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1. Full Text Suramin inhibits Zika virus replication by interfering with virus attachment and release of infectious particles
by Albulescu, Irina C and Kovacikova, Kristina and Tas, Ali and Snijder, Eric J and van Hemert, Martijn J
Antiviral research, ISSN 0166-3542, 07/2017, Volume 143, pp. 230 - 236
Pharmacology & Pharmacy | Life Sciences & Biomedicine | Science & Technology | Virology | Mycophenolic Acid - antagonists & inhibitors | Zika Virus Infection - drug therapy | Cytopathogenic Effect, Viral - drug effects | DNA Replication - drug effects | Cercopithecus aethiops | Glycosylation - drug effects | Virus Internalization - drug effects | Suramin - administration & dosage | Suramin - antagonists & inhibitors | Zika Virus Infection - virology | Time Factors | Flavivirus - drug effects | Mycophenolic Acid - administration & dosage | Vero Cells | Virus Replication - drug effects | Zika Virus - growth & development | RNA, Viral - biosynthesis | Zika Virus - physiology | RNA, Viral - analysis | Zika Virus - drug effects | Virion - drug effects | Virus Attachment - drug effects | Virus Release - drug effects | Animals | RNA, Viral - drug effects | Birth defects | Conjunctivitis | Microbiology | RNA | Guillain-Barre syndrome | Index Medicus
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2. Full Text RAGE-aptamer blocks the development and progression of experimental diabetic nephropathy
by Matsui, Takanori and Higashimoto, Yuichiro and Nishino, Yuri and Nakamura, Nobutaka and Fukami, Kei and Yamagishi, Sho-Ichi
Diabetes (New York, N.Y.), ISSN 0012-1797, 06/2017, Volume 66, Issue 6, pp. 1683 - 1695
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Rats, Wistar | Humans | NADPH Oxidases - metabolism | Male | Receptor for Advanced Glycation End Products - antagonists & inhibitors | Albuminuria | Mesangial Cells - drug effects | Kidney - metabolism | NADPH Oxidases - drug effects | Receptor for Advanced Glycation End Products - genetics | Diabetes Mellitus, Experimental - metabolism | Real-Time Polymerase Chain Reaction | Aptamers, Nucleotide - pharmacology | Fibrosis - genetics | Kidney - drug effects | Enzyme-Linked Immunosorbent Assay | Diabetic Nephropathies - metabolism | Receptor for Advanced Glycation End Products - metabolism | Rats | Chemokine CCL2 - genetics | Glycation End Products, Advanced - drug effects | Gene Expression Regulation - drug effects | Animals | Podocytes - drug effects | Glycation End Products, Advanced - metabolism | Mesangial Cells - pathology | Inflammation - genetics | Receptor for Advanced Glycation End Products - drug effects | Oxidative Stress - drug effects | Chemokine CCL2 - drug effects | Oxidative stress | Development and progression | Research | Streptozocin | Diabetic nephropathies | Advanced glycosylation end products | Kidneys | Peptides | Diabetes mellitus | Glycosylation | Inflammation | Macrophages | Experiments | NAD(P)H oxidase | Molecules | Nephropathy | Rodents | Aptamers | Mesangial cells | Extracellular matrix | Diabetes | Kidney diseases | Monocyte chemoattractant protein 1 | Kidney transplantation | Index Medicus | Abridged Index Medicus
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3. Full Text O-GlcNAc Regulates Pluripotency and Reprogramming by Directly Acting on Core Components of the Pluripotency Network
by Jang, Hyonchol and Kim, Tae Wan and Yoon, Sungho and Choi, Soo-Youn and Kang, Tae-Wook and Kim, Seon-Young and Kwon, Yoo-Wook and Cho, Eun-Jung and Youn, Hong-Duk
Cell stem cell, ISSN 1934-5909, 07/2012, Volume 11, Issue 1, pp. 62 - 74
Cell & Tissue Engineering | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Cell physiology | Molecular and cellular biology | Cell differentiation, maturation, development, hematopoiesis | Embryonic Stem Cells - metabolism | Transcription, Genetic - drug effects | Embryonic Stem Cells - cytology | Humans | Molecular Sequence Data | Gene Regulatory Networks - drug effects | Glycosylation - drug effects | SOXB1 Transcription Factors - metabolism | Octamer Transcription Factor-3 - genetics | Cell Differentiation - genetics | Cellular Reprogramming - genetics | Amino Acid Sequence | Octamer Transcription Factor-3 - chemistry | Mice, Inbred C57BL | Gene Expression Regulation, Developmental - drug effects | Acetylglucosamine - pharmacology | Mutation - genetics | Acetylglucosamine - chemistry | Cellular Reprogramming - drug effects | Pluripotent Stem Cells - metabolism | Animals | Cell Differentiation - drug effects | Models, Biological | Octamer Transcription Factor-3 - metabolism | Pluripotent Stem Cells - drug effects | Cell Proliferation - drug effects | Mice | Index Medicus
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4. Full Text Blockade of receptors of advanced glycation end products ameliorates diabetic osteogenesis of adipose‐derived stem cells through DNA methylation and Wnt signalling pathway
by Zhang, Maorui and Li, Yong and Rao, Pengcheng and Huang, Kui and Luo, Daowen and Cai, Xiaoxiao and Xiao, Jingang
Cell proliferation, ISSN 0960-7722, 10/2018, Volume 51, Issue 5, pp. e12471 - n/a
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Adipogenesis - drug effects | Osteoporosis - drug therapy | Receptor for Advanced Glycation End Products - antagonists & inhibitors | Adipocytes - drug effects | Bone and Bones - drug effects | Adipose Tissue - metabolism | Osteoporosis - metabolism | Bone and Bones - metabolism | Female | Cell Differentiation - physiology | Adult Stem Cells - drug effects | Bone Regeneration - drug effects | Osteogenesis - drug effects | Cells, Cultured | Diabetes Mellitus - drug therapy | Diabetes Mellitus - metabolism | Rats | Glycogen Synthase Kinase 3 beta - metabolism | Rats, Sprague-Dawley | Up-Regulation - drug effects | Adult Stem Cells - metabolism | Animals | Wnt Signaling Pathway - drug effects | Glycation End Products, Advanced - pharmacology | Adipocytes - metabolism | Adipose Tissue - drug effects | DNA Methylation - drug effects | Osteoporosis | Methyltransferases | Methylation | DNA | Stem cells | Wnt protein | Differentiation (biology) | Alizarin | Western blotting | Signal transduction | Receptors | Bone growth | Mineralization | DNA methylation | Bones | Biocompatibility | Age | Deoxyribonucleic acid--DNA | Cbfa-1 protein | Advanced glycosylation end products | Tissue engineering | Diabetes mellitus | DNMT1 protein | Glycosylation | Regeneration | Signaling | Inhibitors | Biomarkers | Diabetes | Immunofluorescence | Osteogenesis | Index Medicus
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5. Full Text Glycemic control by the SGLT2 inhibitor empagliflozin decreases aortic stiffness, renal resistivity index and kidney injury
by Aroor, Annayya R and Das, Nitin A and Carpenter, Andrea J and Habibi, Javad and Jia, Guanghong and Ramirez-Perez, Francisco I and Martinez-Lemus, Luis and Manrique-Acevedo, Camila M and Hayden, Melvin R and Duta, Cornel and Nistala, Ravi and Mayoux, Eric and Padilla, Jaume and Chandrasekar, Bysani and DeMarco, Vincent G
Cardiovascular diabetology, ISSN 1475-2840, 07/2018, Volume 17, Issue 1, pp. 108 - 108
SGLT2 | RECK | Vascular stiffness | Renal resistivity | Pulsatility index | Cardiac & Cardiovascular Systems | Endocrinology & Metabolism | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Kidney - blood supply | Kidney - pathology | Diabetic Nephropathies - etiology | Diabetes Mellitus, Type 2 - genetics | Humans | Sodium-Glucose Transporter 2 Inhibitors - pharmacology | Diabetic Angiopathies - etiology | Endothelium, Vascular - drug effects | Glycosuria - etiology | Diabetic Angiopathies - physiopathology | Kidney - metabolism | Diabetic Nephropathies - physiopathology | Glycosuria - prevention & control | Pulsatile Flow - drug effects | Mice, Mutant Strains | Vascular Resistance - drug effects | Female | Renal Circulation - drug effects | Diabetic Angiopathies - prevention & control | Diabetic Nephropathies - prevention & control | Diabetes Mellitus, Type 2 - complications | Disease Models, Animal | Cell Line | Diabetic Nephropathies - pathology | Glucosides - pharmacology | Kidney - drug effects | Albuminuria - etiology | Sodium-Glucose Transporter 2 - metabolism | Mice, Inbred C57BL | Endothelium, Vascular - physiopathology | Albuminuria - prevention & control | GPI-Linked Proteins - metabolism | Blood Glucose - drug effects | Diabetes Mellitus, Type 2 - blood | Animals | Endothelium, Vascular - metabolism | Vascular Stiffness - drug effects | Benzhydryl Compounds - pharmacology | Vasodilation - drug effects | Blood Glucose - metabolism | Diabetes Mellitus, Type 2 - drug therapy | Renal artery | Control methods | Glucose | Proximal tubules | Vasodilation | Risk factors | Proteins | Hyperglycemia | Reversion | Rodents | Aorta | Blood pressure | Stiffness | Diabetes mellitus (non-insulin dependent) | Hypertension | Glucose transporter | Advanced glycosylation end products | Kidneys | Diabetes mellitus | Health risks | Reabsorption | Glycosylation | Risk analysis | Investigations | Nitric-oxide synthase | Endothelial cells | Endothelium | Weight control | Inhibitors | Sodium | Electrical resistivity | Nitric oxide | Fibrosis | Mice | Diabetes | Kidney diseases | Cardiovascular diseases | Transporter | Index Medicus
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6. Full Text High-throughput decoding of antitrypanosomal drug efficacy and resistance
by Alsford, Sam and Eckert, Sabine and Baker, Nicola and Glover, Lucy and Sanchez-Flores, Alejandro and Leung, Ka Fai and Turner, Daniel J and Field, Mark C and Berriman, Matthew and Horn, David
Nature (London), ISSN 0028-0836, 02/2012, Volume 482, Issue 7384, pp. 232 - 236
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Physicochemical properties. Structure-activity relationships | General pharmacology | Pharmacology. Drug treatments | Biological and medical sciences | Antiparasitic agents | Medical sciences | Antibiotics. Antiinfectious agents. Antiparasitic agents | Lysosomes - drug effects | Trypanosomiasis, African - drug therapy | Melarsoprol - pharmacology | Trypanosoma brucei brucei - metabolism | Endocytosis - drug effects | Humans | Trypanosoma brucei brucei - cytology | Eflornithine - pharmacology | Glycosylation - drug effects | Trypanosoma brucei brucei - enzymology | Trypanosoma brucei brucei - drug effects | Drug Resistance - genetics | Nifurtimox - pharmacology | High-Throughput Screening Assays | Lysosomes - metabolism | RNA Interference | Trypanocidal Agents - pharmacology | Aquaglyceroporins - deficiency | Trypanocidal Agents - therapeutic use | Trypanosomiasis, African - genetics | Suramin - pharmacology | Aquaglyceroporins - metabolism | Pentamidine - pharmacology | Chemotherapy | Care and treatment | Research | Drug resistance | Health aspects | Trypanosomiasis | Cancer | Proteins | Studies | Toxicity | Genomes | Biosynthesis | Genetic testing | Deoxyribonucleic acid--DNA | Index Medicus
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7. Full Text UGT74D1 catalyzes the glucosylation of 2-oxindole-3-acetic acid in the auxin metabolic pathway in arabidopsis
by Tanaka, Keita and Hayashi, Ken-Ichiro and Natsume, Masahiro and Kamiya, Yuji and Sakakibara, Hitoshi and Kawaide, Hiroshi and Kasahara, Hiroyuki
Plant and cell physiology, ISSN 0032-0781, 01/2014, Volume 55, Issue 1, pp. 218 - 228
Plant hormone | Auxin | Metabolism | Arabidopsis | Glucosyltransferase | Life Sciences & Biomedicine | Plant Sciences | Science & Technology | Cell Biology | Arabidopsis - enzymology | Plant Roots - genetics | Glycosylation - drug effects | Indoleacetic Acids - chemistry | Plant Roots - drug effects | Arabidopsis Proteins - metabolism | Plant Roots - physiology | Glucosyltransferases - metabolism | Biosynthetic Pathways - genetics | Biocatalysis - drug effects | Enzyme Induction - drug effects | Gravitropism - drug effects | Glycosyltransferases - biosynthesis | Glucosyltransferases - genetics | Arabidopsis Proteins - genetics | Arabidopsis - drug effects | Indoleacetic Acids - metabolism | Arabidopsis - genetics | Gene Expression Regulation, Plant - drug effects | Metabolic Networks and Pathways - genetics | Biosynthetic Pathways - drug effects | Genes, Plant - genetics | Indoleacetic Acids - pharmacology | Kinetics | Metabolic Networks and Pathways - drug effects | Index Medicus | Regular Papers
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8. Full Text Glycation potentiates α-synuclein-associated neurodegeneration in synucleinopathies
by Vicente Miranda, Hugo and Szego, Éva M and Oliveira, Luís M.A and Breda, Carlo and Darendelioglu, Ekrem and De Oliveira, Rita M and Ferreira, Diana G and Gomes, Marcos A and Rott, Ruth and Oliveira, Márcia and Munari, Francesca and Enguita, Francisco J and Simões, Tânia and Rodrigues, Eva F and Heinrich, Michael and Martins, Ivo C and Zamolo, Irina and Riess, Olaf and Cordeiro, Carlos and Ponces-Freire, Ana and Lashuel, Hilal A and Santos, Nuno C and Lopes, Luisa V and Xiang, Wei and Jovin, Thomas M and Penque, Deborah and Engelender, Simone and Zweckstetter, Markus and Klucken, Jochen and Giorgini, Flaviano and Quintas, Alexandre and Outeiro, Tiago F
Brain (London, England : 1878), ISSN 0006-8950, 05/2017, Volume 140, Issue 5, pp. 1399 - 1419
glycation | neurodegeneration | Parkinson's disease | alpha-synuclein | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | alpha-Synuclein - physiology | Male | Hippocampus - drug effects | Glycosylation - drug effects | alpha-Synuclein - drug effects | Yeasts - physiology | Female | Cell Survival - physiology | Disease Models, Animal | Cell Survival - drug effects | Pyruvaldehyde - pharmacology | Induced Pluripotent Stem Cells - drug effects | Induced Pluripotent Stem Cells - physiology | alpha-Synuclein - toxicity | Drosophila | Cells, Cultured | Enzyme Inhibitors - pharmacology | Rats | Mice, Transgenic | Neurodegenerative Diseases - metabolism | Yeasts - drug effects | Animals | Cell Differentiation - drug effects | Mice | Protein Processing, Post-Translational | Hippocampus - physiology | alpha-Synuclein - metabolism | Protein Aggregation, Pathological - metabolism | Aging - metabolism | Index Medicus | Abridged Index Medicus
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