X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3136) 3136
Publication (362) 362
Newsletter (25) 25
Book Review (21) 21
Newspaper Article (12) 12
Book Chapter (6) 6
Book / eBook (2) 2
Conference Proceeding (2) 2
Data Set (1) 1
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (2121) 2121
nitric oxide synthase (1382) 1382
amino acid oxidoreductases - antagonists & inhibitors (1289) 1289
male (966) 966
rats (954) 954
arginine - analogs & derivatives (953) 953
arginine - pharmacology (913) 913
biochemistry & molecular biology (799) 799
humans (767) 767
amino acid sequence (675) 675
index medicus (648) 648
molecular sequence data (641) 641
nitric oxide (579) 579
kinetics (488) 488
amino acid oxidoreductases - metabolism (473) 473
ng-nitroarginine methyl ester (450) 450
mice (433) 433
female (358) 358
l-arginine (353) 353
omega-n-methylarginine (341) 341
rats, sprague-dawley (341) 341
pharmacology & pharmacy (320) 320
nitroarginine (316) 316
amino acids (311) 311
nitric oxide - physiology (305) 305
nitric oxide - antagonists & inhibitors (299) 299
neurosciences (291) 291
in vitro techniques (290) 290
enzymes (283) 283
research article (280) 280
cells, cultured (278) 278
nitric oxide - metabolism (276) 276
research (258) 258
enzyme inhibitors - pharmacology (257) 257
proteins (250) 250
physiological aspects (243) 243
binding sites (240) 240
rats, wistar (230) 230
substrate specificity (208) 208
relaxing factor (207) 207
oxidoreductases - antagonists & inhibitors (206) 206
expression (200) 200
cell biology (198) 198
inhibition (195) 195
dose-response relationship, drug (190) 190
amino acid oxidoreductases - biosynthesis (180) 180
sequence homology, amino acid (180) 180
multidisciplinary sciences (174) 174
oxidation-reduction (174) 174
oxidoreductases - metabolism (174) 174
cells (173) 173
models, molecular (172) 172
analysis (171) 171
blood pressure - drug effects (170) 170
nitric oxide - biosynthesis (166) 166
base sequence (159) 159
physiology (159) 159
biophysics (155) 155
metabolism (154) 154
rat (154) 154
brain (152) 152
lipids (151) 151
hydrogen-ion concentration (149) 149
purification (147) 147
amino acid oxidoreductases - genetics (144) 144
gene expression (143) 143
release (139) 139
sequence alignment (139) 139
cell line (138) 138
biosynthesis (137) 137
cattle (137) 137
oxidoreductases (137) 137
time factors (136) 136
escherichia-coli (134) 134
amino acids - analysis (132) 132
structure-activity relationship (132) 132
protein binding (131) 131
rabbits (130) 130
activation (127) 127
lipopolysaccharides - pharmacology (125) 125
mutation (125) 125
molecular weight (123) 123
biochemistry (122) 122
alcohol oxidoreductases - antagonists & inhibitors (120) 120
endothelium (118) 118
nitroprusside - pharmacology (118) 118
synthase (118) 118
microbiology (116) 116
protein (116) 116
chemistry (112) 112
article (111) 111
oxidative stress (110) 110
protein conformation (110) 110
identification (107) 107
oxidoreductases - genetics (107) 107
enzyme inhibitors - chemistry (105) 105
signal transduction (104) 104
oxidases (102) 102
catalysis (101) 101
binding (100) 100
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3150) 3150
Japanese (39) 39
German (8) 8
French (7) 7
Russian (7) 7
Spanish (4) 4
Chinese (1) 1
Norwegian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cancer Cell, ISSN 1535-6108, 2011, Volume 19, Issue 1, pp. 17 - 30
IDH1 and IDH2 mutations occur frequently in gliomas and acute myeloid leukemia, leading to simultaneous loss and gain of activities in the production of... 
BREAST-CANCER | TRANSCRIPTIONAL ACTIVITY | IDH2 MUTATIONS | ONCOLOGY | PROLYL HYDROXYLATION | INTEGRATED GENOMIC ANALYSIS | 2-OXOGLUTARATE OXYGENASES | ACUTE MYELOID-LEUKEMIA | HIF-ALPHA | HISTONE DEMETHYLATION | FAMILY | CELL BIOLOGY | Dioxygenases - metabolism | Histone Demethylases - antagonists & inhibitors | Gene Expression - genetics | Caenorhabditis elegans Proteins - chemistry | Humans | Ketoglutaric Acids - chemistry | Glioma - genetics | F-Box Proteins | Oxidoreductases, N-Demethylating - antagonists & inhibitors | Ketoglutaric Acids - pharmacology | Cytosine - metabolism | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Glutarates - chemistry | Oxidoreductases, N-Demethylating - metabolism | DNA-Binding Proteins - antagonists & inhibitors | Glioma - enzymology | Endostatins - metabolism | Models, Molecular | Isocitrate Dehydrogenase - genetics | Histone Demethylases - metabolism | Dioxygenases - antagonists & inhibitors | Amino Acid Substitution - physiology | Procollagen-Proline Dioxygenase - genetics | Cell Line, Tumor | Isocitrate Dehydrogenase - metabolism | Glutarates - pharmacology | Histones - metabolism | Jumonji Domain-Containing Histone Demethylases - metabolism | Caenorhabditis elegans - enzymology | Cytosine - analogs & derivatives | Gene Expression - drug effects | Caenorhabditis elegans Proteins - metabolism | Isocitrate Dehydrogenase - antagonists & inhibitors | Glioma - metabolism | Procollagen-Proline Dioxygenase - metabolism | DNA-Binding Proteins - metabolism | Mixed Function Oxygenases | Biocatalysis - drug effects | Jumonji Domain-Containing Histone Demethylases - antagonists & inhibitors | Jumonji Domain-Containing Histone Demethylases - chemistry | Procollagen-Proline Dioxygenase - antagonists & inhibitors | Ketoglutaric Acids - metabolism | Oxalates - pharmacology | Binding, Competitive | Proto-Oncogene Proteins - metabolism | Proto-Oncogene Proteins - antagonists & inhibitors | Catalytic Domain | Proto-Oncogene Proteins - genetics | Hypoxia-Inducible Factor-Proline Dioxygenases | DNA-Binding Proteins - genetics | Homeodomain Proteins - genetics | Animals | 5-Methylcytosine - metabolism | Caenorhabditis elegans Proteins - antagonists & inhibitors | Glutarates - metabolism
Journal Article
Nature Medicine, ISSN 1078-8956, 09/2010, Volume 16, Issue 9, pp. 1009 - 1017
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 07/2013, Volume 110, Issue 27, pp. E2510 - E2517
A cell-based phenotypic screen for inhibitors of biofilm formation in mycobacteria identified the small molecule TCA1, which has bactericidal activity against... 
Drug resistance | Dual mechanism | MYCOBACTERIUM-TUBERCULOSIS | dual mechanism | BIOSYNTHESIS | MULTIDISCIPLINARY SCIENCES | GROWTH | TOLERANT | drug resistance | INHIBITORS | MODEL | Oxidoreductases - antagonists & inhibitors | Tuberculosis, Pulmonary - microbiology | Antitubercular Agents - chemistry | Bacterial Proteins - chemistry | Biofilms - growth & development | Drug Resistance, Bacterial | Molecular Sequence Data | Carbohydrate Epimerases - antagonists & inhibitors | Tuberculosis, Pulmonary - drug therapy | Thiophenes - administration & dosage | Mycobacterium tuberculosis - drug effects | Oxidoreductases - chemistry | Microbial Sensitivity Tests | Female | Rifampin - administration & dosage | Alcohol Oxidoreductases | Biofilms - drug effects | Amino Acid Sequence | Bacterial Proteins - antagonists & inhibitors | Genes, Bacterial | Benzothiazoles - pharmacology | Oxidoreductases - genetics | Antitubercular Agents - pharmacology | Bacterial Proteins - genetics | Thiophenes - pharmacology | Carbohydrate Epimerases - chemistry | Isoniazid - administration & dosage | Animals | High-Throughput Screening Assays | Mycobacterium tuberculosis - enzymology | Antitubercular Agents - administration & dosage | Benzothiazoles - chemistry | Mice | Mice, Inbred BALB C | Thiophenes - chemistry | Carbohydrate Epimerases - genetics | Benzothiazoles - administration & dosage | Mycobacterium tuberculosis - genetics | Biological Sciences | PNAS Plus
Journal Article
Cell, ISSN 0092-8674, 2002, Volume 109, Issue 7, pp. 887 - 900
Members of the semaphorin family of secreted and transmembrane proteins utilize plexins as neuronal receptors to signal repulsive axon guidance. It remains... 
DOMAIN | MECHANISM | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | TRANSMEMBRANE | FAD-BINDING | SEMAPHORIN-III | GUIDANCE | PROJECTIONS | PROTEINS | DROSOPHILA | CELL BIOLOGY | Oxidoreductases - antagonists & inhibitors | Flavoproteins - chemistry | Cell Adhesion Molecules - genetics | Axons - enzymology | Cytoskeletal Proteins - antagonists & inhibitors | Cytoskeletal Proteins - genetics | Humans | Actins - metabolism | Molecular Sequence Data | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | Oxidoreductases - chemistry | Flavin-Adenine Dinucleotide - metabolism | Flavoproteins - antagonists & inhibitors | Conserved Sequence | Cytoskeletal Proteins - metabolism | Cell Adhesion Molecules, Neuronal - metabolism | Binding Sites | Protein Structure, Tertiary | Amino Acid Sequence | Flavoproteins - metabolism | LIM Domain Proteins | Oxidoreductases - metabolism | Signal Transduction | Flavoproteins - genetics | Oxidoreductases - genetics | Axons - metabolism | Intracellular Signaling Peptides and Proteins | Cytoskeletal Proteins - chemistry | Cell Adhesion Molecules - metabolism | Nerve Tissue Proteins - genetics | Blotting, Western | Cell Adhesion Molecules, Neuronal - genetics | Nerve Tissue Proteins - metabolism | Sequence Homology, Amino Acid | Adaptor Proteins, Signal Transducing | Phenotype | Animals | Semaphorins | Cytoskeleton - metabolism | Drosophila melanogaster - enzymology | Protein Binding | Drosophila Proteins - genetics | Mutation | Proteins | Oxidases | Axons | Cell research | Flavonoids | Analysis | Physiological aspects | Genetic aspects | Oxidoreductases
Journal Article
The Plant Cell, ISSN 1040-4651, 6/2011, Volume 23, Issue 6, pp. 2362 - 2378
Sphingolipids are a class of structural membrane lipids involved in membrane trafficking and cell polarity. Functional analysis of the ceramide synthase family... 
Ceramides | Cell aggregates | Auxins | Lipids | Sphingolipids | Cell membranes | Plants | Fatty acids | Plant cells | Seedlings | CERAMIDE SYNTHASE | FAMILY-MEMBERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLANT-CELLS | SACCHAROMYCES-CEREVISIAE | PLANT SCIENCES | CELL BIOLOGY | AUXIN TRANSPORT | F-SP LYCOPERSICI | FUMONISIN B-1 | LIPID RAFTS | TRANS-GOLGI NETWORK | ROOT-SYSTEM ARCHITECTURE | Oxidoreductases - antagonists & inhibitors | Sphingolipids - chemistry | Cell Polarity | Arabidopsis - physiology | Fumonisins - metabolism | Humans | Molecular Sequence Data | Recombinant Fusion Proteins - metabolism | Endosomes - metabolism | Intracellular Membranes - ultrastructure | Arabidopsis Proteins - metabolism | Isoenzymes - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Amino Acid Sequence | Arabidopsis Proteins - genetics | Ceramides - metabolism | Enzyme Inhibitors - metabolism | Indoleacetic Acids - metabolism | Oxidoreductases - metabolism | Isoenzymes - genetics | Membrane Proteins - genetics | Oxidoreductases - genetics | Arabidopsis - cytology | Sphingolipids - metabolism | Ceramides - chemistry | Protein Synthesis Inhibitors - metabolism | Brefeldin A - metabolism | Arabidopsis - genetics | Secretory Pathway - physiology | Sequence Alignment | Animals | Membrane Proteins - chemistry | Recombinant Fusion Proteins - genetics | Intracellular Membranes - metabolism | Arabidopsis thaliana | Physiological aspects | Genetic aspects | Cell Membrane | Enzyme Inhibitors | Secretory Pathway | Intracellular Membranes | Brefeldin A | Recombinant Fusion Proteins | Life Sciences | Arabidopsis Proteins | Vegetal Biology | Protein Synthesis Inhibitors | Fumonisins | Isoenzymes | Arabidopsis | Membrane Proteins | Oxidoreductases | Indoleacetic Acids | Endosomes
Journal Article
Cell Death and Differentiation, ISSN 1350-9047, 06/2012, Volume 19, Issue 6, pp. 1049 - 1059
WW domain-containing oxidoreductase (WWOX), a putative tumour suppressor, is suggested to be involved in the hyperphosphorylation of Alzheimer's Tau. Tau is a... 
GSK3β | SH-SY5Y | WWOX | Tau | PROTEIN | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | GSK-3 | CELL BIOLOGY | RETINOIC ACID | GSK3-BETA | GSK3 beta | EXPRESSION | ASSOCIATION | Oxidoreductases - antagonists & inhibitors | Phosphorylation | Tumor Suppressor Proteins - antagonists & inhibitors | Humans | Molecular Sequence Data | tau Proteins - metabolism | Glycogen Synthase Kinase 3 beta | Neurons - cytology | Oxidoreductases - chemistry | Microtubules - metabolism | tau Proteins - genetics | RNA Interference | WW Domain-Containing Oxidoreductase | Tumor Suppressor Proteins - chemistry | Neurogenesis - drug effects | Neurons - metabolism | Binding Sites | tau Proteins - antagonists & inhibitors | Tretinoin - pharmacology | Protein Structure, Tertiary | Amino Acid Sequence | Tumor Suppressor Proteins - metabolism | Oxidoreductases - metabolism | Glycogen Synthase Kinase 3 - antagonists & inhibitors | Glycogen Synthase Kinase 3 - metabolism | Molecular Dynamics Simulation | Amino Acid Motifs | Glycogen Synthase Kinase 3 - genetics | Cell Line, Tumor | Protein Binding | RNA, Small Interfering - metabolism | Immunoprecipitation | Neurodegenerative diseases | Axonogenesis | Neurons | Glycogen synthase kinase 3 | Data processing | Alcohol dehydrogenase | reductase | Molecular modelling | Tau protein | Microtubule-associated proteins | Differentiation | Immunofluorescence | oxidoreductase | Alzheimer's disease | Bioinformatics | Retinoic acid | Original Paper
Journal Article
Biochemistry, ISSN 0006-2960, 11/2015, Volume 54, Issue 45, pp. 6815 - 6829
In probing the oxygen reactivity of an Enterococcus faecalis NADH oxidase (Nox; O2 → 2H2O) C42S mutant lacking the Cys42-sulfenic acid (Cys42-SOH) redox... 
GLUTATHIONE-REDUCTASE | ANGSTROM RESOLUTION | ACTIVE-SITE | CATALYTIC-PROPERTIES | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | PARA-HYDROXYBENZOATE HYDROXYLASE | REDOX CENTER | SUPEROXIDE-DISMUTASE | CYSTEINE-SULFENIC ACID | A-DISULFIDE REDUCTASE | Species Specificity | Bacterial Proteins - chemistry | Molecular Sequence Data | Crystallography, X-Ray | Structure-Activity Relationship | Oxidoreductases - chemistry | Streptococcus pyogenes - genetics | Peroxidases - chemistry | NADH, NADPH Oxidoreductases - chemistry | Azides - pharmacology | Azides - metabolism | Enterococcus faecalis - enzymology | Amino Acid Sequence | Bacterial Proteins - antagonists & inhibitors | NADH, NADPH Oxidoreductases - genetics | Catalytic Domain | Oxidation-Reduction | Bacterial Proteins - genetics | Models, Molecular | Multienzyme Complexes - genetics | Cysteine - chemistry | NADH, NADPH Oxidoreductases - isolation & purification | Recombinant Fusion Proteins - chemistry | Multienzyme Complexes - antagonists & inhibitors | Molecular Dynamics Simulation | Multienzyme Complexes - chemistry | Sequence Homology, Amino Acid | Sequence Alignment | Streptococcus pyogenes - enzymology | Flavins - chemistry | Protein Conformation | NADH, NADPH Oxidoreductases - antagonists & inhibitors | Bacterial Proteins - isolation & purification | Multienzyme Complexes - isolation & purification | Azides | Ligands (Biochemistry) | Analysis | NADP (Coenzyme) | Streptococcus pyogenes | Research | Chemical properties
Journal Article
Journal of Antibiotics, ISSN 0021-8820, 02/2014, Volume 67, Issue 2, pp. 147 - 151
Journal Article
Science, ISSN 0036-8075, 9/1999, Volume 285, Issue 5433, pp. 1573 - 1576
A mevalonate-independent pathway of isoprenoid biosynthesis present in Plasmodium falciparum was shown to represent an effective target for chemotherapy of... 
Enzymes | Malaria | Terpenoids | Antimalarials | Amino acids | Apicoplasts | Reports | Parasites | Parasitemia | Dosage | Chromosomes | PARASITE TOXOPLASMA-GONDII | ERYTHROCYTES | HIGHER-PLANTS | APICOMPLEXAN PARASITES | FOSMIDOMYCIN | ISOPENTENYL DIPHOSPHATE | PLASMODIUM-FALCIPARUM | MULTIDISCIPLINARY SCIENCES | 1-DEOXY-D-XYLULOSE 5-PHOSPHATE REDUCTOISOMERASE | TERPENOID BIOSYNTHESIS | MEVALONATE-INDEPENDENT PATHWAY | Oxidoreductases - antagonists & inhibitors | Molecular Sequence Data | Multienzyme Complexes - metabolism | Genes, Protozoan | Organelles - drug effects | Plasmodium falciparum - drug effects | Organophosphorus Compounds - metabolism | Oxidoreductases - chemistry | Terpenes - pharmacology | Plasmodium falciparum - genetics | Cloning, Molecular | Plasmodium falciparum - metabolism | Pentosephosphates - metabolism | Aldose-Ketose Isomerases - metabolism | Fosfomycin - analogs & derivatives | Recombinant Proteins - metabolism | Amino Acid Sequence | Malaria, Falciparum - drug therapy | Aldose-Ketose Isomerases - chemistry | Recombinant Proteins - antagonists & inhibitors | Oxidoreductases - metabolism | Fosfomycin - pharmacology | Oxidoreductases - genetics | Enzyme Inhibitors - pharmacology | Multienzyme Complexes - genetics | Mevalonic Acid - metabolism | Multienzyme Complexes - antagonists & inhibitors | Reverse Transcriptase Polymerase Chain Reaction | Antimalarials - pharmacology | Multienzyme Complexes - chemistry | Malaria, Falciparum - parasitology | Animals | Malaria - parasitology | Hemiterpenes | Mice | Aldose-Ketose Isomerases - genetics | Malaria - drug therapy | Aldose-Ketose Isomerases - antagonists & inhibitors | Organelles - metabolism | Plasmodium | Research | Pharmacology | Biochemistry | Drug therapy
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2018, Volume 293, Issue 10, pp. 3839 - 3848
Journal Article