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

PUM1 mediates the posttranscriptional regulation of human fetal hemoglobin

PUM1介导人类胎儿血红蛋白的转录后调控

Elagooz, Reem; Dhara, Anita R; Gott, Rose M; Adams, Sarah E; White, Rachael A; Ghosh, Arnab; Ganguly, Shinjini; Man, Yuncheng; Owusu-Ansah, Amma; Mian, Omar Y; Gurkan, Umut A; Komar, Anton A; Ramamoorthy, Mahesh; Gnanapragasam, Merlin Nithya

EKLF/KLF1 expression defines a unique macrophage subset during mouse erythropoiesis

EKLF/KLF1表达定义了小鼠红细胞生成过程中一个独特的巨噬细胞亚群

Kaustav Mukherjee ,Li Xue ,Antanas Planutis ,Merlin Nithya Gnanapragasam ,Andrew Chess ,James J Bieker

Survey and evaluation of mutations in the human KLF1 transcription unit

人类KLF1转录单元突变的调查和评估

Gnanapragasam, Merlin Nithya; Crispino, John D; Ali, Abdullah M; Weinberg, Rona; Hoffman, Ronald; Raza, Azra; Bieker, James J

Orchestration of late events in erythropoiesis by KLF1/EKLF

KLF1/EKLF 调控红细胞生成后期事件

Gnanapragasam, Merlin Nithya; Bieker, James J

EKLF/KLF1-regulated cell cycle exit is essential for erythroblast enucleation

EKLF/KLF1调控的细胞周期退出对于成红细胞去核至关重要

Gnanapragasam, Merlin Nithya; McGrath, Kathleen E; Catherman, Seana; Xue, Li; Palis, James; Bieker, James J

A Systems Approach Identifies Essential FOXO3 Functions at Key Steps of Terminal Erythropoiesis

系统方法鉴定 FOXO3 在终末红细胞生成关键步骤中发挥的重要作用

Raymond Liang, Genís Campreciós, Yan Kou, Kathleen McGrath, Roberta Nowak, Seana Catherman, Carolina L Bigarella, Pauline Rimmelé, Xin Zhang, Merlin Nithya Gnanapragasam, James J Bieker, Dmitri Papatsenko, Avi Ma'ayan, Emery Bresnick, Velia Fowler, James Palis, Saghi Ghaffari

Extrinsic and intrinsic control by EKLF (KLF1) within a specialized erythroid niche

EKLF(KLF1)在专门的红细胞生态位中进行内在和外在控制

Li Xue, Mariann Galdass, Merlin Nithya Gnanapragasam, Deepa Manwani, James J Bieker

Mi2β-mediated silencing of the fetal γ-globin gene in adult erythroid cells

Mi2β 介导成人红系细胞中胎儿 γ 珠蛋白基因的沉默

Maria Amaya, Megha Desai, Merlin Nithya Gnanapragasam, Shou Zhen Wang, Sheng Zu Zhu, David C Williams Jr, Gordon D Ginder

Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm

红系转录因子EKLF/KLF1突变导致台湾裔患者发生先天性红细胞生成障碍性贫血IV型:回顾所有已报道病例并建立临床诊断范式

Jaffray, Julie A; Mitchell, W Beau; Gnanapragasam, Merlin Nithya; Seshan, Surya V; Guo, Xinhuo; Westhoff, Connie M; Bieker, James J; Manwani, Deepa

p66Alpha-MBD2 coiled-coil interaction and recruitment of Mi-2 are critical for globin gene silencing by the MBD2-NuRD complex

p66Alpha-MBD2 卷曲螺旋相互作用和 Mi-2 的募集对于 MBD2-NuRD 复合物的珠蛋白基因沉默至关重要

Merlin Nithya Gnanapragasam, J Neel Scarsdale, Maria L Amaya, Heather D Webb, Megha A Desai, Ninad M Walavalkar, Shou Zhen Wang, Sheng Zu Zhu, Gordon D Ginder, David C Williams Jr