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Septins Enable T Cell Contact Guidance via Amoeboid-Mesenchymal Switch.
Zhovmer AS, Manning A, Smith C, Wang J, Ma X, Tsygankov D, Dokholyan NV, Cartagena-Rivera AX, Singh RK, Tabdanov ED. Zhovmer AS, et al. Among authors: manning a. bioRxiv [Preprint]. 2023 Sep 27:2023.09.26.559597. doi: 10.1101/2023.09.26.559597. bioRxiv. 2023. PMID: 37808814 Free PMC article. Preprint.
Publisher Correction: Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.
Huerta-Chagoya A, Schroeder P, Mandla R, Li J, Morris L, Vora M, Alkanaq A, Nagy D, Szczerbinski L, Madsen JGS, Bonàs-Guarch S, Mollandin F, Cole JB, Porneala B, Westerman K, Li JH, Pollin TI, Florez JC, Gloyn AL, Carey DJ, Cebola I, Mirshahi UL, Manning AK, Leong A, Udler M, Mercader JM. Huerta-Chagoya A, et al. Among authors: manning ak. Nat Genet. 2024 Oct 22. doi: 10.1038/s41588-024-01986-2. Online ahead of print. Nat Genet. 2024. PMID: 39438755 Free article. No abstract available.
Multicenter validation of automated detection of paramagnetic rim lesions on brain MRI in multiple sclerosis.
Chen L, Ren Z, Clark KA, Lou C, Liu F, Cao Q, Manning AR, Martin ML, Luskin E, O'Donnell CM, Azevedo CJ, Calabresi PA, Freeman L, Henry RG, Longbrake EE, Oh J, Papinutto N, Bilello M, Song JW, Kaisey M, Sicotte NL, Reich DS, Solomon AJ, Ontaneda D, Sati P, Absinta M, Schindler MK, Shinohara RT; NAIMS Cooperative. Chen L, et al. Among authors: manning ar. J Neuroimaging. 2024 Oct 15. doi: 10.1111/jon.13242. Online ahead of print. J Neuroimaging. 2024. PMID: 39410780
Impact of insurance status on MRI phenotypes in MS.
Martin ML, Robert-Fitzgerald T, Schindler MK, Perrone C, Schultz G, Lynch S, Mirkovic N, Thomas S, Elahi A, Reid D, Moore TM, Baller EB, Satterthwaite TD, Cieslak M, Covitz S, Adebimpe A, Manning A, Markowitz CE, Detre JA, Bar-Or A, Kakara M, Shinohara RT. Martin ML, et al. Among authors: manning a. Mult Scler Relat Disord. 2024 Oct 9;92:105919. doi: 10.1016/j.msard.2024.105919. Online ahead of print. Mult Scler Relat Disord. 2024. PMID: 39406154
Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes.
Huerta-Chagoya A, Schroeder P, Mandla R, Li J, Morris L, Vora M, Alkanaq A, Nagy D, Szczerbinski L, Madsen JGS, Bonàs-Guarch S, Mollandin F, Cole JB, Porneala B, Westerman K, Li JH, Pollin TI, Florez JC, Gloyn AL, Carey DJ, Cebola I, Mirshahi UL, Manning AK, Leong A, Udler M, Mercader JM. Huerta-Chagoya A, et al. Among authors: manning ak. Nat Genet. 2024 Oct 8. doi: 10.1038/s41588-024-01947-9. Online ahead of print. Nat Genet. 2024. PMID: 39379762 Free article.
755 results