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

Intratumoral plasma cells mediate CD8+ T cell infiltration and successful immune checkpoint blockade therapy in de novo MPNSTs

肿瘤内浆细胞介导 CD8+ T 细胞浸润,并促进原发性恶性周围神经鞘瘤 (MPNST) 的免疫检查点阻断疗法成功。

Lingo, Joshua J; Reis, Ryan; Allamargot, Chantal; Raygoza Garay, Juan A; Kaemmer, Courtney A; Elias, Elizabeth C; Voigt, Ellen; Jabbari, Ali; Wilhelm, Connor R; Boyden, Alexander W; Karandikar, Nitin J; Breheny, Patrick; Meyerholz, David K; Dodd, Rebecca D; Houtman, Jon C D; Darbro, Benjamin W; Quelle, Dawn E

A genetic variant in SMAD7 acts as a modifier of LMNA-associated muscular dystrophy, implicating SMAD signaling as a therapeutic target.

SMAD7 基因变异可作为 LMNA 相关肌营养不良症的修饰因子,表明 SMAD 信号传导可作为治疗靶点

Mohar Nathaniel P, Langland Christopher J, Darr Zachary, Viles Jill, Moore Steven A, Darbro Benjamin W, Wallrath Lori L

UDP-glucose dehydrogenase variants cause dystroglycanopathy.

UDP-葡萄糖脱氢酶变异体可导致肌营养不良蛋白病

Reelfs Anna M, Stephan Carrie M, Czech Theresa M, Cox Mary O, Joseph Soumya, Darbro Benjamin W, Moore Steven A, Campbell Kevin P, Mathews Katherine D

Mapping the Evolutionary Space of SARS-CoV-2 Variants to Anticipate Emergence of Subvariants Resistant to COVID-19 Therapeutics

绘制SARS-CoV-2变异株的进化空间图谱,以预测对COVID-19疗法产生耐药性的亚变异株的出现

Rojas Chávez, Roberth Anthony; Fili, Mohammad; Han, Changze; Rahman, Syed A; Bicar, Isaiah G L; Gregory, Sullivan; Helverson, Annika; Hu, Guiping; Darbro, Benjamin W; Das, Jishnu; Brown, Grant D; Haim, Hillel

Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy

杜氏肌营养不良症和贝克尔肌营养不良症中的内含子突变和早期转录终止

Waldrop, Megan A; Moore, Steven A; Mathews, Katherine D; Darbro, Benjamin W; Medne, Livja; Finkel, Richard; Connolly, Anne M; Crawford, Thomas O; Drachman, Daniel; Wein, Nicolas; Habib, Ali A; Krzesniak-Swinarska, Monika A; Zaidman, Craig M; Collins, James J; Jokela, Manu; Udd, Bjarne; Day, John W; Ortiz-Guerrero, Gloria; Statland, Jeff; Butterfield, Russell J; Dunn, Diane M; Weiss, Robert B; Flanigan, Kevin M

A comprehensive list of human microdeletion and microduplication syndromes

人类微缺失和微重复综合征的完整列表

Wetzel, Alyssa S; Darbro, Benjamin W

The emerging role of somatic tumor sequencing in the treatment of urothelial cancer

体细胞肿瘤测序在尿路上皮癌治疗中的新兴作用

Wen, Lexiaochuan; Britton, Cameron J; Garje, Rohan; Darbro, Benjamin W; Packiam, Vignesh T

Data on the utilization of paraneoplastic syndrome autoantibody testing at an academic medical center

学术医疗中心副肿瘤综合征自身抗体检测应用数据

Krasowski, Matthew D; Dolezal, Anna; Steussy, Bryan W; Gailey, Michael P; Darbro, Benjamin W

Combination therapies for MPNSTs targeting RABL6A-RB1 signaling

针对 RABL6A-RB1 信号通路的 MPNST 联合疗法

Kohlmeyer, Jordan L; Gordon, David J; Tanas, Munir R; Dodd, Rebecca D; Monga, Varun; Darbro, Benjamin W; Quelle, Dawn E

Longitudinal phenotype development in a minipig model of neurofibromatosis type 1

小型猪神经纤维瘤病1型模型的纵向表型发展

Uthoff, Johanna; Larson, Jared; Sato, Takashi S; Hammond, Emily; Schroeder, Kimberly E; Rohret, Frank; Rogers, Christopher S; Quelle, Dawn E; Darbro, Benjamin W; Khanna, Rajesh; Weimer, Jill M; Meyerholz, David K; Sieren, Jessica C