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Author Correction: SARS-CoV-2 infection engenders heterogeneous ribonucleoprotein interactions to impede translation elongation in the lungs

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EXPERIMENTAL AND MOLECULAR MEDICINE 2023年第12期55卷 2609-2609页

作者： Kim, Junsoo Youn, Daehwa Choi, Seunghoon Lee, Youn Woo Sumberzul, Dulguun Yoon, Jeongeun Lee, Hanju Bae, Jong Woo Noh, Hyuna On, Dain Hong, Seung-Min An, Se-Hee Jang, Hui Jeong Kim, Seo Yeon Kim, Young Been Hwang, Ji-Yeon Lee, Hyo-Jung Kim, Hong Bin Park, Jun Won Yun, Jun-Won Shin, Jeon-Soo Seo, Jun-Young Nam, Ki Taek Choi, Kang-Seuk Lee, Ho-Young Chang, Hyeshik Seong, Je Kyung Cho, Jun Center for RNA Research Institute for Basic Science (IBS) Seoul National University Seoul Republic of Korea Interdisciplinary Program in Bioinformatics Seoul National University Seoul Republic of Korea Department of Biomedical Science and Engineering Gwangju Institute of Science and Technology (GIST) Gwangju Republic of Korea Korea Mouse Phenotyping Center (KMPC) Seoul National University Seoul Republic of Korea Laboratory of Developmental Biology and Genomics Research Institute for Veterinary Science and BK 21 PLUS Program for Creative Veterinary Science Research College of Veterinary Medicine Seoul National University Seoul Republic of Korea Department of Nuclear Medicine Seoul National University Bundang Hospital Seongnam Republic of Korea School of Biological Sciences Seoul National University Seoul Republic of Korea Laboratory of Avian Diseases Research Institute for Veterinary Science and BK 21 PLUS Program for Creative Veterinary Science Research College of Veterinary Medicine Seoul National University Seoul Republic of Korea Preclinical Research Center Seoul National University Bundang Hospital Seongnam Republic of Korea Department of Periodontology Section of Dentistry Seoul National University Bundang Hospital Seongnam Republic of Korea Department of Internal Medicine Seoul National University Bundang Hospital Seoul National University College of Medicine Seongnam Republic of Korea Division of Biomedical Convergence College of Biomedical Science Kangwon National University ChunCheon Republic of Korea Laboratory of Veterinary Toxicology College of Veterinary Medicine Seoul National University Seoul Republic of Korea Severance Biomedical Science Institute Graduate School of Medical Science Brain Korea 21 Project Yonsei University College of Medicine Seoul Republic of Korea Department of Nuclear Medicine Seoul National University College of Medicine Seoul Republic of Korea Interdisciplinary Program and BIO MAX Institute Seoul National University

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biomedical data and AI

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Science China Life Sciences 2025年第5期68卷 1536-1540页

作者： Hao Xu Shibo Zhou Zefeng Zhu Vincenzo Vitelli Liangyi Chen Ziwei Dai Ning Yang Luhua Lai Shengyong Yang Sergey Ovchinnikov Zhuoran Qiao Sirui Liu Chen Song Jianfeng Pei Han Wen Jianfeng Feng Yaoyao Zhang Zhengwei Xie Yang-Yu Liu Zhiyuan Li Fulai Jin Hao Li Mohammad Lotfollahi Xuegong Zhang Ge Yang Shihua Zhang Ge Gao Pulin Li Qi Liu Jing-Dong Jackie Han Peking-Tsinghua Center for Life Sciences (CLS) Academy for Advanced Interdisciplinary StudiesPeking University Center for Quantitative Biology (CQB) Academy for Advanced Interdisciplinary StudiesPeking University Peking University-Tsinghua University-National Institute of Biological Sciences Joint Graduate Program Academy for Advanced Interdisciplinary StudiesPeking University Department of Physics University of Chicago School of Life Sciences Southern University of Science and Technology Peking University Chengdu Academy for Advanced Interdisciplinary Biotechnologies College of Chemistry and Molecular Engineering Peking University Department of Biotherapy Cancer Center and State Key Laboratory of BiotherapyWest China HospitalSichuan University Department of Biology Massachusetts Institute of Technology Lambic Therapeutics Inc. Changping Laboratory Al for Science Institute Key Laboratory of Computational Neuroscience and Brain-Inspired Intelligence Fudan University Department of Obstetrics and Gynecology West China Second University HospitalSichuan University Peking University International Cancer Institute and Peking University-Yunnan Baiyao International Medical Institute and State Key Laboratory of Natural and Biomimetic Drugs Department of Molecular and Cellular PharmacologySchool of Pharmaceutical SciencesPeking University Health Science CenterPeking University Channing Division of Network Medicine Department of MedicineBrigham and Women's Hospital and Harvard Medical School Center for Artificial Intelligence and Modeling the Carl R.Woese Institute for Genomic BiologyUniversity of Illinois Urbana-Champaign Department of Genetics and Genome Sciences School of Medicine and Department of Computer and Data Sciences and Department of Population and Quantitative Health SciencesCase Western Reserve University Department of Biochemistry and Biophysics University of California Sanger Institute Department of Automation Tsinghua University State Key Laboratory of Multimodal Artificial Intelligence Systems I

The development of artificial intelligence(AI) and the mining of biomedical data complement each other. From the direct use of computer vision results to analyze medical images for disease screening, to now integrating biological knowledge into models and even accelerating the development of new AI based on biological discoveries, the boundaries of both are constantly expanding, and their connections are becoming closer.

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The Process We Call Earth: Relationships Between Dynamic Feedbacks and the Search for Gaiasignatures in a New Paradigm of Earthlikeness

Perspectives of Earth and Space Scientists

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Perspectives of Earth and Space Scientists 2024年第1期5卷

作者： Michael L. Wong Marissa Duckett Emilia S. Hernandez Vahab Rajaei Kayla J. Smith Earth and Planets Laboratory Carnegie Institution for Science Washington DC USA NASA Hubble Fellowship Program Space Telescope Science Institute Baltimore MD USA M. L. Wong Population Biology Ecology and Evolution Graduate Program Graduate Division of Biological & Biomedical Sciences Emory University Atlanta GA USA Department of Earth and Planetary Sciences University of California Davis Davis CA USA Alaska Center for Energy and Power University of Alaska Fairbanks Fairbanks AK USA School of Chemistry and Biochemistry Georgia Institute of Technology Atlanta GA USA NASA Center for the Origins of Life Georgia Institute of Technology Atlanta GA USA Environmental Engineering Program Department of Water Resources Management Central State University Wilberforce OH USA

Standard notions of an “Earthlike” planet rely solely on physical and material properties, like planetary mass, radius, and surface temperature. Here, we introduce a novel, relational perspective on what defines “Earthlikeness.” In our process-based framework, rocky planets are local pockets of free energy that have the potential to drive the emergence of dynamically persistent systems that coevolve with one another. Examples of dynamically persistent planetary phenomena include magnetic dynamos, mantle convection, tectonic regimes, deep volatile cycles, global climate feedbacks, biogeochemical cycles, and the biosphere. When two or more processes couple to one another such that they gain causal efficacy over one another's persistence, some degree of planetary-scale homeostasis may emerge. In astrobiology, Earthlike exoplanets are often considered to be priority targets for the search for life elsewhere. We suggest that a process-based framework for Earthlikeness has the potential to widen our search space and inspire novel planetary-scale biosignatures, or “Gaiasignatures,” that may be essential for detecting exoplanetary biospheres. Additionally, a process-based view of life can influence the development of agnostic biosignatures at all scales. In contrast to the dominant scientific perspective, which has tended to engender a materialistic worldview, relational ontologies may contribute to our scientific understanding of Earth as a network of dynamically persistent systems, humanity as an integral part of nature, and the search for life in the universe. A process-based framework may offer a better gauge of a planetary body's degree of “Earthlikeness” than physical or material considerations The search for life on exoplanets may require looking for “Gaiasignatures”—signs of a biosphere coupling with its geosphere in a dynamically persistent fashion By virtue of contrasting with dominant scientific worldviews, the ontology of relationality intrinsic to a process-bas

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Adjacent segment disease following Dynesys stabilization for lumbar disorders:A case series of mid-and long-term follow-ups

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World Journal of Clinical Cases 2021年第35期9卷 10850-10860页

作者： Kuan-Ju Chen Chien-Ying Lai Lu-Ting Chiu Wei-Sheng Huang Pang-Hsuan Hsiao Chien-Chun Chang Cheng-Jyh Lin Yuan-Shun Lo Yen-Jen Chen Hsien-Te Chen Department of Orthopedic Surgery China Medical University HospitalTaichung City 404Taiwan Spine Center China Medical University HospitalTaichung City 404Taiwan Management Office for Health Data China Medical University HospitalTaichung City 404Taiwan College of Medicine China Medical UniversityTaichung City 404Taiwan School of Chinese Medicine China Medical UniversityTaichung City 404Taiwan Department of Orthopedic Surgery China Medical University HospitalChina Medical UniversityTaichung City 404Taiwan Spine Center China Medical University HospitalChina Medical UniversityTaichung City 404Taiwan Degree Program of Biomedical Science and Engineering National Chiao Tung UniversityHsinchu City 300Taiwan Department of Biological Science and Technology National Chiao Tung UniversityHsinchu City 300Taiwan Department of Orthopedic Surgery China Medical University Beigang HospitalYunlin County 651Taiwan Graduate Institute of Precision Engineering National Chung Hsing UniversityTaichung City 404Taiwan School of Medicine China Medical UniversityTaichung City 404Taiwan Department of Sport Medicine College of Health CareChina Medical UniversityTaichung City 404Taiwan

BACKGROUND Radiologic adjacent segment degeneration(ASDeg)can occur after spinal *** segment disease(ASDis)is defined as the development of new clinical symptoms corresponding to radiographic changes adjacent to the level of previous spinal *** pre-existing ASDeg is generally considered to result in more severe ASDis;nonetheless,whether the ASDeg status before index surgery influences the postoperative risk of revision surgery due to ASDis warrants *** To identify possible risk factors for ASDis and verify the concept that greater preexisting ASDeg leads to more severe *** Data from 212 patients who underwent posterior decompression with Dynesys stabilization from January 2006 to June 2016 were retrospectively *** who underwent surgery for ASDis were categorized as group A(n=13),whereas those who did not were classified as group B(n=199).Survival analysis and Cox proportional hazards models were used to compare the modified Pfirrmann grade,University of California-Los Angeles grade,body mass index,number of Dynesys-instrumented levels,and *** The mean time of reoperation was 7.22(1.65–11.84)years in group A,and the mean follow-up period was 6.09(0.10–12.76)years in group *** significant difference in reoperation risk was observed:Modified Pfirrmann grade 3 vs 4(P=0.53)or 4 vs 5(P=0.46)for the upper adjacent disc,University of California-Los Angeles grade 2 vs 3 for the upper adjacent segment(P=0.66),age of<60 vs>60 years(P=0.9),body mass index<25 vs>25 kg/m2(P=0.3),and sex(P=0.8).CONCLUSION Greater preexisting upper ASDeg was not associated with a higher rate of reoperation for ASDis after Dynesys *** overweight tended to increase reoperation risk after Dynesys surgery for ASDis.

关键词： Adjacent segment degeneration Adjacent segment disease Degenerative lumbar spondylolisthesis Dynamic stabilization Dynesys Spinal stenosis

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Humoral immune response to circulating SARS-CoV-2 variants elicited by inactivated and RBD-subunit vaccines

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细胞研究（英文版） 2021年第7期31卷 732-741页

作者： Yunlong Cao Ayijiang Yisimayi Yali Bai Weijin Huang Xiaofeng Li Zhiying Zhang Tianjiao Yuan Ran An Jing Wang Tianhe Xiao Shuo Du Wenping Ma Liyang Song Yongzheng Li Xiang Li Weiliang Song Jiajing Wu Shuo Liu Xuemei Li Yonghong Zhang Bin Su Xianghua Guo Yangyang Wei Chuanping Gao Nana Zhang Yifei Zhang Yang Dou Xiaoyu Xu Rui Shi Bai Lu Ronghua Jin Yingmin Ma Chengfeng Qin Youchun Wang Yingmei Feng Junyu Xiao Xiaoliang Sunney Xie Beijing Advanced Innovation Center for Genomics (ICG) Peking UniversityBeijingChina Biomedical Pioneering Innovation Center (BIOPIC) Peking UniversityBeijingChina Beijing Advanced Innovation Center for Genomics (ICG) Peking UniversityBeijingChina Biomedical Pioneering Innovation Center (BIOPIC) Peking UniversityBeijingChina School of Life Sciences Peking UniversityBeijingChina Beijing Advanced Innovation Center for Genomics (ICG) Peking UniversityBeijingChina Joint Graduate Program of Peking-Tsinghua-NIBS School of Life SciencesTsinghua UniversityBeijingChina Division of HIV/AIDS and Sex-transmitted Virus Vaccines Institute for Biological Product ControlNational Institutes for Food and Drug Control (NIFDC) and WHO Collaborating Center for Standardization and Evaluation of BiologicalsBeijingChina State Key Laboratory of Pathogen and Biosecurity Beijing Institute of Microbiology and EpidemiologyAcademy of Military Medical SciencesBeijingChina Beijing Advanced Innovation Center for Genomics (ICG) Peking UniversityBeijingChina School of Life Sciences Peking UniversityBeijingChina Beijing Advanced Innovation Center for Genomics (ICG) Peking UniversityBeijingChina Biomedical Pioneering Innovation Center (BIOPIC) Peking UniversityBeijingChina Peking-Tsinghua Center for life Sciences Academy for Advanced Interdisciplinary StudiesPeking UniversityBeijingChina Beijing Youan Hospital Capital Medical UniversityBeijingChina Beijing Advanced Innovation Center for Genomics (ICG) Peking UniversityBeijingChina Peking-Tsinghua Center for life Sciences Academy for Advanced Interdisciplinary StudiesPeking UniversityBeijingChina School of Pharmaceutical Sciences IDG/McGovern Institute for Brain ResearchTsinghua UniversityBeijingChina Vazyme Biotech Co. LtdNanjingJiangsuChina CAS Key Laboratory of Microbial Physiological and Metabolic Engineering Institute of MicrobiologyChinese Academy of SciencesBeijingChina Beijing Ditan Hospital Capital Medical UniversityBeijingChina

SARS-CoV-2 variants could induce immune escape by mutations on the receptor-binding domain (RBD) and N-terminal domain(NTD).Here we report the humoral immune response to circulating SARS-CoV-2 variants,such as 501Y.V2 (B.1.351),of the plasma and neutralizing antibodies (NAbs) elicited by CoronaVac (inactivated vaccine),ZF2001 (RBD-subunit vaccine) and natural *** 86 potent NAbs identified by high-throughput single-cell VDJ sequencing of peripheral blood mononuclear cells from vaccinees and convalescents,near half anti-RBD NAbs showed major neutralization reductions against the K417N/E484K/N501Y mutation combination,with E484K being the dominant ***3-53/VH3-66 recurrent antibodies respond differently to RBD variants,and K417N compromises the majority of neutralizing activity through reduced polar contacts with complementarity determining *** contrast,the 242-244 deletion (242-244A) would abolish most neutralization activity of anti-NTD NAbs by interrupting the conformation of NTD antigenic supersite,indicating a much less diversity of anti-NTD NAbs than anti-RBD *** of convalescents and CoronaVac vaccinees displayed comparable neutralization reductions against pseudo-and authentic 501Y.V2 variants,mainly caused by E484K/N501Y and 242-244△,with the effects being ***,RBD-subunit vaccinees exhibit markedly higher tolerance to 501Y.V2 than convalescents,since the elicited anti-RBD NAbs display a high diversity and are unaffected by NTD ***,an extended gap between the third and second doses of ZF2001 leads to better neutralizing activity and tolerance to 501Y.V2 than the standard three-dose ***,these results suggest that the deployment of RBD-vaccines,through a third-dose boost,may be ideal for combating SARS-CoV-2 variants when necessary,especially for those carrying mutations that disrupt the NTD supersite.

关键词： Cryoelectron microscopy Immunology X-ray crystallography

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Transdermal nanolipoplex simultaneously inhibits subcutaneous melanoma growth and suppresses systemically metastatic melanoma by activating host immunity

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Nanomedicine: Nanotechnology, Biology, and Medicine 2023年 47卷 102628-102628页

作者： Chen, Chia-Hung Weng, Tzu-Han Chuang, Cheng-Hsun Huang, Kai-Yao Huang, Sih-Cheng Chen, Pin-Rong Huang, Hsiao-Hsuan Huang, Ling-Ya Shen, Pei-Chun Chuang, Po-Ya Huang, Hsiao-Yen Wu, Yi-Syuan Chang, Hao-Chiun Weng, Shun-Long Liao, Kuang-Wen Department of Medical Research Hsinchu MacKay Memorial Hospital Hsinchu City30071 Taiwan Dependent of Medical Education MacKay Memorial Hospital Taipei10449 Taiwan Institute of Molecular Medicine and Bioengineering National Yang Ming Chiao Tung University Hsinchu City30068 Taiwan Department of Biological Science and Technology National Yang Ming Chiao Tung University Hsinchu City30068 Taiwan Industrial Development Graduate Program of College of Biological Science and Technology National Yang Ming Chiao Tung University Hsinchu City30068 Taiwan Institute of Bioinformatics and Systems Biology National Yang Ming Chiao Tung University Hsinchu City30068 Taiwan Department of Medicine MacKay Medical College New Taipei City25245 Taiwan Department of Obstetrics and Gynecology Hsinchu MacKay Memorial Hospital Hsinchu City30071 Taiwan MacKay Junior College of Medicine Nursing and Management Taipei City11260 Taiwan Drug Development and Value Creation Research Center College of Dental Medicine Kaohsiung Medical University School of Dentistry Graduate Institute of Medicine College of Medicine Center for Cancer Research Kaohsiung Medical University Kaohsiung City80708 Taiwan Center for Intelligent Drug Systems and Smart Bio-devices National Yang Ming Chiao Tung University Hsinchu City30068 Taiwan Department of Biotechnology and Bioindustry Sciences National Cheng Kung University Tainan City70101 Taiwan Ph.D. Degree Program of Biomedical Science and Engineering National Yang Ming Chiao Tung University Hsinchu City30068 Taiwan

Benefit for clinical melanoma treatments, the transdermal neoadjuvant therapy could reduce surgery region and increase immunotherapy efficacy. Using lipoplex (Lipo-PEG-PEI-complex, LPPC) encapsulated doxorubicin (DOX) and carrying CpG oligodeoxynucleotide;the transdermally administered nano-liposomal drug complex (LPPC-DOX-CpG) would have high cytotoxicity and immunostimulatory activity to suppress systemic metastasis of melanoma. LPPC-DOX-CpG dramatically suppressed subcutaneous melanoma growth by inducing tumor cell apoptosis and recruiting immune cells into the tumor area. Animal studies further showed that the colonization and growth of spontaneously metastatic melanoma cells in the liver and lung were suppressed by transdermal LPPC-DOX-CpG. Furthermore, NGS analysis revealed IFN-γ and NF-κB pathways were triggered to recruit and activate the antigen-presenting-cells and effecter cells, which could activate the anti-tumor responses as the major mechanism responsible for the therapeutic effect of LPPC-DOX-CpG. Finally, we have successfully proved transdermal LPPC-DOX-CpG as a promising penetrative carrier to activate systemic anti-tumor immunity against subcutaneous and metastatic tumor. © 2022

关键词： Tumors

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Corrigendum to "miR-29a-3p-dependent COL3A1 and COL5A1 expression reduction assists sulforaphane to inhibit gastric cancer progression" [Biochem. Pharmacol. 188 (2021) 114539]

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Biochemical pharmacology 2023年 208卷 115389页

作者： Sichong Han Zhe Wang Jining Liu Hui-Min David Wang Qipeng Yuan State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing 100029 PR China. Graduate Institute of Biomedical Engineering National Chung Hsing University Taichung City 402 Taiwan Department of Medical Laboratory Science and Biotechnology China Medical University Taichung City 404 Taiwan Graduate Institute of Medicine College of Medicine Kaohsiung Medical University Kaohsiung City 807 Taiwan College of Food and Biological Engineering Jimei University Xiamen City 361021 Fujia Province PR China Undergraduate Program Study of Biomedical Engineering Physics Department Airlangga University Surabaya City 60115 Indonesia. Electronic address: davidw@dragon.nchu.edu.tw. State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing 100029 PR China. Electronic address: yuanqp@***.

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Transcriptomic analysis of circulating extracellular vesicles during the perioperative period of Fontan and Glenn surgery

npj Cardiovascular Health

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npj Cardiovascular Health 2024年第1期1卷 1-12页

作者： Felipe Takaesu Evan Yang Michael E. Davis Khalid Yasseen Hyun-Ji Park John M. Kelly Christopher K. Breuer Wallace H. Coulter Department of Biomedical Engineering Georgia Institute of Technology & Emory University Atlanta GA USA Biochemistry Cell and Developmental Biology Graduate Training Program Graduate Division of Biological and Biomedical Sciences Laney Graduate School Emory University Atlanta GA USA Children’s Heart Research & Outcomes (HeRO) Center Children’s Healthcare of Atlanta & Emory University Atlanta GA USA Frank H. Netter School of Medicine Quinnipiac University North Haven CT USA Department of Molecular Science and Technology Ajou University Suwon 16499 Korea Center for Regenerative Medicine Abigail Wexner Research Institute at Nationwide Children’s Hospital Columbus OH USA The Heart Center Nationwide Children’s Hospital Columbus OH USA Department of Pediatrics The Ohio State University College of Medicine Columbus OH USA

Single-ventricle defects are treated with the Glenn and Fontan procedures, which offer lifesaving relief but result in lifelong complications. To address the lack of outcome predictors, we conducted an untargeted transcriptomic analysis to identify RNA biomarkers in serum and circulating sEVs from 25 Glenn or Fontan patients with three samples exclusively used for experimental assays. Unsupervised analysis revealed a distinction between pre-op and post-op samples in both surgical groups. Differential gene expression and pathway analysis showed enrichment for pro-angiogenic cargo in post-op sEVs compared to pre-op sEVs. Wound healing assays revealed post-op Fontan sEVs induce a stronger pro-angiogenic response than pre-op Fontan sEVs. A PLSR-guided approach revealed MAPK6, GLE1, hsa-miR-340-5p, and hsa-miR-199b-5p as key transcripts in the observed wound healing response. Lastly, EV-Origin revealed decreased secretion of sEV from cardiac tissue and increased secretion from brain tissue for both Fontan and Glenn samples. This work demonstrates the potential of sEV RNAs as biomarkers for patients with Fontan physiology, enabling quicker diagnosis for Fontan-associated complications.

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Corrigendum to "Mathematical model of modified hybrid pump mechanism for cardiopulmonary resuscitation" [Computer methods and programs in biomedicine 206 (2021) 106106]

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Computer methods and programs in biomedicine 2022年 218卷 106711页

作者： Dong Ah Shin Jung Chan Lee Interdisciplinary Program in Bioengineering Graduate School Seoul National University Seoul 08826 Republic of Korea. Department of Biomedical Engineering College of Medicine and Institute of Medical and Biological Engineering Medical Research Center Seoul National University Seoul 03080 Republic of Korea Institute of BioEngineering Bio-MAX Institute Seoul National University Seoul 08826 Republic of Korea. Electronic address: ljch@snu.ac.kr.

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Tissue clearing and its applications in neuroscience (vol 21, pg 61, 2020)

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NATURE REVIEWS NEUROSCIENCE 2020年第5期21卷 298-298页

作者： Ueda, Hiroki R. Ertuerk, Ali Chung, Kwanghun Gradinaru, Viviana Chedotal, Alain Tomancak, Pavel Keller, Philipp J. Department of Systems Pharmacology University of Tokyo Tokyo Japan Laboratory for Synthetic Biology RIKEN BDR Suita Japan Institute for Stroke and Dementia Research Klinikum der Universität München Ludwig-Maximilian University of Munich Munich Germany Institute of Tissue Engineering and Regenerative Medicine Helmholtz Zentrum München Neuherberg Germany Munich Cluster for Systems Neurology (SyNergy) Munich Germany Institute for Medical Engineering and Science Massachusetts Institute of Technology Cambridge MA USA Picower Institute for Learning and Memory Massachusetts Institute of Technology Cambridge MA USA Department of Chemical Engineering Massachusetts Institute of Technology Cambridge MA USA Department of Brain and Cognitive Sciences Massachusetts Institute of Technology Cambridge MA USA Eli & Edythe Broad Institute of MIT and Harvard Cambridge MA USA Center for NanoMedicine Institute for Basic Science Seoul Republic of Korea Graduate Program of Nano Biomedical Engineering Yonsei-IBS Institute Yonsei University Seoul Republic of Korea Division of Biology and Biological Engineering California Institute of Technology Pasadena CA USA Institut de la Vision Sorbonne Université INSERM CNRS Paris France Max Planck Institute of Molecular Cell Biology and Genetics Dresden Germany IT4Innovations Technical University of Ostrava Ostrava Czech Republic Janelia Research Campus Howard Hughes Medical Institute Ashburn VA USA

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

关键词： Immunological techniques Light-sheet microscopy Neuroscience

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