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Wyszukujesz frazę ""Cells, Cultured"" wg kryterium: Temat


Tytuł :
Senescence-activated enhancer landscape orchestrates the senescence-associated secretory phenotype in murine fibroblasts.
Autorzy :
Guan Y; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.; Institute of Clinical Medicine, Zhanjiang Central Hospital, Guangdong Medical University, Zhanjiang 524000, China.
Zhang C; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.; Center for Bioinformatics, School of Life Sciences and Center for Statistical Science, Peking University, Beijing 100871, China.
Lyu G; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.
Huang X; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.
Zhang X; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.
Zhuang T; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.
Jia L; Center for Bioinformatics, School of Life Sciences and Center for Statistical Science, Peking University, Beijing 100871, China.
Zhang L; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.
Zhang C; China Department of Neurobiology, School of Basic Medical Sciences, Beijing Key Laboratory of Neural Regeneration and Repair, Advanced Innovation Center for Human Brain Protection, Capital Medical University, Beijing 100069, China.
Li C; Center for Bioinformatics, School of Life Sciences and Center for Statistical Science, Peking University, Beijing 100871, China.
Tao W; Key Laboratory of Cell Proliferation and Differentiation, School of Life Sciences, Peking University, Beijing 100871, China.
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Źródło :
Nucleic acids research [Nucleic Acids Res] 2020 Nov 04; Vol. 48 (19), pp. 10909-10923.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cellular Senescence*
Gene Expression Regulation*
Aging/*genetics
Fibroblasts/*cytology
Animals ; Cells, Cultured ; Chromatin/metabolism ; Embryo, Mammalian ; Mice ; Mice, Inbred C57BL ; Rats ; Rats, Sprague-Dawley ; Regulatory Sequences, Nucleic Acid
Czasopismo naukowe
Tytuł :
Urban particulate matter regulates tight junction proteins by inducing oxidative stress via the Akt signal pathway in human nasal epithelial cells.
Autorzy :
Lee DC; Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Department of Otorhinolaryngology-Head and Neck Surgery, Daejeon St. Mary's Hospital, Daeheung-dong, Jung-gu, Daejeon, Republic of Korea. Electronic address: .
Choi H; Clinical Research Institute, Daejeon St. Mary's Hospital, Daeheung-dong, Jung-gu, Daejeon, Republic of Korea. Electronic address: .
Oh JM; Clinical Research Institute, Daejeon St. Mary's Hospital, Daeheung-dong, Jung-gu, Daejeon, Republic of Korea. Electronic address: .
Lee J; Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Department of Otorhinolaryngology-Head and Neck Surgery, Seoul St. Mary's Hospital, 222, Banpo-daero, Seocho-gu, Seoul, Republic of Korea. Electronic address: .
Lee J; Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea; Department of Otorhinolaryngology-Head and Neck Surgery, Daejeon St. Mary's Hospital, Daeheung-dong, Jung-gu, Daejeon, Republic of Korea. Electronic address: .
Lee HY; Division of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, The Catholic University of Korea, Seoul, Republic of Korea. Electronic address: .
Kang JY; Division of Pulmonary, Allergy and Critical Care Medicine, Department of Internal Medicine, The Catholic University of Korea, Seoul, Republic of Korea. Electronic address: .
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Źródło :
Toxicology letters [Toxicol Lett] 2020 Oct 15; Vol. 333, pp. 33-41. Date of Electronic Publication: 2020 Jul 17.
Typ publikacji :
Journal Article
MeSH Terms :
Air Pollutants/*toxicity
Epithelial Cells/*drug effects
Gene Expression Regulation/*drug effects
Nasal Mucosa/*drug effects
Oxidative Stress/*drug effects
Particulate Matter/*toxicity
Proto-Oncogene Proteins c-akt/*metabolism
Tight Junction Proteins/*metabolism
Acetylcysteine/pharmacology ; Cell Survival/drug effects ; Cells, Cultured ; Cytokines/genetics ; Cytokines/metabolism ; Epithelial Cells/metabolism ; Female ; Humans ; Male ; Middle Aged ; Nasal Mucosa/metabolism ; Oxidative Stress/genetics ; Signal Transduction ; Tight Junction Proteins/genetics ; Tight Junctions/drug effects ; Tight Junctions/metabolism ; Turbinates/drug effects ; Turbinates/metabolism ; Urbanization
Czasopismo naukowe
Tytuł :
CD40-miRNA axis controls prospective cell fate determinants during B cell differentiation.
Autorzy :
Salunkhe S; CSIR-Centre for Cellular and Molecular Biology, Hyderabad, 500007, India.
Vaidya T; CSIR-Centre for Cellular and Molecular Biology, Hyderabad, 500007, India. Electronic address: .
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Źródło :
Molecular immunology [Mol Immunol] 2020 Oct; Vol. 126, pp. 46-55. Date of Electronic Publication: 2020 Aug 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
B-Lymphocytes/*physiology
CD40 Antigens/*metabolism
Cell Differentiation/*immunology
Gene Expression Regulation/*immunology
MicroRNAs/*metabolism
Signal Transduction/*immunology
Animals ; Cell Differentiation/drug effects ; Cell Differentiation/genetics ; Cells, Cultured ; Computational Biology ; Datasets as Topic ; Gene Expression Profiling ; Gene Expression Regulation/drug effects ; Male ; Mice ; MicroRNAs/agonists ; Oligonucleotide Array Sequence Analysis ; Primary Cell Culture ; Real-Time Polymerase Chain Reaction ; Signal Transduction/drug effects ; Signal Transduction/genetics
Czasopismo naukowe
Tytuł :
Enhancer RNAs predict enhancer-gene regulatory links and are critical for enhancer function in neuronal systems.
Autorzy :
Carullo NVN; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Phillips Iii RA; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Simon RC; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Soto SAR; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Hinds JE; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Salisbury AJ; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Revanna JS; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Bunner KD; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Ianov L; Civitan International Research Center, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Sultan FA; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Savell KE; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Gersbach CA; Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
Day JJ; Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.; Civitan International Research Center, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
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Źródło :
Nucleic acids research [Nucleic Acids Res] 2020 Sep 25; Vol. 48 (17), pp. 9550-9570.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Enhancer Elements, Genetic*
Gene Expression Regulation*
Neurons/*physiology
RNA/*physiology
Animals ; CREB-Binding Protein/genetics ; CREB-Binding Protein/metabolism ; CRISPR-Cas Systems ; Cells, Cultured ; Chromatin/metabolism ; HEK293 Cells ; Humans ; Neurons/cytology ; Proto-Oncogene Proteins c-fos/genetics ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; RNA, Small Interfering ; Rats ; Reproducibility of Results ; Sequence Analysis, RNA ; Single Molecule Imaging
Czasopismo naukowe
Tytuł :
Proteomics Study on the Differentially Expressed Proteins in c-fos-silenced Cells Exposed to PM 2.5 .
Autorzy :
Cai Y; School of Public Health, University of South China, Hengyang 421001, Hunan, China;Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Zheng K; School of Public Health, University of South China, Hengyang 421001, Hunan, China;Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Li RB; School of Public Health, University of South China, Hengyang 421001, Hunan, China;Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Yu SY; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Liu N; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Ji JJ; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Yang C; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Wu S; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
Qin SJ; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China;Xiangya School of Public Health, Central South University, Changsha 410078, Hunan, China.
Li BR; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China;Xiangya School of Public Health, Central South University, Changsha 410078, Hunan, China.
Zhang ZH; School of Public Health, University of South China, Hengyang 421001, Hunan, China.
Xu XY; Institute of Environment and Health, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong, China.
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Źródło :
Biomedical and environmental sciences : BES [Biomed Environ Sci] 2020 Sep 20; Vol. 33 (9), pp. 680-689.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*
Gene Silencing*
Air Pollutants/*toxicity
Bronchi/*drug effects
Genes, fos/*genetics
Particulate Matter/*toxicity
Respiratory Mucosa/*drug effects
Bronchi/metabolism ; Cells, Cultured ; Humans ; Proteomics ; Respiratory Mucosa/metabolism
Czasopismo naukowe
Tytuł :
Irisin modulates genes associated with severe coronavirus disease (COVID-19) outcome in human subcutaneous adipocytes cell culture.
Autorzy :
de Oliveira M; Department of Internal Clinic, Botucatu Medicine School, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil. Electronic address: .
De Sibio MT; Department of Internal Clinic, Botucatu Medicine School, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Mathias LS; Department of Internal Clinic, Botucatu Medicine School, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Rodrigues BM; Department of Internal Clinic, Botucatu Medicine School, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
Sakalem ME; Department of Anatomy, Londrina State University (UEL), Londrina, Parana, Brazil.
Nogueira CR; Department of Internal Clinic, Botucatu Medicine School, São Paulo State University (UNESP), Botucatu, São Paulo, Brazil.
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Źródło :
Molecular and cellular endocrinology [Mol Cell Endocrinol] 2020 Sep 15; Vol. 515, pp. 110917. Date of Electronic Publication: 2020 Jun 25.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Adipocytes/*drug effects
Fibronectins/*pharmacology
Gene Expression Regulation/*drug effects
ADAM10 Protein/genetics ; ADAM10 Protein/metabolism ; Adipocytes/cytology ; Adipocytes/metabolism ; Amyloid Precursor Protein Secretases/genetics ; Amyloid Precursor Protein Secretases/metabolism ; Betacoronavirus/genetics ; Betacoronavirus/metabolism ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/metabolism ; Cells, Cultured ; Coronavirus Infections/virology ; Fibronectins/genetics ; Fibronectins/metabolism ; Furin/genetics ; Furin/metabolism ; Gene Ontology ; Histone Acetyltransferases/genetics ; Histone Acetyltransferases/metabolism ; Histone Deacetylase 2/genetics ; Histone Deacetylase 2/metabolism ; Humans ; Jumonji Domain-Containing Histone Demethylases/genetics ; Jumonji Domain-Containing Histone Demethylases/metabolism ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Models, Biological ; Molecular Sequence Annotation ; Nuclear Proteins/genetics ; Nuclear Proteins/metabolism ; Obesity/virology ; Pandemics ; Peptidyl-Dipeptidase A/genetics ; Peptidyl-Dipeptidase A/metabolism ; Pneumonia, Viral/virology ; Protein-Serine-Threonine Kinases/antagonists & inhibitors ; Protein-Serine-Threonine Kinases/genetics ; Protein-Serine-Threonine Kinases/metabolism ; Repressor Proteins/genetics ; Repressor Proteins/metabolism ; Signal Transduction ; Sirtuin 1/genetics ; Sirtuin 1/metabolism ; Toll-Like Receptor 3/genetics ; Toll-Like Receptor 3/metabolism ; rab1 GTP-Binding Proteins/genetics ; rab1 GTP-Binding Proteins/metabolism
SCR Disease Name :
COVID-19
Czasopismo naukowe
Tytuł :
Propofol induces mitochondrial-associated protein LRPPRC and protects mitochondria against hypoxia in cardiac cells.
Autorzy :
Zhang Q; Department of Anesthesiology, The First Affiliated Hospital of the University of South China, Hengyang, Hunan Province, P.R. China.
Cai S; Cardiovascular Surgery, The First Affiliated Hospital of the University of South China, Hengyang, Hunan Province, P.R. China.
Guo L; The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan City People's Hospital, Qingyuan, Guangdong Province, P.R. China.
Zhao G; The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan City People's Hospital, Qingyuan, Guangdong Province, P.R. China.
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Źródło :
PloS one [PLoS One] 2020 Sep 08; Vol. 15 (9), pp. e0238857. Date of Electronic Publication: 2020 Sep 08 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation/*drug effects
Hypoxia/*physiopathology
Mitochondria/*drug effects
Mitochondrial Proteins/*metabolism
Myocytes, Cardiac/*drug effects
Propofol/*pharmacology
Protective Agents/*pharmacology
Anesthetics, Intravenous/pharmacology ; Animals ; Apoptosis ; Cells, Cultured ; Membrane Potential, Mitochondrial ; Mitochondria/genetics ; Mitochondria/metabolism ; Mitochondrial Proteins/genetics ; Myocytes, Cardiac/cytology ; Myocytes, Cardiac/metabolism ; Neoplasm Proteins/genetics ; Neoplasm Proteins/metabolism ; Oxidative Stress ; Proto-Oncogene Proteins c-bcl-2 ; Rats ; Reactive Oxygen Species
Czasopismo naukowe
Tytuł :
circPUM1 promotes polycystic ovary syndrome progression by sponging to miR-760.
Autorzy :
Deng L; Department of Gynecology, Hospital of Chengdu University of Traditional Chinese Medicine, No. 39 Shi-er-qiao Road, Chengdu 610072, Sichuan Province, China.
Chen Q; Department of Gynecology, Hospital of Chengdu University of Traditional Chinese Medicine, No. 39 Shi-er-qiao Road, Chengdu 610072, Sichuan Province, China.
Xie J; Department of Gynecology, Hospital of Chengdu University of Traditional Chinese Medicine, No. 39 Shi-er-qiao Road, Chengdu 610072, Sichuan Province, China.
Wei W; Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Hui H; Operating Room, Huai'an Second People's Hospital, The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an, China. Electronic address: .
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Źródło :
Gene [Gene] 2020 Sep 05; Vol. 754, pp. 144903. Date of Electronic Publication: 2020 Jun 12.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*
Granulosa Cells/*pathology
MicroRNAs/*genetics
Polycystic Ovary Syndrome/*pathology
RNA, Circular/*genetics
Apoptosis ; Cell Proliferation ; Cells, Cultured ; Disease Progression ; Female ; Granulosa Cells/drug effects ; Granulosa Cells/metabolism ; Humans ; Hypoglycemic Agents/pharmacology ; Insulin/pharmacology ; Polycystic Ovary Syndrome/genetics ; Polycystic Ovary Syndrome/metabolism
Czasopismo naukowe
Tytuł :
Characterization of 3(3,4-dihydroxy-phenyl) propionic acid as a novel microbiome-derived epigenetic modifier in attenuation of immune inflammatory response in human monocytes.
Autorzy :
Wang J; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, United States; Research and Development Service, Geriatric Research, Education and Clinical Center, James J. Peters Veterans Affairs Medical Center, Bronx, NY, United States.
Blaze J; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, United States.
Haghighi F; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, United States; Research and Development Service, Geriatric Research, Education and Clinical Center, James J. Peters Veterans Affairs Medical Center, Bronx, NY, United States.
Kim-Schulze S; Human Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, New York, United States.
Raval U; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, United States.
Trageser KJ; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, United States.
Pasinetti GM; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, United States; Research and Development Service, Geriatric Research, Education and Clinical Center, James J. Peters Veterans Affairs Medical Center, Bronx, NY, United States. Electronic address: .
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Źródło :
Molecular immunology [Mol Immunol] 2020 Sep; Vol. 125, pp. 172-177. Date of Electronic Publication: 2020 Jul 21.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Gene Expression Regulation/*drug effects
Monocytes/*drug effects
Propionates/*pharmacology
Cells, Cultured ; DNA Methylation/drug effects ; DNA Methylation/genetics ; Down-Regulation ; Gene Expression Regulation/genetics ; Humans ; Interleukin-6/biosynthesis ; Microbiota ; Neuroimmunomodulation/drug effects ; Neuroimmunomodulation/genetics
Czasopismo naukowe
Tytuł :
TLR4-TAK1-p38 MAPK pathway and HDAC6 regulate the expression of sigma-1 receptors in rat primary cultured microglia.
Autorzy :
Iwamoto M; Department of Pharmacology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Japan.
Nakamura Y; Department of Pharmacology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Japan. Electronic address: .
Takemura M; Department of Pharmacology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Japan.
Hisaoka-Nakashima K; Department of Pharmacology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Japan.
Morioka N; Department of Pharmacology, Graduate School of Biomedical & Health Sciences, Hiroshima University, Japan. Electronic address: .
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Źródło :
Journal of pharmacological sciences [J Pharmacol Sci] 2020 Sep; Vol. 144 (1), pp. 23-29. Date of Electronic Publication: 2020 Jul 02.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression/*genetics
Gene Expression Regulation/*genetics
Histone Deacetylase 6/*physiology
MAP Kinase Kinase Kinases/*physiology
MAP Kinase Signaling System/*genetics
MAP Kinase Signaling System/*physiology
Microglia/*metabolism
Neurodegenerative Diseases/*genetics
Receptors, sigma/*genetics
Receptors, sigma/*metabolism
Toll-Like Receptor 4/*physiology
p38 Mitogen-Activated Protein Kinases/*physiology
Animals ; Cells, Cultured ; Down-Regulation/genetics ; MAP Kinase Kinase Kinases/metabolism ; Molecular Targeted Therapy ; Neurodegenerative Diseases/drug therapy ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Rats ; Receptors, sigma/physiology ; Toll-Like Receptor 4/metabolism ; p38 Mitogen-Activated Protein Kinases/metabolism
Czasopismo naukowe
Tytuł :
Circular RNA COL1A2 promotes angiogenesis via regulating miR-29b/VEGF axis in diabetic retinopathy.
Autorzy :
Zou J; Eye Center of Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, PR China; Hunan Key Laboratory of Ophthalmology, Changsha 410008, Hunan Province, PR China.
Liu KC; Eye Center of Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, PR China; Hunan Key Laboratory of Ophthalmology, Changsha 410008, Hunan Province, PR China.
Wang WP; Eye Center of Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, PR China; Hunan Key Laboratory of Ophthalmology, Changsha 410008, Hunan Province, PR China.
Xu Y; Eye Center of Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, PR China; Hunan Key Laboratory of Ophthalmology, Changsha 410008, Hunan Province, PR China. Electronic address: .
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Źródło :
Life sciences [Life Sci] 2020 Sep 01; Vol. 256, pp. 117888. Date of Electronic Publication: 2020 Jun 01.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*/drug effects
Diabetic Retinopathy/*genetics
MicroRNAs/*genetics
Neovascularization, Pathologic/*genetics
RNA, Circular/*metabolism
Vascular Endothelial Growth Factor A/*genetics
Animals ; Base Sequence ; Capillary Permeability/drug effects ; Capillary Permeability/genetics ; Cell Movement/drug effects ; Cell Movement/genetics ; Cell Proliferation/drug effects ; Cell Proliferation/genetics ; Cells, Cultured ; Endothelial Cells/drug effects ; Endothelial Cells/metabolism ; Gene Silencing ; Glucose/toxicity ; Humans ; Male ; Mice, Inbred C57BL ; MicroRNAs/metabolism ; Microvessels/pathology ; Models, Biological ; RNA, Circular/genetics ; Retina/pathology ; Vascular Endothelial Growth Factor A/metabolism
Czasopismo naukowe
Tytuł :
Lnc-M2 controls M2 macrophage differentiation via the PKA/CREB pathway.
Autorzy :
Chen Y; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China; Department of Dermatology, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Li H; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Ding T; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Li J; Department of Pathology, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan People's Hospital, Qingyuan, China.
Zhang Y; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Wang J; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Yang X; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Chong T; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Long Y; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Li X; Shenzhen Key Laboratory of Viral Oncology, Center for Clinical Research and Innovation (CCRI), Shenzhen Hospital, Southern Medical University, Shenzhen, China. Electronic address: .
Gao F; Department of Physiology and Biomedical Engineering and Gastroenterology Research Unit, Enteric Neuroscience Program, Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USA. Electronic address: .
Lyu X; Department of Laboratory Medicine, The Third Affiliated Hospital, Southern Medical University, Guangzhou, China. Electronic address: .
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Źródło :
Molecular immunology [Mol Immunol] 2020 Aug; Vol. 124, pp. 142-152. Date of Electronic Publication: 2020 Jun 19.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation/*immunology
Macrophage Activation/*genetics
Macrophages/*immunology
RNA, Long Noncoding/*genetics
Cell Differentiation/genetics ; Cells, Cultured ; Cyclic AMP Response Element-Binding Protein/metabolism ; Cyclic AMP-Dependent Protein Kinases/metabolism ; Gene Expression Regulation/genetics ; Humans ; Macrophages/metabolism ; RNA, Long Noncoding/metabolism ; STAT3 Transcription Factor/metabolism ; Signal Transduction/immunology
Czasopismo naukowe
Tytuł :
Potential mechanisms of action of celastrol against rheumatoid arthritis: Transcriptomic and proteomic analysis.
Autorzy :
Xinqiang S; Department of Biological Sciences, Xinyang Normal University, Xinyang, China.; Institute for Conservation and Utilization of Agro-Bioresources in Dabie Mountains, Xinyang, China.
Erqin D; Department of Biological Sciences, Xinyang Normal University, Xinyang, China.
Yu Z; Department of Biological Sciences, Xinyang Normal University, Xinyang, China.
Hongtao D; Department of Biological Sciences, Xinyang Normal University, Xinyang, China.
Lei W; Department of Biological Sciences, Xinyang Normal University, Xinyang, China.
Ningning Y; Department of Biological Sciences, Xinyang Normal University, Xinyang, China.
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Źródło :
PloS one [PLoS One] 2020 Jul 29; Vol. 15 (7), pp. e0233814. Date of Electronic Publication: 2020 Jul 29 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Anti-Inflammatory Agents/*pharmacology
Arthritis, Rheumatoid/*drug therapy
Gene Expression Regulation/*drug effects
Proteomics/*methods
Transcriptome/*drug effects
Triterpenes/*pharmacology
Anti-Inflammatory Agents/therapeutic use ; Arthritis, Rheumatoid/genetics ; Arthritis, Rheumatoid/pathology ; Cells, Cultured ; Chromatography, Liquid ; Gene Ontology ; High-Throughput Nucleotide Sequencing ; Humans ; Models, Molecular ; Molecular Docking Simulation ; RNA, Messenger/biosynthesis ; RNA, Messenger/genetics ; Spectrometry, Mass, Electrospray Ionization ; Synoviocytes/drug effects ; Synoviocytes/metabolism ; Tandem Mass Spectrometry ; Triterpenes/therapeutic use
Czasopismo naukowe
Tytuł :
Mesenchymal stromal/stem cells modulate response to experimental sepsis-induced lung injury via regulation of miR-27a-5p in recipient mice.
Autorzy :
Younes N; Critical Care Medicine, The Keenan Research Centre for Biomedical Science of Saint Michael's Hospital, Toronto, Ontario, Canada.
Zhou L; Critical Care Medicine, The Keenan Research Centre for Biomedical Science of Saint Michael's Hospital, Toronto, Ontario, Canada.; Institute of Medical Sciences and Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Amatullah H; Critical Care Medicine, The Keenan Research Centre for Biomedical Science of Saint Michael's Hospital, Toronto, Ontario, Canada.; Institute of Medical Sciences and Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Mei SHJ; Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
Herrero R; Critical Care Service, Hospital Universitario de Getafe-CIBER de Enfermedades Respiratorias (CIBERES), Getafe, Spain.
Lorente JA; Critical Care Service, Hospital Universitario de Getafe-CIBER de Enfermedades Respiratorias (CIBERES), Getafe, Spain.
Stewart DJ; Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
Marsden P; Critical Care Medicine, The Keenan Research Centre for Biomedical Science of Saint Michael's Hospital, Toronto, Ontario, Canada.
Liles WC; Department of Medicine, University of Washington, Seattle, Washington, USA.
Hu P; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Dos Santos CC; Critical Care Medicine, The Keenan Research Centre for Biomedical Science of Saint Michael's Hospital, Toronto, Ontario, Canada .; Institute of Medical Sciences and Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
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Źródło :
Thorax [Thorax] 2020 Jul; Vol. 75 (7), pp. 556-567. Date of Electronic Publication: 2020 Jun 16.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation*
Acute Lung Injury/*genetics
Mesenchymal Stem Cell Transplantation/*methods
MicroRNAs/*genetics
RNA, Messenger/*genetics
Sepsis/*complications
Acute Lung Injury/etiology ; Acute Lung Injury/therapy ; Animals ; Apoptosis ; Cells, Cultured ; Disease Models, Animal ; Male ; Mice ; Mice, Inbred C57BL ; MicroRNAs/biosynthesis ; RNA, Messenger/metabolism ; Signal Transduction
Czasopismo naukowe
Tytuł :
Single-molecule imaging of transcription dynamics in somatic stem cells.
Autorzy :
Wheat JC; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.; Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, New York, NY, USA.
Sella Y; Department of Systems and Computational Biology, Albert Einstein College of Medicine, New York, NY, USA.
Willcockson M; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Skoultchi AI; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.
Bergman A; Department of Systems and Computational Biology, Albert Einstein College of Medicine, New York, NY, USA.; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, New York, NY, USA.; Department of Pathology, Albert Einstein College of Medicine, New York, NY, USA.; Santa Fe Institute, Santa Fe, NM, USA.
Singer RH; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA.; Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, New York, NY, USA.; Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, New York, NY, USA.; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, New York, NY, USA.; Janelia Research Campus of the HHMI, Ashburn, VA, USA.
Steidl U; Department of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA. .; Ruth L. and David S. Gottesman Institute for Stem Cell Research and Regenerative Medicine, Albert Einstein College of Medicine, New York, NY, USA. .; Department of Medicine (Oncology), Albert Einstein College of Medicine-Montefiore Medical Center, New York, NY, USA. .; Albert Einstein Cancer Center, Albert Einstein College of Medicine, New York, NY, USA. .
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Źródło :
Nature [Nature] 2020 Jul; Vol. 583 (7816), pp. 431-436. Date of Electronic Publication: 2020 Jun 24.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation*
Single Molecule Imaging*
Adult Stem Cells/*metabolism
Transcription, Genetic/*genetics
Adult Stem Cells/cytology ; Animals ; Cells, Cultured ; Clone Cells/cytology ; Clone Cells/metabolism ; Female ; GATA1 Transcription Factor/genetics ; GATA2 Transcription Factor/genetics ; Gene Regulatory Networks ; In Situ Hybridization, Fluorescence ; Male ; Mice ; Mice, Inbred C57BL ; Pedigree ; Proto-Oncogene Proteins/genetics ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Stochastic Processes ; Trans-Activators/genetics
Czasopismo naukowe
Tytuł :
AFF1 inhibits adipogenic differentiation via targeting TGM2 transcription.
Autorzy :
Chen Y; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Wang Y; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Lin W; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Sheng R; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Wu Y; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Xu R; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Zhou C; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Yuan Q; State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
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Źródło :
Cell proliferation [Cell Prolif] 2020 Jun; Vol. 53 (6), pp. e12831. Date of Electronic Publication: 2020 May 22.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*
Adipogenesis/*genetics
DNA-Binding Proteins/*metabolism
GTP-Binding Proteins/*genetics
Nuclear Proteins/*metabolism
Transcriptional Elongation Factors/*metabolism
Transglutaminases/*genetics
3T3-L1 Cells ; Animals ; Cells, Cultured ; DNA-Binding Proteins/genetics ; GTP-Binding Proteins/biosynthesis ; GTP-Binding Proteins/metabolism ; Humans ; Mesenchymal Stem Cells/cytology ; Mesenchymal Stem Cells/metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Nuclear Proteins/genetics ; Stem Cells/metabolism ; Transcription, Genetic ; Transcriptional Elongation Factors/genetics ; Transglutaminases/biosynthesis ; Transglutaminases/metabolism
Czasopismo naukowe
Tytuł :
ALS/FTD-associated protein FUS induces mitochondrial dysfunction by preferentially sequestering respiratory chain complex mRNAs.
Autorzy :
Tsai YL; Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Coady TH; Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Lu L; Center for Motor Neuron Biology and Disease, Columbia University, New York, New York 10027, USA.
Zheng D; Department of Microbiology, Biochemistry, and Molecular Genetics, Rutgers New Jersey Medical School, Newark, New Jersey 07103, USA.
Alland I; Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
Tian B; Department of Microbiology, Biochemistry, and Molecular Genetics, Rutgers New Jersey Medical School, Newark, New Jersey 07103, USA.
Shneider NA; Center for Motor Neuron Biology and Disease, Columbia University, New York, New York 10027, USA.
Manley JL; Department of Biological Sciences, Columbia University, New York, New York 10027, USA.
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Źródło :
Genes & development [Genes Dev] 2020 Jun 01; Vol. 34 (11-12), pp. 785-805. Date of Electronic Publication: 2020 May 07.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Amyotrophic Lateral Sclerosis/*genetics
Amyotrophic Lateral Sclerosis/*physiopathology
Gene Expression Regulation/*genetics
Mitochondria/*pathology
RNA, Messenger/*metabolism
RNA-Binding Protein FUS/*genetics
RNA-Binding Protein FUS/*metabolism
Cell Line ; Cell Respiration/genetics ; Cells, Cultured ; Electron Transport/genetics ; Genome, Mitochondrial ; Humans ; Mitochondria/genetics ; Mutation ; Protein Aggregation, Pathological/genetics ; Protein Binding/genetics
Czasopismo naukowe
Tytuł :
TRAF3IP3 negatively regulates cytosolic RNA induced anti-viral signaling by promoting TBK1 K48 ubiquitination.
Autorzy :
Deng M; Oral and Craniofacial Biomedicine PhD Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Craniofacial and Surgery Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Tam JW; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Wang L; Oral and Craniofacial Biomedicine PhD Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Liang K; Oral and Craniofacial Biomedicine PhD Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Li S; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Zhang L; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Sarah W. Stedman Nutrition and Metabolism Center and Duke Molecular Physiology Institute, Duke University Medical Center, Durham, NC, 27710, USA.
Guo H; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Luo X; Department of Periodontics and Oral Medicine, University of Michigan School of Dentistry, University of Michigan Rogel Cancer Center, University of Michigan, Ann Arbor, MI, 48105, USA.
Zhang Y; Department of Dermatology, the Second Affiliated Hospital, School of Medicine, Xi'an Jiaotong University, Xi'an, Shaanxi, 710004, China.
Petrucelli A; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Davis BK; Department of Biology, Franklin and Marshall College, Lancaster, PA, 17604, USA.
Conti BJ; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Biotechnology Center, University of Wisconsin-Madison, Madison, WI, 53706, USA.
June Brickey W; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Ko CC; Oral and Craniofacial Biomedicine PhD Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.; Department of Craniofacial and Surgery Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA.
Lei YL; Department of Periodontics and Oral Medicine, University of Michigan School of Dentistry, University of Michigan Rogel Cancer Center, University of Michigan, Ann Arbor, MI, 48105, USA.
Sun S; Department of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Ting JP; Oral and Craniofacial Biomedicine PhD Program, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA. .; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA. .; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA. .; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, USA. .
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Źródło :
Nature communications [Nat Commun] 2020 May 04; Vol. 11 (1), pp. 2193. Date of Electronic Publication: 2020 May 04.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Gene Expression Regulation*
Carrier Proteins/*genetics
Interferon Type I/*genetics
Membrane Proteins/*genetics
Myeloid Cells/*metabolism
Protein-Serine-Threonine Kinases/*genetics
RNA, Viral/*genetics
Animals ; Carrier Proteins/metabolism ; Cell Line ; Cells, Cultured ; Chlorocebus aethiops ; Cytosol/metabolism ; Cytosol/virology ; HEK293 Cells ; HeLa Cells ; Humans ; Interferon Type I/metabolism ; Jurkat Cells ; Lysine/genetics ; Lysine/metabolism ; Membrane Proteins/metabolism ; Mice, Inbred C57BL ; Mice, Knockout ; Mice, Transgenic ; Myeloid Cells/virology ; Protein-Serine-Threonine Kinases/metabolism ; RNA, Viral/metabolism ; THP-1 Cells ; Ubiquitination ; Vero Cells ; Vesicular stomatitis Indiana virus/genetics ; Vesicular stomatitis Indiana virus/physiology
Czasopismo naukowe
Tytuł :
Cronobacter sakazakii induces necrotizing enterocolitis by regulating NLRP3 inflammasome expression via TLR4.
Autorzy :
Chen Z; Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, PR China.
Zhang Y; Department of Laboratory Medicine, West China Second University Hospital, Sichuan University, Sichuan, PR China.; Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, PR China.
Lin R; Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, PR China.
Meng X; Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, PR China.
Zhao W; Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, PR China.
Shen W; Department of Neonatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, PR China.
Fan H; Department of Microbiology, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, PR China.
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Źródło :
Journal of medical microbiology [J Med Microbiol] 2020 May; Vol. 69 (5), pp. 748-758. Date of Electronic Publication: 2020 Mar 25.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*
Cronobacter sakazakii/*physiology
Enterocolitis, Necrotizing/*genetics
Enterocolitis, Necrotizing/*metabolism
Enterocolitis, Necrotizing/*microbiology
NLR Family, Pyrin Domain-Containing 3 Protein/*genetics
Toll-Like Receptor 4/*metabolism
Animals ; Animals, Newborn ; Cell Cycle/drug effects ; Cell Line ; Cells, Cultured ; Disease Models, Animal ; Enterocolitis, Necrotizing/pathology ; Host-Pathogen Interactions ; Humans ; NF-kappa B/metabolism ; Pyroptosis ; Rats ; Signal Transduction ; Sulfonamides/pharmacology ; Toll-Like Receptor 4/antagonists & inhibitors
Czasopismo naukowe
Tytuł :
1,25(OH)D vitamin D promotes NOS2 expression in response to bacterial and viral PAMPs in primary bovine salivary gland fibroblasts.
Autorzy :
Boylan M; Animal and Bioscience Research Department, Animal and Grassland Research and Innovation Centre, Teagasc, Grange, Ireland.
O'Brien MB; Animal and Bioscience Research Department, Animal and Grassland Research and Innovation Centre, Teagasc, Grange, Ireland.
Beynon C; Animal and Bioscience Research Department, Animal and Grassland Research and Innovation Centre, Teagasc, Grange, Ireland.
Meade KG; Animal and Bioscience Research Department, Animal and Grassland Research and Innovation Centre, Teagasc, Grange, Ireland. .
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Źródło :
Veterinary research communications [Vet Res Commun] 2020 May; Vol. 44 (2), pp. 83-88. Date of Electronic Publication: 2020 May 22.
Typ publikacji :
Journal Article
MeSH Terms :
Fibroblasts/*immunology
Gene Expression Regulation/*drug effects
Immunity, Innate/*drug effects
Nitric Oxide Synthase Type II/*genetics
Vitamin D/*analogs & derivatives
Adjuvants, Immunologic/pharmacology ; Animals ; Cattle ; Cells, Cultured ; Fibroblasts/drug effects ; Pathogen-Associated Molecular Pattern Molecules/pharmacology ; Salivary Glands/cytology ; Vitamin D/pharmacology
Czasopismo naukowe

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