H
Ha Nam Nguyen
Researcher at Johns Hopkins University School of Medicine
Publications - 38
Citations - 6607
Ha Nam Nguyen is an academic researcher from Johns Hopkins University School of Medicine. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 20, co-authored 36 publications receiving 5574 citations. Previous affiliations of Ha Nam Nguyen include Johns Hopkins University & Stanford University.
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Journal ArticleDOI
Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure
Xuyu Qian,Ha Nam Nguyen,Mingxi M. Song,Christopher Hadiono,Sarah C. Ogden,Christy Hammack,Bing Yao,Gregory R. Hamersky,Fadi Jacob,Chun Zhong,Ki Jun Yoon,William J. Jeang,Li Lin,Yujing Li,Jai Thakor,Daniel A. Berg,Ce Zhang,Eunchai Kang,Michael Chickering,David W. Nauen,Cheng-Ying Ho,Cheng-Ying Ho,Zhexing Wen,Kimberly M. Christian,Pei Yong Shi,Brady J. Maher,Hao Wu,Peng Jin,Hengli Tang,Hongjun Song,Guo Li Ming +30 more
TL;DR: A miniaturized spinning bioreactor (SpinΩ) is developed to generate forebrain-specific organoids from human iPSCs that recapitulate key features of human cortical development, including progenitor zone organization, neurogenesis, gene expression, and, notably, a distinct human-specific outer radial glia cell layer.
Journal ArticleDOI
LRRK2 Mutant iPSC-Derived DA Neurons Demonstrate Increased Susceptibility to Oxidative Stress
Ha Nam Nguyen,Blake Byers,Branden J. Cord,Aleksandr Shcheglovitov,James A. Byrne,Prachi Gujar,Kehkooi Kee,Birgitt Schüle,Ricardo E. Dolmetsch,William Langston,Theo D. Palmer,Renee A. Reijo Pera +11 more
TL;DR: Generation of induced pluripotent stem cells that carry the p.G2019S mutation in the Leucine-Rich Repeat Kinase-2 (LRRK2) gene and their differentiation into DA neurons found that DA neurons derived from G2019S-iPSCs showed increased expression of key oxidative stress-response genes and α-synuclein protein.
Journal ArticleDOI
Identification of small-molecule inhibitors of Zika virus infection and induced neural cell death via a drug repurposing screen
Miao Xu,Emily M. Lee,Zhexing Wen,Yichen Cheng,Wei Kai Huang,Xuyu Qian,Julia Tcw,Jennifer Kouznetsova,Sarah C. Ogden,Christy Hammack,Fadi Jacob,Ha Nam Nguyen,Misha Itkin,Catherine Hanna,Paul Shinn,Chase Allen,Samuel G. Michael,Anton Simeonov,Wenwei Huang,Kimberly M. Christian,Alison Goate,Kristen J. Brennand,Ruili Huang,Menghang Xia,Guo Li Ming,Wei Zheng,Hongjun Song,Hengli Tang +27 more
TL;DR: A pan-caspase inhibitor, emricasan, inhibited ZIKV-induced increases in caspase-3 activity and protected human cortical neural progenitors in both monolayer and three-dimensional organoid cultures, and combination treatments using one compound from each category (neuroprotective and antiviral) further increased protection of human neural progensitors and astrocytes from ZIKv-induced cell death.
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Synaptic dysregulation in a human iPS cell model of mental disorders
Zhexing Wen,Ha Nam Nguyen,Ziyuan Guo,Matthew A. Lalli,Xinyuan Wang,Yijing Su,Namshik Kim,Ki Jun Yoon,Jaehoon Shin,Ce Zhang,Georgia Makri,David W. Nauen,Huimei Yu,Elmer Guzman,Cheng Hsuan Chiang,Nadine Yoritomo,Kozo Kaibuchi,Jizhong Zou,Kimberly M. Christian,Linzhao Cheng,Christopher A. Ross,Russell L. Margolis,Gong Chen,Kenneth S. Kosik,Hongjun Song,Guo Li Ming +25 more
TL;DR: This study reveals that a psychiatric disorder relevant mutation causes synapse deficits and transcriptional dysregulation in human neurons and the findings provide new insight into the molecular and synaptic etiopathology of psychiatric disorders.
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Human DAZL, DAZ and BOULE genes modulate primordial germ-cell and haploid gamete formation
TL;DR: It is observed that human DAZL (deleted in azoospermia-like) functions in primordial germ-cell formation, whereas closely related genes DAZ and BOULE promote later stages of meiosis and development of haploid gametes.