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abridged index medicus (79) 79
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protein (71) 71
molecular sequence data (68) 68
apoptosis (66) 66
phosphatidylinositol 3-kinase (66) 66
transport (66) 66
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glucose transport (56) 56
hormones, hormone substitutes, and hormone antagonists (55) 55
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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2014, Volume 111, Issue 14, pp. 5159 - 5164
Journal Article
DIABETES, ISSN 0012-1797, 02/2018, Volume 67, Issue 2, pp. 265 - 277
Mitophagy is a cellular quality-control pathway, which is essential for elimination of unhealthy mitochondria. While mitophagy is critical to pancreatic... 
LIGASE NRDP1 | ERBB3 | PARKIN-MEDIATED MITOPHAGY | INSULIN-SECRETION | GROWTH | ENDOCRINOLOGY & METABOLISM | SUSCEPTIBILITY GENE CLEC16A | DOWN-REGULATION | LENALIDOMIDE | RECEPTOR | AUTOPHAGY | Tissue Banks | Humans | Endosomal Sorting Complexes Required for Transport - genetics | Ubiquitin-Protein Ligases - antagonists & inhibitors | Lectins, C-Type - genetics | Recombinant Fusion Proteins - metabolism | Lectins, C-Type - chemistry | Lectins, C-Type - metabolism | Endopeptidases - chemistry | Insulin-Secreting Cells - metabolism | Ubiquitination - drug effects | Endosomal Sorting Complexes Required for Transport - antagonists & inhibitors | Ubiquitin Thiolesterase - metabolism | Endosomal Sorting Complexes Required for Transport - chemistry | Insulin-Secreting Cells - cytology | Insulin Secretion | Monosaccharide Transport Proteins - metabolism | Ubiquitin Thiolesterase - antagonists & inhibitors | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | Cell Line | Endopeptidases - metabolism | Tissue Culture Techniques | Mice, Inbred C57BL | Cells, Cultured | Endosomal Sorting Complexes Required for Transport - metabolism | Enzyme Inhibitors - pharmacology | Ubiquitin-Protein Ligases - metabolism | Angiogenesis Inhibitors - pharmacology | Mice, Transgenic | Recombinant Fusion Proteins - chemistry | Ubiquitin Thiolesterase - genetics | Ubiquitin-Protein Ligases - chemistry | Mice, Knockout | Insulin - metabolism | Animals | Endopeptidases - genetics | Insulin-Secreting Cells - drug effects | Mitochondrial Degradation - drug effects | Protein Stability - drug effects | Glucose - metabolism | Mice | Monosaccharide Transport Proteins - chemistry | Ubiquitin-Protein Ligases - genetics | Lectins, C-Type - antagonists & inhibitors | Protein Multimerization - drug effects | Ubiquitin Thiolesterase - chemistry | Crosses, Genetic | Ubiquitin | Mitochondria | Pancreatic beta cells | Research | Enzymes | Secretion | Diabetes mellitus | Oxygen consumption | Autophagy | Insulin | Cells | Beta cells | Ubiquitination | Quality control | Diabetes | Pancreas | Ubiquitin-protein ligase | Index Medicus | Abridged Index Medicus | 0711 | Islet Studies
Journal Article
Glycoconjugate Journal, ISSN 0282-0080, 06/2017, Volume 34, Issue 3, pp. 411 - 420
Proteoglycans and glycosaminoglycans modulate numerous cellular processes relevant to tumour progression, including cell proliferation, cell-matrix... 
EXT1 | Galactosyltransferase I | β4GalT7 | Glycosaminoglycans | Solute carriers | UDP-sugars | SYNDECAN-1 CD138 | beta 4GalT7 | BIOCHEMISTRY & MOLECULAR BIOLOGY | NUCLEOTIDE-SUGAR TRANSPORTER | UDP-GLUCOSE DEHYDROGENASE | GLUCURONIC ACID | SYNTHASE 2 | C-MET | ELEGANS VULVAL MORPHOGENESIS | EXPRESSION | BINDING | Heparitin Sulfate - biosynthesis | Dermatan Sulfate - genetics | RNA, Small Interfering - genetics | Cell Proliferation | Chondroitin Sulfates - genetics | Epithelial Cells - metabolism | Hyaluronan Synthases - metabolism | N-Acetyllactosamine Synthase - antagonists & inhibitors | Humans | Hyaluronan Synthases - antagonists & inhibitors | Nucleotide Transport Proteins - antagonists & inhibitors | Gene Expression Regulation, Neoplastic | Extracellular Matrix - metabolism | Heparitin Sulfate - antagonists & inhibitors | N-Acetylglucosaminyltransferases - genetics | Dermatan Sulfate - biosynthesis | Mammary Glands, Human - metabolism | Extracellular Matrix - chemistry | Dermatan Sulfate - analogs & derivatives | Chondroitin Sulfates - biosynthesis | Hyaluronan Synthases - genetics | Hyaluronic Acid - biosynthesis | Isoenzymes - metabolism | Chondroitin Sulfates - antagonists & inhibitors | Monosaccharide Transport Proteins - metabolism | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | Signal Transduction | Cell Survival | Isoenzymes - genetics | Hyaluronic Acid - antagonists & inhibitors | Hyaluronic Acid - genetics | N-Acetyllactosamine Synthase - genetics | Epithelial Cells - pathology | Mammary Glands, Human - pathology | Cell Adhesion | N-Acetylglucosaminyltransferases - metabolism | Nucleotide Transport Proteins - metabolism | Dermatan Sulfate - antagonists & inhibitors | Heparitin Sulfate - genetics | Cell Line, Tumor | N-Acetylglucosaminyltransferases - antagonists & inhibitors | Nucleotide Transport Proteins - genetics | N-Acetyllactosamine Synthase - metabolism | Isoenzymes - antagonists & inhibitors | Cell Movement | RNA, Small Interfering - metabolism | Fibronectins | Physiological aspects | Enzymes | Breast cancer | Sulfates | Hyaluronic acid | Cell proliferation | Motility | Biosynthesis | Fibronectin | Cell adhesion & migration | Hyaluronan | Polysaccharides | Matrix | Compartments | Modulation | Sugar | Saccharides | Heparan sulfate | Proteoglycans | Invasiveness | Interference | siRNA | Adhesion | Substrates | Golgi apparatus | Diseases | Signaling | Depletion | Breast | Sulfate | Viability | Transporter | In vitro methods and tests | Syndecan | Tumors | Cancer | Index Medicus
Journal Article
FEBS Letters, ISSN 0014-5793, 07/2015, Volume 589, Issue 16, pp. 2100 - 2109
Autophagy is a catabolic process involving autophagosome formation via lysosome. However, the initiation step of autophagy is largely unknown. We found an... 
Screening | G6PT | ULK1 | ATG9 | Autophagy modulator | glucose-6-phosphate transporter | N-terminus of Venus vector | chlorogenic acid | BiFC | bimolecular fluorescence complementation | CHA | C-terminus of Venus vector | NEURODEGENERATIVE DISEASE | DISEASE TYPE-IB | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-GROWTH | MACROAUTOPHAGY | MTOR | CELL BIOLOGY | MAMMALIAN ATG PROTEINS | FORMATION SITE | BIOPHYSICS | SIGNALING PATHWAY | AMINO-ACIDS | ANTIPORTER DEFICIENT | Up-Regulation | TOR Serine-Threonine Kinases - metabolism | Vesicular Transport Proteins - metabolism | Humans | Intracellular Signaling Peptides and Proteins - metabolism | Multiprotein Complexes - metabolism | RNA Interference | Intracellular Signaling Peptides and Proteins - genetics | Monosaccharide Transport Proteins - metabolism | Peptide Fragments - genetics | Protein-Serine-Threonine Kinases - metabolism | Monosaccharide Transport Proteins - genetics | Membrane Proteins - genetics | Phagosomes - metabolism | Recombinant Proteins - chemistry | Antiporters - metabolism | Recombinant Fusion Proteins - chemistry | Huntingtin Protein | Peptide Fragments - chemistry | Models, Biological | Protein-Serine-Threonine Kinases - chemistry | Antiporters - antagonists & inhibitors | Hepatocytes - enzymology | Autophagy-Related Proteins | Phagosomes - enzymology | Cricetulus | Hepatocytes - metabolism | Autophagy | Recombinant Fusion Proteins - metabolism | Autophagy-Related Protein-1 Homolog | Mechanistic Target of Rapamycin Complex 1 | Multiprotein Complexes - antagonists & inhibitors | TOR Serine-Threonine Kinases - antagonists & inhibitors | Hepatocytes - cytology | Nerve Tissue Proteins - chemistry | Antiporters - genetics | Membrane Proteins - metabolism | Protein Interaction Domains and Motifs | Monosaccharide Transport Proteins - antagonists & inhibitors | Recombinant Proteins - metabolism | Cell Line | Peptide Fragments - metabolism | Vesicular Transport Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Mutant Proteins - metabolism | Vesicular Transport Proteins - chemistry | Recombinant Proteins - genetics | Nerve Tissue Proteins - genetics | Protein Transport | Nerve Tissue Proteins - metabolism | Animals | Membrane Proteins - chemistry | Intracellular Signaling Peptides and Proteins - chemistry | Mutant Proteins - chemistry | Amino Acid Substitution | Phosphates | Enzymes | Glucose | Analysis | Dextrose | Index Medicus
Journal Article
Genetics, ISSN 0016-6731, 03/2016, Volume 202, Issue 3, pp. 997 - 1012
Action mechanisms of anesthetics remain unclear because of difficulty in explaining how structurally different anesthetics cause similar effects. In... 
Anesthesia | Lipid theory | Glucose transport | Actin | Membrane lipid | glucose transport | CELLS | membrane lipid | TRANSLATION INITIATION | MAJOR FACILITATOR SUPERFAMILY | SACCHAROMYCES-CEREVISIAE | PROTEIN-SYNTHESIS | ISOFLURANE ANESTHESIA | anesthesia | actin | POSITRON-EMISSION-TOMOGRAPHY | GLUCOSE-TRANSPORTER | DRUGS | GENETICS & HEREDITY | lipid theory | EXPRESSION | Gene Expression Regulation, Fungal | Glucose Transport Proteins, Facilitative - metabolism | Saccharomyces cerevisiae - genetics | Saccharomyces cerevisiae Proteins - antagonists & inhibitors | Saccharomyces cerevisiae - drug effects | Saccharomyces cerevisiae Proteins - genetics | Anesthetics, Local - pharmacology | Saccharomyces cerevisiae - metabolism | Culture Media | Phenothiazines - pharmacology | Saccharomyces cerevisiae Proteins - metabolism | Glucose - metabolism | Antipsychotic Agents - pharmacology | Glucose Transport Proteins, Facilitative - genetics | Monosaccharide Transport Proteins - metabolism | Cell Membrane - drug effects | Glucose Transport Proteins, Facilitative - antagonists & inhibitors | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | Usage | Yeast | Analysis | Genetic aspects | Glucose | Brewer's yeast | Anesthetics | Sugars | Dextrose | Phenothiazine | Monosaccharides | Drugs | Lipids | Cell growth | Index Medicus | Investigations
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 10/2015, Volume 59, Issue 10, pp. 6203 - 6209
Journal Article
Virology, ISSN 0042-6822, 2016, Volume 492, pp. 66 - 72
Abstract BK polyomavirus (BKPyV) is a human pathogen that causes polyomavirus-associated nephropathy and hemorrhagic cystitis in transplant patients.... 
Infectious Disease | BKPyV | UGCG | Clathrin | Entry | Endocytosis | Ganglioside | Caveolin | ENDOCYTIC PATHWAY | TRAFFICKING | RECEPTOR | PLASMA-MEMBRANE | RENAL-TRANSPLANT RECIPIENTS | BK VIRUS-INFECTION | REPLICATION | VIROLOGY | POLYOMAVIRUS-ASSOCIATED NEPHROPATHY | PROTEINS | CHOLERA-TOXIN | RNA, Small Interfering - genetics | BK Virus - drug effects | Epithelial Cells - drug effects | Humans | MicroRNAs - metabolism | Virus Internalization - drug effects | Caveolin 2 - antagonists & inhibitors | Clathrin Heavy Chains - metabolism | Kidney Tubules, Proximal - virology | Monosaccharide Transport Proteins - metabolism | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | BK Virus - metabolism | Caveolin 1 - antagonists & inhibitors | Cell Line | Gene Expression Regulation | Caveolin 1 - genetics | BK Virus - genetics | Clathrin Heavy Chains - antagonists & inhibitors | Gangliosides - pharmacology | G(M1) Ganglioside - pharmacology | Caveolin 1 - metabolism | Host-Pathogen Interactions | Caveolin 2 - metabolism | Epithelial Cells - virology | Clathrin Heavy Chains - genetics | MicroRNAs - genetics | Caveolin 2 - genetics | Primary Cell Culture | Kidney Tubules, Proximal - drug effects | RNA, Small Interfering - metabolism | Microbiology | Analysis | Cellulose | Health aspects | Gangliosides | Cells | Medical research | Medicine, Experimental | Index Medicus | entry | clathrin | endocytosis | ganglioside | caveolin
Journal Article
Traffic, ISSN 1398-9219, 03/2008, Volume 9, Issue 3, pp. 380 - 393
Journal Article
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 12/2016, Volume 60, Issue 12, pp. 7407 - 7414
The glucose transporter PfHT is essential to the survival of the malaria parasite Plasmodium falciparum and has been shown to be a druggable target with high... 
LIFE-CYCLE | TARGET | HEXOSE TRANSPORTER | PARASITES | MECHANISM | PLASMODIUM-FALCIPARUM | VALIDATION | MICROBIOLOGY | PHARMACOLOGY & PHARMACY | ANTIMALARIAL | CANCER | EXPRESSION | Glucose Transporter Type 2 - genetics | Small Molecule Libraries - pharmacology | Glucose Transporter Type 4 - metabolism | Species Specificity | Protozoan Proteins - antagonists & inhibitors | Humans | Glucose Transporter Type 1 - metabolism | Tritium | Structure-Activity Relationship | Glucose Transporter Type 3 - metabolism | Plasmodium falciparum - drug effects | Protozoan Proteins - genetics | Glucose Transporter Type 2 - metabolism | Glucose Transporter Type 3 - genetics | Protozoan Proteins - metabolism | HEK293 Cells | Plasmodium falciparum - metabolism | Monosaccharide Transport Proteins - metabolism | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | Gene Expression | Glucose Transporter Type 4 - genetics | Cells, Cultured | Glucose - antagonists & inhibitors | Antimalarials - pharmacology | Erythrocytes - drug effects | Small Molecule Libraries - chemistry | High-Throughput Screening Assays | Glucose Transporter Type 1 - genetics | Antimalarials - chemistry | Erythrocytes - metabolism | Glucose - metabolism | Fluorescence Resonance Energy Transfer - methods | Plasmodium falciparum - growth & development | Erythrocytes - parasitology | Index Medicus
Journal Article
Journal Article
Biochemistry, ISSN 0006-2960, 12/2011, Volume 50, Issue 51, pp. 11009 - 11014
The sucrose permease (CscB) and lactose permease (LacY) of Escherichia colt belong to the oligosaccharide/H+ symporter subfamily of the major facilitator... 
GALACTOPYRANOSIDES | CONSERVATION | SUBSTRATE-BINDING SITE | SPECIFICITY | LACTOSE PERMEASE | LIGAND RECOGNITION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | ACTIVE-TRANSPORT | RESIDUES | SUCROSE PERMEASE | Disaccharides - metabolism | Lactulose - metabolism | Molecular Conformation | Fructose - metabolism | Membrane Transport Proteins - genetics | Symporters - antagonists & inhibitors | Escherichia coli - metabolism | Membrane Transport Proteins - metabolism | Biological Transport - drug effects | Escherichia coli Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - metabolism | Binding Sites - drug effects | Monosaccharide Transport Proteins - antagonists & inhibitors | Monosaccharide Transport Proteins - genetics | Binding, Competitive | Recombinant Proteins - metabolism | Lactulose - analogs & derivatives | Models, Molecular | Recombinant Proteins - chemistry | Escherichia coli Proteins - metabolism | Anilino Naphthalenesulfonates - pharmacology | Cysteine - chemistry | Symporters - chemistry | Glucosides - metabolism | Symporters - metabolism | Membrane Transport Proteins - chemistry | Fructose - analogs & derivatives | Glycosides - metabolism | Symporters - genetics | Escherichia coli Proteins - genetics | Galactosides - metabolism | Alkylation - drug effects | Sulfhydryl Reagents - pharmacology | Monosaccharide Transport Proteins - chemistry | Kinetics | Escherichia coli Proteins - chemistry | Molecular recognition | Microbial enzymes | Research | Oligosaccharides | Structure | Index Medicus | membranes | membrane proteins | transport | H+ symport | sugar | permease
Journal Article