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Fuchen Liu
Fuchen Liu
Qilu Hospital of Shandong University
在 email.sdu.edu.cn 的电子邮件经过验证
标题
引用次数
引用次数
年份
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
M Li, G Santpere, Y Imamura Kawasawa, OV Evgrafov, FO Gulden, ...
Science 362 (6420), eaat7615, 2018
6622018
Zika virus disrupts phospho-TBK1 localization and mitosis in human neuroepithelial stem cells and radial glia
M Onorati, Z Li, F Liu, AMM Sousa, N Nakagawa, M Li, MT Dell’Anno, ...
Cell reports 16 (10), 2576-2592, 2016
3042016
Transcriptome and epigenome landscape of human cortical development modeled in organoids
A Amiri, G Coppola, S Scuderi, F Wu, T Roychowdhury, F Liu, ...
Science 362 (6420), eaat6720, 2018
2762018
Molecular and cellular reorganization of neural circuits in the human lineage
AMM Sousa, Y Zhu, MA Raghanti, RR Kitchen, M Onorati, ...
Science 358 (6366), 1027-1032, 2017
2192017
Control of species-dependent cortico-motoneuronal connections underlying manual dexterity
Z Gu, J Kalambogias, S Yoshioka, W Han, Z Li, YI Kawasawa, ...
Science 357 (6349), 400-404, 2017
1022017
Human neuroepithelial stem cell regional specificity enables spinal cord repair through a relay circuit
MT Dell’Anno, X Wang, M Onorati, M Li, F Talpo, Y Sekine, S Ma, F Liu, ...
Nature communications 9 (1), 3419, 2018
762018
The 7q11. 23 protein DNAJC30 interacts with ATP synthase and links mitochondria to brain development
ATN Tebbenkamp, L Varela, J Choi, MI Paredes, AM Giani, JE Song, ...
Cell 175 (4), 1088-1104. e23, 2018
632018
Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus
PQ Duy, SC Weise, C Marini, XJ Li, D Liang, PJ Dahl, S Ma, A Spajic, ...
Nature neuroscience 25 (4), 458-473, 2022
612022
Unfolded protein response and activated degradative pathways regulation in GNE myopathy
H Li, Q Chen, F Liu, X Zhang, W Li, S Liu, Y Zhao, Y Gong, C Yan
PLoS One 8 (3), e58116, 2013
412013
Idebenone protects against atherosclerosis in apolipoprotein E-deficient mice via activation of the SIRT3-SOD2-mtROS pathway
W Jiang, H Geng, X Lv, J Ma, F Liu, P Lin, C Yan
Cardiovascular Drugs and Therapy 35, 1129-1145, 2021
342021
Dysferlinopathy: mitochondrial abnormalities in human skeletal muscle
F Liu, J Lou, D Zhao, W Li, Y Zhao, X Sun, C Yan
International Journal of Neuroscience 126 (6), 499-509, 2016
302016
Cleavage of potassium channel Kv2. 1 by BACE2 reduces neuronal apoptosis
F Liu, Y Zhang, Z Liang, Q Sun, H Liu, J Zhao, J Xu, J Zheng, Y Yun, X Yu, ...
Molecular psychiatry 23 (7), 1542-1554, 2018
262018
ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme A …
J Xu, D Li, J Lv, X Xu, B Wen, P Lin, F Liu, K Ji, J Shan, H Li, W Li, Y Zhao, ...
Annals of neurology 84 (5), 659-673, 2018
252018
Clinical and molecular genetic analysis in Chinese patients with distal myopathy with rimmed vacuoles
H Li, Q Chen, F Liu, X Zhang, T Liu, W Li, S Liu, Y Zhao, B Wen, T Dai, ...
Journal of human genetics 56 (4), 335-338, 2011
232011
Reversible neuropsychiatric disturbances caused by nitrous oxide toxicity: clinical, imaging and electrophysiological Profiles of 21 patients with 6–12 months follow-up
R Zheng, Q Wang, M Li, F Liu, Y Zhang, B Zhao, Y Sun, D Zhang, C Yan, ...
Neuropsychiatric Disease and Treatment, 2817-2825, 2020
202020
Preresidency publication productivity of US neurosurgery interns
PQ Duy, MD Paranjpe, P Antwi, NS Diab, JK Wang, DNW Kim, ...
World neurosurgery 137, e291-e297, 2020
182020
State MW, Lein ES, Knowles JA, Marques-Bonet T, Sherwood CC, Gerstein MB, Sestan N (2017): Molecular and cellular reorganization of neural circuits in the human lineage
AMM Sousa, Y Zhu, MA Raghanti, RR Kitchen, M Onorati, ...
Science 358, 1027-1032, 0
14
Zika virus disrupts phospho-TBK1 localization and mitosis in human neuroepithelial stem cells and radial glia. Cell Rep 16: 2576–2592
M Onorati, Z Li, F Liu, AMM Sousa, N Nakagawa, M Li, MT Dell’Anno, ...
132016
Novel mitochondrial C15620A variant may modulate the phenotype of mitochondrial G11778A mutation in a Chinese family with Leigh syndrome
K Ji, J Zheng, B Sun, F Liu, J Shan, D Li, YB Luo, Y Zhao, C Yan
Neuromolecular medicine 16, 119-126, 2014
122014
Distal myopathy due to TCAP variants in four unrelated Chinese patients
X Lv, F Gao, T Dai, D Zhao, W Jiang, H Geng, F Liu, P Lin, C Yan
neurogenetics 22, 1-10, 2021
112021
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