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

Snai2 and Snai3 transcriptionally regulate cellular fitness and functionality of T cell lineages through distinct gene programs

Snai2 和 Snai3 通过不同的基因程序转录调控 T 细胞谱系的细胞适应性和功能

Peter D Pioli, Sarah K Whiteside, Janis J Weis, John H Weis

Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3

Snai2 和 Snai3 的条件性缺失导致致命的自身免疫

Peter D Pioli, Xinjian Chen, Janis J Weis, John H Weis

Antagonistic Interplay between MicroRNA-155 and IL-10 during Lyme Carditis and Arthritis

莱姆心肌炎和关节炎期间MicroRNA-155和IL-10之间的拮抗作用

Lochhead, Robert B; Zachary, James F; Dalla Rosa, Luciana; Ma, Ying; Weis, John H; O'Connell, Ryan M; Weis, Janis J

Zfp318 regulates IgD expression by abrogating transcription termination within the Ighm/Ighd locus

Zfp318 通过消除 Ighm/Ighd 基因座内的转录终止来调节 IgD 表达

Peter D Pioli, Irina Debnath, Janis J Weis, John H Weis

Borrelia burgdorferi arthritis-associated locus Bbaa1 regulates Lyme arthritis and K/B×N serum transfer arthritis through intrinsic control of type I IFN production

伯氏疏螺旋体关节炎相关基因位点Bbaa1通过内在调控I型干扰素的产生来调节莱姆关节炎和K/B×N血清转移性关节炎。

Ma, Ying; Bramwell, Kenneth K C; Lochhead, Robert B; Paquette, Jackie K; Zachary, James F; Weis, John H; Teuscher, Cory; Weis, Janis J

Murine complement receptor 1 is required for germinal center B cell maintenance but not initiation

小鼠补体受体 1 是生发中心 B 细胞维持所必需的,但不是启动所必需的

Luke R Donius, Janis J Weis, John H Weis

Generation of a novel Cr2 gene allele by homologous recombination that abrogates production of Cr2 but is sufficient for expression of Cr1

通过同源重组产生新的 Cr2 基因等位基因,该基因可消除 Cr2 的产生,但足以表达 Cr1

Luke R Donius, Christopher M Orlando, Janis J Weis, John H Weis

Snail transcription factors in hematopoietic cell development: a model of functional redundancy

蜗牛转录因子在造血细胞发育中的作用:功能冗余模型

Pioli, Peter D; Weis, John H

Kawasaki disease patients homozygous for the rs12252-C variant of interferon-induced transmembrane protein-3 are significantly more likely to develop coronary artery lesions

川崎病患者中,干扰素诱导跨膜蛋白-3 的 rs12252-C 变异纯合子更容易发生冠状动脉病变。

Bowles, Neil E; Arrington, Cammon B; Hirono, Keiichi; Nakamura, Tsuneyuki; Ngo, Long; Wee, Yin Shen; Ichida, Fukiko; Weis, John H

Bone marrow-induced Mef2c deficiency delays B-cell development and alters the expression of key B-cell regulatory proteins

骨髓诱导的 Mef2c 缺乏会延迟 B 细胞发育并改变关键 B 细胞调节蛋白的表达

Irina Debnath, Kirstin M Roundy, Peter D Pioli, Janis J Weis, John H Weis