Personal information

Activities

Employment (1)

Beckman Research Institute, City of Hope: CA, CA, US

2017-08-01 to present | Postdoctoral researcher (Stem Cell)
Employment
Source: Self-asserted source
Cheng Wang

Education and qualifications (1)

Huazhong University of Science and Technology: Wuhan, Hubei, CN

2012-09-01 to 2015-06-30 | Ph.D. (College of life science)
Education
Source: Self-asserted source
Cheng Wang

Works (16)

Astrocytic response mediated by the CLU risk allele inhibits OPC proliferation and myelination in a human iPSC model

Cell Reports
2023-08 | Journal article
Part of ISSN: 2211-1247
Contributors: Zhenqing Liu; Jianfei Chao; Cheng Wang; Guihua Sun; Daniel Roeth; Wei Liu; Xianwei Chen; Li Li; E Tian; Lizhao Feng et al.
Source: Self-asserted source
Cheng Wang

Compound screen identifies the small molecule Q34 as an inhibitor of SARS-CoV-2 infection

iScience
2022-01-21 | Journal article
Part of ISSN: 2589-0042
Contributors: Qi Cui; Gustavo Garcia; Mingzi Zhang; Cheng Wang; Hongzhi Li; Tao Zhou; Guihua Sun; Vaithilingaraja Arumugaswami; Yanhong Shi; Cheng Wang
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Comparative transcriptomic analysis of SARS-CoV-2 infected cell model systems reveals differential innate immune responses.

Scientific reports
2021-08-25 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Targeting PUS7 suppresses tRNA pseudouridylation and glioblastoma tumorigenesis

Nature Cancer
2021-08-16 | Journal article
Part of ISSN: 2662-1347
Contributors: Qi Cui; Kailin Yin; Xiaoting Zhang; Peng Ye; Xianwei Chen; Jianfei Chao; Haowei Meng; Jiangbo Wei; Daniel Roeth; Li Li et al.
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

ApoE-Isoform-Dependent SARS-CoV-2 Neurotropism and Cellular Response.

Cell stem cell
2021-01-04 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus.

Frontiers in cell and developmental biology
2020-11-04 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Modeling Human Cytomegalovirus-Induced Microcephaly in Human iPSC-Derived Brain Organoids.

Cell reports. Medicine
2020-03-25 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Murine Placental-Fetal Phosphate Dyshomeostasis Caused by an Xpr1 Deficiency Accelerates Placental Calcification and Restricts Fetal Growth in Late Gestation.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
2019-10-25 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

A Novel <i>CDH1</i> Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate.

Genetic testing and molecular biomarkers
2019-10-22 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B.

Epilepsia
2018-07-15 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B.

Scientific reports
2017-12-19 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification.

Movement disorders : official journal of the Movement Disorder Society
2017-05-29 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Molecular mechanism of idiopathic basal ganglia calcification

Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji
2015 | Journal article
EID:

2-s2.0-84942787194

Part of ISSN: 02539772
Contributors: Wang, C.; Xu, X.; Li, L.; Wang, T.; Zhang, M.; Shen, L.; Tang, B.; Liu, J.
Source: Self-asserted source
Cheng Wang via Scopus - Elsevier

Gain-of-function mutations in SCN11A cause familial episodic pain.

American journal of human genetics
2013-10-24 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis.

Nature genetics
2012-02-12 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gamma.

Molecular genetics and metabolism
2010-09-27 | Journal article
Source: Self-asserted source
Cheng Wang
grade
Preferred source (of 2)‎

Peer review (16 reviews for 3 publications/grants)

Review activity for Biochemical genetics. (1)
Review activity for Human genetics. (1)
Review activity for Molecular neurobiology. (14)