Archives of Toxicology, ISSN 0340-5761, 10/2019, Volume 93, Issue 10, pp. 2773 - 2785
Cadmium (Cd) is a ubiquitous environmental metal that is reported to be a “metalloestrogen.” Uterine leiomyomas (fibroids) are estrogen-responsive gynecologic...
Biomedicine, general | Cadmium | Biomedicine | Environmental Health | Uterine leiomyomas | Occupational Medicine/Industrial Medicine | GPER | ERα36 | Pharmacology/Toxicology | EGFR | Cell proliferation | Matrix metalloproteinases | Estrogens | Crosstalk | Menopause | Estrogen receptors | Matrix metalloproteinase | Epidemiology | Human tissues | Neoplasms | Risk factors | Proteins | Signal transduction | Epidermal growth factor | Pathways | Xenoestrogens | Uterus | Metalloproteinase | Pretreatment | Growth factors | Binding | Myometrium | Epidermal growth factor receptors | MAP kinase | Fibroids | Hysterectomy | Risk analysis | Src protein | Gelatinase B | Gelatinase A | Heparin
Biomedicine, general | Cadmium | Biomedicine | Environmental Health | Uterine leiomyomas | Occupational Medicine/Industrial Medicine | GPER | ERα36 | Pharmacology/Toxicology | EGFR | Cell proliferation | Matrix metalloproteinases | Estrogens | Crosstalk | Menopause | Estrogen receptors | Matrix metalloproteinase | Epidemiology | Human tissues | Neoplasms | Risk factors | Proteins | Signal transduction | Epidermal growth factor | Pathways | Xenoestrogens | Uterus | Metalloproteinase | Pretreatment | Growth factors | Binding | Myometrium | Epidermal growth factor receptors | MAP kinase | Fibroids | Hysterectomy | Risk analysis | Src protein | Gelatinase B | Gelatinase A | Heparin
Journal Article
Biochimica et biophysica acta. General subjects, ISSN 0304-4165, 12/2018, Volume 1862, Issue 12, pp. 2806 - 2814
Journal Article
Archives of toxicology, ISSN 0340-5761, 08/2019, Volume 93, Issue 10, p. 2773
Cadmium (Cd) is a ubiquitous environmental metal that is reported to be a "metalloestrogen." Uterine leiomyomas (fibroids) are estrogen-responsive gynecologic...
Leiomyoma | Cadmium | Epidermal growth factor | Analysis | Estrogen | Environmental health | Phenols | Anticoagulants (Medicine) | Cellular signal transduction | G proteins | Epidemiology | Risk factors
Leiomyoma | Cadmium | Epidermal growth factor | Analysis | Estrogen | Environmental health | Phenols | Anticoagulants (Medicine) | Cellular signal transduction | G proteins | Epidemiology | Risk factors
Journal Article
Philosophical Transactions: Biological Sciences, ISSN 0962-8436, 3/2014, Volume 369, Issue 1638, pp. 1 - 9
Humans maintain a constant cell number throughout their lifespan. This equilibrium of cell number is accomplished when cell proliferation and cell death are...
Cell growth | Cell death | HeLa cells | Chloride channels | Ion channels | Potassium channels | Neoplasia | Cells | Apoptosis | Cancer
Cell growth | Cell death | HeLa cells | Chloride channels | Ion channels | Potassium channels | Neoplasia | Cells | Apoptosis | Cancer
Journal Article
genesis, ISSN 1526-954X, 12/2014, Volume 52, Issue 12, pp. 976 - 984
Journal Article
Philosophical Transactions of the Royal Society B: Biological Sciences, ISSN 0962-8436, 03/2014, Volume 369, Issue 1638, p. 20130104
Humans maintain a constant cell number throughout their lifespan. This equilibrium of cell number is accomplished when cell proliferation and cell death are...
Ion channels | Cell death | Apoptosis | Cancer | CELL-VOLUME REGULATION | DEATH RECEPTORS | MITOCHONDRIAL POTASSIUM CHANNEL | CHLORIDE CHANNELS | cell death | apoptosis | OVARIAN-CANCER | ion channels | TUMOR-NECROSIS-FACTOR | KV1.3 CHANNELS | BIOLOGY | LEUKEMIA-CELLS | TARGETING DEATH | cancer | K+ CHANNELS | Neoplasms - metabolism | Cell Death - physiology | Ion Channels - metabolism | Necrosis - physiopathology | Models, Biological | Humans | Signal Transduction - physiology | Apoptosis - physiology | Neoplasms - physiopathology | Review
Ion channels | Cell death | Apoptosis | Cancer | CELL-VOLUME REGULATION | DEATH RECEPTORS | MITOCHONDRIAL POTASSIUM CHANNEL | CHLORIDE CHANNELS | cell death | apoptosis | OVARIAN-CANCER | ion channels | TUMOR-NECROSIS-FACTOR | KV1.3 CHANNELS | BIOLOGY | LEUKEMIA-CELLS | TARGETING DEATH | cancer | K+ CHANNELS | Neoplasms - metabolism | Cell Death - physiology | Ion Channels - metabolism | Necrosis - physiopathology | Models, Biological | Humans | Signal Transduction - physiology | Apoptosis - physiology | Neoplasms - physiopathology | Review
Journal Article
Archives of Biochemistry and Biophysics, ISSN 0003-9861, 2007, Volume 462, Issue 2, pp. 176 - 188
The loss of cell volume or cell shrinkage has been a morphological hallmark of the programmed cell death process known as apoptosis. This isotonic loss of cell...
Apoptotic volume decrease (AVD) | Volume regulation | Chloride | Sodium | Ion channels | Cell shrinkage | Potassium | Apoptosis | potassium | cell shrinkage | BIOCHEMISTRY & MOLECULAR BIOLOGY | apoptosis | ion channels | CULTURED CORTICAL-NEURONS | sodium | TUMOR-NECROSIS-FACTOR | BIOPHYSICS | apoptotic volume decrease (AVD) | chloride | ETOPOSIDE-INDUCED APOPTOSIS | X-RAY-MICROANALYSIS | DEPENDENT POTASSIUM CHANNELS | THYMOCYTE APOPTOSIS | PLASMA-MEMBRANE DEPOLARIZATION | volume regulation | SMOOTH-MUSCLE CELLS | HERG K+ CHANNEL | T-LYMPHOCYTES | Potassium - metabolism | Water-Electrolyte Balance - physiology | Oxidative Stress - physiology | Cell Size | Chlorine - metabolism | Ion Channels - physiology | Cytoprotection - physiology | Sodium - metabolism | Apoptosis Regulatory Proteins - metabolism | Ion Channel Gating - physiology | Models, Biological | Cations | Apoptosis - physiology | Ion Channels | Volume Regulation | Apoptotic Volume Decrease (AVD) | Cell Shrinkage
Apoptotic volume decrease (AVD) | Volume regulation | Chloride | Sodium | Ion channels | Cell shrinkage | Potassium | Apoptosis | potassium | cell shrinkage | BIOCHEMISTRY & MOLECULAR BIOLOGY | apoptosis | ion channels | CULTURED CORTICAL-NEURONS | sodium | TUMOR-NECROSIS-FACTOR | BIOPHYSICS | apoptotic volume decrease (AVD) | chloride | ETOPOSIDE-INDUCED APOPTOSIS | X-RAY-MICROANALYSIS | DEPENDENT POTASSIUM CHANNELS | THYMOCYTE APOPTOSIS | PLASMA-MEMBRANE DEPOLARIZATION | volume regulation | SMOOTH-MUSCLE CELLS | HERG K+ CHANNEL | T-LYMPHOCYTES | Potassium - metabolism | Water-Electrolyte Balance - physiology | Oxidative Stress - physiology | Cell Size | Chlorine - metabolism | Ion Channels - physiology | Cytoprotection - physiology | Sodium - metabolism | Apoptosis Regulatory Proteins - metabolism | Ion Channel Gating - physiology | Models, Biological | Cations | Apoptosis - physiology | Ion Channels | Volume Regulation | Apoptotic Volume Decrease (AVD) | Cell Shrinkage
Journal Article
American Journal of Physiology, ISSN 1040-0605, 09/2012, Volume 303, Issue 5, p. L413
Alveolar epithelial cells are considered to be the primary target of bleomycin-induced lung injury, leading to interstitial fibrosis. The molecular...
Antibiotics | DNA damage | Mitochondrial DNA | Physiology | Drug resistance | Cells | Apoptosis
Antibiotics | DNA damage | Mitochondrial DNA | Physiology | Drug resistance | Cells | Apoptosis
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2003, Volume 278, Issue 40, pp. 39176 - 39184
Cell shrinkage, or the loss of cell volume, is a ubiquitous characteristic of programmed cell death that is observed in all examples of apoptosis, independent...
NEURONAL APOPTOSIS | EFFLUX | INHIBITION | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEGRADATION | MECHANISMS | POTASSIUM | THYMOCYTES | CASPASE ACTIVATION | K+ CHANNELS | LYMPHOCYTES | Chromatin - metabolism | Sodium - chemistry | Jurkat Cells | Humans | Phosphatidylserines - chemistry | Nucleosomes - metabolism | Ions | Lipid Metabolism | DNA - metabolism | Sodium - metabolism | Necrosis | Potassium - chemistry | Microscopy, Confocal | Flow Cytometry | Electrophoresis, Agar Gel | Adenosine Triphosphate - metabolism | Chlorine - chemistry | Caspases - chemistry | Poly(ADP-ribose) Polymerases - chemistry | Microscopy, Fluorescence | Apoptosis
NEURONAL APOPTOSIS | EFFLUX | INHIBITION | BIOCHEMISTRY & MOLECULAR BIOLOGY | DEGRADATION | MECHANISMS | POTASSIUM | THYMOCYTES | CASPASE ACTIVATION | K+ CHANNELS | LYMPHOCYTES | Chromatin - metabolism | Sodium - chemistry | Jurkat Cells | Humans | Phosphatidylserines - chemistry | Nucleosomes - metabolism | Ions | Lipid Metabolism | DNA - metabolism | Sodium - metabolism | Necrosis | Potassium - chemistry | Microscopy, Confocal | Flow Cytometry | Electrophoresis, Agar Gel | Adenosine Triphosphate - metabolism | Chlorine - chemistry | Caspases - chemistry | Poly(ADP-ribose) Polymerases - chemistry | Microscopy, Fluorescence | Apoptosis
Journal Article
BBA - General Subjects, ISSN 0304-4165, 12/2018, Volume 1862, Issue 12, pp. 2806 - 2814
Development of resistance to chemotherapy drugs is a significant problem in treating human malignancies in the clinic. Overexpression of drug efflux proteins,...
Multi-drug resistance | Nitric Oxide | Taxol | Adriamycin | Free radical | P-gp protein | BIOCHEMISTRY & MOLECULAR BIOLOGY | ELECTRON-SPIN RESONANCE | MECHANISMS | FREE-RADICALS | SYNTHASE | ANTICANCER ACTIVITY | OVEREXPRESSION | ETOPOSIDE | BIOPHYSICS | DNA | EXPRESSION | Proteins | Anthracyclines | Nitric oxide | Drug resistance | Drug therapy | Adenosine triphosphatase | Cancer | Index Medicus
Multi-drug resistance | Nitric Oxide | Taxol | Adriamycin | Free radical | P-gp protein | BIOCHEMISTRY & MOLECULAR BIOLOGY | ELECTRON-SPIN RESONANCE | MECHANISMS | FREE-RADICALS | SYNTHASE | ANTICANCER ACTIVITY | OVEREXPRESSION | ETOPOSIDE | BIOPHYSICS | DNA | EXPRESSION | Proteins | Anthracyclines | Nitric oxide | Drug resistance | Drug therapy | Adenosine triphosphatase | Cancer | Index Medicus
Journal Article
Pflügers Archiv - European Journal of Physiology, ISSN 0031-6768, 6/2004, Volume 448, Issue 3, pp. 313 - 318
The mechanism of activation and repression of apoptosis has been a central focus of many studies examining the role of programmed cell death in both normal and...
Ion flux | Sodium | Activation | Programmed cell death | Repression | LifeSciences | Cell shrinkage | Potassium | Apoptosis | NEURONAL APOPTOSIS | PHYSIOLOGY | potassium | cell shrinkage | POTASSIUM CHANNELS | apoptosis | PROGRAMMED CELL-DEATH | sodium | NECROSIS | REGULATORY MECHANISMS | SHRINKAGE | ion flux | repression | SMOOTH-MUSCLE-CELLS | activation | programmed cell death | PLASMA-MEMBRANE DEPOLARIZATION | T-LYMPHOCYTES | K+ CHANNELS | Potassium - metabolism | Animals | Models, Biological | Homeostasis - physiology | Humans | Cell Size | Apoptosis - physiology | Sodium - metabolism | Ions - metabolism | Cells
Ion flux | Sodium | Activation | Programmed cell death | Repression | LifeSciences | Cell shrinkage | Potassium | Apoptosis | NEURONAL APOPTOSIS | PHYSIOLOGY | potassium | cell shrinkage | POTASSIUM CHANNELS | apoptosis | PROGRAMMED CELL-DEATH | sodium | NECROSIS | REGULATORY MECHANISMS | SHRINKAGE | ion flux | repression | SMOOTH-MUSCLE-CELLS | activation | programmed cell death | PLASMA-MEMBRANE DEPOLARIZATION | T-LYMPHOCYTES | K+ CHANNELS | Potassium - metabolism | Animals | Models, Biological | Homeostasis - physiology | Humans | Cell Size | Apoptosis - physiology | Sodium - metabolism | Ions - metabolism | Cells
Journal Article
Molecular and Cellular Endocrinology, ISSN 0303-7207, 03/2019, Volume 484, pp. 59 - 68
The role of ERα36 in regulating BPA's effects and its potential as a risk factor for human uterine fibroids were evaluated. BPA at low concentrations (10 μM -...
Nongenomic signaling | Bisphenol A | Leiomyoma cells | Estrogen receptor alpha36 (ERα36) | Estrogen Receptor alpha36 (ERα36)
Nongenomic signaling | Bisphenol A | Leiomyoma cells | Estrogen receptor alpha36 (ERα36) | Estrogen Receptor alpha36 (ERα36)
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 04/2003, Volume 120, Issue 4, pp. 501 - 511
It is widely believed that epithelial stem cells reside in the hair follicle bulge region. We investigated the hematopoietic stem and progenitor cell marker,...
stem cell | keratinocyte | epidermal | Epidermal | Keratinocyte | Stem cell | LABEL-RETAINING CELLS | EPIDERMAL STEM-CELLS | MOUSE | MONOCLONAL-ANTIBODY | BASAL CELLS | HEMATOPOIETIC PROGENITOR | DERMATOLOGY | IN-VITRO | GENE-EXPRESSION | SKIN | DIFFERENTIATION | Antibody Specificity | Antigens, CD34 - analysis | Integrin alpha6 - analysis | Integrin alpha6 - immunology | Mice, Inbred C57BL | Mice, Transgenic | Keratinocytes - cytology | Stem Cells - cytology | Cell Separation - methods | Keratinocytes - chemistry | Stem Cells - chemistry | Hair Follicle - cytology | Animals | Flow Cytometry | Antigens, CD34 - immunology | Cell Division | Female | Mice | Mice, Inbred BALB C | Antigens, Surface - immunology | Antigens, Surface - analysis
stem cell | keratinocyte | epidermal | Epidermal | Keratinocyte | Stem cell | LABEL-RETAINING CELLS | EPIDERMAL STEM-CELLS | MOUSE | MONOCLONAL-ANTIBODY | BASAL CELLS | HEMATOPOIETIC PROGENITOR | DERMATOLOGY | IN-VITRO | GENE-EXPRESSION | SKIN | DIFFERENTIATION | Antibody Specificity | Antigens, CD34 - analysis | Integrin alpha6 - analysis | Integrin alpha6 - immunology | Mice, Inbred C57BL | Mice, Transgenic | Keratinocytes - cytology | Stem Cells - cytology | Cell Separation - methods | Keratinocytes - chemistry | Stem Cells - chemistry | Hair Follicle - cytology | Animals | Flow Cytometry | Antigens, CD34 - immunology | Cell Division | Female | Mice | Mice, Inbred BALB C | Antigens, Surface - immunology | Antigens, Surface - analysis
Journal Article
Biochemical Pharmacology, ISSN 0006-2952, 10/2015, Volume 97, Issue 3, pp. 256 - 268
In this study, we demonstrate that treatment of T lymphoblastic leukemic Molt4 cells with farnesol activates the apoptosome via the intrinsic pathway of...
ER stress | Molt4 | Gene expression | Leukemia | Apoptosis | LUNG-CARCINOMA CELLS | RISK-FACTORS | DEATH | ENDOPLASMIC-RETICULUM STRESS | SACCHAROMYCES-CEREVISIAE | CYTOCHROME-C | UNFOLDED PROTEIN RESPONSE | SIGNALING PATHWAY | PERILLYL ALCOHOL | MOUSE MODEL | PHARMACOLOGY & PHARMACY | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - pathology | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Farnesol - pharmacology | Humans | Transcriptome - drug effects | Membrane Potential, Mitochondrial - drug effects | Activating Transcription Factor 3 - metabolism | MAP Kinase Signaling System - drug effects | Transfection | Activating Transcription Factor 4 - metabolism | Cell Line, Tumor | Cell Proliferation - drug effects | Transcription Factor CHOP - metabolism | Anticarcinogenic Agents - pharmacology | Proto-Oncogene Proteins c-bcl-2 - genetics | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Cells
ER stress | Molt4 | Gene expression | Leukemia | Apoptosis | LUNG-CARCINOMA CELLS | RISK-FACTORS | DEATH | ENDOPLASMIC-RETICULUM STRESS | SACCHAROMYCES-CEREVISIAE | CYTOCHROME-C | UNFOLDED PROTEIN RESPONSE | SIGNALING PATHWAY | PERILLYL ALCOHOL | MOUSE MODEL | PHARMACOLOGY & PHARMACY | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - pathology | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Farnesol - pharmacology | Humans | Transcriptome - drug effects | Membrane Potential, Mitochondrial - drug effects | Activating Transcription Factor 3 - metabolism | MAP Kinase Signaling System - drug effects | Transfection | Activating Transcription Factor 4 - metabolism | Cell Line, Tumor | Cell Proliferation - drug effects | Transcription Factor CHOP - metabolism | Anticarcinogenic Agents - pharmacology | Proto-Oncogene Proteins c-bcl-2 - genetics | Precursor T-Cell Lymphoblastic Leukemia-Lymphoma - metabolism | Cells
Journal Article
Molecular and Cellular Endocrinology, ISSN 0303-7207, 03/2019, Volume 484, p. 59
The role of ER[alpha]36 in regulating BPA's effects and its potential as a risk factor for human uterine fibroids were evaluated. BPA at low concentrations...
Journal Article
Journal of Immunology, ISSN 0022-1767, 04/2015, Volume 194, Issue 8, pp. 3808 - 3819
Differential display of the integrins CD103 and CD11b are widely used to distinguish two major dendritic cell (DC) subsets in nonlymphoid tissues. CD103(+) DCs...
RESPONSES | MEDIATED-IMMUNITY | CD4 T-CELLS | LYMPHOID-TISSUE | MACROPHAGES | AIRWAY INFLAMMATION | ASTHMA | MICE | IMMUNOLOGY | EXPRESSION | ANTIGEN | Receptor, Anaphylatoxin C5a - genetics | Antigens, CD - immunology | CD11b Antigen - immunology | Gene Expression Regulation - immunology | Monocytes - cytology | Dendritic Cells - immunology | Cell Proliferation - physiology | Dipeptidyl Peptidase 4 - genetics | fms-Like Tyrosine Kinase 3 - immunology | Monocytes - immunology | Antigens, CD - genetics | Mice, Knockout | Organ Specificity - immunology | fms-Like Tyrosine Kinase 3 - genetics | Organ Specificity - genetics | CD11b Antigen - genetics | Animals | Integrin alpha Chains - immunology | Receptor, Anaphylatoxin C5a - immunology | Dendritic Cells - cytology | Mice | Mice, Inbred BALB C | Dipeptidyl Peptidase 4 - immunology | Integrin alpha Chains - genetics
RESPONSES | MEDIATED-IMMUNITY | CD4 T-CELLS | LYMPHOID-TISSUE | MACROPHAGES | AIRWAY INFLAMMATION | ASTHMA | MICE | IMMUNOLOGY | EXPRESSION | ANTIGEN | Receptor, Anaphylatoxin C5a - genetics | Antigens, CD - immunology | CD11b Antigen - immunology | Gene Expression Regulation - immunology | Monocytes - cytology | Dendritic Cells - immunology | Cell Proliferation - physiology | Dipeptidyl Peptidase 4 - genetics | fms-Like Tyrosine Kinase 3 - immunology | Monocytes - immunology | Antigens, CD - genetics | Mice, Knockout | Organ Specificity - immunology | fms-Like Tyrosine Kinase 3 - genetics | Organ Specificity - genetics | CD11b Antigen - genetics | Animals | Integrin alpha Chains - immunology | Receptor, Anaphylatoxin C5a - immunology | Dendritic Cells - cytology | Mice | Mice, Inbred BALB C | Dipeptidyl Peptidase 4 - immunology | Integrin alpha Chains - genetics
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, p. e58417
CD44 is a multifunctional membrane receptor implicated in the regulation of several biological processes, including inflammation. CD44 expression is elevated...
MACROPHAGE ACCUMULATION | RECRUITMENT | OBESITY | OSTEOPONTIN | MULTIDISCIPLINARY SCIENCES | TISSUE | GENE-EXPRESSION | PROFILING REVEALS | HYALURONAN | LIVER STEATOSIS | ROR-ALPHA | Liver - enzymology | Male | Gene Expression Profiling | Body Weight - genetics | Liver - injuries | Panniculitis - genetics | Inflammation - metabolism | Lymphocytes - immunology | Diet, High-Fat | Hyaluronan Receptors - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Fatty Liver - genetics | Lymphocytes - metabolism | Fatty Liver - metabolism | Fatty Liver - prevention & control | Adiposity - genetics | CD3 Complex - metabolism | Hyaluronan Receptors - genetics | Mice, Knockout | Animals | Insulin Resistance - genetics | Inflammation - genetics | Mice | Enzyme Activation | Panniculitis - metabolism | Adipose tissues | Type 2 diabetes | Obesity | Synthesis | Diet | Liver | Genes | Insulin resistance | Triglycerides | Inflammation | Fatty acids | Matrix metalloproteinases | Adipose tissue | Lipids | Kinases | Macrophages | Accumulation | Receptors | Biomedical materials | Fatty liver | CD44 antigen | Rodents | Biocompatibility | Osteopontin | CD36 antigen | Gene expression | Insulin | Biological activity | Steatosis | Collagen | Infiltration | Metabolic disorders | Chemokines
MACROPHAGE ACCUMULATION | RECRUITMENT | OBESITY | OSTEOPONTIN | MULTIDISCIPLINARY SCIENCES | TISSUE | GENE-EXPRESSION | PROFILING REVEALS | HYALURONAN | LIVER STEATOSIS | ROR-ALPHA | Liver - enzymology | Male | Gene Expression Profiling | Body Weight - genetics | Liver - injuries | Panniculitis - genetics | Inflammation - metabolism | Lymphocytes - immunology | Diet, High-Fat | Hyaluronan Receptors - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Fatty Liver - genetics | Lymphocytes - metabolism | Fatty Liver - metabolism | Fatty Liver - prevention & control | Adiposity - genetics | CD3 Complex - metabolism | Hyaluronan Receptors - genetics | Mice, Knockout | Animals | Insulin Resistance - genetics | Inflammation - genetics | Mice | Enzyme Activation | Panniculitis - metabolism | Adipose tissues | Type 2 diabetes | Obesity | Synthesis | Diet | Liver | Genes | Insulin resistance | Triglycerides | Inflammation | Fatty acids | Matrix metalloproteinases | Adipose tissue | Lipids | Kinases | Macrophages | Accumulation | Receptors | Biomedical materials | Fatty liver | CD44 antigen | Rodents | Biocompatibility | Osteopontin | CD36 antigen | Gene expression | Insulin | Biological activity | Steatosis | Collagen | Infiltration | Metabolic disorders | Chemokines
Journal Article