10.3390/diseases4040032. Epub 2016 Oct 19.
Diseases. 2016.
PMID: 28367323
Free PMC article.
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Ataluren stimulates ribosomal selection of near-cognate tRNAs to promote nonsense suppression.
Roy B, Friesen WJ, Tomizawa Y, Leszyk JD, Zhuo J, Johnson B, Dakka J, Trotta CR, Xue X, Mutyam V, Keeling KM, Mobley JA, Rowe SM, Bedwell DM, Welch EM, Jacobson A.
Roy B, et al.
Proc Natl Acad Sci U S A. 2016 Nov 1;113(44):12508-12513. doi: 10.1073/pnas.1605336113. Epub 2016 Oct 4.
Proc Natl Acad Sci U S A. 2016.
PMID: 27702906
Free PMC article.
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Discovery of Clinically Approved Agents That Promote Suppression of Cystic Fibrosis Transmembrane Conductance Regulator Nonsense Mutations.
Mutyam V, Du M, Xue X, Keeling KM, White EL, Bostwick JR, Rasmussen L, Liu B, Mazur M, Hong JS, Falk Libby E, Liang F, Shang H, Mense M, Suto MJ, Bedwell DM, Rowe SM.
Mutyam V, et al.
Am J Respir Crit Care Med. 2016 Nov 1;194(9):1092-1103. doi: 10.1164/rccm.201601-0154OC.
Am J Respir Crit Care Med. 2016.
PMID: 27104944
Free PMC article.
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Identification of the amino acids inserted during suppression of CFTR nonsense mutations and determination of their functional consequences.
Xue X, Mutyam V, Thakerar A, Mobley J, Bridges RJ, Rowe SM, Keeling KM, Bedwell DM.
Xue X, et al.
Hum Mol Genet. 2017 Aug 15;26(16):3116-3129. doi: 10.1093/hmg/ddx196.
Hum Mol Genet. 2017.
PMID: 28575328
Free PMC article.
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A regulated NMD mouse model supports NMD inhibition as a viable therapeutic option to treat genetic diseases.
Echols J, Siddiqui A, Dai Y, Havasi V, Sun R, Kaczmarczyk A, Keeling KM.
Echols J, et al.
Dis Model Mech. 2020 Aug 27;13(8):dmm044891. doi: 10.1242/dmm.044891.
Dis Model Mech. 2020.
PMID: 32737261
Free PMC article.
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