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1. Full Text Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels
by Tin, Adrienne and Li, Yong and Li, Yong and Brody, Jennifer A and Brody, Jennifer A and Nutile, Teresa and Nutile, Teresa and Chu, Audrey Y and Chu, Audrey Y and Huffman, Jennifer E and Huffman, Jennifer E and Yang, Qiong and Yang, Qiong and Chen, Ming-Huei and Chen, Ming-Huei and Robinson-Cohen, Cassianne and Macé, Aurélien and Liu, Jun and Demirkan, Ayşe and Sorice, Rossella and Sorice, Rossella and Sedaghat, Sanaz and Swen, Melody and Yu, Bing and Yu, Bing and Ghasemi, Sahar and Ghasemi, Sahar and Teumer, Alexanda and Teumer, Alexanda and Vollenweider, Peter and Ciullo, Marina and Ciullo, Marina and Li, Meng and Uitterlinden, André G and Uitterlinden, André G and Kraaij, Robert and Kraaij, Robert and Amin, Najaf and van Rooij, Jeroen and Kutalik, Zoltán and Dehghan, Abbas and Dehghan, Abbas and McKnight, Barbara and van Duijn, Cornelia M and Morrison, Alanna and Morrison, Alanna and Psaty, Bruce M and Boerwinkle, Eric and Boerwinkle, Eric and Fox, Caroline S and Fox, Caroline S and Woodward, Owen M and Köttgen, Anna and Köttgen, Anna
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 4228 - 11
Elevated serum urate levels can cause gout, an excruciating disease with suboptimal treatment. Previous GWAS identified common variants with modest effects on... 
GENETIC-VARIATION | RISK-FACTORS | HYPERURICEMIA | GOUT | MULTIDISCIPLINARY SCIENCES | LINKAGE ANALYSIS | LOCI | CHRONIC KIDNEY-DISEASE | IDENTIFICATION | GENOME-WIDE ASSOCIATION | TRANSPORTER 9 HSLC2A9 | Glucose Transport Proteins, Facilitative - metabolism | Genetic Predisposition to Disease | Meta-Analysis as Topic | Organic Cation Transport Proteins - metabolism | Protein Structure, Secondary | Humans | Organic Anion Transporters - chemistry | Organic Cation Transport Proteins - chemistry | Glucose Transport Proteins, Facilitative - chemistry | Organic Anion Transporters - metabolism | Kidney Function Tests | Exome - genetics | Organic Anion Transporters - genetics | Uric Acid - blood | Glucose Transport Proteins, Facilitative - genetics | Organic Cation Transport Proteins - genetics | Proteins | Sequences | Kidneys | Medical treatment | Gout | Uric acid | Gene mapping | Peptide mapping | Protein structure | Lead poisoning | Index Medicus
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2. Full Text Structure of a eukaryotic SWEET transporter in a homotrimeric complex
by Tao, Yuyong and Cheung, Lily S and Li, Shuo and Eom, Joon-Seob and Chen, Li-Qing and Xu, Yan and Perry, Kay and Frommer, Wolf B and Feng, Liang and Stanford Univ., CA (United States) and Carnegie Inst. of Science, Stanford, CA (United States)
Nature, ISSN 0028-0836, 11/2015, Volume 527, Issue 7577, pp. 259 - 263
Eukaryotes rely on efficient distribution of energy and carbon skeletons between organs in the form of sugars. Glucose in animals and sucrose in plants serve... 
SUGAR TRANSPORTER | PROTEIN | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | RESOLUTION | AMMONIUM UPTAKE | CRYSTALLOGRAPHY | NUTRITION | ARABIDOPSIS | BACTERIAL | OLIGOMERIZATION | Glucose Transport Proteins, Facilitative - metabolism | Arabidopsis Proteins - genetics | Arabidopsis - chemistry | Protein Structure, Secondary | Humans | Protein Multimerization | Models, Molecular | Crystallography, X-Ray | Oryza - chemistry | Structure-Activity Relationship | Glucose Transport Proteins, Facilitative - chemistry | Arabidopsis Proteins - metabolism | Phloem | Arabidopsis Proteins - chemistry | Biological Transport | Oryza - genetics | Plant Proteins - chemistry | HEK293 Cells | Protein Structure, Quaternary | Monosaccharide Transport Proteins - chemistry | Plant Proteins - metabolism | Glucose Transport Proteins, Facilitative - genetics | Monosaccharide Transport Proteins - metabolism | Monosaccharide Transport Proteins - genetics | Energy metabolism | Bioenergetics | Carrier proteins | Biological transport | Genetic aspects | Glucose | Observations | Properties | Dextrose | Proteins | Plasma | Eukaryotes | Mutation | Crystal structure | Index Medicus | X-ray crystallography | Transporters | BASIC BIOLOGICAL SCIENCES
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3. Full Text Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
by De Backer, Julie and Gardella, Rita and Loeys, Bart and Dietz, Harry C and Willaert, Andy and Callewaert, Bert and Forsyth, Ramses and Colombi, Marina and De Paepe, Anne and Barlati, Sergio and Wessels, Marja W and Fox, Joyce E and Willems, Patrick J and Zoppi, Nicoletta and Facchetti, Fabio and Kambouris, Marios and Mancini, Grazia M S and Coucke, Paul J
Nature Genetics, ISSN 1061-4036, 04/2006, Volume 38, Issue 4, pp. 452 - 457
Arterial tortuosity syndrome (ATS) is an autosomal recessive disorder characterized by tortuosity, elongation, stenosis and aneurysm formation in the major... 
VERSICAN | GROWTH-FACTORS | SEQUENCE | GENETICS & HEREDITY | FANCONI-BICKEL-SYNDROME | SMOOTH-MUSCLE-CELLS | CANDIDATE GENE | TRAITS | SLC2A10 GLUT10 | FAMILY | Amino Acid Sequence | Humans | Molecular Sequence Data | Vascular Diseases - genetics | Male | Chromosome Mapping | Arteries - pathology | Glucose Transport Proteins, Facilitative - chemistry | Sequence Homology, Amino Acid | Pedigree | Glucose Transport Proteins, Facilitative - physiology | Female | Neovascularization, Pathologic - genetics | Glucose Transport Proteins, Facilitative - genetics | Mutation | Chromosomes, Human, Pair 20 | Complications and side effects | Gene mutations | Connective tissue diseases | Physiological aspects | Genetic aspects | Diagnosis | Research | Neovascularization | Identification and classification | Risk factors | Signal transduction | Cardiovascular disease | Index Medicus
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4. Full Text Trehalose inhibits solute carrier 2A (SLC2A) proteins to induce autophagy and prevent hepatic steatosis
by DeBosch, Brian J and Heitmeier, Monique R and Mayer, Allyson L and Higgins, Cassandra B and Crowley, Jan R and Kraft, Thomas E and Chi, Maggie and Newberry, Elizabeth P and Chen, Zhouji and Finck, Brian N and Davidson, Nicholas O and Yarasheski, Kevin E and Hruz, Paul W and Moley, Kelle H
Science Signaling, ISSN 1945-0877, 02/2016, Volume 9, Issue 416, pp. ra21 - ra21
Trehalose is a naturally occurring disaccharide that has gained attention for its ability to induce cellular autophagy and mitigate diseases related to... 
INSULIN | MICE | GLUCOSE TRANSPORTERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHREBP | CELL BIOLOGY | Fatty Liver - genetics | Glucose Transport Proteins, Facilitative - metabolism | AMP-Activated Protein Kinases - metabolism | Fatty Liver - metabolism | Fatty Liver - pathology | Humans | Autophagy | Hep G2 Cells | Mice, Knockout | Trehalose - metabolism | Animals | HEK293 Cells | Mice | Glucose Transport Proteins, Facilitative - genetics | AMP-Activated Protein Kinases - genetics | Index Medicus
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5. Full Text Crystal structure of a glucose/H+symporter and its mechanism of action
by Cristina V. Iancu and Jamillah Zamoon and Sang Bum Woo and Alexander Aleshin and Jun-yong Choe
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2013, Volume 110, Issue 44, pp. 17862 - 17867
Glucose transporters are required to bring glucose into cells, where it is an essential energy source and precursor in protein and lipid synthesis. These... 
Active transport | Biochemical mechanisms | Facilitative glucose transport proteins | Symporters | Escherichia coli | Counterflow | Biochemistry | Cytochalasins | Crystal structure | P branes | GLUT1 | SITE | PROTEIN | GLUT | MULTIDISCIPLINARY SCIENCES | EXOFACIAL LIGAND-BINDING | ESCHERICHIA-COLI | MONOSACCHARIDE TRANSPORTERS | COLI MEMBRANE-VESICLES | FAMILY | INHIBITION | sugar transporter | solute-carrier 2A | membrane protein | major facilitator superfamily | CYTOCHALASIN-B | Cytochalasin B - pharmacology | Mutagenesis, Site-Directed | Colforsin - pharmacology | Humans | Crystallization | Staphylococcus epidermidis - chemistry | Models, Molecular | Glucose Transport Proteins, Facilitative - chemistry | Staphylococcus epidermidis - genetics | Sequence Homology | Mutagenesis | Phloretin - pharmacology | Cloning, Molecular | Protein Conformation | Biological Transport - physiology | Glucose Transport Proteins, Facilitative - genetics | Glucose Transport Proteins, Facilitative - antagonists & inhibitors | Gram-positive bacteria | Lipids | Glucose | Molecular structure | Protein synthesis | Index Medicus | Biological Sciences
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6. Full Text Host programmed death ligand 1 is dominant over programmed death ligand 2 expression in regulating graft-versus-host disease lethality
by Saha, Asim and Saha, Asim and Aoyama, Kazutoshi and Aoyama, Kazutoshi and Taylor, Patricia A and Taylor, Patricia A and Koehn, Brent H and Koehn, Brent H and Veenstra, Rachelle G and Veenstra, Rachelle G and Panoskaltsis-Mortari, Angela and Panoskaltsis-Mortari, Angela and Munn, David H and Munn, David H and Murphy, William J and Murphy, William J and Azuma, Miyuki and Azuma, Miyuki and Yagita, Hideo and Yagita, Hideo and Fife, Brian T and Fife, Brian T and Sayegh, Mohammed H and Sayegh, Mohammed H and Najafian, Nader and Najafian, Nader and Socie, Gerard and Socie, Gerard and Ahmed, Rafi and Ahmed, Rafi and Freeman, Gordon J and Freeman, Gordon J and Sharpe, Arlene H and Sharpe, Arlene H and Blazar, Bruce R and Blazar, Bruce R
Blood, ISSN 0006-4971, 2013, Volume 122, Issue 17, pp. 3062 - 3073
Programmed death 1 (PD-1) and its ligands, PD-L1 and PD-L2, play an important role in the maintenance of peripheral tolerance. We explored the role of PD-1... 
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | BONE-MARROW-TRANSPLANTATION | T-CELL-ACTIVATION | GASTROINTESTINAL-TRACT | ENDOTHELIAL-CELLS | IN-VIVO | TNF-ALPHA | HEMATOLOGY | PD-1 | GAMMA-DEPENDENT MECHANISM | LYMPHOCYTES | Glucose Transport Proteins, Facilitative - metabolism | Liver - pathology | Cell Proliferation | Spleen - immunology | Programmed Cell Death 1 Ligand 2 Protein - metabolism | Intestines - metabolism | Graft vs Host Disease - metabolism | CD4-Positive T-Lymphocytes - pathology | Graft vs Host Disease - immunology | Intestines - immunology | CD4-Positive T-Lymphocytes - immunology | Liver - immunology | Glucose Transport Proteins, Facilitative - immunology | Graft vs Host Disease - mortality | Bone Marrow Transplantation | Apoptosis Regulatory Proteins - genetics | Glucose Transport Proteins, Facilitative - genetics | Spleen - pathology | Transplantation Tolerance - immunology | Acute Disease | Apoptosis Regulatory Proteins - immunology | Intestines - pathology | Programmed Cell Death 1 Ligand 2 Protein - genetics | Liver - metabolism | CD4-Positive T-Lymphocytes - metabolism | Gene Expression Regulation | Oxidative Phosphorylation | Programmed Cell Death 1 Receptor - metabolism | B7-H1 Antigen - genetics | B7-H1 Antigen - immunology | Apoptosis Regulatory Proteins - metabolism | Graft vs Host Disease - pathology | Programmed Cell Death 1 Ligand 2 Protein - immunology | B7-H1 Antigen - metabolism | Animals | Spleen - metabolism | Peripheral Tolerance - immunology | Survival Analysis | Glycolysis | Mice | Programmed Cell Death 1 Receptor - immunology | Programmed Cell Death 1 Receptor - genetics | Index Medicus | Abridged Index Medicus | Transplantation
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7. Full Text Plasma Urate Level Is Directly Regulated by a Voltage-driven Urate Efflux Transporter URATv1 (SLC2A9) in Humans
by Naohiko Anzai and Kimiyoshi Ichida and Promsuk Jutabha and Toru Kimura and Ellappan Babu and Chun Ji Jin and Sunena Srivastava and Kenichiro Kitamura and Ichiro Hisatome and Hitoshi Endou and Hiroyuki Sakurai
Journal of Biological Chemistry, ISSN 0021-9258, 10/2008, Volume 283, Issue 40, pp. 26834 - 26838
Hyperuricemia is a significant factor in a variety of diseases, including gout and cardiovascular diseases. Although renal excretion largely determines plasma... 
RENAL HYPOURICEMIA | FACILITATORS | CLONING | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUT9 | IDENTIFICATION | EXCRETION | APICAL MEMBRANE | EXPRESSION | URIC-ACID | FAMILY | Glucose Transport Proteins, Facilitative - metabolism | Gene Expression | Uric Acid - metabolism | Cardiovascular Diseases - metabolism | Organic Cation Transport Proteins - metabolism | Humans | Xenopus laevis | Hyperuricemia - metabolism | Mutation, Missense | Cardiovascular Diseases - genetics | Hyperuricemia - etiology | Oocytes | Organic Anion Transporters - metabolism | Hyperuricemia - genetics | Cardiovascular Diseases - complications | Organic Anion Transporters - genetics | Animals | Models, Biological | Kidney Tubules, Proximal - metabolism | Female | Glucose Transport Proteins, Facilitative - genetics | Organic Cation Transport Proteins - genetics | Ion Transport - genetics | Index Medicus
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8. Full Text Isoform-selective inhibition of facilitative glucose transporters: Elucidation of the molecular mechanism of HIV protease inhibitor binding
by Hresko, Richard C and Kraft, Thomas E and Tzekov, Anatoly and Wildman, Scott A and Hruz, Paul W
Journal of Biological Chemistry, ISSN 0021-9258, 06/2014, Volume 289, Issue 23, pp. 16100 - 16113
Pharmacologic HIV protease inhibitors (PIs) and structurally related oligopeptides are known to reversibly bind and inactivate the insulin-responsive... 
GLUT1 | CELLS | SCANNING-MUTAGENESIS | LIGAND-BINDING | STRUCTURAL BASIS | INSULIN-RESISTANCE | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MULTIPLE SEQUENCE ALIGNMENTS | SURFACE | CYTOCHALASIN-B | Glucose Transport Proteins, Facilitative - metabolism | Amino Acid Sequence | Cell Line | Humans | HIV Protease Inhibitors - metabolism | Indinavir - pharmacology | HIV Protease Inhibitors - pharmacology | Sequence Homology, Amino Acid | Protein Isoforms - metabolism | Cloning, Molecular | Glucose Transport Proteins, Facilitative - genetics | Glucose Transport Proteins, Facilitative - antagonists & inhibitors | Protein Isoforms - antagonists & inhibitors | Indinavir - metabolism | Protein Isoforms - genetics | Index Medicus | Protein Chimeras | HIV | Photoaffinity Labeling | Monosaccharide Transport Protein | Membrane Biology | Insulin Resistance | Glucose Transport | Homology Modeling | HIV Protease Inhibitor
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9. Full Text The uric acid transporter SLC2A9 is a direct target gene of the tumor suppressor p53 contributing to antioxidant defense
by Itahana, Y and Han, R and Barbier, S and Lei, Z and Rozen, S and Itahana, K
Oncogene, ISSN 0950-9232, 04/2015, Volume 34, Issue 14, pp. 1799 - 1810
Only humans and higher primates have high uric acid blood levels. Although high uric acid causes gout, it has been linked with human longevity because of its... 
URATE OXIDASE | APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA-DAMAGE | IDENTIFICATION | CANCER | CELL BIOLOGY | ONCOLOGY | ARF | GLUCOSE | IN-VIVO | DISEASE | GENETICS & HEREDITY | GLUT9 | DNA Damage - drug effects | Glucose Transport Proteins, Facilitative - metabolism | Reactive Oxygen Species - metabolism | Uric Acid - metabolism | Oxidative Stress | Antioxidants - metabolism | Humans | Probenecid - pharmacology | Tumor Suppressor Protein p53 - metabolism | Neoplasms - mortality | Tumor Suppressor Protein p53 - genetics | Hep G2 Cells | Biological Transport | Neoplasms - genetics | RNA Interference | Cell Line, Tumor | DNA Damage - genetics | RNA, Small Interfering | Glucose Transport Proteins, Facilitative - genetics | Neoplasms - pathology | Glucose Transport Proteins, Facilitative - antagonists & inhibitors | Reactive oxygen species | Genetic aspects | Tumor proteins | Properties | Carcinogenesis | Health aspects | Antioxidants | Acids | Genes | Tumors | Index Medicus
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10. Full Text Noise-mean relationship in mutated promoters
by Hornung, Gil and Bar-Ziv, Raz and Rosin, Dalia and Tokuriki, Nobuhiko and Tawfik, Dan S and Oren, Moshe and Barkai, Naama
Genome Research, ISSN 1088-9051, 12/2012, Volume 22, Issue 12, pp. 2409 - 2417
Gene expression depends on the frequency of transcription events (burst frequency) and on the number of mRNA molecules made per event (burst size). Both... 
FLUCTUATING ENVIRONMENTS | SINGLE CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | TRANSCRIPTION | SACCHAROMYCES-CEREVISIAE | YEAST | VARIABILITY | OPEN READING FRAMES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | GENE-EXPRESSION NOISE | REVEALS | Gene Expression Regulation, Fungal | Glucose Transport Proteins, Facilitative - metabolism | Glycerol-3-Phosphate Dehydrogenase (NAD+) - metabolism | Saccharomyces cerevisiae - genetics | Heat-Shock Proteins - metabolism | RNA, Messenger - genetics | Nucleosomes - metabolism | Nucleosomes - genetics | Binding Sites - genetics | Saccharomyces cerevisiae Proteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | RNA, Messenger - metabolism | DNA-Binding Proteins - metabolism | Saccharomyces cerevisiae - metabolism | Transcription Factors - metabolism | Heat-Shock Proteins - genetics | Saccharomyces cerevisiae Proteins - metabolism | TATA Box - genetics | Glucose Transport Proteins, Facilitative - genetics | Mutation | Glycerol-3-Phosphate Dehydrogenase (NAD+) - genetics | Gene mutations | Yeast fungi | Genetic variation | Genetic aspects | Research | Genetic transcription | Gene expression | Index Medicus
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11. Full Text Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes
by Matsuo, Hirotaka and Yamamoto, Ken and Nakaoka, Hirofumi and Nakayama, Akiyoshi and Sakiyama, Masayuki and Chiba, Toshinori and Takahashi, Atsushi and Nakamura, Takahiro and Nakashima, Hiroshi and Takada, Yuzo and Danjoh, Inaho and Shimizu, Seiko and Abe, Junko and Kawamura, Yusuke and Terashige, Sho and Ogata, Hiraku and Tatsukawa, Seishiro and Yin, Guang and Okada, Rieko and Morita, Emi and Naito, Mariko and Tokumasu, Atsumi and Onoue, Hiroyuki and Iwaya, Keiichi and Ito, Toshimitsu and Takada, Tappei and Inoue, Katsuhisa and Kato, Yukio and Nakamura, Yukio and Sakurai, Yutaka and Suzuki, Hiroshi and Kanai, Yoshikatsu and Hosoya, Tatsuo and Hamajima, Nobuyuki and Inoue, Ituro and Kubo, Michiaki and Ichida, Kimiyoshi and Ooyama, Hiroshi and Shimizu, Toru and Shinomiya, Nariyoshi
Annals of the Rheumatic Diseases, ISSN 0003-4967, 04/2016, Volume 75, Issue 4, pp. 652 - 659
ObjectiveGout, caused by hyperuricaemia, is a multifactorial disease. Although genome-wide association studies (GWASs) of gout have been reported, they... 
SERUM URATE CONCENTRATIONS | FASTING GLUCOSE | CORNICHON PROTEINS | RENAL HYPOURICEMIA | GLUCOKINASE-REGULATORY-PROTEIN | AMPA RECEPTORS | CARDIOVASCULAR-DISEASE | TYPE-2 DIABETES RISK | GENETIC-LOCI | RHEUMATOLOGY | URIC-ACID LEVELS | Myosin Light Chains - genetics | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Male | Case-Control Studies | Uric Acid - urine | ATP-Binding Cassette Transporters - genetics | Gout - urine | Adult | Glucose Transport Proteins, Facilitative - genetics | Neoplasm Proteins - genetics | Hyperuricemia - complications | ATP Binding Cassette Transporter, Subfamily G, Member 2 | Genetic Predisposition to Disease | Genome-Wide Association Study | Membrane Proteins - genetics | Cardiac Myosins - genetics | Japan | Gout - etiology | Hyperuricemia - genetics | Hyperuricemia - urine | Adaptor Proteins, Signal Transducing - genetics | Aged | Gout - genetics | Polymorphism, Single Nucleotide | Egg Proteins - genetics | Genome-wide association studies | Usage | Care and treatment | Hyperuricemia | Gout | Causes of | Single nucleotide polymorphisms | Research | Studies | Hospitals | Collaboration | Quality control | Genomes | Uric acid | Metabolic disorders | Methods | Index Medicus | Gene Polymorphism | Clinical and Epidemiological Research | Arthritis | 1506
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12. Full Text Multiple myeloma exhibits novel dependence on GLUT4, GLUT8, and GLUT11: Implications for glucose transporter-directed therapy
by McBrayer, Samuel K and Cheng, Javelin C and Singhal, Seema and Krett, Nancy L and Rosen, Steven T and Shanmugam, Mala
Blood, ISSN 0006-4971, 05/2012, Volume 119, Issue 20, pp. 4686 - 4697
Multiple myeloma is one of numerous malignancies characterized by increased glucose consumption, a phenomenon with significant prognostic implications in this... 
CANCER-CELLS | GLYCOLYSIS | APOPTOSIS | INHIBITION | METABOLISM | INSULIN-RESISTANCE | MCL-1 | GROWTH | DRUG-RESISTANCE | HEMATOLOGY | EXPRESSION | Glucose Transport Proteins, Facilitative - metabolism | Off-Label Use | Cell Proliferation | Glucose Transporter Type 4 - metabolism | Humans | Cell Survival - genetics | Biological Availability | HIV Protease Inhibitors - pharmacology | Glucose Transporter Type 4 - physiology | Multiple Myeloma - therapy | Molecular Targeted Therapy - trends | Ritonavir - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Glucose Transport Proteins, Facilitative - genetics | Drug Evaluation, Preclinical | Gene Expression Regulation, Neoplastic - physiology | Molecular Targeted Therapy - methods | Glucose Transporter Type 4 - antagonists & inhibitors | Glucose Transporter Type 4 - genetics | Cells, Cultured | Multiple Myeloma - metabolism | Disease Progression | Multiple Myeloma - pathology | Glucose - pharmacokinetics | Glucose Transport Proteins, Facilitative - physiology | Cell Line, Tumor | Glucose - metabolism | Primary Cell Culture | Glucose Transport Proteins, Facilitative - antagonists & inhibitors | Multiple Myeloma - genetics | Index Medicus | Abridged Index Medicus | Lymphoid Neoplasia
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