日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Early detection of aberrant cell fate and repair using circulating progenitor cells in patients with heterotopic ossification

利用循环祖细胞对异位骨化患者的异常细胞命运进行早期检测和修复

Nunez, Johanna; Holtz, Matilda; Korlakunta, Sneha; Kang, Hanil; Lin, Florence; Stowe, Hannah; Pagani, Chase A; Shah, Achira; Jeffery, Elise C; Elhamad, Meriam; Nazemidashtarjandi, Saeed; Tower, Robert; Choi, Ji Hae; Kang, Heeseog; Callan, Alexandra; Chen, Antonia F; Ayata, Cenk; Toner, Mehmet; Levi, Benjamin; Karabacak, N Murat

Thrombospondin 1 and 2 regulate mesenchymal progenitor cell fate and matrix organization.

血小板反应蛋白 1 和 2 调节间充质祖细胞的命运和基质组织。

Hunter Madysen K, Korlakunta Sneha, Vishlaghi Neda, Mittal Monisha, Cragg Kyle, Juan Conan, Pagani Chase A, Sun Yuxiao, Lammlin Lindsey, Kessell Karen, Feist Dylan, Choi Ji Hae, Hsieh Meng-Lun, Saikia Jahnu, Duvall Craig L, Kang Heeseog, Alford Andrea I, Hankenson Kurt D, Tower Robert J, Maerz Tristan, Levi Benjamin

Maternal CENP-C restores centromere symmetry in mammalian zygotes to ensure proper chromosome segregation.

母源 CENP-C 可恢复哺乳动物合子着丝粒的对称性,以确保染色体的正确分离。

Tower Catherine A, Manske Gabriel, Ferrell Emily L, Anbarci Dilara N, Jorgensen Kelsey, Ma Binbin, Aboelenain Mansour, Ranjan Rajesh, Chakraborty Saikat, Moritz Lindsay, Das Arunika, Boiani Michele, Black Ben E, Chavez Shawn, Marsh Erica E, Shikanov Ariella, Schindler Karen, Chen Xin, Hammoud Saher Sue

Splicing variants in MYRF cause partial loss of function in the retinal pigment epithelium leading to nanophthalmos

MYRF基因的剪接变异会导致视网膜色素上皮细胞部分功能丧失,从而导致小眼球症。

Rozumek, Gabrielle M; Brinkmeier, Michelle L; Guan, Bin; Wang, Su Qing; Tower, Catherine; Yang, Nina T; Lim, Rachel S; Kong, Dejuan; Soden, Daniel; Zhang, Qitao; Han, John Ys; Miller, Jason Ml; Dong, Lijin; Hannum, D Ford; Moroi, Sayoko E; Richards, Julia E; Hufnagel, Robert B; Prasov, Lev

Integrative spatial multi-omics reveal niche-specific inflammatory signaling and differentiation hierarchies in AML

整合空间多组学揭示急性髓系白血病中特定微环境的炎症信号传导和分化层级

Dasdemir, Enes; Veletic, Ivo; Ly, Christopher P; Quesada, Andres E; Pacheco, Christopher D; Jelloul, Fatima Z; Borges, Pamella; Basu, Sreyashi; Jindal, Sonali; Wang, Zhiqiang; Lazar, Alexander; Wani, Khalida M; Antunes, Dinler A; Reville, Patrick K; Gunaratne, Preethi H; Tower, Robert J; Sharma, Padmanee; Abbas, Hussein A

Effect of Bunion Surgery on Fall Risk: A Nationwide Database Study of 127,990 Older Adults with Hallux Valgus

拇外翻手术对跌倒风险的影响:一项针对127,990名患有拇外翻的老年人的全国数据库研究

Fleischer, Adam; Albright, Rachel; Bhatt, Zalak; Abuali, Neveen; Tower, Dyane; Weil, Lowell

Spatial transcriptomics in bone research: navigating hype and hurdles

骨骼研究中的空间转录组学:应对炒作与挑战

Sokolowskei, Dimitri; Shah, Achira; Trostle, Alexander J; Juan, Conan; Sammarco, Mimi C; Tower, Robert J

Examination of Peer Interactions During Cooperative and Competitive Board Games Among Children with Attention-Deficit/Hyperactivity Disorder on and off Methylphenidate

对服用和未服用哌甲酯的注意力缺陷/多动障碍儿童在合作和竞争性棋盘游戏中同伴互动情况的研究

Jusko, Morgan L; Merrill, Brittany M; Sutton, Emily R; Sikov, Jennifer; Edmondson, Grant; Hayes, Timothy; Tower, Devon; Boeckel, Amy; Fabiano, Gregory A

Risk of revision and other complications in total ankle arthroplasty do not differ by surgeon specialty: Analysis of the PearlDiver healthcare claims database from 2010 to 2023

全踝关节置换术的翻修风险和其他并发症风险并不因外科医生的专科不同而有所差异:基于2010年至2023年PearlDiver医疗保健索赔数据库的分析

Fleischer, Adam E; Albright, Rachel H; Patel, Khushiben; Santiago, Hector; Hook, Jonathan; Tower, Dyane; Weil, Lowell Jr

Suppressive Genetic Interactions Between Haploinsufficient Mitochondrial Genes Encoded in the 22q11.2 Microdeletion Locus Define Brain and Cardiac Phenotypes.

22q11.2 微缺失位点编码的单倍体不足线粒体基因之间的抑制性遗传相互作用决定了大脑和心脏表型。

Wynne Meghan, Zlatic Stephanie A, Park Austin S, Crocker Amanda, Mendez-Vazquez Hadassah, Liporace Eliana, Gokhale Avanti, Tower-Gilchrist Cristy, Robinette Maxine, Purcell Ryan H, Bassell Gary J, Werner Erica, Kwong Jennifer Q, Faundez Victor