Nature Immunology, ISSN 1529-2908, 11/2012, Volume 13, Issue 11, pp. 1092 - 1100
Germinal centers (GCs) are sites of intense B cell proliferation and are central for T cell dependent antibody responses. However, the role of c-Myc, a key...
PROTOONCOGENE EXPRESSION | SEQUESTRATION | PATHOGENESIS | CENTER B-CELLS | RESPONSES | ORIGIN | BCL6 | GENE-EXPRESSION | DIFFERENTIATION | IMMUNOLOGY | TRANSCRIPTION FACTOR | Cell Cycle - genetics | Green Fluorescent Proteins | Translocation, Genetic | Cell Proliferation | Germinal Center - immunology | Genetic Loci | Lymphoma - metabolism | Signal Transduction - immunology | T-Lymphocytes - metabolism | Cell Transformation, Neoplastic - genetics | Cell Cycle - immunology | Gene Deletion | B-Lymphocyte Subsets - immunology | Lymphoma - pathology | B-Lymphocytes - pathology | T-Lymphocytes - pathology | B-Lymphocytes - metabolism | Genes, Reporter | Gene Expression Regulation - immunology | Lymphoma - genetics | Proto-Oncogene Proteins c-myc - immunology | Mice, Transgenic | Signal Transduction - genetics | Germinal Center - pathology | Cell Transformation, Neoplastic - immunology | Animals | B-Lymphocytes - immunology | Germinal Center - metabolism | Proto-Oncogene Proteins c-myc - deficiency | T-Lymphocytes - immunology | Mice | Proto-Oncogene Proteins c-myc - genetics | Immunization | Care and treatment | Cell cycle | Development and progression | Genetic aspects | Lymphomas | Research | Genetic transcription | Genetic regulation
PROTOONCOGENE EXPRESSION | SEQUESTRATION | PATHOGENESIS | CENTER B-CELLS | RESPONSES | ORIGIN | BCL6 | GENE-EXPRESSION | DIFFERENTIATION | IMMUNOLOGY | TRANSCRIPTION FACTOR | Cell Cycle - genetics | Green Fluorescent Proteins | Translocation, Genetic | Cell Proliferation | Germinal Center - immunology | Genetic Loci | Lymphoma - metabolism | Signal Transduction - immunology | T-Lymphocytes - metabolism | Cell Transformation, Neoplastic - genetics | Cell Cycle - immunology | Gene Deletion | B-Lymphocyte Subsets - immunology | Lymphoma - pathology | B-Lymphocytes - pathology | T-Lymphocytes - pathology | B-Lymphocytes - metabolism | Genes, Reporter | Gene Expression Regulation - immunology | Lymphoma - genetics | Proto-Oncogene Proteins c-myc - immunology | Mice, Transgenic | Signal Transduction - genetics | Germinal Center - pathology | Cell Transformation, Neoplastic - immunology | Animals | B-Lymphocytes - immunology | Germinal Center - metabolism | Proto-Oncogene Proteins c-myc - deficiency | T-Lymphocytes - immunology | Mice | Proto-Oncogene Proteins c-myc - genetics | Immunization | Care and treatment | Cell cycle | Development and progression | Genetic aspects | Lymphomas | Research | Genetic transcription | Genetic regulation
Journal Article
BMC Cancer, ISSN 1471-2407, 2016, Volume 16, Issue 1
The single hotspot mutation AKT1 [G49A:E17K] has been described in several cancers, with the highest incidence observed in breast cancer. However, its precise...
mutation | AKT1 | Breast cancer | Blood-based mutation detection | Complications and side effects | Care and treatment | Gene mutations | Menopause | Metastasis | Diagnosis | Research | Health aspects
mutation | AKT1 | Breast cancer | Blood-based mutation detection | Complications and side effects | Care and treatment | Gene mutations | Menopause | Metastasis | Diagnosis | Research | Health aspects
Journal Article
Nature Medicine, ISSN 1078-8956, 05/2010, Volume 16, Issue 5, pp. 571 - 579
Mammalian genomes contain many repetitive elements, including long terminal repeats (LTRs), which have long been suspected to have a role in tumorigenesis....
MEDICINE, RESEARCH & EXPERIMENTAL | REED-STERNBERG CELLS | DNA HYPOMETHYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECEPTOR | KAPPA-B | STIMULATING FACTOR-I | CELL BIOLOGY | BREAST-CANCER | B-CELLS | DIFFERENTIAL TRANSCRIPTION | GENE | HODGKIN LYMPHOMA | Gene Expression | Tumor Suppressor Proteins - metabolism | Hodgkin Disease - genetics | Humans | Lymphoma - genetics | Repressor Proteins - genetics | Phosphoproteins - genetics | Colony-Stimulating Factors - genetics | Lymphoma, B-Cell - genetics | Phosphoproteins - metabolism | Proto-Oncogenes - genetics | Tumor Suppressor Proteins - genetics | Macrophage Colony-Stimulating Factor - genetics | Terminal Repeat Sequences | Repressor Proteins - metabolism | Development and progression | Lymphomas | Genetic aspects | Research | Gene expression | Health aspects | Oncogenes | Medical research | Cellular biology | Genomics
MEDICINE, RESEARCH & EXPERIMENTAL | REED-STERNBERG CELLS | DNA HYPOMETHYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECEPTOR | KAPPA-B | STIMULATING FACTOR-I | CELL BIOLOGY | BREAST-CANCER | B-CELLS | DIFFERENTIAL TRANSCRIPTION | GENE | HODGKIN LYMPHOMA | Gene Expression | Tumor Suppressor Proteins - metabolism | Hodgkin Disease - genetics | Humans | Lymphoma - genetics | Repressor Proteins - genetics | Phosphoproteins - genetics | Colony-Stimulating Factors - genetics | Lymphoma, B-Cell - genetics | Phosphoproteins - metabolism | Proto-Oncogenes - genetics | Tumor Suppressor Proteins - genetics | Macrophage Colony-Stimulating Factor - genetics | Terminal Repeat Sequences | Repressor Proteins - metabolism | Development and progression | Lymphomas | Genetic aspects | Research | Gene expression | Health aspects | Oncogenes | Medical research | Cellular biology | Genomics
Journal Article
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 2606 - 2606
Journal Article
JAMA Neurology, ISSN 2168-6149, 03/2014, Volume 71, Issue 3, pp. 306 - 314
IMPORTANCE It remains unclear whether vitamin D insufficiency, which is common in individuals with multiple sclerosis (MS), has an adverse effect on MS...
GENETIC-DETERMINANTS | RELAPSE RISK | 25-HYDROXYVITAMIN D | DOUBLE-BLIND | INTERFERON BETA-1B | CLINICALLY ISOLATED SYNDROMES | PLACEBO-CONTROLLED TRIAL | DIAGNOSTIC-CRITERIA | AUTOIMMUNE ENCEPHALOMYELITIS | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | Predictive Value of Tests | Recurrence | Demyelinating Diseases - blood | Follow-Up Studies | Multiple Sclerosis - blood | Humans | Risk Factors | Male | Biomarkers - blood | Disease Progression | Randomized Controlled Trials as Topic | Vitamin D - blood | Magnetic Resonance Imaging | Time Factors | Multiple Sclerosis - pathology | Adult | Female | Vitamin D - analogs & derivatives | Demyelinating Diseases - pathology | Demyelinating Diseases - drug therapy | Multiple Sclerosis - drug therapy | Life Sciences | Neurons and Cognition
GENETIC-DETERMINANTS | RELAPSE RISK | 25-HYDROXYVITAMIN D | DOUBLE-BLIND | INTERFERON BETA-1B | CLINICALLY ISOLATED SYNDROMES | PLACEBO-CONTROLLED TRIAL | DIAGNOSTIC-CRITERIA | AUTOIMMUNE ENCEPHALOMYELITIS | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | Predictive Value of Tests | Recurrence | Demyelinating Diseases - blood | Follow-Up Studies | Multiple Sclerosis - blood | Humans | Risk Factors | Male | Biomarkers - blood | Disease Progression | Randomized Controlled Trials as Topic | Vitamin D - blood | Magnetic Resonance Imaging | Time Factors | Multiple Sclerosis - pathology | Adult | Female | Vitamin D - analogs & derivatives | Demyelinating Diseases - pathology | Demyelinating Diseases - drug therapy | Multiple Sclerosis - drug therapy | Life Sciences | Neurons and Cognition
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2016, Volume 113, Issue 18, pp. 5065 - 5070
Although canonical NF-κB signaling is crucial to generate a normal mature B-cell compartment, its role in the persistence of resting mature B cells is...
SURVIVAL | RECEPTOR SIGNALS | follicular B cells | ACTIVATION | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | IMMUNOGLOBULIN | canonical signaling | PROLIFERATION | MAINTENANCE | NF-kappa B | persistence | MICE | EXPRESSION | LYMPHOCYTES | Signal Transduction - immunology | B-Lymphocytes - cytology | Animals | B-Lymphocytes - immunology | Mice, Inbred C57BL | Cells, Cultured | NF-kappa B - immunology | Mice | Cell Survival - immunology | Biological Sciences | NF-κB
SURVIVAL | RECEPTOR SIGNALS | follicular B cells | ACTIVATION | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | IMMUNOGLOBULIN | canonical signaling | PROLIFERATION | MAINTENANCE | NF-kappa B | persistence | MICE | EXPRESSION | LYMPHOCYTES | Signal Transduction - immunology | B-Lymphocytes - cytology | Animals | B-Lymphocytes - immunology | Mice, Inbred C57BL | Cells, Cultured | NF-kappa B - immunology | Mice | Cell Survival - immunology | Biological Sciences | NF-κB
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 12/2017, Volume 35, Issue 35, pp. 3898 - 3905
PurposePhosphatidylinositol 3-kinase (PI3K) signaling is critical for the proliferation and survival of malignant B cells. Copanlisib, a pan-class I PI3K...
BAY 80-6946 | ADVANCED SOLID TUMORS | PI3K-DELTA | RESPONSE CRITERIA | ONCOLOGY | IDELALISIB | PI3K INHIBITORS | 1ST-IN-HUMAN PHASE-I | CHRONIC LYMPHOCYTIC-LEUKEMIA | MALIGNANCIES | FOLLICULAR LYMPHOMA | Isoenzymes | Phosphatidylinositol 3-Kinase - antagonists & inhibitors | Humans | Middle Aged | Transcriptome | Male | Protein Kinase Inhibitors - adverse effects | Lymphoma, B-Cell - genetics | Protein Kinase Inhibitors - therapeutic use | Pyrimidines - therapeutic use | Quinazolines - therapeutic use | Lymphoma, B-Cell - enzymology | Pyrimidines - adverse effects | Quinazolines - adverse effects | Aged, 80 and over | Adult | Female | Aged | Lymphoma, B-Cell - drug therapy | Index Medicus
BAY 80-6946 | ADVANCED SOLID TUMORS | PI3K-DELTA | RESPONSE CRITERIA | ONCOLOGY | IDELALISIB | PI3K INHIBITORS | 1ST-IN-HUMAN PHASE-I | CHRONIC LYMPHOCYTIC-LEUKEMIA | MALIGNANCIES | FOLLICULAR LYMPHOMA | Isoenzymes | Phosphatidylinositol 3-Kinase - antagonists & inhibitors | Humans | Middle Aged | Transcriptome | Male | Protein Kinase Inhibitors - adverse effects | Lymphoma, B-Cell - genetics | Protein Kinase Inhibitors - therapeutic use | Pyrimidines - therapeutic use | Quinazolines - therapeutic use | Lymphoma, B-Cell - enzymology | Pyrimidines - adverse effects | Quinazolines - adverse effects | Aged, 80 and over | Adult | Female | Aged | Lymphoma, B-Cell - drug therapy | Index Medicus
Journal Article
Gastroenterology, ISSN 0016-5085, 05/2019, Volume 156, Issue 6, pp. 1731 - 1741
In a phase 3 trial (RESORCE), regorafenib increased overall survival compared with placebo in patients with hepatocellular carcinoma (HCC) previously treated...
Time to Progression | NGS | Predictive | Prognostic Factor | ANGIOGENESIS | CLASSIFICATION | MUTATIONS | SORAFENIB | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | VEGFA | Development and progression | Care and treatment | Hepatoma | Biological markers | Analysis | Blood proteins
Time to Progression | NGS | Predictive | Prognostic Factor | ANGIOGENESIS | CLASSIFICATION | MUTATIONS | SORAFENIB | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | VEGFA | Development and progression | Care and treatment | Hepatoma | Biological markers | Analysis | Blood proteins
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2014, Volume 111, Issue 42, pp. E4513 - E4522
Deregulated transcription factor (TF) activities are commonly observed in hematopoietic malignancies. Understanding tumorigenesis therefore requires...
SYSTEM | FACTOR-BINDING | ACTIVATION | MULTIDISCIPLINARY SCIENCES | GENE-REGULATION | INDUCTION | NF-KAPPA-B | EXPRESSION | STERNBERG CELLS | T-CELLS | GENOME | Chromatin - metabolism | Oligonucleotide Array Sequence Analysis | Hodgkin Disease - genetics | Humans | Gene Expression Regulation, Neoplastic | Interferon Regulatory Factors - metabolism | NF-kappa B - metabolism | Gene Expression Profiling | Transcription Factor AP-1 - metabolism | Lymphoma - metabolism | B-Lymphocytes - cytology | Cytokines - metabolism | Hodgkin Disease - metabolism | Inflammation | Spleen - cytology | Chemotaxis | Plasmids - metabolism | Amino Acid Motifs | Cell Lineage | Deoxyribonuclease I - metabolism | Animals | Lymphoma, Non-Hodgkin - metabolism | Cell Line, Tumor | Leukocytes, Mononuclear - cytology | Chemokines - metabolism | Mice | PNAS Plus | Biological Sciences
SYSTEM | FACTOR-BINDING | ACTIVATION | MULTIDISCIPLINARY SCIENCES | GENE-REGULATION | INDUCTION | NF-KAPPA-B | EXPRESSION | STERNBERG CELLS | T-CELLS | GENOME | Chromatin - metabolism | Oligonucleotide Array Sequence Analysis | Hodgkin Disease - genetics | Humans | Gene Expression Regulation, Neoplastic | Interferon Regulatory Factors - metabolism | NF-kappa B - metabolism | Gene Expression Profiling | Transcription Factor AP-1 - metabolism | Lymphoma - metabolism | B-Lymphocytes - cytology | Cytokines - metabolism | Hodgkin Disease - metabolism | Inflammation | Spleen - cytology | Chemotaxis | Plasmids - metabolism | Amino Acid Motifs | Cell Lineage | Deoxyribonuclease I - metabolism | Animals | Lymphoma, Non-Hodgkin - metabolism | Cell Line, Tumor | Leukocytes, Mononuclear - cytology | Chemokines - metabolism | Mice | PNAS Plus | Biological Sciences
Journal Article
Multiple Sclerosis, ISSN 1352-4585, 04/2019, Volume 25, Issue 4, pp. 565 - 573
BACKGROUND: Treatment of multiple sclerosis (MS) with interferon β can lead to the development of antibodies directed against interferon β that interfere with...
interferon beta | anti-drug antibodies | genetic variation | Multiple sclerosis | HLA-DRB1 | genome-wide association study | GENOTYPE | GUIDELINES | LINKS | NEUROSCIENCES | CLINICAL NEUROLOGY | IMMUNOGENICITY | THERAPY | MULTIPLE-SCLEROSIS | Immunoglobulins | Clinical trials | Antibodies | Genomes | Single-nucleotide polymorphism | Patients | Genetic variance | Genetic markers | Alleles | Drb1 protein | Histocompatibility antigen HLA | Interferon
interferon beta | anti-drug antibodies | genetic variation | Multiple sclerosis | HLA-DRB1 | genome-wide association study | GENOTYPE | GUIDELINES | LINKS | NEUROSCIENCES | CLINICAL NEUROLOGY | IMMUNOGENICITY | THERAPY | MULTIPLE-SCLEROSIS | Immunoglobulins | Clinical trials | Antibodies | Genomes | Single-nucleotide polymorphism | Patients | Genetic variance | Genetic markers | Alleles | Drb1 protein | Histocompatibility antigen HLA | Interferon
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 05/2017, Volume 35, Issue 15_suppl, pp. 4078 - 4078
Journal Article
Cancer Cell, ISSN 1535-6108, 08/2012, Volume 22, Issue 2, pp. 167 - 179
In Burkitt lymphoma (BL), a germinal center B-cell-derived tumor, the pro-apoptotic properties of c-MYC must be counterbalanced. Predicting that survival...
PATHOGENESIS | ACTIVATION | SIGNATURES | ONCOLOGY | B-CELL LYMPHOMAS | CYCLIN D3 | C-MYC | RECEPTOR | MICE | P53 | CELL BIOLOGY | Burkitt Lymphoma - enzymology | B-Lymphocytes - enzymology | Humans | Mice, Inbred C57BL | Gene Expression Regulation, Neoplastic | Germinal Center - enzymology | Molecular Sequence Data | Phosphatidylinositol 3-Kinases - metabolism | Signal Transduction - genetics | Germinal Center - pathology | Cell Transformation, Neoplastic - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Burkitt Lymphoma - pathology | Phosphatidylinositol 3-Kinases - genetics | Animals | Cell Transformation, Neoplastic - genetics | Base Sequence | Burkitt Lymphoma - genetics | Cell Line, Tumor | Mice | Proto-Oncogene Proteins c-myc - genetics | B-Lymphocytes - pathology | Enzyme Activation | Cell Transformation, Neoplastic - pathology | Medical colleges | Lymphomas | Gene expression | Genes | Medical informatics
PATHOGENESIS | ACTIVATION | SIGNATURES | ONCOLOGY | B-CELL LYMPHOMAS | CYCLIN D3 | C-MYC | RECEPTOR | MICE | P53 | CELL BIOLOGY | Burkitt Lymphoma - enzymology | B-Lymphocytes - enzymology | Humans | Mice, Inbred C57BL | Gene Expression Regulation, Neoplastic | Germinal Center - enzymology | Molecular Sequence Data | Phosphatidylinositol 3-Kinases - metabolism | Signal Transduction - genetics | Germinal Center - pathology | Cell Transformation, Neoplastic - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Burkitt Lymphoma - pathology | Phosphatidylinositol 3-Kinases - genetics | Animals | Cell Transformation, Neoplastic - genetics | Base Sequence | Burkitt Lymphoma - genetics | Cell Line, Tumor | Mice | Proto-Oncogene Proteins c-myc - genetics | B-Lymphocytes - pathology | Enzyme Activation | Cell Transformation, Neoplastic - pathology | Medical colleges | Lymphomas | Gene expression | Genes | Medical informatics
Journal Article
Cell Reports, ISSN 2211-1247, 05/2015, Volume 11, Issue 5, pp. 715 - 726
Diffuse large B cell lymphoma (DLBCL) is a complex disease comprising diverse subtypes and genetic profiles. Possibly because of the prevalence of genetic...
MULTIPLE-MYELOMA | ALPHA PROTEOLYSIS | ACTIVATION | PATHWAY | BAFF-RECEPTOR | DIFFUSE | GENE-EXPRESSION | SURVIVAL SIGNALS | LYMPHOMA | PLASMA-CELL DIFFERENTIATION | CELL BIOLOGY | B-Lymphocytes - cytology | Lymphoma, Large B-Cell, Diffuse - pathology | Signal Transduction | Cell Survival | Humans | Gene Expression Regulation, Neoplastic | Protein-Serine-Threonine Kinases - genetics | NF-kappa B - metabolism | TNF Receptor-Associated Factor 3 - metabolism | Lymphoma, Large B-Cell, Diffuse - metabolism | DNA-Binding Proteins - genetics | DNA-Binding Proteins - deficiency | Mice, Knockout | DNA-Binding Proteins - metabolism | Animals | B-Lymphocytes - immunology | TNF Receptor-Associated Factor 3 - genetics | Cell Line, Tumor | Cell Differentiation | Mice | B-Lymphocytes - metabolism | Protein-Serine-Threonine Kinases - metabolism | Proto-Oncogene Proteins c-bcl-6
MULTIPLE-MYELOMA | ALPHA PROTEOLYSIS | ACTIVATION | PATHWAY | BAFF-RECEPTOR | DIFFUSE | GENE-EXPRESSION | SURVIVAL SIGNALS | LYMPHOMA | PLASMA-CELL DIFFERENTIATION | CELL BIOLOGY | B-Lymphocytes - cytology | Lymphoma, Large B-Cell, Diffuse - pathology | Signal Transduction | Cell Survival | Humans | Gene Expression Regulation, Neoplastic | Protein-Serine-Threonine Kinases - genetics | NF-kappa B - metabolism | TNF Receptor-Associated Factor 3 - metabolism | Lymphoma, Large B-Cell, Diffuse - metabolism | DNA-Binding Proteins - genetics | DNA-Binding Proteins - deficiency | Mice, Knockout | DNA-Binding Proteins - metabolism | Animals | B-Lymphocytes - immunology | TNF Receptor-Associated Factor 3 - genetics | Cell Line, Tumor | Cell Differentiation | Mice | B-Lymphocytes - metabolism | Protein-Serine-Threonine Kinases - metabolism | Proto-Oncogene Proteins c-bcl-6
Journal Article
Structure, ISSN 0969-2126, 04/2013, Volume 21, Issue 4, pp. 550 - 559
GTPases of immunity-associated proteins (GIMAPs) are regulators of lymphocyte survival and homeostasis. We previously determined the structural basis of...
SURVIVAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | G-PROTEINS | TUMOR-CELLS | 3 DIMENSIONS | CELL BIOLOGY | IAN FAMILY | BIOPHYSICS | GENE | TOXOPLASMA-GONDII | HODGKIN LYMPHOMA | T-CELL DEVELOPMENT | BINDING | Cell Line | GTP-Binding Proteins - chemistry | Humans | Crystallization | Models, Molecular | Ultracentrifugation | Reverse Transcriptase Polymerase Chain Reaction | GTP Phosphohydrolases - chemistry | Hydrolysis | GTP Phosphohydrolases - metabolism | Membrane Proteins - chemistry | T-Lymphocytes - metabolism | Calorimetry | Protein Conformation | Membrane Proteins - metabolism | Dimerization | Enzyme Activation - physiology | Lipid Metabolism - physiology | Microscopy, Fluorescence | GTP-Binding Proteins - metabolism | Proteins | Crystals | Non-Hodgkin's lymphomas | G proteins | Structure | T cells
SURVIVAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | G-PROTEINS | TUMOR-CELLS | 3 DIMENSIONS | CELL BIOLOGY | IAN FAMILY | BIOPHYSICS | GENE | TOXOPLASMA-GONDII | HODGKIN LYMPHOMA | T-CELL DEVELOPMENT | BINDING | Cell Line | GTP-Binding Proteins - chemistry | Humans | Crystallization | Models, Molecular | Ultracentrifugation | Reverse Transcriptase Polymerase Chain Reaction | GTP Phosphohydrolases - chemistry | Hydrolysis | GTP Phosphohydrolases - metabolism | Membrane Proteins - chemistry | T-Lymphocytes - metabolism | Calorimetry | Protein Conformation | Membrane Proteins - metabolism | Dimerization | Enzyme Activation - physiology | Lipid Metabolism - physiology | Microscopy, Fluorescence | GTP-Binding Proteins - metabolism | Proteins | Crystals | Non-Hodgkin's lymphomas | G proteins | Structure | T cells
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 05/2016, Volume 113, Issue 18, p. 5065
Although canonical NF-...B signaling is crucial to generate a normal mature B-cell compartment, its role in the persistence of resting mature B cells is...
Signal transduction | Gene expression | Cells
Signal transduction | Gene expression | Cells
Journal Article
JAMA Neurology, ISSN 2168-6149, 12/2015, Volume 72, Issue 12, pp. 1458 - 1465
IMPORTANCE: Low serum 25-hydroxyvitamin D (25[OH]D) levels are associated with an increased risk of multiple sclerosis (MS) as well as with increased disease...
CONTROLLED-TRIAL | DETERMINANTS | RELAPSE RISK | D SUPPLEMENTATION | 25-HYDROXYVITAMIN D | DOUBLE-BLIND | CLINICAL NEUROLOGY | Disability Evaluation | Age Factors | Double-Blind Method | HLA-DRB1 Chains - genetics | Multiple Sclerosis - blood | Humans | Middle Aged | Genotype | Male | Multiple Sclerosis - genetics | Disease Progression | Vitamin D - blood | Dose-Response Relationship, Drug | Vitamin D-Binding Protein - genetics | Time Factors | Interferon beta-1b - therapeutic use | Adult | Female | Vitamin D - analogs & derivatives | Retrospective Studies | Adjuvants, Immunologic - therapeutic use | Longitudinal Studies | Multiple Sclerosis - drug therapy
CONTROLLED-TRIAL | DETERMINANTS | RELAPSE RISK | D SUPPLEMENTATION | 25-HYDROXYVITAMIN D | DOUBLE-BLIND | CLINICAL NEUROLOGY | Disability Evaluation | Age Factors | Double-Blind Method | HLA-DRB1 Chains - genetics | Multiple Sclerosis - blood | Humans | Middle Aged | Genotype | Male | Multiple Sclerosis - genetics | Disease Progression | Vitamin D - blood | Dose-Response Relationship, Drug | Vitamin D-Binding Protein - genetics | Time Factors | Interferon beta-1b - therapeutic use | Adult | Female | Vitamin D - analogs & derivatives | Retrospective Studies | Adjuvants, Immunologic - therapeutic use | Longitudinal Studies | Multiple Sclerosis - drug therapy
Journal Article
Plant Molecular Biology, ISSN 0167-4412, 3/2007, Volume 63, Issue 4, pp. 505 - 517
We have isolated two Arabidopsis thaliana genes, AtGpp1 and AtGpp2, showing homology with the yeast low molecular weight phosphatases GPP1 and GPP2, which have...
Life Sciences | Plant Pathology | Biochemistry, general | Glycerol-3-phosphate | Arabidopsis | Glycerol-3-phosphatases | Plant Sciences | Transgenic plants | Stress | Glycerol metabolism | Glycerol-3- phosphatases | PHOSPHOMONOESTERASE | transgenic plants | stress | LOCALIZATION | GLYCEROL-3-PHOSPHATE DEHYDROGENASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | SACCHAROMYCES-CEREVISIAE | glycerol-3-phosphate | PLANT SCIENCES | YEAST | COMPANION CELLS | GENE | glycerol-3-phosphatases | glycerol metabolism | EXPRESSION | Physiological aspects | Proteins | Oxidative stress
Life Sciences | Plant Pathology | Biochemistry, general | Glycerol-3-phosphate | Arabidopsis | Glycerol-3-phosphatases | Plant Sciences | Transgenic plants | Stress | Glycerol metabolism | Glycerol-3- phosphatases | PHOSPHOMONOESTERASE | transgenic plants | stress | LOCALIZATION | GLYCEROL-3-PHOSPHATE DEHYDROGENASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | SACCHAROMYCES-CEREVISIAE | glycerol-3-phosphate | PLANT SCIENCES | YEAST | COMPANION CELLS | GENE | glycerol-3-phosphatases | glycerol metabolism | EXPRESSION | Physiological aspects | Proteins | Oxidative stress
Journal Article