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Year | Number of Results |
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2022 | 4 |
2023 | 1 |
2024 | 2 |
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MUTATIONEXPLORER- A WEBSERVER FOR MUTATION OF PROTEINS AND 3D VISUALIZATION OF ENERGETIC IMPACTS.
bioRxiv [Preprint]. 2024 Feb 28:2023.03.23.533926. doi: 10.1101/2023.03.23.533926.
bioRxiv. 2024.
PMID: 38464310
Free PMC article.
Updated.
Preprint.
Approximating Projections of Conformational Boltzmann Distributions with AlphaFold2 Predictions: Opportunities and Limitations.
Brown BP, Stein RA, Meiler J, Mchaourab HS.
Brown BP, et al.
J Chem Theory Comput. 2024 Feb 13;20(3):1434-1447. doi: 10.1021/acs.jctc.3c01081. Epub 2024 Jan 12.
J Chem Theory Comput. 2024.
PMID: 38215214
Free PMC article.
Item in Clipboard
Approximating conformational Boltzmann distributions with AlphaFold2 predictions.
Brown BP, Stein RA, Meiler J, Mchaourab H.
Brown BP, et al.
bioRxiv [Preprint]. 2023 Aug 7:2023.08.06.552168. doi: 10.1101/2023.08.06.552168.
bioRxiv. 2023.
PMID: 37609301
Free PMC article.
Updated.
Preprint.
Item in Clipboard
Allele-specific activation, enzyme kinetics, and inhibitor sensitivities of EGFR exon 19 deletion mutations in lung cancer.
Brown BP, Zhang YK, Kim S, Finneran P, Yan Y, Du Z, Kim J, Hartzler AL, LeNoue-Newton ML, Smith AW, Meiler J, Lovly CM.
Brown BP, et al.
Proc Natl Acad Sci U S A. 2022 Jul 26;119(30):e2206588119. doi: 10.1073/pnas.2206588119. Epub 2022 Jul 22.
Proc Natl Acad Sci U S A. 2022.
PMID: 35867821
Free PMC article.
Item in Clipboard
An Active Learning Framework Improves Tumor Variant Interpretation.
Blee AM, Li B, Pecen T, Meiler J, Nagel ZD, Capra JA, Chazin WJ.
Blee AM, et al.
Cancer Res. 2022 Aug 3;82(15):2704-2715. doi: 10.1158/0008-5472.CAN-21-3798.
Cancer Res. 2022.
PMID: 35687855
Free PMC article.
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Integration of Protein Structure and Population-Scale DNA Sequence Data for Disease Gene Discovery and Variant Interpretation.
Li B, Jin B, Capra JA, Bush WS.
Li B, et al.
Annu Rev Biomed Data Sci. 2022 Aug 10;5:141-161. doi: 10.1146/annurev-biodatasci-122220-112147. Epub 2022 May 4.
Annu Rev Biomed Data Sci. 2022.
PMID: 35508071
Review.
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Confirmation of association of TGFBI p.Ser591Phe mutation with variant lattice corneal dystrophy.
Choo CH, Chung DD, Ledwitch KV, Kassels A, Meiler J, Aldave AJ.
Choo CH, et al.
Ophthalmic Genet. 2022 Aug;43(4):530-533. doi: 10.1080/13816810.2022.2050766. Epub 2022 Mar 22.
Ophthalmic Genet. 2022.
PMID: 35315300
Free PMC article.
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