| Year |
Citation |
Score |
| 2024 |
Stock AJ, Gonzalez Paredes P, de Almeida LP, Kosanke SD, Chetlur S, Budde H, Wakenight P, Zwingman TA, Rosen ABI, Allenspach EJ, Millen KJ, Buckner JH, Rawlings DJ, Gorman JA. The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner. Frontiers in Immunology. 15: 1349601. PMID 38487540 DOI: 10.3389/fimmu.2024.1349601 |
0.558 |
|
| 2024 |
Stock AJ, Gonzalez-Paredes P, Previato de Almeida L, Kosanke SD, Chetlur S, Budde H, Wakenight P, Zwingman TA, Rosen AB, Allenspach E, Millen KJ, Buckner JH, Rawlings DJ, Gorman JA. The IFIH1-A946T risk variant promotes diabetes in a sex-dependent manner. Biorxiv : the Preprint Server For Biology. PMID 38328221 DOI: 10.1101/2024.01.20.576482 |
0.558 |
|
| 2023 |
Nguyen ED, Fard VN, Kim BY, Collins S, Galey M, Nelson BR, Wakenight P, Gable SM, McKenna A, Bammler TK, MacDonald J, Okamura DM, Shendure J, Beier DR, Ramirez JM, et al. GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse (Acomys cahirinus). G3 (Bethesda, Md.). PMID 37552705 DOI: 10.1093/g3journal/jkad177 |
0.544 |
|
| 2023 |
Nguyen ED, Fard VN, Kim BY, Collins S, Galey M, Nelson BR, Wakenight P, Gable SM, McKenna A, Bammler TK, MacDonald J, Okamura DM, Shendure J, Beier DR, Ramirez JM, et al. GENOME REPORT: Chromosome-scale genome assembly of the African spiny mouse ( ). Biorxiv : the Preprint Server For Biology. PMID 37066261 DOI: 10.1101/2023.04.03.535372 |
0.544 |
|
| 2022 |
Wei AD, Wakenight P, Zwingman TA, Bard AM, Sahai N, Willemsen MH, Schelhaas HJ, Stegmann APA, Verhoeven JS, de Man SA, Wessels MW, Kleefstra T, Shinde DN, Helbig KL, Basinger A, et al. Human KCNQ5 de novo Mutations Underlie Epilepsy and Intellectual Disability. Journal of Neurophysiology. PMID 35583973 DOI: 10.1152/jn.00509.2021 |
0.507 |
|
| 2021 |
Okamura DM, Brewer CM, Wakenight P, Bahrami N, Bernardi K, Tran A, Olson J, Shi X, Yeh SY, Piliponsky A, Collins SJ, Nguyen ED, Timms AE, MacDonald JW, Bammler TK, et al. Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis. Iscience. 24: 103269. PMID 34849462 DOI: 10.1016/j.isci.2021.103269 |
0.552 |
|
| 2021 |
Brewer CM, Nelson BR, Wakenight P, Collins SJ, Okamura DM, Dong XR, Mahoney WM, McKenna A, Shendure J, Timms A, Millen KJ, Majesky MW. Adaptations in Hippo-Yap signaling and myofibroblast fate underlie scar-free ear appendage wound healing in spiny mice. Developmental Cell. PMID 34610329 DOI: 10.1016/j.devcel.2021.09.008 |
0.536 |
|
| 2013 |
Lehoczky JA, Thomas PE, Patrie KM, Owens KM, Villarreal LM, Galbraith K, Washburn J, Johnson CN, Gavino B, Borowsky AD, Millen KJ, Wakenight P, Law W, Van Keuren ML, Gavrilina G, et al. A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice. Plos Genetics. 9: e1003967. PMID 24339789 DOI: 10.1371/Journal.Pgen.1003967 |
0.551 |
|
| 2010 |
Swanson DJ, Steshina EY, Wakenight P, Aldinger KA, Goldowitz D, Millen KJ, Chizhikov VV. Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele. The European Journal of Neuroscience. 32: 707-16. PMID 20722722 DOI: 10.1111/J.1460-9568.2010.07330.X |
0.528 |
|
| 2010 |
Singla V, Hunkapiller J, Santos N, Seol AD, Norman AR, Wakenight P, Skarnes WC, Reiter JF. Floxin, a resource for genetically engineering mouse ESCs. Nature Methods. 7: 50-2. PMID 19966808 DOI: 10.1038/Nmeth.1406 |
0.333 |
|
| 2001 |
Mitchell KJ, Pinson KI, Kelly OG, Brennan J, Zupicich J, Scherz P, Leighton PA, Goodrich LV, Lu X, Avery BJ, Tate P, Dill K, Pangilinan E, Wakenight P, Tessier-Lavigne M, et al. Functional analysis of secreted and transmembrane proteins critical to mouse development. Nature Genetics. 28: 241-9. PMID 11431694 DOI: 10.1038/90074 |
0.423 |
|
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