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  1. Article ; Online: Association between tumor necrosis factor-α -308 Gauss/A polymorphism and risk of silicosis and coal workers pneumoconiosis in Chinese population.

    Yang, Li-Teng / Liu, Xin / Wu, Gao-Hui / Chen, Li-Fang

    Inhalation toxicology

    2018  Volume 30, Issue 6, Page(s) 213–217

    Abstract: Background: Many studies have attempted to clarify the association between TNF-a -308G/A polymorphism and pneumoconiosis, but there has been no definite consensus to date. To further assess the effects of TNF-a -308G/A polymorphism on the risk of ... ...

    Abstract Background: Many studies have attempted to clarify the association between TNF-a -308G/A polymorphism and pneumoconiosis, but there has been no definite consensus to date. To further assess the effects of TNF-a -308G/A polymorphism on the risk of pneumoconiosis, a meta-analysis was performed in Chinese population.
    Methods: We searched the related literature in PubMed and Chinese databases through June 2018. The strength of the associations was assessed used pooled odds ratios (ORs) and 95% confidence intervals (CIs).
    Results: Nine case-control studies including 730 silicosis cases, 457 coal workers pneumoconiosis cases and 2429 controls were identified according to the inclusion criteria. In the total analyses, a significantly elevated risk was found in allelic model (OR = 1.41, 95% CI = 1.16-1.71). In the subgroup analyses by geographic area and type of pneumoconiosis, significant results were found both in North China (A versus G, OR = 1.33, CI = 1.05-1.69) and South China (A versus G, OR = 1.56, CI = 1.14-2.15); significant results were also found in silicosis (A versus G, OR = 1.40, CI = 1.11-1.78) and coal worker pneumoconiosis (A versus G, OR = 1.42, CI = 1.03-1.96).
    Conclusion: This meta-analysis suggested that TNF-a gene -308 G/A polymorphism is associated with increased silicosis and coal workers pneumoconiosis risk in the Chinese population, and further studies in other ethnic groups are required for definite conclusions.
    MeSH term(s) Anthracosis/genetics ; Asian Continental Ancestry Group/genetics ; Case-Control Studies ; Humans ; Polymorphism, Genetic ; Risk Factors ; Silicosis/genetics ; Tumor Necrosis Factor-alpha/genetics
    Chemical Substances Tumor Necrosis Factor-alpha
    Language English
    Publishing date 2018-09-26
    Publishing country England
    Document type Journal Article ; Meta-Analysis
    ZDB-ID 1038809-6
    ISSN 1091-7691 ; 0895-8378
    ISSN (online) 1091-7691
    ISSN 0895-8378
    DOI 10.1080/08958378.2018.1494766
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The transcription factor XBP1 in dendritic cells promotes the T

    Yang, Gui / Zeng, Xian-Hai / Geng, Xiao-Rui / Liu, Jiang-Qi / Mo, Li-Hua / Luo, Xiang-Qian / Liu, Hua-Zhen / Zhang, Yuan-Yi / Yang, Li-Teng / Huang, Qin-Miao / Xiao, Xiao-Jun / Liu, Jie / Xu, Ling-Zhi / Liu, Da-Bo / Liu, Xiao-Yu / Liu, Zhi-Qiang / Yang, Ping-Chang

    Science signaling

    2023  Volume 16, Issue 791, Page(s) eabm9454

    Abstract: Dendritic cells (DCs) that express T cell immunoglobulin domain molecule-4 (TIM4), a cell surface receptor for phosphatidylserine, induce T helper 2 ( ... ...

    Abstract Dendritic cells (DCs) that express T cell immunoglobulin domain molecule-4 (TIM4), a cell surface receptor for phosphatidylserine, induce T helper 2 (T
    MeSH term(s) Humans ; Interleukin-2/metabolism ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Th2 Cells ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Hypersensitivity/genetics ; Hypersensitivity/metabolism ; Dendritic Cells/metabolism ; Particulate Matter/metabolism ; X-Box Binding Protein 1/genetics
    Chemical Substances Interleukin-2 ; Transcription Factors ; Membrane Proteins ; Particulate Matter ; XBP1 protein, human ; X-Box Binding Protein 1
    Language English
    Publishing date 2023-06-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2417226-1
    ISSN 1937-9145 ; 1945-0877
    ISSN (online) 1937-9145
    ISSN 1945-0877
    DOI 10.1126/scisignal.abm9454
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Chimeric antigen-guiding extracellular vesicles eliminate antigen-specific Th2 cells in subjects with food allergy.

    Zhang, Yuan-Yi / Mo, Li-Hua / Yang, Gui / Liu, Jiang-Qi / Liu, Zhi-Qiang / Yang, Li-Teng / Ran, Pi-Xin / Liu, Zhi-Gang / Yang, Ping-Chang

    The World Allergy Organization journal

    2021  Volume 14, Issue 3, Page(s) 100522

    Abstract: Background: Antigen (Ag)-specific T helper (Th)2 cells play a central role in food allergy (FA) pathogenesis. Methods can be used to eliminate Ag-specific Th2 cells that are currently lacking. This study aims to eliminate the Ag-specific Th2 cells with ... ...

    Abstract Background: Antigen (Ag)-specific T helper (Th)2 cells play a central role in food allergy (FA) pathogenesis. Methods can be used to eliminate Ag-specific Th2 cells that are currently lacking. This study aims to eliminate the Ag-specific Th2 cells with a novel nanoparticle, the mEV (modified extracellular vesicles, that carry a chimeric antigen peptide, MHC II and caspase 3) in a murine FA model.
    Methods: mEVs were generated by exposing dendritic cells (DC) to ovalbumin (OVA, a specific Ag) and recombinant caspase 3 (Casp3) in the culture overnight. Exosomes were purified from culture supernatant by the magnetic antibody approach. A murine FA model was developed with OVA as the specific Ag.
    Results: Purified mEVs had the molecular markers of extracellular vesicle, CD81, CD63, and CD9, cleaved Casp3 and MHC II/OVA complexes. mEVs specifically bound to the surface of Ag-specific CD4
    Conclusions: mEVs carry Ag/MHC II complexes and Casp3, that can induce Ag-specific Th2 cell apoptosis. Administration of mEV can efficiently suppress experimental FA. The results suggest that the mEVs have the translational potential to be used in the treatment of FA and other allergic diseases.
    Language English
    Publishing date 2021-02-24
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2581968-9
    ISSN 1939-4551
    ISSN 1939-4551
    DOI 10.1016/j.waojou.2021.100522
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: T cell activator-carrying extracellular vesicles induce antigen-specific regulatory T cells.

    Mo, Li-Hua / Han, Hai-Yang / Jin, Qiao-Ruo / Song, Yan-Nan / Wu, Gao-Hui / Zhang, Youming / Yang, Li-Teng / Liu, Tao / Liu, Zhi-Gang / Feng, Yan / Yang, Ping-Chang

    Clinical and experimental immunology

    2021  Volume 206, Issue 2, Page(s) 129–140

    Abstract: The mechanism of antigen-specific regulatory T cell ( ... ...

    Abstract The mechanism of antigen-specific regulatory T cell (T
    MeSH term(s) Animals ; Antigens/immunology ; Disease Models, Animal ; Extracellular Vesicles/immunology ; Lymphocyte Activation ; Mice ; Rhinitis, Allergic/immunology ; T-Lymphocytes, Regulatory/immunology
    Chemical Substances Antigens
    Language English
    Publishing date 2021-08-30
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 218531-3
    ISSN 1365-2249 ; 0009-9104 ; 0964-2536
    ISSN (online) 1365-2249
    ISSN 0009-9104 ; 0964-2536
    DOI 10.1111/cei.13655
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Epithelial cell-derived CD83 restores immune tolerance in the airway mucosa by inducing regulatory T-cell differentiation.

    Mo, Li-Hua / Luo, Xiang-Qian / Yang, Gui / Liu, Jiang-Qi / Yang, Li-Teng / Liu, Zhi-Qiang / Wang, Shuai / Liu, Da-Bo / Liu, Zhi-Gang / Yang, Ping-Chang

    Immunology

    2021  Volume 163, Issue 3, Page(s) 310–322

    Abstract: The mechanism of generation of regulatory T cells (Treg) remains incompletely understood. Recent studies show that CD83 has immune regulatory functions. This study aims to investigate the role of epithelial cell-derived CD83 in the restoration of immune ... ...

    Abstract The mechanism of generation of regulatory T cells (Treg) remains incompletely understood. Recent studies show that CD83 has immune regulatory functions. This study aims to investigate the role of epithelial cell-derived CD83 in the restoration of immune tolerance in the airway mucosa by inducing the Treg differentiation. In this study, CD83 and ovalbumin (OVA)-carrying exosomes were generated from airway epithelial cells. An airway allergy mouse model was developed to test the role of CD83/OVA-carrying exosomes in the suppression of airway allergy by inducing Treg generation. We observed that mouse airway epithelial cells expressed CD83 that could be up-regulated by CD40 ligand. The CD83 deficiency in epithelial cells retarded the Treg generation in the airway mucosa. CD83 up-regulated transforming growth factor-β-inducible early gene 1 expression in CD4
    MeSH term(s) Allergens/immunology ; Animals ; Antigens, CD/metabolism ; Cell Differentiation ; Disease Models, Animal ; Epithelial Cells/metabolism ; Exosomes/metabolism ; Hypersensitivity/immunology ; Immune Tolerance ; Immunoglobulins/metabolism ; Lymphocyte Activation ; Membrane Glycoproteins/metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Ovalbumin/immunology ; Respiratory Hypersensitivity/immunology ; Respiratory Mucosa/immunology ; T-Lymphocytes, Regulatory/immunology ; CD83 Antigen
    Chemical Substances Allergens ; Antigens, CD ; Immunoglobulins ; Membrane Glycoproteins ; Ovalbumin (9006-59-1)
    Language English
    Publishing date 2021-02-28
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80124-0
    ISSN 1365-2567 ; 0019-2805 ; 0953-4954
    ISSN (online) 1365-2567
    ISSN 0019-2805 ; 0953-4954
    DOI 10.1111/imm.13317
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Specific antigen-guiding exosomes inhibit food allergies by inducing regulatory T cells.

    Yu, Dian / Liu, Jiang-Qi / Mo, Li-Hua / Luo, Xiang-Qian / Liu, Zhi-Qiang / Wu, Gao-Hui / Yang, Li-Teng / Liu, Da-Bo / Wang, Shuai / Liu, Zhi-Gang / Yang, Ping-Chang

    Immunology and cell biology

    2020  Volume 98, Issue 8, Page(s) 639–649

    Abstract: The therapies for food allergy (FA) need to be improved. The generation of inducible regulatory T cells (Tregs) can support immune tolerance in the body. This study aims to suppress experimental FA by inducing Tregs through the employment of modified ... ...

    Abstract The therapies for food allergy (FA) need to be improved. The generation of inducible regulatory T cells (Tregs) can support immune tolerance in the body. This study aims to suppress experimental FA by inducing Tregs through the employment of modified exosomes (mExosomes). In this study, mExosomes were prepared by incubating dendritic cells with interleukin (IL)-2 and ovalbumin (OVA, used as a specific antigen) in the culture. Exosomes were purified from culture supernatant and used as the mExosomes. A murine FA model was developed to test the effects of mExosomes on the generation of Tregs in the mouse intestinal tissues and inhibiting FA. The results showed that mExosomes, which carried IL-2 and a complex of OVA peptide-major histocompatibility complex class II on the surface of exosomes, bound to OVA-specific CD4
    MeSH term(s) Animals ; Dendritic Cells ; Exosomes/immunology ; Food Hypersensitivity/immunology ; Food Hypersensitivity/prevention & control ; Immune Tolerance ; Interleukin-2/immunology ; Intestines/immunology ; Mice ; Mice, Inbred BALB C ; Ovalbumin ; T-Lymphocytes, Regulatory/immunology
    Chemical Substances Interleukin-2 ; Ovalbumin (9006-59-1)
    Language English
    Publishing date 2020-07-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 284057-1
    ISSN 1440-1711 ; 0818-9641
    ISSN (online) 1440-1711
    ISSN 0818-9641
    DOI 10.1111/imcb.12347
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  7. Article ; Online: FcγRI plays a critical role in patients with ulcerative colitis relapse.

    Li, Yan / Zhang, Yuan-Yi / Yang, Li-Teng / Liu, Jiang-Qi / Zhou, Chuan / Liu, Zhi-Qiang / Yang, Gui / Mo, Li-Hua / Liu, Zhi-Gang / Feng, Bai-Sui / Yang, Ping-Chang

    European journal of immunology

    2020  Volume 51, Issue 2, Page(s) 459–470

    Abstract: Ulcerative colitis (UC) is a disease that frequently relapses and affects more than 0.1% general population; the underlying mechanism is poorly understood. Published data show that polymorphonuclear neutrophils (PMN) contribute to the pathogenesis of UC. ...

    Abstract Ulcerative colitis (UC) is a disease that frequently relapses and affects more than 0.1% general population; the underlying mechanism is poorly understood. Published data show that polymorphonuclear neutrophils (PMN) contribute to the pathogenesis of UC. This study aims to identify antigen (Ag)-specific PMNs and investigate their role in UC relapse. In this study, the correlation between PMN activities and UC relapse was assessed in a group of UC patients. A UC mouse model was developed to expand the findings of UC patient study. The results showed that a positive correlation was detected between the high PMN activities and the food Ag-specific IgG amounts in colon biopsies of UC patients. UC patient-derived Ag-specific PMNs could be activated upon exposure to food specific Ag. The Ag/FcγRI complexes were detected on the surface of PMNs in UC patients. Re-exposure of sensitized PMNs to specific Ag triggered PMN activation and induced UC-like inflammation in the mouse colon. We conclude that FcγRI plays a critical role in UC relapse. Inhibition of FcγRI can efficiently inhibits experimental UC.
    MeSH term(s) Adult ; Animals ; Cells, Cultured ; Colitis, Ulcerative/metabolism ; Colitis, Ulcerative/pathology ; Colon/metabolism ; Colon/pathology ; Female ; Humans ; Immunoglobulin G/metabolism ; Inflammation/metabolism ; Inflammation/pathology ; Male ; Mice ; Mice, Inbred C57BL ; Neutrophil Activation/physiology ; Neutrophils/metabolism ; Neutrophils/pathology ; Reactive Oxygen Species/metabolism ; Receptors, IgG/metabolism ; Recurrence
    Chemical Substances Immunoglobulin G ; Reactive Oxygen Species ; Receptors, IgG
    Language English
    Publishing date 2020-11-16
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 120108-6
    ISSN 1521-4141 ; 0014-2980
    ISSN (online) 1521-4141
    ISSN 0014-2980
    DOI 10.1002/eji.202048622
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Integrin αvβ6 cooperates with resiquimod to restore antigen-specific immune tolerance in airway allergy.

    Ma, Fei / Zhang, Yuan-Yi / Yang, Gui / Mo, Li-Hua / Liu, Da-Bo / Yang, Li-Teng / Liu, Zhi-Gang / Ning, Yan / Yang, Ping-Chang

    Immunology letters

    2020  Volume 230, Page(s) 49–58

    Abstract: Background: Integrin αvβ6 can convert the transforming growth factor (TGF)-β precursor to the mature form. Resiquimod (R848) can generate TGF-β-producing regulatory T cells (Treg). Thus, to concurrent administration of specific antigen and R848 may ... ...

    Abstract Background: Integrin αvβ6 can convert the transforming growth factor (TGF)-β precursor to the mature form. Resiquimod (R848) can generate TGF-β-producing regulatory T cells (Treg). Thus, to concurrent administration of specific antigen and R848 may generate antigen-specific Tregs, that is expected to restore immune tolerance in subjects with airway allergic diseases (AAD).
    Methods: A bio-nanoparticle, designated Rexo, containing an antigen/MHC II complex and R848, was naturally assembled in dendritic cells, that was released as an exosome. An AAD mouse model was developed used to test the effects of Rexo on restoring the immune tolerance in the airways.
    Results: Exposure to R848 failed to induce Tregs in the β6-deficient mouse airway tissues, that were successfully induced in wild type mice. The results were validated inin vitro experiments. R848 activated the TLR7/MyD88/p38 signal pathway to increase the αvβ6 levels in CD4
    Conclusions: Rexos can inhibit experimental AAD via inducing antigen-specific Tregs to restore immune tolerance in the airway tissues, suggesting that Rexos have the translational potential to be used in the treatment of AAD.
    MeSH term(s) Allergens/immunology ; Allergens/metabolism ; Animals ; Antigen Presentation ; Antigens, Neoplasm/genetics ; Antigens, Neoplasm/metabolism ; Dendritic Cells/immunology ; Exosomes/immunology ; Exosomes/metabolism ; Histocompatibility Antigens Class II/metabolism ; Imidazoles/therapeutic use ; Immune Tolerance ; Integrins/genetics ; Integrins/metabolism ; Membrane Glycoproteins/metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; Nanoparticles ; Respiratory Hypersensitivity/drug therapy ; Signal Transduction ; T-Lymphocytes, Regulatory/immunology ; Toll-Like Receptor 7/metabolism ; Transforming Growth Factor beta/metabolism
    Chemical Substances Allergens ; Antigens, Neoplasm ; Histocompatibility Antigens Class II ; Imidazoles ; Integrins ; Membrane Glycoproteins ; Tlr7 protein, mouse ; Toll-Like Receptor 7 ; Transforming Growth Factor beta ; integrin alphavbeta6 ; resiquimod (V3DMU7PVXF)
    Language English
    Publishing date 2020-12-29
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 445150-8
    ISSN 1879-0542 ; 0165-2478
    ISSN (online) 1879-0542
    ISSN 0165-2478
    DOI 10.1016/j.imlet.2020.12.011
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  9. Article ; Online: Modulating oxidative stress counteracts specific antigen-induced regulatory T-cell apoptosis in mice.

    Zhang, Yuan-Yi / Feng, Bai-Sui / Zhang, Huanping / Yang, Gui / Jin, Qiao-Ruo / Luo, Xiang-Qian / Ma, Na / Huang, Qin-Miao / Yang, Li-Teng / Zhang, Guo-Hao / Liu, Da-Bo / Yu, Yong / Liu, Zhi-Gang / Zheng, Peng-Yuan / Yang, Ping-Chang

    European journal of immunology

    2021  Volume 51, Issue 7, Page(s) 1748–1761

    Abstract: Treg are known to have a central role in orchestrating immune responses, but less is known about the destiny of Treg after being activated by specific Ags. This study aimed to investigate the role of superoxide dismutase, an active molecule in the ... ...

    Abstract Treg are known to have a central role in orchestrating immune responses, but less is known about the destiny of Treg after being activated by specific Ags. This study aimed to investigate the role of superoxide dismutase, an active molecule in the regulation of oxidative stress in the body, in the prevention of Treg apoptosis induced by specific Ags. Ag-specific Tregs were isolated from the DO11.10 mouse intestine. A food allergy mouse model was developed with ovalbumin as the specific Ag and here, we observed that exposure to specific Ag induced Treg apoptosis through converting the precursor of TGF-β to its mature form inside the Tregs. Oxidative stress was induced in Tregs upon exposure to specific Ags, in which Smad3 bound the latency-associated peptide to induce its degradation, converting the TGF-β precursor to its mature form, TGF-β. Suppressing oxidative stress in Tregs alleviated the specific Ag-induced Treg apoptosis in in vitro experiments and suppressed experimental food allergy by preventing the specific Ag-induced Treg apoptosis in the intestine. In conclusion, exposure to specific Ags induces Treg apoptosis and it can be prevented by upregulating superoxide dismutase or suppressing reactive oxidative species in Tregs.
    MeSH term(s) Animals ; Antigens/immunology ; Apoptosis/immunology ; Lymphocyte Activation/immunology ; Mice ; Mice, Inbred BALB C ; Ovalbumin/immunology ; Oxidative Stress/immunology ; Smad3 Protein/immunology ; Superoxide Dismutase/immunology ; T-Lymphocytes, Regulatory/immunology ; Transforming Growth Factor beta/immunology ; Up-Regulation/immunology
    Chemical Substances Antigens ; Smad3 Protein ; Transforming Growth Factor beta ; Ovalbumin (9006-59-1) ; Superoxide Dismutase (EC 1.15.1.1)
    Language English
    Publishing date 2021-04-16
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 120108-6
    ISSN 1521-4141 ; 0014-2980
    ISSN (online) 1521-4141
    ISSN 0014-2980
    DOI 10.1002/eji.202049112
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  10. Article ; Online: Dust-mite-derived protein disulfide isomerase suppresses airway allergy by inducing tolerogenic dendritic cells.

    Liu, Xiaoyu / Wang, Yuwei / Chen, Desheng / Ji, Shuyu / Yang, Li-Teng / Huang, Qinmiao / Guan, Lvxin / Chang, Kexin / Li, Dan / Yuan, Ruyi / Ouyang, Chunyan / Hu, Tian-Yong / Liu, Zhi-Qiang / Sun, Baoqing / Xu, Guorong / Liu, Zhi-Gang / Yang, Ping-Chang

    The Journal of biological chemistry

    2021  Volume 296, Page(s) 100585

    Abstract: House dust mites (HDMs) are a potent allergen source that are commonly found in human living environments. While HDMs are known to induce allergic diseases in humans, such as asthma, its other biological activities related to human health are less ... ...

    Abstract House dust mites (HDMs) are a potent allergen source that are commonly found in human living environments. While HDMs are known to induce allergic diseases in humans, such as asthma, its other biological activities related to human health are less understood. Our laboratory recently purified the HDM protein PDI (protein disulfide isomerase). In this study, we assess the role of PDI in contributing to immune regulation. Using mass spectrometry, we analyzed the complexes of DEC205 and HDM extracts, and the role of PDI in the induction of tolerogenic dendritic cells (DCs) was assessed in human cell culture experiments and verified in a murine model. We found that more than 20 HDM-derived proteins, including PDI, bound to DCs by forming complexes with DEC205. Additionally, DEC205-mediated the endocytosis of PDI. HDM-derived PDI (HDM-PDI) promoted Foxp3 expression in DCs. HDM-PDI-primed DCs also showed tolerogenic properties that induced regulatory T cell development, indicating that the primed DCs were tolerogenic DCs. Our results suggested that the PDI/DEC205/TIEG1/Foxp3 signal pathway activation was involved in the HDM-PDI-induced Foxp3 expression in DCs. Finally, we found that HDM-PDI competitively counteracted the Th2 cytokines to restore DC's tolerogenicity, and administration of HDM-PDI could suppress experimental asthma. In conclusion, our data suggest that HDM-PDI contributes to immune regulation by inducing tolerogenic DC development. Administration of HDM-PDI can alleviate experimental asthma. These findings demonstrate that HDM-PDI has translational potential to be used in the treatment of immune disorders such as asthma.
    MeSH term(s) Animals ; Cytokines/metabolism ; Dendritic Cells/immunology ; Dendritic Cells/metabolism ; Hypersensitivity/immunology ; Hypersensitivity/metabolism ; Hypersensitivity/therapy ; Mice ; Protein Disulfide-Isomerases/metabolism ; Pyroglyphidae/enzymology ; Respiratory System/immunology
    Chemical Substances Cytokines ; Protein Disulfide-Isomerases (EC 5.3.4.1)
    Language English
    Publishing date 2021-03-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1016/j.jbc.2021.100585
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