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BBA - Molecular Cell Research, ISSN 0167-4889, 02/2014, Volume 1843, Issue 2, pp. 372 - 386
(CRNDE) is a novel gene that is activated early in colorectal cancer but whose regulation and functions are unknown. CRNDE transcripts are recognized as long... 
lncRNA | IGF1 | Insulin | CRNDE | Colorectal cancer | Warburg effect | LncRNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | IncRNA | CELL-PROLIFERATION | GLUCOSE-TRANSPORT | MUSCLE-CELLS | CELL BIOLOGY | COLON-CANCER | RECTAL-CANCER | COLORECTAL-CANCER | MUTATIONS | CARBOHYDRATE-METABOLISM | EXPRESSION | GROWTH-FACTOR-I | Insulin-Like Growth Factor I - pharmacology | Glucose Transporter Type 4 - metabolism | TOR Serine-Threonine Kinases - metabolism | Colorectal Neoplasms - genetics | Humans | Phosphatidylinositol 3-Kinases - metabolism | RNA, Messenger - metabolism | raf Kinases - metabolism | RNA Interference | Metabolism - drug effects | Insulin-Like Growth Factor II - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Proto-Oncogene Proteins c-akt - metabolism | Colorectal Neoplasms - metabolism | Metabolism - genetics | Insulin - pharmacology | RNA, Messenger - genetics | RNA, Long Noncoding - genetics | Signal Transduction - genetics | Transcriptome - genetics | Down-Regulation - drug effects | Down-Regulation - genetics | Insulin-Like Growth Factor II - metabolism | Gene Expression Regulation - drug effects | Insulin - metabolism | Lactates - metabolism | Signal Transduction - drug effects | Models, Biological | Cell Line, Tumor | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Colorectal Neoplasms - pathology | RNA, Long Noncoding - metabolism | Insulin-Like Growth Factor I - metabolism | Mitogen-Activated Protein Kinases - metabolism | RNA, Small Interfering - metabolism | RNA | Genes | Analysis | Physiological aspects | Glucose | Gene expression | Dextrose | Epigenetic inheritance
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 05/2012, Volume 109, Issue 19, pp. E1192 - E1200
Plants must effectively defend against biotic and abiotic stresses to survive in nature. However, this defense is costly and is often accompanied by... 
Light response | Disease resistance | Plant growth | Plant defense | Plant immunity | plant growth | TRANSCRIPTION FACTORS | ARABIDOPSIS-THALIANA | CYTOCHROME-P450 MONOOXYGENASE | PROTEIN | MULTIDISCIPLINARY SCIENCES | RECEPTOR | RESPONSES | plant defense | disease resistance | GENE | light response | REPRESSOR | plant immunity | ALPHA-AMYLASE | RICE | Arabidopsis - growth & development | Oryza - metabolism | Seedlings - genetics | Arabidopsis Proteins - metabolism | DNA-Binding Proteins - metabolism | Proteolysis - drug effects | Oryza - growth & development | Basic Helix-Loop-Helix Transcription Factors - metabolism | Oryza - genetics | Plants - genetics | RNA Interference | Gibberellins - metabolism | Plant Proteins - metabolism | Repressor Proteins - metabolism | Arabidopsis Proteins - genetics | Basic Helix-Loop-Helix Transcription Factors - genetics | Plant Development | F-Box Proteins - metabolism | Repressor Proteins - genetics | Signal Transduction - genetics | Cyclopentanes - pharmacology | Seedlings - drug effects | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Arabidopsis - metabolism | Arabidopsis - genetics | Transcription Factors - metabolism | Oxylipins - metabolism | Plant Proteins - genetics | Two-Hybrid System Techniques | Gene Expression Regulation, Plant - drug effects | Plants - metabolism | Signal Transduction - drug effects | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Oxylipins - pharmacology | Gibberellins - pharmacology | Protein Binding | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Cyclopentanes - metabolism | Signal Transduction - physiology | Mutation | Plant Growth Regulators - metabolism | F-Box Proteins - genetics | Plant Growth Regulators - pharmacology | Seedlings - metabolism | Proteins | Signal transduction | Flowers & plants | Hormones | Binding sites | Index Medicus | Biological Sciences | PNAS Plus
Journal Article
Nature Communications, ISSN 2041-1723, 2015, Volume 6, Issue 1, pp. 7629 - 7629
Bile acids are signalling molecules, which activate the transmembrane receptor TGR5 and the nuclear receptor FXR. BA sequestrants (BAS) complex bile acids in... 
GLP-1 SECRETION | FXR | BILE-ACID RECEPTORS | GLUCOSE-HOMEOSTASIS | OBESITY | MULTIDISCIPLINARY SCIENCES | RAT SMALL-INTESTINE | MICE | TYPE-2 DIABETES-MELLITUS | METABOLIC-RATE | EXPRESSION | Colon - cytology | Intestinal Mucosa - metabolism | Sequestering Agents - pharmacology | Humans | Ileum - metabolism | RNA, Messenger - metabolism | Colesevelam Hydrochloride - pharmacology | Obesity - genetics | Glucagon-Like Peptide 1 - genetics | Jejunum - metabolism | Insulin-Secreting Cells - metabolism | Proglucagon - drug effects | Diet, High-Fat | Jejunum - cytology | Enteroendocrine Cells - metabolism | Ileum - cytology | Proglucagon - metabolism | Insulin Secretion | Glucagon-Like Peptide 1 - metabolism | Signal Transduction | Bile Acids and Salts - metabolism | Nuclear Proteins - metabolism | Receptors, Cytoplasmic and Nuclear - genetics | Colon - metabolism | Mice, Knockout | Obesity - metabolism | Transcription Factors - metabolism | Insulin - metabolism | Animals | Glycolysis | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Mice, Obese | Mice | Proglucagon - genetics | Receptors, G-Protein-Coupled - genetics | Blood Glucose - metabolism | Anticholesteremic Agents - pharmacology | Intestines - cytology | Index Medicus | Cell and Molecular Biology | Endokrinologi och diabetes | Multidisciplinary Sciences | Cell- och molekylärbiologi | Endocrinology and Diabetes
Journal Article
The EMBO Journal, ISSN 0261-4189, 07/2004, Volume 23, Issue 13, pp. 2544 - 2553
Bach1 is a transcriptional repressor of heme oxygenase‐1 and β‐globin genes, both of which are known to be transcriptionally induced by heme. To test the... 
heme oxygenase | Maf | globin | heme | oxidative stress | Globin | Oxidative stress | Heme | Heme oxygenase | CELLS | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | INDUCTION | OXYGENASE-1 GENE | LEUCINE ZIPPER PROTEIN | CELL BIOLOGY | CADMIUM | SMALL MAF | TRANSCRIPTION FACTOR NF-E2 | BINDING | Immunohistochemistry | Heme - metabolism | Transcription Factors - chemistry | Humans | Leucine Zippers | Molecular Sequence Data | Globins - metabolism | Recombinant Fusion Proteins - metabolism | DNA-Binding Proteins - metabolism | Cell Nucleus - metabolism | Chromatin Immunoprecipitation | Heme Oxygenase-1 | Transcription, Genetic | Active Transport, Cell Nucleus | Hemin - pharmacology | Heme Oxygenase (Decyclizing) - metabolism | Dimerization | Heme Oxygenase (Decyclizing) - genetics | Genes, Reporter | Repressor Proteins - metabolism | Fibroblasts - metabolism | Amino Acid Sequence | Cell Line | Green Fluorescent Proteins - metabolism | Zinc Fingers | Gene Expression Regulation | Glutathione Transferase - metabolism | Alanine - metabolism | Nuclear Proteins - metabolism | Recombinant Fusion Proteins - chemistry | Transcription Factors - genetics | Fanconi Anemia Complementation Group Proteins | Amino Acid Motifs | MafK Transcription Factor | Membrane Proteins | Transcription Factors - metabolism | Karyopherins - metabolism | Escherichia coli - genetics | Plasmids | Fibroblasts - drug effects | Erythroid-Specific DNA-Binding Factors | Spectrophotometry | Basic-Leucine Zipper Transcription Factors | Amino Acid Substitution | Receptors, Cytoplasmic and Nuclear - metabolism | Index Medicus
Journal Article
American Journal of Physiology - Endocrinology and Metabolism, ISSN 0193-1849, 07/2016, Volume 311, Issue 1, pp. E224 - E235
Increased availability of lipids may conserve muscle protein during catabolic stress. Our study was designed to define 1) intracellular mechanisms leading to... 
Human | Protein breakdown | Obesity | Fasting | Subcutaneous adipose tissue | Lipolysis | Skeletal muscle | ADIPOSE TRIGLYCERIDE LIPASE | PHYSIOLOGY | HORMONE-SENSITIVE LIPASE | MUSCLE | fasting | sub-cutaneous adipose tissue | AMINO-ACID | protein breakdown | GROWTH-HORMONE | FAT-CELLS | ENDOCRINOLOGY & METABOLISM | WHOLE-BODY | LEUCINE TURNOVER | lipolysis | skeletal muscle | human | obesity | DECREASED EXPRESSION | 1-Acylglycerol-3-Phosphate O-Acyltransferase - genetics | Phosphorylation | TOR Serine-Threonine Kinases - metabolism | Humans | Sterol Esterase - metabolism | Male | Muscle, Skeletal - metabolism | Autophagy-Related Protein-1 Homolog - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | RNA, Messenger - metabolism | Obesity - genetics | Case-Control Studies | Lipolysis - genetics | Young Adult | Adipose Tissue - metabolism | 1-Acylglycerol-3-Phosphate O-Acyltransferase - metabolism | Forearm | Time Factors | Muscle Proteins - metabolism | Adult | Lipid Metabolism - genetics | Urea - metabolism | Fasting - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Cell Cycle Proteins - metabolism | Ubiquitin-Protein Ligases - metabolism | Lipase - metabolism | Obesity - metabolism | Cross-Over Studies | Tripartite Motif Proteins - metabolism | Autophagy-Related Protein-1 Homolog - genetics | Lipase - genetics | Protein metabolism | Physiological aspects | Physiological research | Lipid metabolism | Research | Biological control systems | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 05/2004, Volume 279, Issue 19, pp. 20314 - 20326
Hepatic glucokinase (GK) catalyzes the phosphorylation of glucose to glucose 6-phosphate (G6P), a step which is essential for glucose metabolism in liver as... 
FATTY-ACID-SYNTHASE | GLUCOSE-HOMEOSTASIS | CARBOHYDRATE RESPONSE ELEMENT | RAT HEPATOCYTES | STEROL REGULATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ELEMENT-BINDING PROTEIN-1C | PYRUVATE-KINASE GENE | TRANSCRIPTION FACTOR | CARNITINE-PALMITOYLTRANSFERASE-I | TRANSGENIC MICE | Glucokinase - physiology | Liver - enzymology | Fatty Acid Synthases - metabolism | Immunoblotting | Hepatocytes - metabolism | RNA, Messenger - metabolism | DNA-Binding Proteins - metabolism | Cell Nucleus - metabolism | Glycogen - metabolism | Time Factors | CCAAT-Enhancer-Binding Proteins - physiology | Adenoviridae - genetics | Transcription, Genetic | Pentosephosphates - metabolism | RNA - metabolism | CCAAT-Enhancer-Binding Proteins - metabolism | DNA-Binding Proteins - physiology | Pyruvate Kinase - metabolism | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Carbohydrate Metabolism | Cells, Cultured | Gene Expression Regulation | Lipid Metabolism | Mice, Transgenic | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Nuclear Proteins | Transcription Factors - metabolism | Blotting, Northern | Animals | Proteins - metabolism | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors | Glucose - metabolism | Mice | Kinetics | Sterol Regulatory Element Binding Protein 1 | Glucose-6-Phosphate - metabolism | Acetyl-CoA Carboxylase - metabolism | Microscopy, Fluorescence | RNA, Small Interfering - metabolism | Index Medicus
Journal Article
Developmental Cell, ISSN 1534-5807, 10/2016, Volume 39, Issue 1, pp. 13 - 27
Journal Article
Free Radical Biology and Medicine, ISSN 0891-5849, 03/2016, Volume 92, pp. 152 - 162
The effects of physiological oxygen tension on Nuclear Factor-E2-Related Factor 2 (Nrf2)-regulated redox signaling remain poorly understood. We report the... 
NQO1 | Bach1 | Solute Carrier Family 7-anionic amino acid transporter light chain xCT | Coronary artery | HO-1 | Redox signaling | Endothelial cells | Normoxia | GCL | Physiological oxygen tension | Mitochondria | Nuclear Factor-E2-Related Factor 2, Nrf2 | Glutathione reductase GR | Thioredoxin reductase-1 | Sequestosome-1 | Glutathione | Physiologicaloxygentension | NuclearFactor-E2-RelatedFactor2,Nrf2 | Redoxsignaling | transporterlightchainxCT | Solute CarrierFamily7-anionicaminoacid | Thioredoxinreductase-1 | REPRESSOR BACH1 | ENDOCRINOLOGY & METABOLISM | SMOOTH-MUSCLE-CELLS | HEME OXYGENASE-1 | MOLECULAR-BASIS | KEAP1-NRF2 SYSTEM | NQ01 | OXIDATIVE STRESS | STEM-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | VASCULAR ENDOTHELIUM | SENSING MECHANISMS | TRANSCRIPTION FACTOR NRF2 | Heme Oxygenase-1 - metabolism | Basic-Leucine Zipper Transcription Factors - metabolism | Reactive Oxygen Species - metabolism | Glutathione - metabolism | Antioxidants - metabolism | Humans | NAD(P)H Dehydrogenase (Quinone) - genetics | Oxygen - metabolism | Coronary Vessels - metabolism | DNA-Binding Proteins - metabolism | Kelch-Like ECH-Associated Protein 1 - genetics | Heme Oxygenase-1 - genetics | Fanconi Anemia Complementation Group Proteins - metabolism | Amino Acid Transport System y+ - metabolism | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | NF-E2-Related Factor 2 - genetics | Glutamate-Cysteine Ligase - metabolism | Endothelial Cells - metabolism | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Kelch-Like ECH-Associated Protein 1 - metabolism | Basic-Leucine Zipper Transcription Factors - genetics | DNA-Binding Proteins - genetics | Veins - metabolism | NF-E2-Related Factor 2 - metabolism | NAD(P)H Dehydrogenase (Quinone) - metabolism | Genetic research | Physiological aspects | Genes | Endothelium | Surface active agents | RNA | Amino acids | DNA binding proteins | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 04/2012, Volume 484, Issue 7394, pp. 333 - 338
The prevalence of obesity and type 2 diabetes is increasing worldwide and threatens to shorten lifespan. Impaired insulin action in peripheral tissues is a... 
DIABETES-MELLITUS | FATTY-ACID SYNTHESIS | GENE | INSULIN-RESISTANCE | LIPOGENESIS | MULTIDISCIPLINARY SCIENCES | CARBOHYDRATE-RESPONSE ELEMENT | LIVER | BINDING-PROTEIN CHREBP | UCSC GENOME BROWSER | TRANSGENIC MICE | Transcription Factors - chemistry | Diabetes Mellitus - genetics | Humans | Male | RNA, Messenger - metabolism | Adipose Tissue - metabolism | Protein Isoforms - chemistry | Nuclear Proteins - deficiency | Lipogenesis | Body Mass Index | Glucose Transporter Type 4 - genetics | Adipose Tissue - pathology | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - chemistry | Genotype | Glucose - pharmacology | Nuclear Proteins - chemistry | Mice, Knockout | Insulin - metabolism | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics | Insulin Resistance - genetics | Glucose - metabolism | Mice | Blood Glucose - metabolism | Homeostasis - genetics | Cohort Studies | Diabetes Mellitus - blood | Body Weight | Glucose Transporter Type 4 - metabolism | Transcription Factors - deficiency | Adipose Tissue - cytology | Molecular Sequence Data | Obesity - genetics | Promoter Regions, Genetic - genetics | Protein Isoforms - metabolism | Adiposity | Female | Nuclear Proteins - genetics | Insulin - pharmacology | Glucose Intolerance - genetics | Cross-Sectional Studies | Gene Expression Regulation - genetics | RNA, Messenger - genetics | Cells, Cultured | Diabetes Mellitus - metabolism | Nuclear Proteins - metabolism | Transcription Factors - genetics | Obesity - metabolism | Transcription Factors - metabolism | Animals | Glucose Transporter Type 4 - biosynthesis | Adipocytes - metabolism | Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism | Protein Isoforms - genetics | Index Medicus
Journal Article
Cancer Cell, ISSN 1535-6108, 05/2017, Volume 31, Issue 5, pp. 711 - 723.e4
Effector T cells have the capability of recognizing and killing cancer cells. However, whether tumors can become immune resistant through exclusion of effector... 
T cell-inflamed tumor microenvironment | non-T cell-inflamed tumor microenvironment | immunotherapy resistance | immune escape | adoptive T cell transfer | METASTATIC MELANOMA | RESPONSES | IMMUNITY | MECHANISM | ONCOLOGY | CANCER REGRESSION | REJECTION | ANTIGENS | MICE | BLOCKADE | EXPRESSION | CELL BIOLOGY | Chemotaxis, Leukocyte | Tumor Escape | Basic-Leucine Zipper Transcription Factors - metabolism | Cell Proliferation | Dendritic Cells - immunology | Tumor Microenvironment | T-Lymphocytes - transplantation | Antigens, CD - metabolism | Repressor Proteins - deficiency | T-Lymphocytes - metabolism | Time Factors | Basic-Leucine Zipper Transcription Factors - deficiency | CD8-Positive T-Lymphocytes - metabolism | Dendritic Cells - metabolism | Repressor Proteins - metabolism | Melanoma - metabolism | Skin Neoplasms - pathology | Immunotherapy, Adoptive - methods | Signal Transduction | Skin Neoplasms - immunology | Skin Neoplasms - therapy | Repressor Proteins - genetics | Genotype | Integrin alpha Chains - metabolism | Basic-Leucine Zipper Transcription Factors - genetics | Melanoma - pathology | Tumor Burden | beta Catenin - metabolism | Mice, Knockout | Skin Neoplasms - metabolism | Phenotype | Animals | Melanoma - immunology | Chemokine CXCL9 - metabolism | Cell Line, Tumor | Immunologic Memory | T-Lymphocytes - immunology | CD8-Positive T-Lymphocytes - immunology | Melanoma - therapy | Chemokine CXCL10 - metabolism | Dendritic cells | T cells | Cancer | Immunotherapy | Index Medicus | Adoptive T cell transfer
Journal Article
Science, ISSN 0036-8075, 7/2012, Volume 337, Issue 6090, pp. 93 - 96
The transport of pyruvate, the end product of glycolysis, into mitochondria is an essential process that provides the organelle with a major oxidative fuel.... 
Essential amino acids | Yeasts | Lactates | Cell growth | Mitochondria | Dehydrogenases | REPORTS | Mitochondrial membranes | Amino acids |