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Wyszukujesz frazę ""Glucose Transport Proteins, Facilitative"" wg kryterium: Temat


Tytuł :
Let-7a-5p inhibits triple-negative breast tumor growth and metastasis through GLUT12-mediated warburg effect.
Autorzy :
Shi Y; Medical School of Guizhou University, Guiyang, 550025, China; Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, 100850, China.
Zhang Y; Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, 100850, China.
Ran F; Medical School of Guizhou University, Guiyang, 550025, China; Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, 100850, China.
Liu J; Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, 100850, China.
Lin J; Department of Oncology, Fourth Medical Center of Chinese PLA General Hospital, Beijing, 100048, China.
Hao X; Department of General Surgery, First Medical Center of Chinese PLA General Hospital, Beijing, 100853, China. Electronic address: .
Ding L; Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, 100850, China. Electronic address: .
Ye Q; Medical School of Guizhou University, Guiyang, 550025, China; Department of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, 100850, China. Electronic address: .
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Źródło :
Cancer letters [Cancer Lett] 2020 Dec 28; Vol. 495, pp. 53-65. Date of Electronic Publication: 2020 Sep 15.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Warburg Effect, Oncologic*
Glucose Transport Proteins, Facilitative/*genetics
MicroRNAs/*genetics
Triple Negative Breast Neoplasms/*pathology
3' Untranslated Regions ; Animals ; Cell Line, Tumor ; Cell Movement ; Cell Proliferation ; Female ; Gene Expression Regulation, Neoplastic ; Glucose Transport Proteins, Facilitative/metabolism ; Glycolysis ; Humans ; Mice ; Neoplasm Metastasis ; Neoplasm Transplantation ; Prognosis ; Triple Negative Breast Neoplasms/genetics ; Triple Negative Breast Neoplasms/metabolism ; Up-Regulation
Czasopismo naukowe
Tytuł :
Monosomy-3 Alters the Expression Profile of the Glucose Transporters GLUT1-3 in Uveal Melanoma.
Autorzy :
Maaßen T; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Vardanyan S; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Brosig A; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Merz H; Reference Center for Lymph Node Pathology and Haematopathology, 23562 Lübeck, Germany.
Ranjbar M; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Kakkassery V; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Grisanti S; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Tura A; Department of Ophthalmology, University of Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2020 Dec 08; Vol. 21 (24). Date of Electronic Publication: 2020 Dec 08.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Pair 3/*genetics
Glucose Transport Proteins, Facilitative/*genetics
Melanoma/*genetics
Uveal Neoplasms/*genetics
Aged ; Aged, 80 and over ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Cells, Cultured ; Female ; Glucose Transport Proteins, Facilitative/metabolism ; Humans ; Male ; Melanoma/metabolism ; Melanoma/pathology ; Middle Aged ; Neoplasm Metastasis ; Neoplastic Cells, Circulating/metabolism ; Uveal Neoplasms/metabolism ; Uveal Neoplasms/pathology
SCR Disease Name :
Uveal melanoma
Czasopismo naukowe
Tytuł :
The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis.
Autorzy :
Lukkunaprasit T; Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, 270 Rama VI Rd., Ratchathewi, Bangkok, 10400, Thailand.; Department of Pharmacology, College of Pharmacy, Rangsit University, Pathum Thani, Thailand.
Rattanasiri S; Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, 270 Rama VI Rd., Ratchathewi, Bangkok, 10400, Thailand. .
Turongkaravee S; Social and Administrative Pharmacy Excellence Research (SAPER) Unit, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Suvannang N; Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, 270 Rama VI Rd., Ratchathewi, Bangkok, 10400, Thailand.
Ingsathit A; Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, 270 Rama VI Rd., Ratchathewi, Bangkok, 10400, Thailand.
Attia J; Centre for Clincial Epidemiology and Biostatistics, School of Medicine and Public Health, Faculty of Health and Medicine, University of Newcastle, and Hunter Medical Research Institute, Newcastle, NSW, Australia.
Thakkinstian A; Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, 270 Rama VI Rd., Ratchathewi, Bangkok, 10400, Thailand.
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Źródło :
BMC medical genetics [BMC Med Genet] 2020 Oct 21; Vol. 21 (1), pp. 210. Date of Electronic Publication: 2020 Oct 21.
Typ publikacji :
Journal Article; Meta-Analysis; Systematic Review
MeSH Terms :
Polymorphism, Single Nucleotide*
ATP Binding Cassette Transporter, Subfamily G, Member 2/*genetics
Glucose Transport Proteins, Facilitative/*genetics
Gout/*genetics
Hyperuricemia/*genetics
Neoplasm Proteins/*genetics
Uric Acid/*blood
ATP Binding Cassette Transporter, Subfamily G, Member 2/blood ; Alleles ; Asian Continental Ancestry Group ; European Continental Ancestry Group ; Female ; Gene Expression ; Gene Frequency ; Genotype ; Glucose Transport Proteins, Facilitative/blood ; Gout/blood ; Gout/diagnosis ; Gout/ethnology ; Humans ; Hyperuricemia/blood ; Hyperuricemia/diagnosis ; Hyperuricemia/ethnology ; Male ; Neoplasm Proteins/blood ; Odds Ratio
Czasopismo naukowe
Tytuł :
Identification of GLUT12/SLC2A12 as a urate transporter that regulates the blood urate level in hyperuricemia model mice.
Autorzy :
Toyoda Y; Department of Pharmacy, The University of Tokyo Hospital, Bunkyo-ku, 113-8655 Tokyo, Japan.
Takada T; Department of Pharmacy, The University of Tokyo Hospital, Bunkyo-ku, 113-8655 Tokyo, Japan; .
Miyata H; Department of Pharmacy, The University of Tokyo Hospital, Bunkyo-ku, 113-8655 Tokyo, Japan.
Matsuo H; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, 359-8513 Saitama, Japan.
Kassai H; Laboratory of Animal Resources, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, 113-0033 Tokyo, Japan.
Nakao K; Laboratory of Animal Resources, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, 113-0033 Tokyo, Japan.
Nakatochi M; Division of Public Health Informatics, Department of Integrative Health Science, Nagoya University Graduate School of Medicine, 461-8673 Nagoya, Japan.
Kawamura Y; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, 359-8513 Saitama, Japan.
Shimizu S; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, 359-8513 Saitama, Japan.
Shinomiya N; Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, Tokorozawa, 359-8513 Saitama, Japan.
Ichida K; Department of Pathophysiology, Tokyo University of Pharmacy and Life Sciences, Hachioji, 192-0392 Tokyo, Japan.
Hosoyamada M; Department of Human Physiology and Pathology, Faculty of Pharma-Sciences, Teikyo University, Itabashi-ku, 173-8605 Tokyo, Japan.
Aiba A; Laboratory of Animal Resources, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, 113-0033 Tokyo, Japan.
Suzuki H; Department of Pharmacy, The University of Tokyo Hospital, Bunkyo-ku, 113-8655 Tokyo, Japan.
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Źródło :
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2020 Aug 04; Vol. 117 (31), pp. 18175-18177. Date of Electronic Publication: 2020 Jul 20.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Glucose Transport Proteins, Facilitative/*metabolism
Hyperuricemia/*blood
Uric Acid/*blood
Animals ; Gene Expression Regulation ; Glucose Transport Proteins, Facilitative/genetics ; Mice ; Mice, Knockout ; Uric Acid/metabolism
Czasopismo naukowe
Tytuł :
Anaerobic glucose consumption is accelerated at non-proliferating elevated temperatures through upregulation of a glucose transporter gene in Corynebacterium glutamicum.
Autorzy :
Uchikura H; Faculty of Natural System, Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan.
Toyoda K; Research Institute of Innovative Technology for the Earth, Kizugawa, Kyoto, Japan.
Matsuzawa H; Faculty of Natural System, Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan.
Mizuno H; Faculty of Natural System, Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan.
Ninomiya K; Faculty of Natural System, Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan.; Institute for Frontier Science Initiative, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa, 920-1192, Japan.
Takahashi K; Faculty of Natural System, Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan.
Inui M; Research Institute of Innovative Technology for the Earth, Kizugawa, Kyoto, Japan.
Tsuge Y; Faculty of Natural System, Institute of Science and Engineering, Kanazawa University, Kanazawa, Ishikawa, Japan. .; Institute for Frontier Science Initiative, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa, 920-1192, Japan. .
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Źródło :
Applied microbiology and biotechnology [Appl Microbiol Biotechnol] 2020 Aug; Vol. 104 (15), pp. 6719-6729. Date of Electronic Publication: 2020 Jun 17.
Typ publikacji :
Journal Article
MeSH Terms :
Hot Temperature*
Metabolic Networks and Pathways*
Corynebacterium glutamicum/*genetics
Glucose/*metabolism
Glucose Transport Proteins, Facilitative/*genetics
Anaerobiosis ; Biological Transport ; Corynebacterium glutamicum/metabolism ; Gene Expression ; Gene Expression Profiling ; Glucose Transport Proteins, Facilitative/metabolism ; Up-Regulation
Czasopismo naukowe
Tytuł :
Regulation of aerobic glycolysis to decelerate tumor proliferation by small molecule inhibitors targeting glucose transporters.
Autorzy :
Gao M; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, China.; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.
Huang J; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, China.; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.
Jiang X; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.; State Key Laboratory of Membrane Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.; Department of Molecular Biology, Princeton University, Princeton, NJ, 08544, USA.
Yuan Y; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.; State Key Laboratory of Membrane Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Pang H; School of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China.
Luo S; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, China.; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.
Wang N; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.; State Key Laboratory of Membrane Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Yao C; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, China.; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.
Lin Z; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, China.; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.
Pu D; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.; School of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China.
Zhang S; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.; State Key Laboratory of Membrane Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Sun P; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.; State Key Laboratory of Membrane Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Liu Z; Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing, 100084, China.; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China.; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China.
Xiao Y; Laboratory Medicine Center, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Wang Q; Laboratory Medicine Center, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Hu Z; School of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China.
Yin H; Tsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing, 100084, China. .; Beijing Advanced Innovation Center for Structural Biology, Tsinghua University, Beijing, 100084, China. .; School of Pharmaceutical Sciences, Tsinghua University, Beijing, 100084, China. .
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Źródło :
Protein & cell [Protein Cell] 2020 Jun; Vol. 11 (6), pp. 446-451.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Antineoplastic Agents/*pharmacology
Cell Proliferation/*drug effects
Glucose Transport Proteins, Facilitative/*antagonists & inhibitors
Glycolysis/*drug effects
Neoplasms/*drug therapy
Small Molecule Libraries/*pharmacology
Aerobiosis/drug effects ; Glucose Transport Proteins, Facilitative/metabolism ; Humans ; Neoplasms/metabolism ; Neoplasms/pathology
Raport
Tytuł :
Glucose transporter 10 modulates adipogenesis via an ascorbic acid-mediated pathway to protect mice against diet-induced metabolic dysregulation.
Autorzy :
Jiang CL; Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Jen WP; Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Tsao CY; Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Chang LC; Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Chen CH; Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Lee YC; Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
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Źródło :
PLoS genetics [PLoS Genet] 2020 May 26; Vol. 16 (5), pp. e1008823. Date of Electronic Publication: 2020 May 26 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
DNA Methylation*/drug effects
Adipose Tissue, White/*metabolism
Ascorbic Acid/*metabolism
Diabetes Mellitus, Type 2/*genetics
Diet, High-Fat/*adverse effects
Glucose Transport Proteins, Facilitative/*genetics
3T3-L1 Cells ; Adipogenesis ; Adult ; Aged ; Animals ; CCAAT-Enhancer-Binding Proteins/genetics ; Diabetes Mellitus, Type 2/metabolism ; Disease Models, Animal ; Female ; Gene Expression Regulation/drug effects ; Glucose Transport Proteins, Facilitative/metabolism ; Glycated Hemoglobin A/metabolism ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Middle Aged ; Mutation ; PPAR gamma/genetics
Czasopismo naukowe
Tytuł :
Effects of Metformin and Sitagliptin Monotherapy on Expression of Intestinal and Renal Sweet Taste Receptors and Glucose Transporters in a Rat Model of Type 2 Diabetes.
Autorzy :
Zhang M; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Feng R; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Yue J; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Qian C; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Yang M; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Liu W; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Rayner CK; Centre of Research Excellence in Translating Nutritional Science to Good Health, University of Adelaide, Adelaide, Australia.; Department of Gastroenterology and Hepatology, Royal Adelaide Hospital, Adelaide, Australia.
Ma J; Department of Endocrinology and Metabolism, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
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Źródło :
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme [Horm Metab Res] 2020 May; Vol. 52 (5), pp. 329-335. Date of Electronic Publication: 2020 Apr 06.
Typ publikacji :
Journal Article
MeSH Terms :
Diabetes Mellitus, Type 2/*drug therapy
Glucose Transport Proteins, Facilitative/*metabolism
Intestine, Small/*metabolism
Kidney/*metabolism
Metformin/*pharmacology
Receptors, G-Protein-Coupled/*metabolism
Sitagliptin Phosphate/*pharmacology
Taste/*drug effects
Animals ; Diabetes Mellitus, Type 2/genetics ; Disease Models, Animal ; Gene Expression Regulation/drug effects ; Glucose Transport Proteins, Facilitative/genetics ; Insulin Resistance/genetics ; Intestine, Small/drug effects ; Kidney/drug effects ; Metformin/therapeutic use ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Rats, Zucker ; Receptors, G-Protein-Coupled/genetics ; Signal Transduction/drug effects ; Signal Transduction/genetics ; Sitagliptin Phosphate/therapeutic use
Czasopismo naukowe
Tytuł :
Revisiting the Schistosoma japonicum life cycle transcriptome for new insights into lung schistosomula development.
Autorzy :
King M; School of Biological Sciences, Queen's University Belfast, Belfast, BT9 5DL, UK.
Carson J; School of Biological Sciences, Queen's University Belfast, Belfast, BT9 5DL, UK.
Stewart MT; School of Biological Sciences, Queen's University Belfast, Belfast, BT9 5DL, UK.
Gobert GN; School of Biological Sciences, Queen's University Belfast, Belfast, BT9 5DL, UK. Electronic address: .
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Źródło :
Experimental parasitology [Exp Parasitol] 2021 Apr; Vol. 223, pp. 108080. Date of Electronic Publication: 2021 Feb 04.
Typ publikacji :
Journal Article; Systematic Review
MeSH Terms :
Life Cycle Stages*
Lung/*parasitology
Lung Diseases, Parasitic/*parasitology
Schistosoma japonicum/*growth & development
Schistosomiasis japonica/*parasitology
Transcriptome/*physiology
Analysis of Variance ; Animals ; Cell Degranulation/physiology ; Datasets as Topic ; Glucose Transport Proteins, Facilitative/physiology ; Host-Parasite Interactions ; Lung Diseases, Parasitic/immunology ; Neutrophils/physiology ; Peptide Elongation Factor 1/physiology ; Schistosoma japonicum/genetics ; Schistosoma japonicum/immunology ; Schistosomiasis japonica/immunology
Czasopismo naukowe
Tytuł :
Comprehensive in silico Study of GLUT10: Prediction of Possible Substrate Binding Sites and Interacting Molecules.
Autorzy :
Hosen MJ; Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet-3114, Bangladesh.
Hasan M; Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet-3114, Bangladesh.; Department of Pharmaceuticals and Industrial Biotechnology, Sylhet Agricultural University, Sylhet- 3100, Bangladesh.; CANSi Research Institute, Bioinformatics Laboratory, Sylhet, Bangladesh.
Chakraborty S; Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet-3114, Bangladesh.; CANSi Research Institute, Bioinformatics Laboratory, Sylhet, Bangladesh.
Abir RA; Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet-3114, Bangladesh.; CANSi Research Institute, Bioinformatics Laboratory, Sylhet, Bangladesh.
Zubaer A; CANSi Research Institute, Bioinformatics Laboratory, Sylhet, Bangladesh.; Department of Microbiology, University of Manitoba, Winnipeg, MB, Canada.
Coucke P; Center for Medical Genetics, Ghent University Hospital, Corneel Heymanslaan 10, Ghent 9000, Belgium.
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Źródło :
Current pharmaceutical biotechnology [Curr Pharm Biotechnol] 2020; Vol. 21 (2), pp. 117-130.
Typ publikacji :
Journal Article
MeSH Terms :
Glucose Transport Proteins, Facilitative/*chemistry
Muscles/*enzymology
Arteries/abnormalities ; Binding Sites ; Biological Transport ; Crystallography, X-Ray ; Databases, Factual ; Glucose Transport Proteins, Facilitative/genetics ; Glucose Transport Proteins, Facilitative/metabolism ; Humans ; Joint Instability/genetics ; Metabolomics ; Molecular Docking Simulation ; Mutation ; Skin Diseases, Genetic/genetics ; Substrate Specificity ; Vascular Malformations/genetics
SCR Disease Name :
Arterial Tortuosity Syndrome
Czasopismo naukowe
Tytuł :
Baicalein alleviates hyperuricemia by promoting uric acid excretion and inhibiting xanthine oxidase.
Autorzy :
Chen Y; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Zhao Z; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Li Y; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Yang Y; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Li L; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Jiang Y; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Lin C; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Cao Y; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Zhou P; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Tian Y; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China.
Wu T; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China. Electronic address: .
Pang J; Guangdong Provincial Key Laboratory of Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, Guangdong, 510515, China. Electronic address: .
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Źródło :
Phytomedicine : international journal of phytotherapy and phytopharmacology [Phytomedicine] 2021 Jan; Vol. 80, pp. 153374. Date of Electronic Publication: 2020 Oct 09.
Typ publikacji :
Journal Article
MeSH Terms :
Flavanones/*pharmacology
Hyperuricemia/*drug therapy
Uric Acid/*urine
Xanthine Oxidase/*antagonists & inhibitors
Animals ; Antioxidants/pharmacology ; Disease Models, Animal ; Enzyme Inhibitors/pharmacology ; Flavanones/chemistry ; Flavanones/metabolism ; Glucose Transport Proteins, Facilitative/chemistry ; Glucose Transport Proteins, Facilitative/genetics ; Glucose Transport Proteins, Facilitative/metabolism ; HEK293 Cells ; Humans ; Hyperuricemia/chemically induced ; Kidney/drug effects ; Kidney/metabolism ; Liver/drug effects ; Male ; Mice ; Molecular Docking Simulation ; Organic Anion Transporters/chemistry ; Organic Anion Transporters/genetics ; Organic Anion Transporters/metabolism ; Organic Cation Transport Proteins/chemistry ; Organic Cation Transport Proteins/genetics ; Organic Cation Transport Proteins/metabolism ; Oxonic Acid/toxicity ; Uric Acid/blood
Czasopismo naukowe
Tytuł :
Asp symporter.
Autorzy :
Seica AFS; Laboratoire de Bioélectrochimie et Spectroscopie, UMR 7140, CMC, Université de Strasbourg CNRS, Strasbourg, France.
Iancu CV; Department of Chemistry, East Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, North Carolina, USA.
Pfeilschifter B; University of Regensburg, Institute of Biophysics and Physical Biochemistry, Regensburg, Germany.
Madej MG; University of Regensburg, Institute of Biophysics and Physical Biochemistry, Regensburg, Germany.
Choe JY; Department of Chemistry, East Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, North Carolina, USA; Department of Biochemistry and Molecular Biology, Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois, USA. Electronic address: .
Hellwig P; Laboratoire de Bioélectrochimie et Spectroscopie, UMR 7140, CMC, Université de Strasbourg CNRS, Strasbourg, France.
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Źródło :
The Journal of biological chemistry [J Biol Chem] 2020 Nov 06; Vol. 295 (45), pp. 15253-15261. Date of Electronic Publication: 2020 Aug 28.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Protons*
Aspartic Acid/*metabolism
Glucose Transport Proteins, Facilitative/*chemistry
Glucose Transport Proteins, Facilitative/*metabolism
Staphylococcus epidermidis/*chemistry
Symporters/*chemistry
Symporters/*metabolism
Biological Transport ; Glucose/metabolism ; Hydrogen-Ion Concentration
Czasopismo naukowe
Tytuł :
Evidence that hindbrain astrocytes in the rat detect low glucose with a glucose transporter 2-phospholipase C-calcium release mechanism.
Autorzy :
Rogers RC; Laboratory of Autonomic Neuroscience, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Burke SJ; Laboratory of Immunogenetics, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Collier JJ; Laboratory of Islet Biology and Inflammation, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
Ritter S; Department of Veterinary and Comparative Anatomy, Pharmacology and Physiology, Washington State University, Pullman, Washington.
Hermann GE; Laboratory of Autonomic Neuroscience, Pennington Biomedical Research Center, Baton Rouge, Louisiana.
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Źródło :
American journal of physiology. Regulatory, integrative and comparative physiology [Am J Physiol Regul Integr Comp Physiol] 2020 Jan 01; Vol. 318 (1), pp. R38-R48. Date of Electronic Publication: 2019 Oct 09.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Astrocytes/*physiology
Calcium/*metabolism
Glucose/*metabolism
Glucose Transport Proteins, Facilitative/*metabolism
Rhombencephalon/*cytology
Type C Phospholipases/*metabolism
Anilides/pharmacology ; Animals ; Antioxidants/pharmacology ; Boron Compounds/pharmacology ; Calcium/pharmacology ; Dantrolene/pharmacology ; Estrenes/pharmacology ; Glucose Transport Proteins, Facilitative/antagonists & inhibitors ; Phlorhizin/pharmacology ; Prodrugs ; Pyrrolidinones/pharmacology ; Quercetin/pharmacology ; Rats ; Rats, Long-Evans ; Type C Phospholipases/antagonists & inhibitors
Czasopismo naukowe
Tytuł :
The Solute Carrier Family 2 Genes Are Potential Prognostic Biomarkers in Acute Myeloid Leukemia.
Autorzy :
Lai B; Department of Hematology, Ningbo First Hospital, Ningbo, Zhejiang Province, China.
Lai Y; Department of Hematology, Ningbo First Hospital, Ningbo, Zhejiang Province, China.
Zhang Y; Department of Hematology, Ningbo First Hospital, Ningbo, Zhejiang Province, China.
Zhou M; Department of Hematology, Ningbo First Hospital, Ningbo, Zhejiang Province, China.
Sheng L; Department of Hematology, Ningbo First Hospital, Ningbo, Zhejiang Province, China.
OuYang G; Department of Hematology, Ningbo First Hospital, Ningbo, Zhejiang Province, China.
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Źródło :
Technology in cancer research & treatment [Technol Cancer Res Treat] 2020 Jan-Dec; Vol. 19, pp. 1533033819894308.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Gene Expression Regulation, Neoplastic*
Biomarkers, Tumor/*genetics
Glucose Transport Proteins, Facilitative/*genetics
Glucose Transporter Type 5/*genetics
Leukemia, Myeloid, Acute/*genetics
Leukemia, Myeloid, Acute/*pathology
Databases, Genetic/statistics & numerical data ; Female ; Gene Expression Profiling ; Glucose Transport Proteins, Facilitative/metabolism ; Glucose Transporter Type 5/metabolism ; Humans ; Leukemia, Myeloid, Acute/metabolism ; Male ; Middle Aged ; Prognosis ; Survival Rate
Czasopismo naukowe
Tytuł :
Investigation of the Role of Glucose Decorated Chitosan and PLGA Nanoparticles as Blocking Agents to Glucose Transporters of Tumor Cells.
Autorzy :
Abolhasani A; Department of Biotechnology, University of Isfahan, Isfahan, Iran.
Biria D; Department of Biotechnology, University of Isfahan, Isfahan, Iran.
Abolhasani H; Department of Physiology and Pharmacology, Qom University of Medical Sciences, Qom, Iran.
Zarrabi A; Department of Biotechnology, University of Isfahan, Isfahan, Iran.
Komeili T; Department of Physiology and Pharmacology, Qom University of Medical Sciences, Qom, Iran.
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Źródło :
International journal of nanomedicine [Int J Nanomedicine] 2019 Dec 04; Vol. 14, pp. 9535-9546. Date of Electronic Publication: 2019 Dec 04 (Print Publication: 2019).
Typ publikacji :
Journal Article
MeSH Terms :
Antineoplastic Agents/*pharmacology
Chitosan/*chemistry
Drug Delivery Systems/*methods
Glucose/*chemistry
Glucose Transport Proteins, Facilitative/*antagonists & inhibitors
Nanoparticles/*chemistry
Antineoplastic Agents/administration & dosage ; Apoptosis/drug effects ; Drug Stability ; Glucose Transport Proteins, Facilitative/genetics ; Glucose Transporter Type 1/antagonists & inhibitors ; Glucose Transporter Type 1/genetics ; Glucose Transporter Type 4/genetics ; HT29 Cells ; Humans ; Molecular Targeted Therapy/methods ; Nanoparticles/therapeutic use ; Polylactic Acid-Polyglycolic Acid Copolymer/chemistry
Czasopismo naukowe
Tytuł :
Aged garlic extract and S-allylcysteine increase the GLUT3 and GCLC expression levels in cerebral ischemia.
Autorzy :
Gomez CD; Department of Physiology and Pharmacology, University of Calgary, Canada.
Aguilera P; Laboratory of Cerebral Vascular Pathology, National Institute of Neurology and Neurosurgery 'Manuel Velasco Suárez', Mexico City, Mexico.
Ortiz-Plata A; Laboratory of Experimental Neuropathology, National Institute of Neurology and Neurosurgery, Mexico City, Mexico.
López FN; Laboratory of Cerebral Vascular Pathology, National Institute of Neurology and Neurosurgery 'Manuel Velasco Suárez', Mexico City, Mexico.
Chánez-Cárdenas ME; Laboratory of Cerebral Vascular Pathology, National Institute of Neurology and Neurosurgery 'Manuel Velasco Suárez', Mexico City, Mexico.
Flores-Alfaro E; Laboratory of Clinical and Molecular Epidemiology, Faculty of Biological and Chemical Sciences, Universidad Autónoma de Guerrero, Chilpancingo, Mexico.
Ruiz-Tachiquín ME; Medical Research Unit on Human Genetics, Pediatrics Hospital, Mexican Institute of Social Security (IMSS), Mexico City, Mexico.
Espinoza-Rojo M; Laboratory of Molecular and Genomic Biology, Faculty of Biological Chemical Sciences, Universidad Autónoma de Guerrero, Chilpancingo, Mexico.
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Źródło :
Advances in clinical and experimental medicine : official organ Wroclaw Medical University [Adv Clin Exp Med] 2019 Dec; Vol. 28 (12), pp. 1609-1614.
Typ publikacji :
Journal Article
MeSH Terms :
Brain Ischemia*/metabolism
Garlic*/chemistry
Neuroprotective Agents*/therapeutic use
Glucose Transport Proteins, Facilitative/*metabolism
Glutamate-Cysteine Ligase/*metabolism
Animals ; Antioxidants/metabolism ; Antioxidants/pharmacology ; Cysteine/analogs & derivatives ; Cysteine/pharmacology ; Glucose Transport Proteins, Facilitative/drug effects ; Glutamate-Cysteine Ligase/drug effects ; Male ; Plant Extracts/pharmacology ; Rats ; Rats, Wistar ; Reperfusion Injury/metabolism
Czasopismo naukowe
Tytuł :
A forskolin-conjugated insulin analog targeting endogenous glucose-transporter for glucose-responsive insulin delivery.
Autorzy :
Wang J; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA. , University of California, Los Angeles, CA 90095, USA.
Wang Z; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA. , University of California, Los Angeles, CA 90095, USA.
Yu J; Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC 27514, USA.
Zhang Y; Joint Department of Biomedical Engineering, University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC 27514, USA.
Zeng Y; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA. , University of California, Los Angeles, CA 90095, USA.
Gu Z; Department of Bioengineering, University of California, Los Angeles, CA 90095, USA. , University of California, Los Angeles, CA 90095, USA and Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA 90024, USA and Center for Minimally Invasive Therapeutics, University of California, Los Angeles, CA 90095, USA.
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Źródło :
Biomaterials science [Biomater Sci] 2019 Nov 01; Vol. 7 (11), pp. 4508-4513. Date of Electronic Publication: 2019 Oct 14.
Typ publikacji :
Journal Article
MeSH Terms :
Drug Delivery Systems*
Colforsin/*pharmacology
Diabetes Mellitus, Experimental/*drug therapy
Diabetes Mellitus, Type 1/*drug therapy
Glucose/*metabolism
Glucose Transport Proteins, Facilitative/*antagonists & inhibitors
Hypoglycemic Agents/*pharmacology
Insulin/*pharmacology
Animals ; Colforsin/administration & dosage ; Diabetes Mellitus, Experimental/metabolism ; Diabetes Mellitus, Type 1/metabolism ; Glucose Tolerance Test ; Glucose Transport Proteins, Facilitative/metabolism ; Hypoglycemic Agents/administration & dosage ; Injections, Subcutaneous ; Insulin/administration & dosage ; Insulin/metabolism ; Mice
Czasopismo naukowe
Tytuł :
Identification and characterisation of two high-affinity glucose transporters from the spoilage yeast Brettanomyces bruxellensis.
Autorzy :
Tiukova IA; Division of Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Kemigården 4, 412 96 Gothenburg, Sweden.
Møller-Hansen I; The Novo Nordisk Foundation for Biosustainability, Technical University of Denmark, Building 220, 2800 Kongens Lyngby, Denmark.
Belew ZM; Department of Plant and Environmental Sciences, DynaMo Center, Copenhagen Plant Science Center, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg, Denmark.
Darbani B; The Novo Nordisk Foundation for Biosustainability, Technical University of Denmark, Building 220, 2800 Kongens Lyngby, Denmark.
Boles E; Institute of Molecular Biosciences, Faculty of Biological Sciences, Goethe University Frankfurt, Max-von-Laue Straße 9, 60438, Frankfurt am Main, Germany.
Nour-Eldin HH; Department of Plant and Environmental Sciences, DynaMo Center, Copenhagen Plant Science Center, University of Copenhagen, Thorvaldsensvej 40, 1871 Frederiksberg, Denmark.
Linder T; Department of Molecular Sciences, Swedish University of Agricultural Sciences, Almas allé 5, 750 07 Uppsala, Sweden.
Nielsen J; Division of Systems and Synthetic Biology, Department of Biology and Biological Engineering, Chalmers University of Technology, Kemigården 4, 412 96 Gothenburg, Sweden.
Borodina I; The Novo Nordisk Foundation for Biosustainability, Technical University of Denmark, Building 220, 2800 Kongens Lyngby, Denmark.
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Źródło :
FEMS microbiology letters [FEMS Microbiol Lett] 2019 Sep 01; Vol. 366 (17).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Brettanomyces/*genetics
Brettanomyces/*metabolism
Glucose Transport Proteins, Facilitative/*genetics
Glucose Transport Proteins, Facilitative/*metabolism
Base Sequence ; Biological Transport ; Brettanomyces/classification ; Carbohydrate Metabolism ; Cloning, Molecular ; Ethanol/metabolism ; Fermentation ; Gene Expression ; Glucose/metabolism ; Glucose Transport Proteins, Facilitative/chemistry ; Multigene Family ; Oocytes/metabolism ; Phylogeny ; Sequence Analysis, Protein
Czasopismo naukowe
Tytuł :
Power of two: combination of therapeutic approaches involving glucose transporter (GLUT) inhibitors to combat cancer.
Autorzy :
Tilekar K; Department of Pharmaceutical Chemistry, Bharati Vidyapeeth's College of Pharmacy, Navi Mumbai, Maharashtra, India.
Upadhyay N; Department of Pharmaceutical Chemistry, Bharati Vidyapeeth's College of Pharmacy, Navi Mumbai, Maharashtra, India.
Iancu CV; East Carolina Diabetes and Obesity Institute, Department of Chemistry, East Carolina University, Greenville, NC, USA.
Pokrovsky V; Laboratory of Combined Therapy, N.N. Blokhin Cancer Research Center, Moscow, Russia; Department of Biochemistry, People's Friendship University, Moscow, Russia.
Choe JY; East Carolina Diabetes and Obesity Institute, Department of Chemistry, East Carolina University, Greenville, NC, USA.
Ramaa CS; Department of Pharmaceutical Chemistry, Bharati Vidyapeeth's College of Pharmacy, Navi Mumbai, Maharashtra, India. Electronic address: .
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Źródło :
Biochimica et biophysica acta. Reviews on cancer [Biochim Biophys Acta Rev Cancer] 2020 Dec; Vol. 1874 (2), pp. 188457. Date of Electronic Publication: 2020 Oct 21.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Antineoplastic Agents/*therapeutic use
Glucose Transport Proteins, Facilitative/*antagonists & inhibitors
Neoplasms/*drug therapy
Animals ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; Clinical Trials as Topic ; Drug Synergism ; Glycolysis/drug effects ; Humans ; Molecular Structure ; Neoplasms/metabolism
Czasopismo naukowe
Tytuł :
Phospholipid effects on SGLT1-mediated glucose transport in rabbit ileum brush border membrane vesicles.
Autorzy :
Ebel H; Institute of Clinical Physiology/Nutritional Medicine, Dept. of Gastroenterology, Rheumatology, and Infectious Diseases, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Fromm A; Institute of Clinical Physiology/Nutritional Medicine, Dept. of Gastroenterology, Rheumatology, and Infectious Diseases, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Günzel D; Institute of Clinical Physiology/Nutritional Medicine, Dept. of Gastroenterology, Rheumatology, and Infectious Diseases, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Fromm M; Institute of Clinical Physiology/Nutritional Medicine, Dept. of Gastroenterology, Rheumatology, and Infectious Diseases, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Schulzke JD; Institute of Clinical Physiology/Nutritional Medicine, Dept. of Gastroenterology, Rheumatology, and Infectious Diseases, Charité - Universitätsmedizin Berlin, Hindenburgdamm 30, 12203 Berlin, Germany. Electronic address: .
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Źródło :
Biochimica et biophysica acta. Biomembranes [Biochim Biophys Acta Biomembr] 2019 Oct 01; Vol. 1861 (10), pp. 182985. Date of Electronic Publication: 2019 May 11.
Typ publikacji :
Journal Article
MeSH Terms :
Glucose Transport Proteins, Facilitative/*metabolism
Membrane Fluidity/*drug effects
Sodium-Glucose Transporter 1/*metabolism
Animals ; Biological Transport ; Fatty Acids/metabolism ; Fluorescence Polarization/methods ; Glucose/metabolism ; Glucose Transport Proteins, Facilitative/physiology ; Ileum/metabolism ; Intestine, Small/metabolism ; Male ; Microvilli/metabolism ; Microvilli/physiology ; Phosphatidic Acids/chemistry ; Phosphatidylcholines/chemistry ; Phosphatidylinositols/chemistry ; Phospholipids/metabolism ; Phospholipids/physiology ; Rabbits ; Sodium/metabolism ; Sodium-Glucose Transporter 1/physiology ; Transport Vesicles/metabolism ; Transport Vesicles/physiology
Czasopismo naukowe

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