Biochemical Journal, ISSN 0264-6021, 2016, Volume 473, Issue 13, pp. 1895 - 1904
GDF-15 (growth/differentiation factor 15) is a novel member of the TGF (transforming growth factor)-β superfamily that has critical roles in the central and...
TβRII | Akt/mTOR | 1.3 | GDF-15 | Ca | ERK | Nifedipine - pharmacology | Calcium Channels - metabolism | TOR Serine-Threonine Kinases - metabolism | Calcium - metabolism | Cells, Cultured | Rats | Extracellular Signal-Regulated MAP Kinases - metabolism | Calcium Channel Blockers - pharmacology | Rats, Sprague-Dawley | Animals | Signal Transduction - drug effects | Cerebellum - cytology | Growth Differentiation Factor 15 - pharmacology | Neurons - metabolism | Neurons - drug effects | Oncogene Protein v-akt - metabolism | [Ca2+]i | mTOR | Akt | Cav1.3
TβRII | Akt/mTOR | 1.3 | GDF-15 | Ca | ERK | Nifedipine - pharmacology | Calcium Channels - metabolism | TOR Serine-Threonine Kinases - metabolism | Calcium - metabolism | Cells, Cultured | Rats | Extracellular Signal-Regulated MAP Kinases - metabolism | Calcium Channel Blockers - pharmacology | Rats, Sprague-Dawley | Animals | Signal Transduction - drug effects | Cerebellum - cytology | Growth Differentiation Factor 15 - pharmacology | Neurons - metabolism | Neurons - drug effects | Oncogene Protein v-akt - metabolism | [Ca2+]i | mTOR | Akt | Cav1.3
Journal Article
European Journal of Immunology, ISSN 0014-2980, 07/2012, Volume 42, Issue 7, pp. 1796 - 1803
Notch proteins play an important role in embryonic development and cell‐fate decisions. Notch influences also the activation and differentiation of peripheral...
Immune regulation | Regulatory T cells | TGF‐βRII | Notch signaling | TGF-βRII | DOMAIN | DELTA-4 | IMMUNOSUPPRESSION | DIFFERENTIATION | LIGAND | IMMUNOLOGY | TGF-ss RII | HEMATOPOIETIC PROGENITORS | Up-Regulation | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - immunology | Humans | Transcriptional Activation | Immunoblotting | RNA - genetics | T-Lymphocytes, Regulatory - immunology | Calcium-Binding Proteins - immunology | Serrate-Jagged Proteins | Leukocytes, Mononuclear - immunology | T-Lymphocytes, Regulatory - cytology | Jagged-1 Protein | Smad Proteins - immunology | Signal Transduction | Protein-Serine-Threonine Kinases - genetics | Receptor, Notch1 - immunology | Membrane Proteins - immunology | Smad Proteins - genetics | RNA - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Basic Helix-Loop-Helix Transcription Factors - immunology | Leukocytes, Mononuclear - cytology | Protein-Serine-Threonine Kinases - immunology | Intercellular Signaling Peptides and Proteins - immunology | Life Sciences | Biochemistry, Molecular Biology
Immune regulation | Regulatory T cells | TGF‐βRII | Notch signaling | TGF-βRII | DOMAIN | DELTA-4 | IMMUNOSUPPRESSION | DIFFERENTIATION | LIGAND | IMMUNOLOGY | TGF-ss RII | HEMATOPOIETIC PROGENITORS | Up-Regulation | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - immunology | Humans | Transcriptional Activation | Immunoblotting | RNA - genetics | T-Lymphocytes, Regulatory - immunology | Calcium-Binding Proteins - immunology | Serrate-Jagged Proteins | Leukocytes, Mononuclear - immunology | T-Lymphocytes, Regulatory - cytology | Jagged-1 Protein | Smad Proteins - immunology | Signal Transduction | Protein-Serine-Threonine Kinases - genetics | Receptor, Notch1 - immunology | Membrane Proteins - immunology | Smad Proteins - genetics | RNA - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Basic Helix-Loop-Helix Transcription Factors - immunology | Leukocytes, Mononuclear - cytology | Protein-Serine-Threonine Kinases - immunology | Intercellular Signaling Peptides and Proteins - immunology | Life Sciences | Biochemistry, Molecular Biology
Journal Article
Journal of Clinical Laboratory Analysis, ISSN 0887-8013, 07/2019, Volume 33, Issue 6, pp. e22904 - n/a
Background Graves' disease (GD) is a common autoimmune disease characterized by genetic and environmental factors. Fcγ receptors (FcγRs) are involved in...
FcγRII | autoimmunity | Graves' disease | CD32B | FcγR | THYROCYTES | IIB | MONOCYTES | IMMUNOGLOBULIN | MECHANISMS | Fc gamma RII | MEMORY B-CELLS | LUPUS | DYSREGULATION | Fc gamma R | INFECTION | MEDICAL LABORATORY TECHNOLOGY | COMPLEMENT RECEPTORS | Flow cytometry | Immunoglobulins | Immune response | Therapeutic applications | Leukocytes (mononuclear) | Environmental factors | CD14 antigen | Western blotting | Monocytes | CD16 antigen | Isotypes | Peripheral blood mononuclear cells | Autoimmune diseases
FcγRII | autoimmunity | Graves' disease | CD32B | FcγR | THYROCYTES | IIB | MONOCYTES | IMMUNOGLOBULIN | MECHANISMS | Fc gamma RII | MEMORY B-CELLS | LUPUS | DYSREGULATION | Fc gamma R | INFECTION | MEDICAL LABORATORY TECHNOLOGY | COMPLEMENT RECEPTORS | Flow cytometry | Immunoglobulins | Immune response | Therapeutic applications | Leukocytes (mononuclear) | Environmental factors | CD14 antigen | Western blotting | Monocytes | CD16 antigen | Isotypes | Peripheral blood mononuclear cells | Autoimmune diseases
Journal Article
European Journal of Obstetrics & Gynecology and Reproductive Biology, ISSN 0301-2115, 2013, Volume 169, Issue 1, pp. 28 - 32
Abstract Objective First, to determine if microRNA-17 and -19b are expressed in villous samples at early stages of pregnancy. Second, to determine whether...
Obstetrics and Gynecology | Villous sample | miRNA-19b | PTEN | CREB-1 | microRNA | Early pregnancy | TGF-β1 | TGFβ-RII | miRNA-17 | TGF beta-RII | TGF-beta 1 | MIR-17-92 | CELL-PROLIFERATION | MISCARRIAGE | CANCER | OBSTETRICS & GYNECOLOGY | INVASION | REPRODUCTIVE BIOLOGY | SPONTANEOUS-ABORTION | POLYCISTRON | DIFFERENTIATION | CLUSTER | Placenta - metabolism | Pregnancy | PTEN Phosphohydrolase - genetics | Abortion, Spontaneous - genetics | Down-Regulation | Humans | Adult | Female | MicroRNAs - biosynthesis | Placentation - genetics | RNA, Messenger - metabolism | Case-Control Studies | Transforming growth factors | Pregnant women | MicroRNA
Obstetrics and Gynecology | Villous sample | miRNA-19b | PTEN | CREB-1 | microRNA | Early pregnancy | TGF-β1 | TGFβ-RII | miRNA-17 | TGF beta-RII | TGF-beta 1 | MIR-17-92 | CELL-PROLIFERATION | MISCARRIAGE | CANCER | OBSTETRICS & GYNECOLOGY | INVASION | REPRODUCTIVE BIOLOGY | SPONTANEOUS-ABORTION | POLYCISTRON | DIFFERENTIATION | CLUSTER | Placenta - metabolism | Pregnancy | PTEN Phosphohydrolase - genetics | Abortion, Spontaneous - genetics | Down-Regulation | Humans | Adult | Female | MicroRNAs - biosynthesis | Placentation - genetics | RNA, Messenger - metabolism | Case-Control Studies | Transforming growth factors | Pregnant women | MicroRNA
Journal Article
Molecular Cancer, ISSN 1476-4598, 05/2013, Volume 12, Issue 1, pp. 38 - 38
Background: Infection with high-risk human papillomavirus (HR-HPV) genotypes, mainly HPV16 and HPV18, is a major risk factor for cervical cancer and...
Human papillomavirus | SMAD | TGFβ signaling | HPV16 E5 | TGFβRII | ONCOPROTEIN | HOMEOSTASIS | PROTEIN | HUMAN-PAPILLOMAVIRUS TYPE-16 | TGF beta signaling | MESSENGER-RNA EXPRESSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | KERATINOCYTE CELL-LINE | CHROMOSOMAL INSTABILITY | TGF beta RII | ONCOLOGY | NEOPLASIA | GROWTH | INFECTION | Cervical Intraepithelial Neoplasia - pathology | Gene Expression | Signal Transduction | Humans | RNA, Messenger - genetics | Gene Expression Regulation, Neoplastic | Neoplasm Grading | Transforming Growth Factor beta - genetics | Time Factors | Cervical Intraepithelial Neoplasia - metabolism | Female | Oncogene Proteins, Viral - genetics | Cervical Intraepithelial Neoplasia - genetics | Smad Proteins - metabolism | Transforming Growth Factor beta - metabolism | Oncogene Proteins, Viral - metabolism | Viral proteins | RNA | Development and progression | Genetic aspects | Cellular signal transduction | Transforming growth factors | Papillomavirus infections | Health aspects | Risk factors | Cervical cancer | Proteins | Phosphorylation | Epidermal growth factor | Cytokines | Rodents | Homeostasis | Infections | Acquisitions & mergers | Cancer | Oncogene Proteins, Viral | Life Sciences | Smad Proteins | RNA, Messenger | Cervical Intraepithelial Neoplasia | Transforming Growth Factor beta
Human papillomavirus | SMAD | TGFβ signaling | HPV16 E5 | TGFβRII | ONCOPROTEIN | HOMEOSTASIS | PROTEIN | HUMAN-PAPILLOMAVIRUS TYPE-16 | TGF beta signaling | MESSENGER-RNA EXPRESSION | BIOCHEMISTRY & MOLECULAR BIOLOGY | KERATINOCYTE CELL-LINE | CHROMOSOMAL INSTABILITY | TGF beta RII | ONCOLOGY | NEOPLASIA | GROWTH | INFECTION | Cervical Intraepithelial Neoplasia - pathology | Gene Expression | Signal Transduction | Humans | RNA, Messenger - genetics | Gene Expression Regulation, Neoplastic | Neoplasm Grading | Transforming Growth Factor beta - genetics | Time Factors | Cervical Intraepithelial Neoplasia - metabolism | Female | Oncogene Proteins, Viral - genetics | Cervical Intraepithelial Neoplasia - genetics | Smad Proteins - metabolism | Transforming Growth Factor beta - metabolism | Oncogene Proteins, Viral - metabolism | Viral proteins | RNA | Development and progression | Genetic aspects | Cellular signal transduction | Transforming growth factors | Papillomavirus infections | Health aspects | Risk factors | Cervical cancer | Proteins | Phosphorylation | Epidermal growth factor | Cytokines | Rodents | Homeostasis | Infections | Acquisitions & mergers | Cancer | Oncogene Proteins, Viral | Life Sciences | Smad Proteins | RNA, Messenger | Cervical Intraepithelial Neoplasia | Transforming Growth Factor beta
Journal Article
Oncology Reports, ISSN 1021-335X, 01/2016, Volume 35, Issue 1, pp. 398 - 408
MicroRNAs (miRNAs), a class of small non-coding RNA molecules, are associated with a variety of human cancers. Currently, little data are available regarding...
MiR-590-5p | Microarray | Vulvar squamous cell carcinoma | TGFβRII | MiRNA | CANCER CELLS | miR-590-5p | MICRORNAS | vulvar squamous cell carcinoma | TRENDS | microarray | INVASION | TGF beta RII | INHIBITION | ONCOLOGY | PATHWAY | GROWTH | GENES | miRNA | DIFFERENTIATION | DECREASED EXPRESSION | Up-Regulation | Receptors, Transforming Growth Factor beta - genetics | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Protein-Serine-Threonine Kinases - genetics | Gene Expression Profiling - methods | Smad Proteins - genetics | Neoplasm Metastasis | Vulvar Neoplasms - pathology | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | Vulvar Neoplasms - genetics | Vulvar Neoplasms - metabolism | Aged, 80 and over | Cell Line, Tumor | Female | MicroRNAs - genetics | Protein-Serine-Threonine Kinases - metabolism
MiR-590-5p | Microarray | Vulvar squamous cell carcinoma | TGFβRII | MiRNA | CANCER CELLS | miR-590-5p | MICRORNAS | vulvar squamous cell carcinoma | TRENDS | microarray | INVASION | TGF beta RII | INHIBITION | ONCOLOGY | PATHWAY | GROWTH | GENES | miRNA | DIFFERENTIATION | DECREASED EXPRESSION | Up-Regulation | Receptors, Transforming Growth Factor beta - genetics | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Protein-Serine-Threonine Kinases - genetics | Gene Expression Profiling - methods | Smad Proteins - genetics | Neoplasm Metastasis | Vulvar Neoplasms - pathology | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | Vulvar Neoplasms - genetics | Vulvar Neoplasms - metabolism | Aged, 80 and over | Cell Line, Tumor | Female | MicroRNAs - genetics | Protein-Serine-Threonine Kinases - metabolism
Journal Article
BIOCHEMICAL JOURNAL, ISSN 0264-6021, 07/2016, Volume 473, pp. 1895 - 1904
GDF-15 (growth/differentiation factor 15) is a novel member of the TGF (transforming growth factor)-beta superfamily that has critical roles in the central and...
CELLS | SIGNALING PATHWAYS | PROTEIN | [Ca2+](i) | Ca(v)1.3 | T beta RII | BIOCHEMISTRY & MOLECULAR BIOLOGY | OUTWARD K+ CURRENT | TGF-BETA SUPERFAMILY | Akt/mTOR | GATED CALCIUM-CHANNELS | HIPPOCAMPAL-NEURONS | GDF-15 | INHIBITORY CYTOKINE-1 | IN-VIVO | NA+ CURRENT | ERK
CELLS | SIGNALING PATHWAYS | PROTEIN | [Ca2+](i) | Ca(v)1.3 | T beta RII | BIOCHEMISTRY & MOLECULAR BIOLOGY | OUTWARD K+ CURRENT | TGF-BETA SUPERFAMILY | Akt/mTOR | GATED CALCIUM-CHANNELS | HIPPOCAMPAL-NEURONS | GDF-15 | INHIBITORY CYTOKINE-1 | IN-VIVO | NA+ CURRENT | ERK
Journal Article
American Journal of Physiology - Regulatory Integrative and Comparative Physiology, ISSN 0363-6119, 07/2016, Volume 311, Issue 1, pp. R79 - R88
Adipose tissue PKA has roles in adipogenesis, lipolysis, and mitochondrial function. PKA transduces the cAMP signal downstream of G protein-coupled receptors,...
Protein kinase A | Energy expenditure | Adipose | Uncoupling protein 1 | PHYSIOLOGY | GLUCOSE CONTROL | BROWN ADIPOCYTES | TISSUE | RII-BETA-SUBUNIT | CELL-SIZE | adipose | ADULT HUMANS | energy expenditure | uncoupling protein 1 | CYCLIC-AMP | WHITE FAT | OBESITY | GENE-EXPRESSION | protein kinase A | Uncoupling Protein 1 - drug effects | Cyclic AMP-Dependent Protein Kinases - pharmacology | Mice, Inbred C57BL | Insulin Resistance | Adipose Tissue, White - metabolism | Glucose Intolerance | Uncoupling Protein 1 - biosynthesis | Adipose Tissue - metabolism | Insulin-Secreting Cells - metabolism | Animals | Cyclic AMP-Dependent Protein Kinases - genetics | Adiposity | Adiponectin - genetics | Diet, High-Fat | Adiponectin - metabolism | Adipose Tissue, Brown - metabolism | Mice | Energy Metabolism - physiology | Health Status | Weight Gain | Adipose tissues | Physiological aspects | Metabolism | Observations | Protein kinases | Obesity, Diabetes and Energy Homeostasis
Protein kinase A | Energy expenditure | Adipose | Uncoupling protein 1 | PHYSIOLOGY | GLUCOSE CONTROL | BROWN ADIPOCYTES | TISSUE | RII-BETA-SUBUNIT | CELL-SIZE | adipose | ADULT HUMANS | energy expenditure | uncoupling protein 1 | CYCLIC-AMP | WHITE FAT | OBESITY | GENE-EXPRESSION | protein kinase A | Uncoupling Protein 1 - drug effects | Cyclic AMP-Dependent Protein Kinases - pharmacology | Mice, Inbred C57BL | Insulin Resistance | Adipose Tissue, White - metabolism | Glucose Intolerance | Uncoupling Protein 1 - biosynthesis | Adipose Tissue - metabolism | Insulin-Secreting Cells - metabolism | Animals | Cyclic AMP-Dependent Protein Kinases - genetics | Adiposity | Adiponectin - genetics | Diet, High-Fat | Adiponectin - metabolism | Adipose Tissue, Brown - metabolism | Mice | Energy Metabolism - physiology | Health Status | Weight Gain | Adipose tissues | Physiological aspects | Metabolism | Observations | Protein kinases | Obesity, Diabetes and Energy Homeostasis
Journal Article
Breast Cancer Research and Treatment, ISSN 0167-6806, 1/2015, Volume 149, Issue 2, pp. 467 - 477
Perturbations of transforming growth factor-beta (TGF-β) signaling are pivotal to tumorigenesis and tumor progression through their effects on cell...
TGF-βRII | Prognosis | Medicine & Public Health | TGF-β signaling | pSmad2 | Oncology | Breast cancer | MOLECULAR CHARACTERIZATION | SMAD2 | CELLS | LOCALIZATION | RECOGNITION | PHOSPHORYLATION | MICROSATELLITE INSTABILITY | TGF-beta RII | INACTIVATION | TGF-beta signaling | ONCOLOGY | II RECEPTOR | KINASE RECEPTOR | Immunohistochemistry | Gene Expression | Receptors, Transforming Growth Factor beta - genetics | Humans | Middle Aged | Risk Factors | Protein-Serine-Threonine Kinases - genetics | Smad2 Protein - metabolism | Cytoplasm - metabolism | Tumor Burden | Breast Neoplasms - metabolism | Breast Neoplasms - therapy | Neoplasm Grading | Receptors, Transforming Growth Factor beta - metabolism | Breast Neoplasms - pathology | China | Smad2 Protein - genetics | Adult | Breast Neoplasms - mortality | Female | Aged | Neoplasm Staging | Protein-Serine-Threonine Kinases - metabolism
TGF-βRII | Prognosis | Medicine & Public Health | TGF-β signaling | pSmad2 | Oncology | Breast cancer | MOLECULAR CHARACTERIZATION | SMAD2 | CELLS | LOCALIZATION | RECOGNITION | PHOSPHORYLATION | MICROSATELLITE INSTABILITY | TGF-beta RII | INACTIVATION | TGF-beta signaling | ONCOLOGY | II RECEPTOR | KINASE RECEPTOR | Immunohistochemistry | Gene Expression | Receptors, Transforming Growth Factor beta - genetics | Humans | Middle Aged | Risk Factors | Protein-Serine-Threonine Kinases - genetics | Smad2 Protein - metabolism | Cytoplasm - metabolism | Tumor Burden | Breast Neoplasms - metabolism | Breast Neoplasms - therapy | Neoplasm Grading | Receptors, Transforming Growth Factor beta - metabolism | Breast Neoplasms - pathology | China | Smad2 Protein - genetics | Adult | Breast Neoplasms - mortality | Female | Aged | Neoplasm Staging | Protein-Serine-Threonine Kinases - metabolism
Journal Article
Experimental Cell Research, ISSN 0014-4827, 01/2018, Volume 362, Issue 1, pp. 121 - 131
Two different types of FcRs for IgG are constitutively expressed on the surface of human neutrophils, namely, FcγRIIA (CD32a) and FcγRIIIB (CD16b). Unlike...
Shp-2 | CD16b | Neutrophil | CD32a | SIGNAL-TRANSDUCTION PATHWAYS | RESPIRATORY BURST | PHAGOCYTOSIS | CHEMOKINES | DISTINCT | INVOLVEMENT | RECEPTOR | TYROSINE PHOSPHATASES | CELL BIOLOGY | FC-GAMMA-RII | ONCOLOGY | KINASE ACTIVATION | Phosphorylation - physiology | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - metabolism | Cyclodextrins - metabolism | Cytokines - metabolism | Membrane Microdomains - metabolism | Humans | GPI-Linked Proteins - metabolism | Receptors, IgG - metabolism | Syk Kinase - metabolism | Adult | Signal Transduction - physiology | Apoptosis - physiology | Neutrophils - metabolism
Shp-2 | CD16b | Neutrophil | CD32a | SIGNAL-TRANSDUCTION PATHWAYS | RESPIRATORY BURST | PHAGOCYTOSIS | CHEMOKINES | DISTINCT | INVOLVEMENT | RECEPTOR | TYROSINE PHOSPHATASES | CELL BIOLOGY | FC-GAMMA-RII | ONCOLOGY | KINASE ACTIVATION | Phosphorylation - physiology | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - metabolism | Cyclodextrins - metabolism | Cytokines - metabolism | Membrane Microdomains - metabolism | Humans | GPI-Linked Proteins - metabolism | Receptors, IgG - metabolism | Syk Kinase - metabolism | Adult | Signal Transduction - physiology | Apoptosis - physiology | Neutrophils - metabolism
Journal Article
Tumor Biology, ISSN 1010-4283, 6/2015, Volume 36, Issue 6, pp. 4819 - 4824
Lung cancer is the leading cause of cancer-related death worldwide. Transforming growth factor-β receptor II (TGF-βRII) plays an important role in the...
Cancer Research | Biomedicine | TGF-βRII | A549 cells | Simvastatin | ERK | APOPTOSIS | ACTIVATION | TGF-beta RII | RECEPTOR | SUPPRESSION | STATINS | FAMILY | ONCOLOGY | PATHWAY | GROWTH | PROMOTES | Lung Neoplasms - genetics | Cell Survival - drug effects | Lung Neoplasms - drug therapy | Receptors, Transforming Growth Factor beta - genetics | Simvastatin - administration & dosage | Humans | Protein-Serine-Threonine Kinases - genetics | Lung Neoplasms - pathology | Sesquiterpenes - administration & dosage | Extracellular Signal-Regulated MAP Kinases - biosynthesis | Extracellular Signal-Regulated MAP Kinases - genetics | Protein-Serine-Threonine Kinases - biosynthesis | Receptors, Transforming Growth Factor beta - biosynthesis | Cell Line, Tumor | Cell Proliferation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Polyisoprenyl Phosphates - administration & dosage
Cancer Research | Biomedicine | TGF-βRII | A549 cells | Simvastatin | ERK | APOPTOSIS | ACTIVATION | TGF-beta RII | RECEPTOR | SUPPRESSION | STATINS | FAMILY | ONCOLOGY | PATHWAY | GROWTH | PROMOTES | Lung Neoplasms - genetics | Cell Survival - drug effects | Lung Neoplasms - drug therapy | Receptors, Transforming Growth Factor beta - genetics | Simvastatin - administration & dosage | Humans | Protein-Serine-Threonine Kinases - genetics | Lung Neoplasms - pathology | Sesquiterpenes - administration & dosage | Extracellular Signal-Regulated MAP Kinases - biosynthesis | Extracellular Signal-Regulated MAP Kinases - genetics | Protein-Serine-Threonine Kinases - biosynthesis | Receptors, Transforming Growth Factor beta - biosynthesis | Cell Line, Tumor | Cell Proliferation - drug effects | Gene Expression Regulation, Neoplastic - drug effects | Polyisoprenyl Phosphates - administration & dosage
Journal Article
Parasites and Vectors, ISSN 1756-3305, 05/2016, Volume 9, Issue 1, p. 278
Background: Echinococcus granulosus infection causes cystic echinococcosis (CE); the generation of liver fibrosis around the parasitic larval cyst...
HSC | miR-19 | TβRII | Liver fibrosis | Echinococcus granulosus | MECHANISM | T beta RII | MICRORNAS | TROPICAL MEDICINE | HEPATIC STELLATE CELLS | GROWTH | MICE | INFECTION | IN-VIVO TREATMENT | PROGRESSION | PARASITOLOGY | Liver - pathology | Humans | Middle Aged | Cells, Cultured | Cyst Fluid - physiology | Hepatic Stellate Cells - metabolism | Cystic Fibrosis - parasitology | Male | Gene Expression Regulation - drug effects | Young Adult | Animals | Echinococcus - physiology | Liver Cirrhosis - parasitology | MicroRNAs - drug effects | Adult | Female | Cell Proliferation - drug effects | MicroRNAs - genetics | Echinococcosis - parasitology | Hepatic Stellate Cells - drug effects | Complications and side effects | Liver diseases | MicroRNA | Fibrosis | Development and progression | Genetic aspects | Properties | Gene expression | Health aspects | Echinococcosis
HSC | miR-19 | TβRII | Liver fibrosis | Echinococcus granulosus | MECHANISM | T beta RII | MICRORNAS | TROPICAL MEDICINE | HEPATIC STELLATE CELLS | GROWTH | MICE | INFECTION | IN-VIVO TREATMENT | PROGRESSION | PARASITOLOGY | Liver - pathology | Humans | Middle Aged | Cells, Cultured | Cyst Fluid - physiology | Hepatic Stellate Cells - metabolism | Cystic Fibrosis - parasitology | Male | Gene Expression Regulation - drug effects | Young Adult | Animals | Echinococcus - physiology | Liver Cirrhosis - parasitology | MicroRNAs - drug effects | Adult | Female | Cell Proliferation - drug effects | MicroRNAs - genetics | Echinococcosis - parasitology | Hepatic Stellate Cells - drug effects | Complications and side effects | Liver diseases | MicroRNA | Fibrosis | Development and progression | Genetic aspects | Properties | Gene expression | Health aspects | Echinococcosis
Journal Article
Experimental Cell Research, ISSN 0014-4827, 09/2014, Volume 327, Issue 1, pp. 24 - 36
The role of EGF and TGF-β1 in thyroid cancer is still not clearly defined. TGF-β1 inhibited the cellular growth and migration of follicular (FTC-133) and...
TGF-β1 | TβRII | ErbB receptors | Human thyroid carcinoma | EGF | Receptor, Epidermal Growth Factor - genetics | Receptors, Transforming Growth Factor beta - genetics | Cell Proliferation | Epidermal Growth Factor - genetics | Gene Expression - genetics | Humans | Middle Aged | RNA, Messenger - genetics | Protein-Serine-Threonine Kinases - genetics | Male | Transforming Growth Factor beta1 - genetics | Cell Movement - genetics | Young Adult | Thyroid Neoplasms - genetics | Cell Line, Tumor | Adult | Carcinoma - genetics | Female | Aged | Cadherins - genetics | MESSENGER-RNA | PHENOTYPE | THYROID | CELL PROLIFERATION | ANIMAL TISSUES | RECEPTORS | 60 APPLIED LIFE SCIENCES | ADENOMAS | HEMATOXYLIN | PLANT GROWTH
TGF-β1 | TβRII | ErbB receptors | Human thyroid carcinoma | EGF | Receptor, Epidermal Growth Factor - genetics | Receptors, Transforming Growth Factor beta - genetics | Cell Proliferation | Epidermal Growth Factor - genetics | Gene Expression - genetics | Humans | Middle Aged | RNA, Messenger - genetics | Protein-Serine-Threonine Kinases - genetics | Male | Transforming Growth Factor beta1 - genetics | Cell Movement - genetics | Young Adult | Thyroid Neoplasms - genetics | Cell Line, Tumor | Adult | Carcinoma - genetics | Female | Aged | Cadherins - genetics | MESSENGER-RNA | PHENOTYPE | THYROID | CELL PROLIFERATION | ANIMAL TISSUES | RECEPTORS | 60 APPLIED LIFE SCIENCES | ADENOMAS | HEMATOXYLIN | PLANT GROWTH
Journal Article
Life Sciences, ISSN 0024-3205, 08/2015, Volume 134, Issue 1, pp. 63 - 67
A variety of evidence suggests that vitamin D can prevent the development of multiple sclerosis (MS). TGF-β pathway genes also play important roles in MS....
Multiple sclerosis | TGF-β2 | TGF-βRII | Vitamin D | TGF-βRI | Tgf-β2 tgf-βri tgf-βrii multiple sclerosis vitamin D | Humans | Middle Aged | Gene Expression Regulation | Male | Transforming Growth Factor beta2 - biosynthesis | Protein-Serine-Threonine Kinases - biosynthesis | RNA, Messenger - biosynthesis | Receptors, Transforming Growth Factor beta - biosynthesis | Multiple Sclerosis - pathology | Adult | Female | Vitamin D - metabolism | Real-Time Polymerase Chain Reaction | Multiple Sclerosis - metabolism
Multiple sclerosis | TGF-β2 | TGF-βRII | Vitamin D | TGF-βRI | Tgf-β2 tgf-βri tgf-βrii multiple sclerosis vitamin D | Humans | Middle Aged | Gene Expression Regulation | Male | Transforming Growth Factor beta2 - biosynthesis | Protein-Serine-Threonine Kinases - biosynthesis | RNA, Messenger - biosynthesis | Receptors, Transforming Growth Factor beta - biosynthesis | Multiple Sclerosis - pathology | Adult | Female | Vitamin D - metabolism | Real-Time Polymerase Chain Reaction | Multiple Sclerosis - metabolism
Journal Article
LIFE SCIENCES, ISSN 0024-3205, 08/2015, Volume 134, pp. 63 - 67
Aim: A variety of evidence suggests that vitamin D can prevent the development of multiple sclerosis (MS). TGF-beta pathway genes also play important roles in...
SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | TGF-beta 2 | Multiple sclerosis | SIGNALING PATHWAYS | INCREASES | TGF-beta RII | DERMAL PAPILLA CELLS | TGF-beta RI | ELEMENT | Vitamin D | GENE-EXPRESSION | PHARMACOLOGY & PHARMACY | 1,25-DIHYDROXYVITAMIN D-3 | D-RECEPTOR | DIFFERENTIATION | INHIBITOR
SURVIVAL | MEDICINE, RESEARCH & EXPERIMENTAL | TGF-beta 2 | Multiple sclerosis | SIGNALING PATHWAYS | INCREASES | TGF-beta RII | DERMAL PAPILLA CELLS | TGF-beta RI | ELEMENT | Vitamin D | GENE-EXPRESSION | PHARMACOLOGY & PHARMACY | 1,25-DIHYDROXYVITAMIN D-3 | D-RECEPTOR | DIFFERENTIATION | INHIBITOR
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2013, Volume 8, Issue 4, p. e62851
CD23, the low affinity receptor for immunoglobulin E (IgE), has been proposed to play a critical role in the regulation of IgE production, based on altered IgE...
B-CELL DEVELOPMENT | GENETIC-VARIATION | MULTIDISCIPLINARY SCIENCES | MOUSE | LYMPHOCYTE RECEPTOR | MICE | 129/SVJ | C57BL/6 | Amyloid Precursor Protein Secretases - genetics | Spleen - immunology | Immunoglobulin E - biosynthesis | Open Reading Frames | Male | Mice, 129 Strain | RNA, Messenger - metabolism | Immunoglobulin E - blood | Female | Membrane Proteins - metabolism | B-Lymphocytes - metabolism | Membrane Proteins - genetics | Mice, Inbred C57BL | RNA, Messenger - genetics | ADAM10 Protein | Mice, Transgenic | Spleen - cytology | Receptors, IgE - genetics | Chromosomes, Mammalian | Mice, Knockout | ADAM Proteins - metabolism | Amyloid Precursor Protein Secretases - metabolism | Phenotype | Animals | B-Lymphocytes - immunology | Receptors, IgE - metabolism | Intracellular Space - metabolism | Mice | Mutation | ADAM Proteins - genetics | RNA | Analysis | Genes | Immunoglobulin E | Genetic aspects | B cells | Flow cytometry | Animal models | Immunoglobulins | Transgenic mice | Rheumatology | Inflammation | Gene expression | Blood | Immunology | CD23 antigen | Lymphocytes B | Rodents | Chromosome 8 | Lectins | Laboratory animals | Klinisk medicin | mice | mutagenesis | lymphocyte | Clinical Medicine | mouse | murine cd23 | immunoglobulin-e | receptor | hyper ige | fc-epsilon-rii | b-cell development | genetic-variation
B-CELL DEVELOPMENT | GENETIC-VARIATION | MULTIDISCIPLINARY SCIENCES | MOUSE | LYMPHOCYTE RECEPTOR | MICE | 129/SVJ | C57BL/6 | Amyloid Precursor Protein Secretases - genetics | Spleen - immunology | Immunoglobulin E - biosynthesis | Open Reading Frames | Male | Mice, 129 Strain | RNA, Messenger - metabolism | Immunoglobulin E - blood | Female | Membrane Proteins - metabolism | B-Lymphocytes - metabolism | Membrane Proteins - genetics | Mice, Inbred C57BL | RNA, Messenger - genetics | ADAM10 Protein | Mice, Transgenic | Spleen - cytology | Receptors, IgE - genetics | Chromosomes, Mammalian | Mice, Knockout | ADAM Proteins - metabolism | Amyloid Precursor Protein Secretases - metabolism | Phenotype | Animals | B-Lymphocytes - immunology | Receptors, IgE - metabolism | Intracellular Space - metabolism | Mice | Mutation | ADAM Proteins - genetics | RNA | Analysis | Genes | Immunoglobulin E | Genetic aspects | B cells | Flow cytometry | Animal models | Immunoglobulins | Transgenic mice | Rheumatology | Inflammation | Gene expression | Blood | Immunology | CD23 antigen | Lymphocytes B | Rodents | Chromosome 8 | Lectins | Laboratory animals | Klinisk medicin | mice | mutagenesis | lymphocyte | Clinical Medicine | mouse | murine cd23 | immunoglobulin-e | receptor | hyper ige | fc-epsilon-rii | b-cell development | genetic-variation
Journal Article