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

Tabular foundation model predicts alternative lengthening of telomeres (ALT) and identifies SMARCAL1 as a target in ALT-driven cancers

表格基础模型预测端粒替代延长(ALT),并将SMARCAL1确定为ALT驱动型癌症的靶点

Bennett, D; Wierdl, M; Chakraborty, S; Johnson, J D; Akingbehin, V; Estevez-Prado, D; Feng, Y; Morsby, J J; Harper, J; Mohammad Nezhady, M A; Pan, M; Ocasio-Martinez, N; Catlett, J L; Nations, T B; Dharia, N V; Robichaud, A; Herman, A; Zhang, S; Kelly, J; Steele, J; Rusch, M; Wienand, K; Campbell, C D; Alexe, G; Vazquez, F; Getz, G; Roberts, Cwm; Mullighan, C G; Sweet-Cordero, E A; Reynolds, C P; Koneru, B; Shelat, A A; Durbin, A D; Bernstein, E; Ma, X; Stegmaier, K; Geeleher, P; Guenther, L M

Enhanced Risk Stratification for Children and Young Adults with B-Cell Acute Lymphoblastic Leukemia: A Children's Oncology Group Report

儿童和青少年B细胞急性淋巴细胞白血病风险分层强化:儿童肿瘤协作组报告

DelRocco, N J; Loh, M L; Borowitz, M J; Gupta, S; Rabin, K R; Zweidler-McKay, P; Maloney, K W; Mattano, L A; Larsen, E; Angiolillo, A; Schore, R J; Burke, M J; Salzer, W L; Wood, B L; Carroll, A J; Heerema, N A; Reshmi, S C; Gastier-Foster, J M; Harvey, R; Chen, I M; Roberts, K G; Mullighan, C G; Willman, C; Winick, N; Carroll, W L; Rau, R E; Teachey, D T; Hunger, S P; Raetz, E A; Devidas, M; Kairalla, J A

Novel ALK fusion in anaplastic large cell lymphoma involving EEF1G, a subunit of the eukaryotic elongation factor-1 complex

间变性大细胞淋巴瘤中发现一种新的ALK融合基因,该基因涉及真核延伸因子-1复合物的亚基EEF1G。

Palacios, G; Shaw, T I; Li, Y; Singh, R K; Valentine, M; Sandlund, J T; Lim, M S; Mullighan, C G; Leventaki, V

PU.1 cooperates with IRF4 and IRF8 to suppress pre-B-cell leukemia

PU.1 与 IRF4 和 IRF8 协同作用抑制前 B 细胞白血病

Pang, S H M; Minnich, M; Gangatirkar, P; Zheng, Z; Ebert, A; Song, G; Dickins, R A; Corcoran, L M; Mullighan, C G; Busslinger, M; Huntington, N D; Nutt, S L; Carotta, S

IDH1 and IDH2 mutations in pediatric acute leukemia.

儿童急性白血病中的 IDH1 和 IDH2 突变

Andersson A K, Miller D W, Lynch J A, Lemoff A S, Cai Z, Pounds S B, Radtke I, Yan B, Schuetz J D, Rubnitz J E, Ribeiro R C, Raimondi S C, Zhang J, Mullighan C G, Shurtleff S A, Schulman B A, Downing J R

Fas gene promoter polymorphisms in primary Sjögren's syndrome

原发性干燥综合征中Fas基因启动子多态性

Mullighan, C G; Heatley, S; Lester, S; Rischmueller, M; Gordon, T P; Bardy, P G

Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?

对男性 CVID 患者进行 Btk 基因突变评估:有多少人被误诊?

Weston, S A; Prasad, M L; Mullighan, C G; Chapel, H; Benson, E M

A rapid method of haplotyping HFE mutations and linkage disequilibrium in a Caucasoid population

一种快速检测高加索人群中HFE基因突变和连锁不平衡单倍型的方法

Mullighan, C G; Bunce, M; Fanning, G C; Marshall, S E; Welsh, K I