Nehal Patel相关文献与解析，生知库 | 链接生命科学的每一步

PRMT5 inhibition promotes osteogenic differentiation of mesenchymal stromal cells and represses basal interferon stimulated gene expression

PRMT5 抑制促进间充质基质细胞的成骨分化并抑制基础干扰素刺激的基因表达

期刊:Bone

影响因子:3.5

doi:10.1016/j.bone.2018.08.025

Satya K Kota, Coco Roening, Nehal Patel, Savithri B Kota, Roland Baron

A Size-Selective Intracellular Delivery Platform

尺寸选择性细胞内递送平台

期刊:Small

影响因子:13

doi:10.1002/smll.201601155

May Tun Saung, Armon Sharei, Viktor A Adalsteinsson, Nahyun Cho, Tushar Kamath, Camilo Ruiz, Jesse Kirkpatrick, Nehal Patel, Mari Mino-Kenudson, Sarah P Thayer, Robert Langer, Klavs F Jensen, Andrew S Liss, J Christopher Love

Growth arrest in the ribosomopathy, Bowen-Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression

核糖体病（鲍恩-康拉迪综合征）中的生长停滞是由于细胞增殖急剧减少和有丝分裂进程缺陷造成的

期刊:

影响因子:3.3

doi:10.1016/j.bbadis.2015.02.007

Joy Armistead, Nehal Patel, Xiaoli Wu, Richard Hemming, Biswajit Chowdhury, Gagandeep Singh Basra, Marc R Del Bigio, Hao Ding, Barbara Triggs-Raine

Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay

EMG1 突变导致 Bowen-Conradi 综合征，导致细胞增殖率降低，同时伴有 G2/M 停滞和 18S rRNA 处理延迟

期刊:

影响因子:

doi:10.1016/j.bbacli.2014.05.002

Joy Armistead, Richard Hemming, Nehal Patel, Barbara Triggs-Raine

De-repression of FOXO3a death axis by microRNA-132 and -212 causes neuronal apoptosis in Alzheimer's disease

microRNA-132 和 -212 解除 FOXO3a 死亡轴的抑制会导致阿尔茨海默病中的神经元凋亡

期刊:Human Molecular Genetics

影响因子:3.1

doi:10.1093/hmg/ddt164

Hon-Kit Andus Wong, Tatiana Veremeyko, Nehal Patel, Cynthia A Lemere, Dominic M Walsh, Christine Esau, Charles Vanderburg, Anna M Krichevsky

Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome

核糖体生物合成所必需的基因 EMG1 突变导致 Bowen-Conradi 综合征

期刊:American Journal of Human Genetics

影响因子:8.1

doi:10.1016/j.ajhg.2009.04.017

Joy Armistead, Sunita Khatkar, Britta Meyer, Brian L Mark, Nehal Patel, Gail Coghlan, Ryan E Lamont, Shuangbo Liu, Jill Wiechert, Peter A Cattini, Peter Koetter, Klaus Wrogemann, Cheryl R Greenberg, Karl-Dieter Entian, Teresa Zelinski, Barbara Triggs-Raine

信号转导

发表日期：2009

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An unexpected finding during microscopy for urinary hemosiderin

在尿液含铁血黄素显微镜检查中意外发现

PRMT5 inhibition promotes osteogenic differentiation of mesenchymal stromal cells and represses basal interferon stimulated gene expression

PRMT5 抑制促进间充质基质细胞的成骨分化并抑制基础干扰素刺激的基因表达

A Size-Selective Intracellular Delivery Platform

尺寸选择性细胞内递送平台

Growth arrest in the ribosomopathy, Bowen-Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression

核糖体病（鲍恩-康拉迪综合征）中的生长停滞是由于细胞增殖急剧减少和有丝分裂进程缺陷造成的

Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay

EMG1 突变导致 Bowen-Conradi 综合征，导致细胞增殖率降低，同时伴有 G2/M 停滞和 18S rRNA 处理延迟

De-repression of FOXO3a death axis by microRNA-132 and -212 causes neuronal apoptosis in Alzheimer's disease

microRNA-132 和 -212 解除 FOXO3a 死亡轴的抑制会导致阿尔茨海默病中的神经元凋亡

Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome

核糖体生物合成所必需的基因 EMG1 突变导致 Bowen-Conradi 综合征