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  1. Article ; Online: Corrigendum to "Qing Chang Hua Shi granule ameliorate inflammation in experimental rats and cell model of ulcerative colitis through MEK/ERK signaling pathway" [Biomed. Pharmacother. 116 (2019) 108967].

    Zhu, Lei / Dai, Lu-Ming / Shen, Hong / Gu, Pei-Qing / Zheng, Kai / Liu, Ya-Jun / Zhang, Lu / Cheng, Jia-Fei

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2023  Volume 163, Page(s) 114854

    Language English
    Publishing date 2023-05-12
    Publishing country France
    Document type Published Erratum
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2023.114854
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: [Research progress on strontium isotope-traced plant remains production areas and implications for traceability of Dao-di herbs in Forbidden City of the Qing Dynasty].

    Jiang, Yun-Lu / Peng, Hua-Sheng / Yang, Bin

    Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica

    2024  Volume 49, Issue 1, Page(s) 39–45

    Abstract: ... than 1 000 relics of medicinal materials from the Forbidden City of the Qing Dynasty, which are rare ... materials in the Forbidden City of the Qing Dynasty helps avoid external strontium contamination, making ... on medicinal materials from the Forbidden City of the Qing Dynasty: creating strontium isotope ratio maps ...

    Abstract Strontium isotope(~(87)S/~(86)Sr) tracing technology has been widely used in animal remains and origin of modern food origin sources. However, due to the problems of sample contamination and cleaning, this technology has been applied less frequently in the tracing of plant remains. The Palace Museum preserves more than 1 000 relics of medicinal materials from the Forbidden City of the Qing Dynasty, which are rare precious materials for the study of Dao-di herbs. The well-preserved environment of these medicinal materials in the Forbidden City of the Qing Dynasty helps avoid external strontium contamination, making it possible to introduce strontium isotope technology in their tracing research. On this basis, this study discussed the principle of strontium isotope tracing technology and summarized the current research progress on tracing plant remains using strontium isotope. In addition, this study discussed three key problems and their respective solutions encountered when applying strontium isotope technology to the tracing research on medicinal materials from the Forbidden City of the Qing Dynasty: creating strontium isotope ratio maps, dealing with the wide range of traceable results, and addressing the sample contamination and cleaning challenges. The literature and historical materials of the Qing Dynasty are the important basis for understanding the distribution and application of Dao-di herbs in the Qing Dynasty. Based on literature research, the use of strontium isotope to trace the producing area of medicinal materials in the Forbidden City of the Qing Dynasty can provide physical evidence for relevant research. The combined evidence of historical materials and medicinal relics is expected to provide a new perspective for the study of Dao-di herbs in the Qing Dynasty and also provide a reference for the study of the revolution of Dao-di herbs producing areas.
    MeSH term(s) Drugs, Chinese Herbal ; Medicine, Chinese Traditional ; Plants, Medicinal ; Technology ; Strontium Isotopes ; China
    Chemical Substances Drugs, Chinese Herbal ; Strontium Isotopes
    Language Chinese
    Publishing date 2024-02-25
    Publishing country China
    Document type English Abstract ; Journal Article
    ZDB-ID 1004649-5
    ISSN 1001-5302 ; 0254-0029
    ISSN 1001-5302 ; 0254-0029
    DOI 10.19540/j.cnki.cjcmm.20230902.101
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Developing a digital archive system for imperial Chinese robe in the Qing Dynasty.

    Su, Miao / Li, Saiquan / Lu, Yan / Yang, Limei / Duan, Yiting / Xiao, Kaida / Pointer, Michael / Luo, Ming Ronnier / Liu, Xiaoxuan

    Frontiers in neuroscience

    2022  Volume 16, Page(s) 971169

    Abstract: ... to achieve accurate color reproduction. Taking the Imperial Chinese robes in the Qing Dynasty as an example ...

    Abstract The digital archive of cultural heritage provides new opportunities for the protection of the cultural heritage and the development of online museums. One of the essential requirements for the digitization is to achieve accurate color reproduction. Taking the Imperial Chinese robes in the Qing Dynasty as an example, this study aims to develop a digital achieve system to digitize the robes using a high-end imaging system and accurately reproduce their color properties on a display. Currently, there has been very limited study focused on the color reproduction of silk fabrics or other textile materials. The conventional color management process using a traditional color chart, however, may not be suitable for the reproduction of silk fabrics because they have very high gloss. To address this difficulty, a unique "Qianlong Palette" color chart, consisting of 210 silk fabric samples, has been specifically produced for optimizing the color reproduction of silk fabrics and a color image reproduction system has been developed for the digitization and archiving of the clothing fabric for the royal court. Color characterization models using both the "Qianlong Palette" color chart and the traditional color chart, and different mapping methods, are compared and the model with highest accuracy used in a self-programmed interface for automatically processing textile images in the future. Finally, the digital archive system has been validated using six garments of silk fabric relics. The color differences after the color image reproduction are all less than 3.00ΔE*
    Language English
    Publishing date 2022-07-28
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2411902-7
    ISSN 1662-453X ; 1662-4548
    ISSN (online) 1662-453X
    ISSN 1662-4548
    DOI 10.3389/fnins.2022.971169
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Qing-Re-Chu-shi decoction ameliorates 2,4-dinitrochlorobenzene-induced atopic dermatitis in NC/Nga mice through anti-inflammation and immunoregulatory mechanisms.

    Meng, YuJiao / Liu, Yu / Guo, Jianning / Guo, Xiaoyao / Han, Xuyang / Zhang, Lu / Di, Tingting / Zhao, Jingxia / Wang, Yan / Li, Ping

    Journal of ethnopharmacology

    2024  Volume 323, Page(s) 117702

    Abstract: Ethnopharmacological relevance: Qing-Re-Chu-Shi Decoction (QRCSD), a traditional Chinese herbal ...

    Abstract Ethnopharmacological relevance: Qing-Re-Chu-Shi Decoction (QRCSD), a traditional Chinese herbal formula, has been employed as a complementary and alternative therapy for inflammatory skin diseases. However, its active constituents and the mechanistic basis of its action on atopic dermatitis remain in adequately understood.
    Aim of the study: Atopic dermatitis (AD) is an allergic dermatitis marked by eczematous lesions and pruritus. The study aimed to elucidate the underlying effects of QRCSD on AD and to identify the components responsible for its therapeutic efficacy in a mouse model.
    Materials and methods: Network pharmacology and UPLC-mass analysis were used to anticipate the pharmacological mechanisms and to identify active components of QRCSD, respectively. A DNCB-induced AD-like model was established in NC/Nga mice. QRCSD or prednisolone (as a positive control) was administered via gavage every other day from day14 to day 21. Dermatitis severity score, scratching behavior, skin barrier function, spleen index, Th1/Th2 lymphocyte ratio, and serum IgE levels were evaluated. Protein arrays, including 40 inflammatory cytokines, were performed on skin lesions, followed by confirmation experiments of Western blotting in dorsal skin lesions.
    Results: The construction of a QRCSD-AD-Network and topological analysis firstly proposed potential targets of QRCSD acting on AD. Animal experiments demonstrated that oral administration of QRCSD ameliorated AD-like lesions, reduced epidermal thickness and mast cell count, decreased serum IgE levels, augmented tight junction protein (Claudin 1, Occludin) levels, and regulated the Th1/Th2 balance in the spleen, as well as spleen index. Elevated levels of interleukin (IL)-4, IL-5, IL-6, IL-17, and Eotaxin were revealed in AD-like skin lesions by protein arrays. Western blotting confirmed that the phosphorylation levels of ERK, P38, JNK, STAT3 and P65 were downregulated, and IL-6 expression was also reduced following QRCSD treatment.
    Conclusions: The study enhances the understanding of the anti-inflammatory and immunomodulatory effects of QRCSD, showcasing its significant protective role against atopic dermatitis. Treatment with QRCSD may be considered as a viable candidate for complementary and alternative therapy in managing atopic dermatitis.
    MeSH term(s) Mice ; Animals ; Dermatitis, Atopic/chemically induced ; Dermatitis, Atopic/drug therapy ; Dermatitis, Atopic/pathology ; Dinitrochlorobenzene/toxicity ; Skin/pathology ; Interleukin-6/metabolism ; Cytokines/metabolism ; Anti-Inflammatory Agents/adverse effects ; Immunoglobulin E
    Chemical Substances Dinitrochlorobenzene ; Interleukin-6 ; Cytokines ; Anti-Inflammatory Agents ; Immunoglobulin E (37341-29-0)
    Language English
    Publishing date 2024-01-03
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2024.117702
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Study on the Mechanism of Qing-Fei-Shen-Shi Decoction on Asthma Based on Integrated 16S rRNA Sequencing and Untargeted Metabolomics.

    Hu, Haibo / Zhao, Guojing / Wang, Kun / Han, Ping / Ye, Haiyan / Wang, Fengchan / Liu, Na / Zhou, Peixia / Lu, Xuechao / Zhou, Zhaoshan / Cui, Huantian

    Evidence-based complementary and alternative medicine : eCAM

    2023  Volume 2023, Page(s) 1456844

    Abstract: Qing-Fei-Shen-Shi decoction (QFSS) consists of ...

    Abstract Qing-Fei-Shen-Shi decoction (QFSS) consists of
    Language English
    Publishing date 2023-02-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2171158-6
    ISSN 1741-4288 ; 1741-427X
    ISSN (online) 1741-4288
    ISSN 1741-427X
    DOI 10.1155/2023/1456844
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: [Characteristics, origin, and processing of Poria in Qing Dynasty Palace:evidence of both historical relics and documents].

    Yao, Ting / Peng, Hua-Sheng / Guan, Xue-Ling / Jin, Yan / Li, Feng-Yuan / Yuan, Yuan / Huang, Lu-Qi

    Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica

    2023  Volume 48, Issue 11, Page(s) 3118–3123

    Abstract: ... The royal medical records of the Qing Dynasty include multiple medicinal materials of Fu Ling, such as Bai ... Ling in the Qing Dynasty Pa-lace was mainly from the tribute paid of the officials in Yunnan-Guizhou ... region. The tribute situation was stable in the whole Qing Dynasty, and changed in the late Qing Dynasty ...

    Abstract Poria(Fu Ling) is a bulk traditional Chinese medicine(TCM)with a long history and complex varieties. The royal medical records of the Qing Dynasty include multiple medicinal materials of Fu Ling, such as Bai Fu Ling(white Poria), Chi Fu Ling(rubra Poria), and Zhu Fu Ling(Poria processed with cinnabaris). The Palace Museum preserves 6 kinds of specimens including Fu Ling Ge(dried Poria), Bai Fu Ling, Chi Fu Ling, Zhu Fu Ling, Bai Fu Shen(white Poria cum Radix Pini), and Fu Shen Mu(Poria cum Radix Pini). After trait identification and textual research, we found that Fu Ling Ge was an intact sclerotium, which was processed into Fu Ling Pi(Poriae Cutis), Bai Fu Ling and other medicinal materials in the Palace. The Fu Ling in the Qing Dynasty Pa-lace was mainly from the tribute paid of the officials in Yunnan-Guizhou region. The tribute situation was stable in the whole Qing Dynasty, and changed in the late Qing Dynasty. The cultural relics of Fu Ling in the Qing Dynasty Palace confirm with the archival documents such as the royal medical records and herbal medicine books, providing precious historical materials for understanding Fu Ling in the Qing Dynasty and a basis for the restoration of the processing of the Fu Ling in the Qing Dynasty Palace.
    MeSH term(s) Animals ; Poria ; China ; Books ; Coleoptera ; Medical Records ; Wolfiporia
    Language Chinese
    Publishing date 2023-06-29
    Publishing country China
    Document type English Abstract ; Journal Article
    ZDB-ID 1004649-5
    ISSN 1001-5302 ; 0254-0029
    ISSN 1001-5302 ; 0254-0029
    DOI 10.19540/j.cnki.cjcmm.20230215.101
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Network Pharmacology and Experimental Validation to Explore the Mechanism of Qing-Jin-Hua-Tan-Decoction Against Acute Lung Injury.

    Xiao, Shunli / Liu, Lu / Sun, Zhengxiao / Liu, Xiaoqian / Xu, Jing / Guo, Zhongyuan / Yin, Xiaojie / Liao, Fulong / Xu, Jun / You, Yun / Zhang, Tiejun

    Frontiers in pharmacology

    2022  Volume 13, Page(s) 891889

    Abstract: Qing-Jin-Hua-Tan-Decoction (QJHTD), a classic famous Chinese ancient prescription, has been used ...

    Abstract Qing-Jin-Hua-Tan-Decoction (QJHTD), a classic famous Chinese ancient prescription, has been used for treatment of pulmonary diseases since Ming Dynasty. A total of 22 prototype compounds of QJHTD absorbed into rat blood were chosen as candidates for the pharmacological network analysis and molecular docking. The targets from the intersection of compound target and ALI disease targets were used for GO and KEGG enrichment analyses. Molecular docking was adopted to further verify the interactions between 22 components and the top 20 targets with higher degree values in the component-target-pathway network.
    Language English
    Publishing date 2022-07-08
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587355-6
    ISSN 1663-9812
    ISSN 1663-9812
    DOI 10.3389/fphar.2022.891889
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Modified Qing' e Pills exerts anti-osteoporosis effects and prevents bone loss by enhancing type H blood vessel formation.

    Lu, Junjie / Hu, Desheng / Ma, Chen / Xu, Xiaojuan / Shen, Lin / Rong, Jianhui / Zhao, Jia / Shuai, Bo

    Frontiers in endocrinology

    2022  Volume 13, Page(s) 998971

    Abstract: Objective: To explore whether the modified Qing' e Pills (MQEP) exerts anti-osteoporotic effects ...

    Abstract Objective: To explore whether the modified Qing' e Pills (MQEP) exerts anti-osteoporotic effects and prevents bone loss by enhancing angiogenesis.
    Methods: Network pharmacology was used to assess whether MQEP has a pro-angiogenic capacity and to predict its potential targets. Human umbilical vein endothelial cells were treated with glucocorticoids and MQEP to assess cell viability. The expression of angiotensin II type 1 receptor, angiotensin II type 2 receptor, and angiotensin converting enzyme, which are associated with the activation of the renin-angiotensin-aldosterone system, and the expression of vascular endothelial growth factor and hypoxia-inducible factor 1 alpha, which are associated with the formation of type H blood vessels, were examined by western blot and RT-qPCR. Thereafter, the glucocorticoid-induced osteoporosis model was established and intervened with MQEP. Femur scanning was performed with micro-computed tomography; trabecular spacing, trabecular thickness, and trabecular number were observed and calculated; the expression of nuclear factor-kappa B ligand and osteoprotegerin was detected by ELISA, and the ratio was calculated to evaluate the degree of bone resorption. Finally, type H blood vessels that were highly coupled to osteogenic cells were identified by immunohistochemistry staining and flow cytometry.
    Results: This is the first study to reveal and confirm that MQEP could prevent bone loss in glucocorticoid-induced osteoporosis by promoting the expression of hypoxia-inducible factor 1 alpha and vascular endothelial growth factor, which are highly associated with type H blood vessel formation.
    Conclusion: MQEP exerts anti-osteoporosis effects and prevents bone loss by alleviating vascular injury caused by renin-angiotensin-aldosterone system activation and promoting type H blood vessel formation.
    MeSH term(s) Bone Diseases, Metabolic ; Endothelial Cells/metabolism ; Glucocorticoids/adverse effects ; Humans ; Hypoxia-Inducible Factor 1/metabolism ; Ligands ; Osteoporosis/chemically induced ; Osteoporosis/drug therapy ; Osteoporosis/prevention & control ; Osteoprotegerin/metabolism ; Peptidyl-Dipeptidase A/metabolism ; Receptor, Angiotensin, Type 1/metabolism ; Receptor, Angiotensin, Type 2/metabolism ; Vascular Endothelial Growth Factor A/metabolism ; Vascular System Injuries ; X-Ray Microtomography
    Chemical Substances Glucocorticoids ; Hypoxia-Inducible Factor 1 ; Ligands ; Osteoprotegerin ; Receptor, Angiotensin, Type 1 ; Receptor, Angiotensin, Type 2 ; Vascular Endothelial Growth Factor A ; Peptidyl-Dipeptidase A (EC 3.4.15.1)
    Language English
    Publishing date 2022-09-06
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2592084-4
    ISSN 1664-2392
    ISSN 1664-2392
    DOI 10.3389/fendo.2022.998971
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: The analysis of Modified Qing' E Formula on the differential expression of exosomal miRNAs in the femoral head bone tissue of mice with steroid-induced ischemic necrosis of femoral head.

    Zhu, Wei / Zhang, Faxue / Lu, Junjie / Ma, Chen / Shen, Lin / Hu, Desheng / Xu, Xiaojuan / Shuai, Bo

    Frontiers in endocrinology

    2022  Volume 13, Page(s) 954778

    Abstract: ... of Modified Qing' E Formula (MQEF) on steroid-induced ischemic necrosis of the femoral head (INFH) model ...

    Abstract Objective: To investigate the differential expression of exosomal miRNAs in the bone marrow tissue of Modified Qing' E Formula (MQEF) on steroid-induced ischemic necrosis of the femoral head (INFH) model.
    Methods: Steroid hormones were used to establish the INFH model and treated with MQEF. After successful modeling, femoral tissue exosomes were isolated for miRNA sequencing to obtain femoral tissue exosomal differential miRNAs. By GO analysis and KEGG analysis of the differential genes in both groups, the major exosomal miRNAs of MQEF exerting anti-INFH as well as the major signaling pathways were identified. Next, a quantitative metabolomic validation of MQEF with broad targeting was performed to obtain the main active components of MQEF and to perform biological analysis and signaling pathway prediction of the active components by network pharmacology. Finally, the sequencing results were validated by using RT-qPCR. The results of miRNA sequencing were verified by double examination of network pharmacology and RT-qPCR, and the exosomal miRNAs regulated by the anti-INFH effect of MQEF and the specific signaling pathway of the effect were clarified.
    Results: A total of 65,389 target genes were predicted in the exosomes of two groups of mice, and 18 significant differentially expressed miRNAs were obtained, of which 14 were up-regulated and 4 down-regulated. GO enrichment analysis showed that these predicted target genes were enriched in 12371 biological processes, 1727 cell components, and 4112 molecular functions. KEGG analysis showed that the predicted miRNA target genes were annotated to 342 signal pathways, in which the highly enriched pathways closely related to bone metabolism were PI3K-Akt signal pathway, MAPK signal pathway, and Wnt signal pathway. The most significantly up-regulated miRNAs were miR-185-3p and miR-1b-5p and the most significantly down-regulated miRNAs were miR-129b-5p and miR-223-5p, of which the targeted genes were closely related to the PI3K-Akt signal pathway. MQEF aqueous decoction extract targeted metabolomics quantitatively combined with network pharmacology predicted targets also closely related to PI3K-Akt signaling pathway. Real-time quantitative PCR validation showed that miR-185-3p was up-regulated 7.2-fold and miR-129b-5p was down-regulated 2.2-fold in the treatment group, and the difference was significant (P < 0.05).
    Conclusions: MQEF can regulate exosomal miRNA expression in steroid-induced INFH models, miR-185-3p or miR-129b-5p/PI3K-Akt signal axis may be part of the mechanism of MQEF against steroid-induced INFH.
    MeSH term(s) Animals ; Femur Head/pathology ; Femur Head Necrosis/chemically induced ; Femur Head Necrosis/genetics ; Mice ; MicroRNAs/genetics ; Phosphatidylinositol 3-Kinases ; Proto-Oncogene Proteins c-akt ; Steroids/adverse effects
    Chemical Substances MicroRNAs ; Steroids ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language English
    Publishing date 2022-08-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2592084-4
    ISSN 1664-2392
    ISSN 1664-2392
    DOI 10.3389/fendo.2022.954778
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Qing Chang Hua Shi granule ameliorate inflammation in experimental rats and cell model of ulcerative colitis through MEK/ERK signaling pathway.

    Zhu, Lei / Dai, Lu-Ming / Shen, Hong / Gu, Pei-Qing / Zheng, Kai / Liu, Ya-Jun / Zhang, Lu / Cheng, Jia-Fei

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2019  Volume 116, Page(s) 108967

    Abstract: Ulcerative colitis (UC), a bowel disease with significant morbidity, is associated with inflammation. In this study, the effect of Qingchang Huashi granule (QCHS) on UC and its underlying mechanisms were explored using both animal and cell culture ... ...

    Abstract Ulcerative colitis (UC), a bowel disease with significant morbidity, is associated with inflammation. In this study, the effect of Qingchang Huashi granule (QCHS) on UC and its underlying mechanisms were explored using both animal and cell culture experiments. A rat UC model was induced with trinitro-benzene-sulfonic acid (TNBS), concentrations of the cytokines IL-1α, IL-6, IL-8, IL-1β, and TNF-α were significantly up-regulated and the concentrations of IL-4, IL-10, and IL-13 were significantly down-regulated compared with the control group (P < 0.05). In contrast, the QCHS and salicylazosulfapyridine (SASP) groups reversed these modulations (P < 0.05). A UC cell model in HT-29 cells was generated using TNF-α combined with lipopolysaccharide treatment. Cells treated with QCHS were used to investigate the possible mechanisms. The expression of apoptosis-related proteins, including Bax/Bcl-2, caspase-3, caspase-9, Fas/Fas-L, and Rafl in the QCHS and SASP groups, were significantly lower than that in the control group in both animal and cell experiments (P < 0.05). In addition, the in vitro results indicate changes in these indicators mediate the MEK/ERK signaling pathways via SGK1. Our results suggested that QCHS could be beneficial in preventing UC progression as an alternative drug for UC treatment.
    MeSH term(s) Animals ; Apoptosis/drug effects ; Biomarkers/metabolism ; Colitis, Ulcerative/drug therapy ; Colitis, Ulcerative/enzymology ; Colitis, Ulcerative/pathology ; Colon/drug effects ; Colon/pathology ; Cytokines/metabolism ; Disease Models, Animal ; Drugs, Chinese Herbal/pharmacology ; Drugs, Chinese Herbal/therapeutic use ; Female ; Gene Silencing ; HT29 Cells ; Humans ; Immediate-Early Proteins/metabolism ; Inflammation/pathology ; Lipopolysaccharides ; MAP Kinase Signaling System/drug effects ; Male ; Models, Biological ; Protein Serine-Threonine Kinases/metabolism ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Rats, Sprague-Dawley
    Chemical Substances Biomarkers ; Cytokines ; Drugs, Chinese Herbal ; Immediate-Early Proteins ; Lipopolysaccharides ; RNA, Messenger ; Protein Serine-Threonine Kinases (EC 2.7.11.1) ; serum-glucocorticoid regulated kinase (EC 2.7.11.1)
    Language English
    Publishing date 2019-05-16
    Publishing country France
    Document type Journal Article
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2019.108967
    Database MEDical Literature Analysis and Retrieval System OnLINE

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