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Wyszukujesz frazę ""Histone Deacetylase 1"" wg kryterium: Temat


Tytuł :
The glial-specific hypermethylated 3' untranslated region of histone deacetylase 1 may modulates several signal pathways in Alzheimer's disease.
Autorzy :
Lv L; Department of Cardio-Vascular Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China.
Zhang D; Department of General Surgery, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510030, China.
Hua P; Department of Cardio-Vascular Surgery, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China. Electronic address: .
Yang S; Biobank and Bioinformatics Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou 510120, China. Electronic address: .
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Źródło :
Life sciences [Life Sci] 2021 Jan 15; Vol. 265, pp. 118760. Date of Electronic Publication: 2020 Nov 16.
Typ publikacji :
Journal Article
MeSH Terms :
3' Untranslated Regions*
Signal Transduction*
Alzheimer Disease/*metabolism
Histone Deacetylase 1/*metabolism
Neuroglia/*metabolism
Alzheimer Disease/enzymology ; DNA Methylation ; Gene Expression Regulation ; Histone Deacetylase 1/physiology ; Humans ; Neuroglia/enzymology ; Protein Interaction Maps
Czasopismo naukowe
Tytuł :
Glioma-initiating cells at tumor edge gain signals from tumor core cells to promote their malignancy.
Autorzy :
Bastola S; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Pavlyukov MS; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, 117997, Russian Federation.
Yamashita D; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Ghosh S; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Cho H; Research Institute for Future Medicine, Seoul, 06351, Republic of Korea.; Institute for Refractory Cancer Research, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, 06351, Republic of Korea.
Kagaya N; Biomedical Information Research Center, National Institute of Advanced Industrial Science and Technology, 2-4-7 Aomi, Koto-ku, Tokyo, 135-0064, Japan.
Zhang Z; Department of Radiation Oncology, University of Alabama at Birmingham, Birmingham, AL, 35233, USA.
Minata M; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Lee Y; Research Institute for Future Medicine, Seoul, 06351, Republic of Korea.; Institute for Refractory Cancer Research, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, 06351, Republic of Korea.
Sadahiro H; Department of Neurosurgery, Yamaguchi University, Yamaguchi, Japan.
Yamaguchi S; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Komarova S; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Yang E; Department of Radiation Oncology, University of Alabama at Birmingham, Birmingham, AL, 35233, USA.
Markert J; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Nabors LB; Department of Neurology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Bhat K; Department of Translational Molecular Pathology and Brain Tumor Center, The University of Texas, M.D. Anderson Cancer Center, Houston, TX, 77030, USA.
Lee J; Department of Chemical and Biomolecular Engineering, Ohio State University, Columbus, OH, 43210, USA.
Chen Q; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.; Department of Integrative medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, People's Republic of China.
Crossman DK; Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Shin-Ya K; Biomedical Information Research Center, National Institute of Advanced Industrial Science and Technology, 2-4-7 Aomi, Koto-ku, Tokyo, 135-0064, Japan.
Nam DH; Department of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, 06351, Republic of Korea.; Department of Health Science and Technology, Samsung Advanced Institute for Health Science and Technology, Sungkyunkwan University, Seoul, 06351, Republic of Korea.
Nakano I; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, 35294, USA. .; Research and Development Center for Precision Medicine, Tsukuba University, Tsukuba, Japan. .
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Źródło :
Nature communications [Nat Commun] 2020 Sep 16; Vol. 11 (1), pp. 4660. Date of Electronic Publication: 2020 Sep 16.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Antigens, CD/*metabolism
Brain Neoplasms/*pathology
Glioblastoma/*pathology
Histone Deacetylase 1/*metabolism
Neoplasm Proteins/*metabolism
Animals ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Brain Neoplasms/genetics ; Brain Neoplasms/metabolism ; Brain Neoplasms/mortality ; Female ; GPI-Linked Proteins/metabolism ; Gene Expression Regulation, Neoplastic ; Glioblastoma/genetics ; Glioblastoma/metabolism ; Glioblastoma/mortality ; Histone Deacetylase 1/antagonists & inhibitors ; Histone Deacetylase 1/genetics ; Histone Deacetylase 2/genetics ; Histone Deacetylase 2/metabolism ; Humans ; Mice, SCID ; Phenylbutyrates/pharmacology ; Signal Transduction ; Tumor Microenvironment ; Xenograft Model Antitumor Assays
Czasopismo naukowe
Tytuł :
Histone deacetylase HDA-1 modulates mitochondrial stress response and longevity.
Autorzy :
Shao LW; Beijing Advanced Innovation Center for Genomics, State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.; Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, 100871, Beijing, China.
Peng Q; Laboratory of Bioinformatics and Genomic Medicine, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.
Dong M; Beijing Advanced Innovation Center for Genomics, State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.; Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, 100871, Beijing, China.
Gao K; Beijing Advanced Innovation Center for Genomics, State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.
Li Y; Laboratory of Bioinformatics and Genomic Medicine, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.
Li Y; Beijing Advanced Innovation Center for Genomics, State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China.; Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University, 100871, Beijing, China.
Li CY; Laboratory of Bioinformatics and Genomic Medicine, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China. .
Liu Y; Beijing Advanced Innovation Center for Genomics, State Key Laboratory of Membrane Biology, Beijing Key Laboratory of Cardiometabolic Molecular Medicine, Institute of Molecular Medicine, Peking University, 100871, Beijing, China. .
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Źródło :
Nature communications [Nat Commun] 2020 Sep 15; Vol. 11 (1), pp. 4639. Date of Electronic Publication: 2020 Sep 15.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Longevity*
Caenorhabditis elegans/*enzymology
Caenorhabditis elegans Proteins/*metabolism
Histone Deacetylase 1/*metabolism
Histone Deacetylase 2/*metabolism
Histone Deacetylases/*metabolism
Mitochondria/*enzymology
Animals ; Caenorhabditis elegans/genetics ; Caenorhabditis elegans/growth & development ; Caenorhabditis elegans Proteins/genetics ; Histone Deacetylase 1/genetics ; Histone Deacetylase 2/genetics ; Histone Deacetylases/genetics ; Macaca mulatta ; Stress, Physiological ; Unfolded Protein Response
Czasopismo naukowe
Tytuł :
The histone deacetylase HDAC1 activates HIF1α/VEGFA signal pathway in colorectal cancer.
Autorzy :
Chen C; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
Wei M; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
Wang C; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
Sun D; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
Liu P; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
Zhong X; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
He Q; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China.
Yu W; Department of General Surgery, Qilu Hospital of Shandong University, 107 West Wenhua Road, Jinan, China. Electronic address: .
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Źródło :
Gene [Gene] 2020 Sep 05; Vol. 754, pp. 144851. Date of Electronic Publication: 2020 Jun 07.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation, Neoplastic*
Colorectal Neoplasms/*pathology
Histone Deacetylase 1/*metabolism
Hypoxia-Inducible Factor 1, alpha Subunit/*metabolism
Neovascularization, Pathologic/*pathology
Vascular Endothelial Growth Factor A/*metabolism
Animals ; Apoptosis ; Biomarkers, Tumor ; Cell Cycle ; Cell Movement ; Cell Proliferation ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/metabolism ; Disease Progression ; Histone Deacetylase 1/genetics ; Humans ; Hypoxia-Inducible Factor 1, alpha Subunit/genetics ; Male ; Mice ; Mice, Nude ; Neoplasm Invasiveness ; Neovascularization, Pathologic/genetics ; Neovascularization, Pathologic/metabolism ; Prognosis ; Signal Transduction ; Tumor Cells, Cultured ; Vascular Endothelial Growth Factor A/genetics ; Xenograft Model Antitumor Assays
Czasopismo naukowe
Tytuł :
HOXD3 was negatively regulated by YY1 recruiting HDAC1 to suppress progression of hepatocellular carcinoma cells via ITGA2 pathway.
Autorzy :
Wang L; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Gao Y; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Yan'an Key Laboratory of Chronic Disease Prevention and Research, Yan'an, China.
Zhao X; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Guo C; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Wang X; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Yang Y; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Han C; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Zhao L; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Qin Y; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Liu L; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Huang C; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Institute of Genetics and Developmental Biology, School of Basic Medical Sciences, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Cardiovascular Research Center, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Wang W; Department of Cell Biology and Genetics, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center, Xi'an, China.; Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
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Źródło :
Cell proliferation [Cell Prolif] 2020 Aug; Vol. 53 (8), pp. e12835. Date of Electronic Publication: 2020 Jun 17.
Typ publikacji :
Journal Article
MeSH Terms :
Carcinoma, Hepatocellular/*genetics
Gene Expression Regulation, Neoplastic/*genetics
Histone Deacetylase 1/*metabolism
Homeodomain Proteins/*metabolism
Liver Neoplasms/*genetics
Transcription Factors/*metabolism
YY1 Transcription Factor/*metabolism
Apoptosis/physiology ; Cell Movement/physiology ; Cell Proliferation/physiology ; Histone Deacetylase 1/genetics ; Humans ; RNA, Long Noncoding/metabolism
Czasopismo naukowe
Tytuł :
The polycomb group protein PCGF6 mediates germline gene silencing by recruiting histone-modifying proteins to target gene promoters.
Autorzy :
Liu M; State Key Laboratory of Pharmaceutical Biotechnology and MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center, Nanjing University, Nanjing, China.
Zhu Y; State Key Laboratory of Pharmaceutical Biotechnology and MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center, Nanjing University, Nanjing, China.
Xing F; College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.
Liu S; State Key Laboratory of Pharmaceutical Biotechnology and MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center, Nanjing University, Nanjing, China.
Xia Y; School of Biomedical Sciences, Chinese University of Hong Kong, Hong Kong, China.
Jiang Q; Department of Sports Medicine and Adult Reconstructive Surgery, Nanjing Drum Tower Hospital Affiliated to Medical School of Nanjing University, Nanjing, China.
Qin J; State Key Laboratory of Pharmaceutical Biotechnology and MOE Key Laboratory of Model Animals for Disease Study, Model Animal Research Center, Nanjing University, Nanjing, China .
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Źródło :
The Journal of biological chemistry [J Biol Chem] 2020 Jul 10; Vol. 295 (28), pp. 9712-9724. Date of Electronic Publication: 2020 Jun 01.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Silencing*
Histone Deacetylase 1/*metabolism
Histone Deacetylase 2/*metabolism
Histone-Lysine N-Methyltransferase/*metabolism
Mouse Embryonic Stem Cells/*metabolism
Polycomb Repressive Complex 1/*metabolism
Animals ; Cell Line ; Histone Deacetylase 1/genetics ; Histone Deacetylase 2/genetics ; Histone-Lysine N-Methyltransferase/genetics ; Histones ; Mice ; Mice, Knockout ; Polycomb Repressive Complex 1/genetics ; RNA-Seq
Czasopismo naukowe
Tytuł :
Inhibition of PHLDA2 transcription by DNA methylation and YY1 in goat placenta.
Autorzy :
Wang R; Chongqing Engineering Research Center for Herbivores Resource Protection and Utilization, College of Animal Science and Technology, Southwest University, Chongqing 400715, PR China.
Su L; Epigenetic Research Laboratory, Institute for Interdisciplinary Research, Jianghan University, Wuhan, Hubei 430056, PR China.
Yu S; Chongqing Engineering Research Center for Herbivores Resource Protection and Utilization, College of Animal Science and Technology, Southwest University, Chongqing 400715, PR China.
Ma X; Chongqing Engineering Research Center for Herbivores Resource Protection and Utilization, College of Animal Science and Technology, Southwest University, Chongqing 400715, PR China.
Jiang C; Chongqing Engineering Research Center for Herbivores Resource Protection and Utilization, College of Animal Science and Technology, Southwest University, Chongqing 400715, PR China. Electronic address: .
Yu Y; Chongqing Engineering Research Center for Herbivores Resource Protection and Utilization, College of Animal Science and Technology, Southwest University, Chongqing 400715, PR China.
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Źródło :
Gene [Gene] 2020 May 20; Vol. 739, pp. 144512. Date of Electronic Publication: 2020 Feb 26.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Expression Regulation*
Goats/*genetics
Histone Deacetylase 1/*metabolism
Histone Deacetylases/*metabolism
Nuclear Proteins/*metabolism
YY1 Transcription Factor/*metabolism
Animals ; CpG Islands/genetics ; DNA Methylation ; Female ; Histone Deacetylase 1/genetics ; Histone Deacetylases/genetics ; Nuclear Proteins/genetics ; Placenta ; Pregnancy ; Promoter Regions, Genetic/genetics ; YY1 Transcription Factor/genetics
Czasopismo naukowe
Tytuł :
Activation of β-Catenin Signaling and its Crosstalk With Estrogen and Histone Deacetylases in Human Uterine Fibroids.
Autorzy :
Ali M; Department of Obstetrics and Gynecology, University of Illinois at Chicago, Chicago, Illinois.; Department of Surgery, University of Illinois at Chicago, Chicago, Illinois.; Clinical Pharmacy Department, Faculty of Pharmacy, ASU, Cairo, Egypt.
Shahin SM; Clinical Pharmacy Department, Faculty of Pharmacy, ASU, Cairo, Egypt.
Sabri NA; Clinical Pharmacy Department, Faculty of Pharmacy, ASU, Cairo, Egypt.
Al-Hendy A; Department of Obstetrics and Gynecology, University of Illinois at Chicago, Chicago, Illinois.; Department of Surgery, University of Illinois at Chicago, Chicago, Illinois.
Yang Q; Department of Obstetrics and Gynecology, University of Illinois at Chicago, Chicago, Illinois.; Department of Surgery, University of Illinois at Chicago, Chicago, Illinois.
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Źródło :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2020 Apr 01; Vol. 105 (4).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Biomarkers/*metabolism
Estrogens/*pharmacology
Histone Deacetylase 1/*metabolism
Leiomyoma/*pathology
Receptors, Estrogen/*metabolism
beta Catenin/*metabolism
Cyclin D1/genetics ; Cyclin D1/metabolism ; Female ; Histone Deacetylase 1/antagonists & inhibitors ; Histone Deacetylase 1/genetics ; Histone Deacetylase Inhibitors/pharmacology ; Humans ; Leiomyoma/drug therapy ; Leiomyoma/metabolism ; Receptors, Androgen/genetics ; Receptors, Androgen/metabolism ; Receptors, Estrogen/genetics ; Signal Transduction ; Tumor Cells, Cultured ; beta Catenin/genetics
Czasopismo naukowe
Tytuł :
HDAC1 and HDAC2 regulate anti-inflammatory effects of anesthetic isoflurane in human monocytes.
Autorzy :
Guo X; Department of Anesthesia and Pain Medicine, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China.; School of Medicine, South China University of Technology, Guangzhou, China.; Department of Anesthesiology, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ, USA.
Deng J; Department of Anesthesia and Pain Medicine, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China.; School of Medicine, South China University of Technology, Guangzhou, China.
Zheng B; Department of Anesthesia and Pain Medicine, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China.; School of Medicine, South China University of Technology, Guangzhou, China.
Liu H; Department of Cardiology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou Institute of Cardiovascular Disease, Guangzhou, China.
Zhang Y; School of Medicine, South China University of Technology, Guangzhou, China.; Department of Ophthalmology, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China.
Ying Y; Department of Anesthesia and Pain Medicine, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China.; School of Medicine, South China University of Technology, Guangzhou, China.
Jia J; Department of Anesthesiology, Guangdong Women and Children Hospital, Guangzhou, China.
Ruan X; Department of Anesthesia and Pain Medicine, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou, China.; School of Medicine, South China University of Technology, Guangzhou, China.
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Źródło :
Immunology and cell biology [Immunol Cell Biol] 2020 Apr; Vol. 98 (4), pp. 318-331. Date of Electronic Publication: 2020 Feb 25.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Anesthetics, Inhalation/*pharmacology
Histone Deacetylase 1/*metabolism
Histone Deacetylase 2/*metabolism
Inflammation/*metabolism
Isoflurane/*pharmacology
Monocytes/*metabolism
Cell Line ; Gene Silencing ; Histone Deacetylase 1/antagonists & inhibitors ; Histone Deacetylase 1/genetics ; Histone Deacetylase 2/antagonists & inhibitors ; Histone Deacetylase 2/genetics ; Histone Deacetylase Inhibitors/pharmacology ; Histone Deacetylases/genetics ; Histone Deacetylases/metabolism ; Humans ; Hydroxamic Acids/pharmacology ; Inflammation/immunology ; Interleukin-1beta/metabolism ; Interleukin-8/metabolism ; Lipopolysaccharides/pharmacology ; Monocytes/drug effects ; NF-kappa B/metabolism ; Tumor Necrosis Factor-alpha/metabolism
Czasopismo naukowe
Tytuł :
Histone deacetylases 1 and 2 silence cryptic transcription to promote mitochondrial function during cardiogenesis.
Autorzy :
Milstone ZJ; Cardiovascular Medicine, UMass Medical School, Worcester, MA 01605, USA.; Department of Medicine, UMass Medical School, Worcester, MA 01605, USA.
Saheera S; Cardiovascular Medicine, UMass Medical School, Worcester, MA 01605, USA.; Department of Medicine, UMass Medical School, Worcester, MA 01605, USA.
Bourke LM; Cardiovascular Medicine, UMass Medical School, Worcester, MA 01605, USA.; Department of Medicine, UMass Medical School, Worcester, MA 01605, USA.
Shpilka T; Department of Molecular, Cell, and Cancer Biology, UMass Medical School, Worcester, MA 01605, USA.
Haynes CM; Department of Molecular, Cell, and Cancer Biology, UMass Medical School, Worcester, MA 01605, USA.
Trivedi CM; Cardiovascular Medicine, UMass Medical School, Worcester, MA 01605, USA.; Department of Medicine, UMass Medical School, Worcester, MA 01605, USA.; Department of Molecular, Cell, and Cancer Biology, UMass Medical School, Worcester, MA 01605, USA.; Li-Weibo Institute for Rare Diseases Research, UMass Medical School, Worcester, MA 01605, USA.
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Źródło :
Science advances [Sci Adv] 2020 Apr 10; Vol. 6 (15), pp. eaax5150. Date of Electronic Publication: 2020 Apr 10 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms :
Gene Expression Regulation*
Heart/*embryology
Histone Deacetylase 1/*metabolism
Histone Deacetylase 2/*metabolism
Mitochondria/*genetics
Mitochondria/*metabolism
Organogenesis/*genetics
Animals ; Histone Deacetylase 1/genetics ; Histone Deacetylase 2/genetics ; Mice ; Mice, Knockout ; Mice, Transgenic ; Models, Biological ; Transcription, Genetic
Czasopismo naukowe
Tytuł :
Epigenetic regulation of defense genes by histone deacetylase1 in human cell line-derived macrophages promotes intracellular survival of Leishmania donovani.
Autorzy :
Roy G; MolecularParasitology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Brar HK; MolecularParasitology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Muthuswami R; Chromatin Remodeling Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
Madhubala R; MolecularParasitology Laboratory, School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
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Źródło :
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2020 Apr 10; Vol. 14 (4), pp. e0008167. Date of Electronic Publication: 2020 Apr 10 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Epigenesis, Genetic*
Cytoplasm/*metabolism
Histone Deacetylase 1/*genetics
Leishmania donovani/*pathogenicity
Leishmaniasis/*genetics
Macrophages/*parasitology
Cell Line ; Chromatin Assembly and Disassembly ; Cytoplasm/parasitology ; DNA Methylation ; Down-Regulation ; Gene Expression Regulation ; Gene Silencing ; Histone Deacetylase 1/metabolism ; Histones/genetics ; Histones/metabolism ; Host-Parasite Interactions/genetics ; Humans ; Monocytes/metabolism ; Monocytes/parasitology ; Protein Processing, Post-Translational ; RNA, Messenger/metabolism ; RNA, Small Interfering/metabolism ; THP-1 Cells
Czasopismo naukowe
Tytuł :
Molecular mechanisms underlying eicosapentaenoic acid inhibition of HDAC1 and DNMT expression and activity in carcinoma cells.
Autorzy :
Ceccarelli V; Department of Experimental Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy.
Ronchetti S; Department of Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy.
Marchetti MC; Department of Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy.
Calvitti M; Department of Experimental Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy.
Riccardi C; Department of Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy.
Grignani F; Department of Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy.
Vecchini A; Department of Experimental Medicine, P.le L. Severi, 1, University of Perugia, 06132 Perugia, Italy. Electronic address: .
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Źródło :
Biochimica et biophysica acta. Gene regulatory mechanisms [Biochim Biophys Acta Gene Regul Mech] 2020 Feb; Vol. 1863 (2), pp. 194481. Date of Electronic Publication: 2020 Jan 08.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Antineoplastic Agents/*pharmacology
DNA (Cytosine-5-)-Methyltransferase 1/*antagonists & inhibitors
Eicosapentaenoic Acid/*pharmacology
Epigenesis, Genetic/*drug effects
Gene Expression Regulation, Neoplastic/*drug effects
Histone Deacetylase 1/*antagonists & inhibitors
Animals ; Cell Line, Tumor ; CpG Islands ; DNA/metabolism ; DNA (Cytosine-5-)-Methyltransferase 1/metabolism ; Genes, Tumor Suppressor ; Histone Deacetylase 1/metabolism ; Kruppel-Like Transcription Factors/biosynthesis ; Kruppel-Like Transcription Factors/genetics ; Liver Neoplasms, Experimental/genetics ; Liver Neoplasms, Experimental/metabolism ; PPAR gamma/metabolism ; Rats
Czasopismo naukowe
Tytuł :
LncRNA HRCEG, regulated by HDAC1, inhibits cells proliferation and epithelial-mesenchymal-transition in gastric cancer.
Autorzy :
Wu S; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Wu E; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Wang D; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Niu Y; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Yue H; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Zhang D; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Luo J; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; University of Chinese Academy of Sciences, Beijing, 100049, China. Electronic address: .
Chen R; Key Laboratory of RNA Biology, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China; University of Chinese Academy of Sciences, Beijing, 100049, China; Guangdong Geneway Decoding Bio-Tech Co. Ltd, Foshan, 528316, China. Electronic address: .
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Źródło :
Cancer genetics [Cancer Genet] 2020 Feb; Vol. 241, pp. 25-33. Date of Electronic Publication: 2020 Jan 08.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation, Neoplastic*
Histone Deacetylase 1/*metabolism
RNA, Long Noncoding/*metabolism
Stomach Neoplasms/*genetics
Cell Line, Tumor ; Cell Movement/genetics ; Cell Proliferation/genetics ; Epithelial-Mesenchymal Transition/genetics ; Female ; Gastrectomy ; Gene Knockdown Techniques ; Histone Deacetylase 1/genetics ; Humans ; Neoplasm Invasiveness/genetics ; RNA, Long Noncoding/genetics ; RNA, Small Interfering/metabolism ; Stomach/pathology ; Stomach/surgery ; Stomach Neoplasms/pathology ; Stomach Neoplasms/surgery
Czasopismo naukowe
Tytuł :
ARID1A influences HDAC1/BRD4 activity, intrinsic proliferative capacity and breast cancer treatment response.
Autorzy :
Nagarajan S; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Rao SV; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.; Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
Sutton J; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Cheeseman D; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Dunn S; Wellcome Trust Sanger Institute, Hinxton, UK.
Papachristou EK; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Prada JG; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Couturier DL; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Kumar S; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Kishore K; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Chilamakuri CSR; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Glont SE; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Archer Goode E; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Brodie C; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Guppy N; The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK.
Natrajan R; The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, UK.
Bruna A; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Caldas C; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Russell A; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Siersbæk R; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Yusa K; Wellcome Trust Sanger Institute, Hinxton, UK.; Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Chernukhin I; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK.
Carroll JS; CRUK Cambridge Institute, University of Cambridge, Cambridge, UK. .
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Źródło :
Nature genetics [Nat Genet] 2020 Feb; Vol. 52 (2), pp. 187-197. Date of Electronic Publication: 2020 Jan 06.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms/*drug therapy
Cell Cycle Proteins/*metabolism
DNA-Binding Proteins/*metabolism
Histone Deacetylase 1/*metabolism
Transcription Factors/*metabolism
Acetylation ; Animals ; Breast Neoplasms/mortality ; Breast Neoplasms/pathology ; Cell Cycle Proteins/genetics ; Cell Proliferation ; Clustered Regularly Interspaced Short Palindromic Repeats ; DNA-Binding Proteins/genetics ; Drug Resistance, Neoplasm/genetics ; Estrogen Receptor alpha/genetics ; Estrogen Receptor alpha/metabolism ; Female ; Gene Expression Regulation, Neoplastic ; Hepatocyte Nuclear Factor 3-alpha/genetics ; Hepatocyte Nuclear Factor 3-alpha/metabolism ; Histone Deacetylase 1/genetics ; Humans ; MCF-7 Cells ; Mice, Inbred NOD ; Transcription Factors/genetics ; Xenograft Model Antitumor Assays
Czasopismo naukowe
Tytuł :
The topology of chromatin-binding domains in the NuRD deacetylase complex.
Autorzy :
Millard CJ; The Leicester Institute of Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 7RH, UK.
Fairall L; The Leicester Institute of Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 7RH, UK.
Ragan TJ; The Leicester Institute of Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 7RH, UK.
Savva CG; The Leicester Institute of Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 7RH, UK.
Schwabe JWR; The Leicester Institute of Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester LE1 7RH, UK.
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Źródło :
Nucleic acids research [Nucleic Acids Res] 2020 Dec 16; Vol. 48 (22), pp. 12972-12982.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromatin/*genetics
DNA-Binding Proteins/*genetics
Mi-2 Nucleosome Remodeling and Deacetylase Complex/*genetics
Repressor Proteins/*genetics
Retinoblastoma-Binding Protein 4/*genetics
Trans-Activators/*genetics
Amino Acid Sequence/genetics ; Cryoelectron Microscopy ; DNA-Binding Proteins/ultrastructure ; Histone Deacetylase 1/genetics ; Histone Deacetylase 1/ultrastructure ; Histone Deacetylases/genetics ; Histone Deacetylases/ultrastructure ; Humans ; Mi-2 Nucleosome Remodeling and Deacetylase Complex/ultrastructure ; Nucleosomes/genetics ; Nucleosomes/ultrastructure ; Protein Binding/genetics ; Protein Domains/genetics ; Repressor Proteins/ultrastructure ; Retinoblastoma-Binding Protein 4/ultrastructure ; Trans-Activators/ultrastructure
Czasopismo naukowe
Tytuł :
Inhibition of histone deacetylase 1 (HDAC1) and HDAC2 enhances CRISPR/Cas9 genome editing.
Autorzy :
Liu B; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Chen S; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Rose A; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Chen D; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Cao F; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Zwinderman M; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Kiemel D; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.; Department of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, 69120, Germany.
Aïssi M; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Dekker FJ; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
Haisma HJ; Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.
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Źródło :
Nucleic acids research [Nucleic Acids Res] 2020 Jan 24; Vol. 48 (2), pp. 517-532.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
CRISPR-Cas Systems/*genetics
Gene Editing/*methods
Histone Deacetylase 1/*genetics
Histone Deacetylase 2/*genetics
Acetylation/drug effects ; CRISPR-Associated Protein 9/genetics ; Chromatin/genetics ; DNA End-Joining Repair/genetics ; Gene Knockout Techniques ; Histone Deacetylase 1/antagonists & inhibitors ; Histone Deacetylase 2/antagonists & inhibitors ; Histone Deacetylase Inhibitors/chemistry ; Histone Deacetylase Inhibitors/pharmacology ; Histones/chemistry ; Histones/genetics ; Humans
Czasopismo naukowe
Tytuł :
β-Hydroxybutyrate Ameliorates Aβ-Induced Downregulation of TrkA Expression by Inhibiting HDAC1/3 in SH-SY5Y Cells.
Autorzy :
Li X; Department of Nutrition and Food Hygiene, School of Public Health, China Medical University, Shenyang, China.
Zhan Z; Department of Nutrition and Food Hygiene, School of Public Health, China Medical University, Shenyang, China.; Department of Nutrition and Food Hygiene, School of Public Health, Jinzhou Medical University, Jinzhou, China.
Zhang J; Department of Nutrition and Food Hygiene, School of Public Health, China Medical University, Shenyang, China.
Zhou F; Department of Nutrition and Food Hygiene, School of Public Health, China Medical University, Shenyang, China.
An L; Department of Nutrition and Food Hygiene, School of Public Health, China Medical University, Shenyang, China.
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Źródło :
American journal of Alzheimer's disease and other dementias [Am J Alzheimers Dis Other Demen] 2020 Jan-Dec; Vol. 35, pp. 1533317519883496. Date of Electronic Publication: 2019 Oct 24.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Down-Regulation*
Histone Deacetylase 1*
3-Hydroxybutyric Acid/*pharmacology
Amyloid beta-Peptides/*metabolism
Receptor Protein-Tyrosine Kinases/*metabolism
Alzheimer Disease/metabolism ; Cell Culture Techniques ; Humans
Czasopismo naukowe
Tytuł :
CHD7 and 53BP1 regulate distinct pathways for the re-ligation of DNA double-strand breaks.
Autorzy :
Rother MB; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Pellegrino S; Department of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.
Smith R; Univ Rennes, CNRS, IGDR (Institut de génétique et développement de Rennes)-UMR 6290, BIOSIT-UMS3480, F-35000, Rennes, France.
Gatti M; Department of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.
Meisenberg C; The Institute of Cancer Research, Royal Cancer Hospital, London, UK.
Wiegant WW; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Luijsterburg MS; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Imhof R; Department of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland.
Downs JA; The Institute of Cancer Research, Royal Cancer Hospital, London, UK.
Vertegaal ACO; Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, The Netherlands.
Huet S; Univ Rennes, CNRS, IGDR (Institut de génétique et développement de Rennes)-UMR 6290, BIOSIT-UMS3480, F-35000, Rennes, France.; Institut Universitaire de France, Paris, France.
Altmeyer M; Department of Molecular Mechanisms of Disease, University of Zurich, Zurich, Switzerland. .
van Attikum H; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands. .
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Źródło :
Nature communications [Nat Commun] 2020 Nov 13; Vol. 11 (1), pp. 5775. Date of Electronic Publication: 2020 Nov 13.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
DNA Breaks, Double-Stranded*
DNA Helicases/*metabolism
DNA-Binding Proteins/*metabolism
Tumor Suppressor p53-Binding Protein 1/*metabolism
Cell Line, Tumor ; Chromatin/metabolism ; DNA End-Joining Repair ; DNA Ligase ATP/metabolism ; Green Fluorescent Proteins/metabolism ; Histone Deacetylase 1/metabolism ; Humans ; Ku Autoantigen/metabolism ; Poly (ADP-Ribose) Polymerase-1 ; Ubiquitin-Protein Ligases/metabolism
Czasopismo naukowe
Tytuł :
Zingiber officinale Roscoe rhizome extract alleviates neuropathic pain by inhibiting neuroinflammation in mice.
Autorzy :
Borgonetti V; Department of Neuroscience, Psychology, Drug Research and Child Health (NEUROFARBA), Section of Pharmacology, University of Florence, Viale G. Pieraccini 6, 50139 Florence, Italy.
Governa P; Department of Biotechnology, Chemistry and Pharmacy - Department of Excellence 2018-2022, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.
Biagi M; Department of Physical Sciences, Earth and Environment, University of Siena, Strada Laterina 8, 53100 Siena, Italy.
Pellati F; Department of Life Science, University of Modena and Reggio Emilia, Via G. Campi 103, 41125 Modena, Italy.
Galeotti N; Department of Neuroscience, Psychology, Drug Research and Child Health (NEUROFARBA), Section of Pharmacology, University of Florence, Viale G. Pieraccini 6, 50139 Florence, Italy,. Electronic address: .
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Źródło :
Phytomedicine : international journal of phytotherapy and phytopharmacology [Phytomedicine] 2020 Nov; Vol. 78, pp. 153307. Date of Electronic Publication: 2020 Aug 19.
Typ publikacji :
Journal Article
MeSH Terms :
Analgesics, Non-Narcotic/*pharmacology
Ginger/*chemistry
Neuralgia/*drug therapy
Plant Extracts/*chemistry
Plant Extracts/*pharmacology
Administration, Oral ; Analgesics, Non-Narcotic/administration & dosage ; Analgesics, Non-Narcotic/chemistry ; Animals ; Cytokines/metabolism ; Disease Models, Animal ; Histone Deacetylase 1/metabolism ; Hyperalgesia/drug therapy ; Inflammation/drug therapy ; Locomotion/drug effects ; Male ; Mice, Inbred Strains ; Neuralgia/metabolism ; Plant Extracts/administration & dosage ; Rhizome/chemistry ; Spinal Cord/drug effects
Czasopismo naukowe
Tytuł :
Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway.
Autorzy :
Suda K; Department of Applied Biology, Advanced Insect Research Promotion Center, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan.
Muraoka Y; Department of Applied Biology, Advanced Insect Research Promotion Center, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan.
Ortega-Yáñez A; Departamento de Genética del Desarrollo Y Fisiología Molecular Instituto de Biotecnología, Universidad Nacional Autónoma de México, Mexico.
Yoshida H; Department of Applied Biology, Advanced Insect Research Promotion Center, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan. Electronic address: .
Kizu F; Department of Information Science, Advanced Insect Research Promotion Center, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan.
Hochin T; Department of Information Science, Advanced Insect Research Promotion Center, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan.
Kimura H; Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama, Japan.
Yamaguchi M; Department of Applied Biology, Advanced Insect Research Promotion Center, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, 606-8585, Japan. Electronic address: .
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Źródło :
Experimental cell research [Exp Cell Res] 2019 Dec 15; Vol. 385 (2), pp. 111673. Date of Electronic Publication: 2019 Oct 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Epigenesis, Genetic*
Locomotion*
Drosophila Proteins/*genetics
Drosophila Proteins/*metabolism
Histone Deacetylase 1/*metabolism
Mitochondrial Diseases/*genetics
Mitochondrial Proteins/*genetics
Motor Neurons/*metabolism
Phosphate Transport Proteins/*genetics
Animals ; Cells, Cultured ; Drosophila melanogaster ; Histone Code ; Histone Deacetylase 1/genetics ; Humans ; Motor Neurons/pathology ; Motor Neurons/physiology
Czasopismo naukowe

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