X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (952) 952
index medicus (873) 873
cystathionine gamma-lyase - metabolism (749) 749
hydrogen sulfide - metabolism (620) 620
hydrogen sulfide (612) 612
humans (535) 535
male (487) 487
rats (411) 411
mice (374) 374
biochemistry & molecular biology (368) 368
cystathionine gamma-lyase (326) 326
cystathionine beta-synthase - metabolism (292) 292
h2s (291) 291
cystathionine gamma-lyase - genetics (284) 284
oxidative stress (272) 272
cysteine (244) 244
enzymes (235) 235
hydrogen-sulfide (221) 221
cystathionine beta-synthase (206) 206
hydrogen sulfide - pharmacology (197) 197
metabolism (197) 197
cysteine - metabolism (188) 188
nitric-oxide (179) 179
female (173) 173
physiological aspects (170) 170
cell biology (162) 162
equipment and supplies (159) 159
homocysteine (149) 149
physiology (149) 149
cystathionine-gamma-lyase (147) 147
glycine - analogs & derivatives (138) 138
cystathionine gamma-lyase - antagonists & inhibitors (135) 135
pharmacology & pharmacy (131) 131
research (129) 129
glycine - pharmacology (127) 127
cystathionine γ-lyase (123) 123
expression (123) 123
rats, sprague-dawley (123) 123
signal transduction (122) 122
glutathione (120) 120
disease models, animal (118) 118
inflammation (118) 118
alkynes - pharmacology (116) 116
sulfides - pharmacology (113) 113
liver - metabolism (111) 111
proteins (111) 111
apoptosis (110) 110
rats, wistar (109) 109
liver - enzymology (106) 106
mice, inbred c57bl (106) 106
nitric oxide (106) 106
mice, knockout (104) 104
endocrinology & metabolism (102) 102
article (100) 100
cells, cultured (99) 99
cystathionine-beta-synthase (98) 98
hypertension (98) 98
methionine (98) 98
gene expression (97) 97
nitric-oxide synthase (97) 97
inhibition (96) 96
gamma-lyase (95) 95
rodents (95) 95
research article (93) 93
rat (92) 92
cystathionine beta-synthase - genetics (91) 91
kinetics (91) 91
lyases - metabolism (90) 90
hydrogen (89) 89
microbiology (88) 88
in-vitro (87) 87
glutathione - metabolism (86) 86
liver (85) 85
multidisciplinary sciences (82) 82
analysis (81) 81
cells (81) 81
sulfur (80) 80
medicine (79) 79
methionine - metabolism (79) 79
smooth-muscle-cells (79) 79
amino acids (78) 78
biosynthesis (77) 77
ischemia-reperfusion injury (77) 77
biology (76) 76
escherichia-coli (76) 76
dose-response relationship, drug (75) 75
nitric oxide - metabolism (75) 75
sulfurtransferases - metabolism (75) 75
activation (74) 74
enzyme inhibitors - pharmacology (74) 74
health aspects (73) 73
cystathionine-γ-lyase (68) 68
cell line (67) 67
signal transduction - drug effects (67) 67
3-mercaptopyruvate sulfurtransferase (66) 66
neurosciences (66) 66
hydrogen sulfide - blood (65) 65
sulfides - metabolism (63) 63
sulfide (62) 62
vasorelaxant (62) 62
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1488) 1488
Chinese (27) 27
Japanese (24) 24
Ukrainian (6) 6
French (3) 3
Polish (3) 3
German (2) 2
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature, ISSN 0028-0836, 2014, Volume 508, Issue 7498, pp. 96 - 100
Journal Article
Cardiovascular Research, ISSN 0008-6363, 06/2010, Volume 86, Issue 3, pp. 487 - 495
Cystathionine gamma-lyase (CSE)-derived H2S plays an important role in regulating cell growth. Lack of CSE expression results in development of hypertension.... 
Hydrogen sulfide | Hypertension | Smooth muscle cell | Cystathionine gamma-lyase | Apoptosis | CARDIAC & CARDIOVASCULAR SYSTEMS | SPONTANEOUSLY HYPERTENSIVE-RATS | RECEPTOR-LIKE-RECEPTOR | H2S | PROLIFERATION | HYDROGEN-SULFIDE | VASORELAXANT | GROWTH-FACTOR | GENETIC-HYPERTENSION | EXPRESSION | Cyclin D1 - metabolism | Phosphorylation | Oligonucleotide Array Sequence Analysis | Myocytes, Smooth Muscle - pathology | Mesenteric Arteries - pathology | Male | Receptors, Calcitonin - genetics | Calcitonin Receptor-Like Protein | RNA, Messenger - metabolism | Time Factors | Polymerase Chain Reaction | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Cystathionine gamma-Lyase - genetics | Myocytes, Smooth Muscle - drug effects | Aorta - enzymology | Cystathionine gamma-Lyase - deficiency | Muscle, Smooth, Vascular - drug effects | Hydrogen Sulfide - pharmacology | Myocytes, Smooth Muscle - enzymology | Mice, Inbred C57BL | Cells, Cultured | Intercellular Signaling Peptides and Proteins - genetics | Gene Expression Profiling - methods | Blotting, Western | Mice, Knockout | Aorta - pathology | Heparin-binding EGF-like Growth Factor | Muscle, Smooth, Vascular - pathology | Animals | Mitogen-Activated Protein Kinase 3 - metabolism | Cell Proliferation - drug effects | Mice | Integrin beta1 - genetics | Mesenteric Arteries - enzymology | Muscle, Smooth, Vascular - enzymology | Mitogen-Activated Protein Kinase 1 - metabolism
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2014, Volume 9, Issue 11, p. e113038
Hydrogen sulfide (H2S) is an important gaseous signaling molecule that functions in physiological and pathological conditions, such as atherosclerosis. H2S... 
CELLS | OXIDATIVE STRESS | PROTEIN | ADIPONECTIN | DONOR | MULTIDISCIPLINARY SCIENCES | H2S | P53 | Blood Pressure | Hydrogen Sulfide - metabolism | Up-Regulation | Body Weight | Apolipoproteins E - deficiency | Oxidative Stress | Cystathionine gamma-Lyase - metabolism | NF-kappa B - metabolism | Aorta - metabolism | Apolipoproteins E - metabolism | Atherosclerosis - etiology | Leptin - blood | Lipids - blood | Myocardium - metabolism | Cystathionine gamma-Lyase - genetics | Glutathione Peroxidase - metabolism | Atherosclerosis - pathology | Down-Regulation | Mice, Inbred C57BL | Tumor Suppressor Protein p53 - metabolism | Mice, Transgenic | Mice, Knockout | Plaque, Atherosclerotic - physiopathology | Adiponectin - blood | Aorta - pathology | Animals | Apolipoproteins E - genetics | Mice | Hydrogen sulfide | Proteins | Genes | Atherosclerosis | Genetic engineering | Health aspects | Sulfide | Oxidative stress | Regulations | Phosphorylation | Laboratories | Hydrogen | Weaning | Body weight | p53 Protein | Smooth muscle | Kinases | Atherogenic diet | Apolipoprotein E | Rodents | Surgery | Aorta | Peroxidase | Blood pressure | Hydrogen ion concentration | Plaques | Cardiovascular system | NF-κB protein | Preservation | Transgenic mice | Blood vessels | Inflammation | Gene expression | Cholesterol | Biological activity | Medicine | Signaling | Overexpression | Diet | Arteriosclerosis | Stem cells | Apoptosis | Veins & arteries
Journal Article
Antioxidants & Redox Signaling, ISSN 1523-0864, 11/2017, Volume 27, Issue 13, pp. 931 - 944
Aims: The pathogenic mechanisms for the higher prevalence of allergic asthma in children than in adults have not been settled. The aim of the present study is... 
Original Research Communications | Type-2 immune response | S-sulfhydration | Gasotransmitter | Asthma | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | H2S | PERSISTENT ASTHMA | CELL-FATE | asthma | HYDROGEN-SULFIDE | CHILDHOOD ASTHMA | IMMUNE-SYSTEM | ENDOCRINOLOGY & METABOLISM | gasotransmitter | K-ATP CHANNEL | AIRWAY SMOOTH-MUSCLE | BIRTH COHORT | type-2 immune response | Hydrogen Sulfide - metabolism | Fetal Blood - immunology | Leukocytes, Mononuclear - metabolism | Asthma - metabolism | Age Factors | Cytokines - metabolism | Humans | Cells, Cultured | Cystathionine gamma-Lyase - metabolism | Fetal Blood - cytology | Fetal Blood - metabolism | Asthma - chemically induced | Mice, Knockout | Animals | Gene Expression Regulation, Developmental | Leukocytes, Mononuclear - immunology | Ovalbumin - adverse effects | Asthma - immunology | Leukocytes, Mononuclear - cytology | Mice | Cystathionine gamma-Lyase - genetics | GATA3 Transcription Factor - metabolism | Cystathionine gamma-Lyase - deficiency | Disease Models, Animal | Allergy | Cysteine | Causes of | Extracellular matrix | Cellular signal transduction | Research | Allergic reaction | Sulfide | Innovations | Leukocytes (mononuclear) | Blood | Hydrogen sulfide | Proteins | Cord blood | Splenocytes | Rodents | Peripheral blood mononuclear cells | Inhibition | Children | Supplementation | Age | Immune system | Translocation | Ovalbumin | Abundance | T cell receptors | GATA-3 protein | Biomarkers | Adults | Umbilical cord | Differentiation | Hydrogen production
Journal Article
Antioxidants & Redox Signaling, ISSN 1523-0864, 01/2016, Volume 24, Issue 3, pp. 129 - 140
Aims: To investigate the regulation of hepatic glucose production by cystathionine γ-lyase (CSE)-generated hydrogen sulfide (H 2 S) in hepatic glucose... 
Original Research Communications | BINDING PROTEIN-BETA | RAT-LIVER | GLYCOGEN-METABOLISM | HEPATIC GLUCONEOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL PRIMARY CULTURES | COACTIVATOR PGC-1 | ENDOCRINOLOGY & METABOLISM | H2S | HYDROGEN-SULFIDE | ENERGY-METABOLISM | PHOSPHOENOLPYRUVATE CARBOXYKINASE GTP | Cyclic AMP-Dependent Protein Kinases - metabolism | Hydrogen Sulfide - metabolism | Receptors, Glucocorticoid - antagonists & inhibitors | CCAAT-Enhancer-Binding Protein-beta - genetics | Liver - metabolism | Carbazoles - administration & dosage | Cystathionine gamma-Lyase - metabolism | Hepatocytes - metabolism | Transcription Factors - genetics | CCAAT-Enhancer-Binding Protein-beta - metabolism | Mice, Knockout | Transcription Factors - metabolism | Animals | Cyclic AMP-Dependent Protein Kinases - genetics | Gluconeogenesis - genetics | Pyrroles - administration & dosage | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Glucose - metabolism | Mice | Cystathionine gamma-Lyase - genetics | Cyclic AMP - metabolism | Hydrogen sulfide | Genetically modified mice | Glucose metabolism | Care and treatment | Analysis | Metabolic syndrome X | Research | Health aspects | Protein kinase A | Transcription factors | Adenosine monophosphate | Glucocorticoids | Liver | Innovations | Cyclic AMP | Activation | CCAAT/enhancer-binding protein | Glucose | Metabolism | Kinases | Fructose | Proteins | Organic chemistry | Hepatocytes | Adenosine kinase | Physiology | Glucose-6-phosphatase | Metabolic disorders | Gluconeogenesis
Journal Article
Circulation, ISSN 0009-7322, 06/2013, Volume 127, Issue 25, pp. 2514 - 2522
BACKGROUND—The exact etiology of preeclampsia is unknown, but there is growing evidence of an imbalance in angiogenic growth factors and abnormal placentation.... 
fms-like tyrosine kinase-1 | placental growth factor | hydrogen sulfide | angiogenesis | vascular endothelial growth factor | preeclampsia | fetal development | CARDIAC & CARDIOVASCULAR SYSTEMS | SOLUBLE ENDOGLIN | RISK | ANGIOGENIC FACTORS | WOMEN | SERUM CONCENTRATIONS | TYROSINE KINASE-1 | PREGNANCIES | VASORELAXANT | PERIPHERAL VASCULAR DISEASE | GROWTH-FACTOR | MOUSE PLACENTA | Endothelium, Vascular - cytology | Hydrogen Sulfide - metabolism | Pregnancy Complications, Cardiovascular - physiopathology | Pregnancy, Animal | Glycine - analogs & derivatives | Glycine - adverse effects | Humans | Cystathionine gamma-Lyase - metabolism | Pregnancy Proteins - metabolism | Organothiophosphorus Compounds - pharmacology | Pre-Eclampsia - physiopathology | Antigens, CD - metabolism | Hypertension - etiology | Placenta Diseases - etiology | Young Adult | Endoglin | Pregnancy Complications, Cardiovascular - metabolism | Fetal Development - physiology | Hypertension - chemically induced | Adult | Alkynes - pharmacology | Female | Pre-Eclampsia - metabolism | Organ Culture Techniques | Disease Models, Animal | Fetal Development - drug effects | Mice, Inbred C57BL | Cells, Cultured | Morpholines - pharmacology | Receptors, Cell Surface - metabolism | Vascular Endothelial Growth Factor Receptor-1 - metabolism | Placenta Diseases - physiopathology | Hypertension - metabolism | Hydrogen Sulfide - antagonists & inhibitors | Placenta - drug effects | Placenta - metabolism | Pregnancy | Neovascularization, Physiologic - physiology | Placenta - physiopathology | Animals | Glycine - pharmacology | Endothelium, Vascular - metabolism | Adolescent | Placenta Growth Factor | Mice | Placenta Diseases - metabolism | Alkynes - adverse effects | Pregnancy Complications, Cardiovascular - etiology
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2016, Volume 11, Issue 8, p. e0160521
Journal Article
Cellular Signalling, ISSN 0898-6568, 12/2014, Volume 26, Issue 12, pp. 2801 - 2808
Journal Article
Journal Article