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Mesothelin is a novel cell surface disease marker and potential therapeutic target in acute myeloid leukemia.
Kaeding AJ, Barwe SP, Gopalakrishnapillai A, Ries RE, Alonzo TA, Gerbing RB, Correnti C, Loken MR, Broderson LE, Pardo L, Le QH, Tang T, Leonti AR, Smith JL, Chou CK, Xu M, Triche T, Kornblau SM, Kolb EA, Tarlock K, Meshinchi S. Kaeding AJ, et al. Among authors: xu m. Blood Adv. 2021 May 11;5(9):2350-2361. doi: 10.1182/bloodadvances.2021004424. Blood Adv. 2021. PMID: 33938941 Free PMC article.
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia.
Wei Q, Fan W, Li HF, Wanga PS, Xu M, Dong HL, Yu H, Lyu J, Luo WJ, Chen DF, Ge W, Wu ZY. Wei Q, et al. Among authors: xu m. J Genet Genomics. 2025 Jan 14:S1673-8527(25)00019-0. doi: 10.1016/j.jgg.2025.01.004. Online ahead of print. J Genet Genomics. 2025. PMID: 39814172
The role of lipid metabolism in cognitive impairment.
Xu M, Wang L, Meng Y, Kang G, Jiang Q, Yan T, Che F. Xu M, et al. Arq Neuropsiquiatr. 2025 Jan;83(1):1-13. doi: 10.1055/s-0044-1792097. Epub 2025 Jan 15. Arq Neuropsiquiatr. 2025. PMID: 39814004 Review.
3D genomic features across >50 diverse cell types reveal insights into the genomic architecture of childhood obesity.
Trang KB, Pahl MC, Pippin JA, Su C, Littleton SH, Sharma P, Kulkarni NN, Ghanem LR, Terry NA, O'Brien JM, Wagley Y, Hankenson KD, Jermusyk A, Hoskins J, Amundadottir LT, Xu M, Brown K, Anderson S, Yang W, Titchenell P, Seale P, Kaestner KH, Cook L, Levings M, Zemel BS, Chesi A, Wells AD, Grant SFA. Trang KB, et al. Among authors: xu m. Elife. 2025 Jan 15;13:RP95411. doi: 10.7554/eLife.95411. Elife. 2025. PMID: 39813287
22,462 results
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