European Journal of Immunology, ISSN 0014-2980, 12/2012, Volume 42, Issue 12, pp. 3346 - 3357
Attraction of neutrophils to sites of infection or tissue injury is an essential prerequisite for an efficient innate immune response. Herein, we provide novel...
Chemotaxis | Lipocalin‐2 (Lcn2) | polymorphonuclear neutrophils (PMNs) | Lipocalin-2 (Lcn2) | Polymorphonuclear neutrophils (PMNs) | NGAL | HUMAN NEUTROPHIL GELATINASE | PROTEIN | RECEPTOR | IRON | GELATINASE-ASSOCIATED LIPOCALIN | IMMUNOLOGY | ISCHEMIA-REPERFUSION INJURY | ADHESION | INFECTION | EXPRESSION | Oncogene Proteins - genetics | Humans | Salmonella Infections - genetics | Salmonella Infections - immunology | Male | Acute-Phase Proteins - genetics | Paracrine Communication - immunology | Lipocalins - genetics | Proto-Oncogene Proteins - immunology | Chemotaxis - immunology | Oncogene Proteins - immunology | Proto-Oncogene Proteins - pharmacology | Lipocalins - pharmacology | Salmonella typhimurium - immunology | Neutrophils - immunology | Oncogene Proteins - pharmacology | Paracrine Communication - genetics | Proto-Oncogene Proteins - genetics | Inflammation - immunology | Chemotaxis - drug effects | Chemotaxis - genetics | Mice, Knockout | Animals | Lipocalin-2 | Lipocalins - immunology | Paracrine Communication - drug effects | Inflammation - genetics | Mice | Acute-Phase Proteins - pharmacology | Acute-Phase Proteins - immunology | Medical research | Rodents
Chemotaxis | Lipocalin‐2 (Lcn2) | polymorphonuclear neutrophils (PMNs) | Lipocalin-2 (Lcn2) | Polymorphonuclear neutrophils (PMNs) | NGAL | HUMAN NEUTROPHIL GELATINASE | PROTEIN | RECEPTOR | IRON | GELATINASE-ASSOCIATED LIPOCALIN | IMMUNOLOGY | ISCHEMIA-REPERFUSION INJURY | ADHESION | INFECTION | EXPRESSION | Oncogene Proteins - genetics | Humans | Salmonella Infections - genetics | Salmonella Infections - immunology | Male | Acute-Phase Proteins - genetics | Paracrine Communication - immunology | Lipocalins - genetics | Proto-Oncogene Proteins - immunology | Chemotaxis - immunology | Oncogene Proteins - immunology | Proto-Oncogene Proteins - pharmacology | Lipocalins - pharmacology | Salmonella typhimurium - immunology | Neutrophils - immunology | Oncogene Proteins - pharmacology | Paracrine Communication - genetics | Proto-Oncogene Proteins - genetics | Inflammation - immunology | Chemotaxis - drug effects | Chemotaxis - genetics | Mice, Knockout | Animals | Lipocalin-2 | Lipocalins - immunology | Paracrine Communication - drug effects | Inflammation - genetics | Mice | Acute-Phase Proteins - pharmacology | Acute-Phase Proteins - immunology | Medical research | Rodents
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 02/2015, Volume 30, Issue 2, pp. 357 - 368
ABSTRACT Mechanical loading represents a crucial factor in the regulation of skeletal homeostasis. Its reduction causes loss of bone mass, eventually leading...
LCN2 | UNLOADING | OSTEOCLASTS | ADIPOKINE | MECHANICAL FORCES | OSTEOBLASTS | Unloading | Osteoclasts | Mechanical forces | Adipokine | Osteoblasts | NGAL | PROTEIN | MOUSE | MUSCULAR-DYSTROPHY | IRON | GELATINASE-ASSOCIATED LIPOCALIN | ISCHEMIA-REPERFUSION INJURY | MODELED MICROGRAVITY | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | NEUTROPHIL-GELATINASE | Oncogene Proteins - genetics | Humans | Male | Acute-Phase Proteins - genetics | Paralysis - pathology | Lipocalins - blood | Lipocalins - genetics | HEK293 Cells | Adult | Cell Differentiation | Mechanotransduction, Cellular - genetics | Disease Models, Animal | Bed Rest | Osteoclasts - pathology | Mice, Inbred C57BL | Gene Expression Regulation | Proto-Oncogene Proteins - genetics | Hindlimb Suspension | Osteoclasts - metabolism | Osteoblasts - pathology | Bone and Bones - physiopathology | Phenotype | Animals | Lipocalin-2 | Paralysis - physiopathology | Osteoblasts - metabolism | Proto-Oncogene Proteins - blood | Homeostasis - genetics | Osteogenesis | Osteoporosis | Exercise | RNA | Analysis | Genes | Homeostasis | Physiological aspects
LCN2 | UNLOADING | OSTEOCLASTS | ADIPOKINE | MECHANICAL FORCES | OSTEOBLASTS | Unloading | Osteoclasts | Mechanical forces | Adipokine | Osteoblasts | NGAL | PROTEIN | MOUSE | MUSCULAR-DYSTROPHY | IRON | GELATINASE-ASSOCIATED LIPOCALIN | ISCHEMIA-REPERFUSION INJURY | MODELED MICROGRAVITY | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | NEUTROPHIL-GELATINASE | Oncogene Proteins - genetics | Humans | Male | Acute-Phase Proteins - genetics | Paralysis - pathology | Lipocalins - blood | Lipocalins - genetics | HEK293 Cells | Adult | Cell Differentiation | Mechanotransduction, Cellular - genetics | Disease Models, Animal | Bed Rest | Osteoclasts - pathology | Mice, Inbred C57BL | Gene Expression Regulation | Proto-Oncogene Proteins - genetics | Hindlimb Suspension | Osteoclasts - metabolism | Osteoblasts - pathology | Bone and Bones - physiopathology | Phenotype | Animals | Lipocalin-2 | Paralysis - physiopathology | Osteoblasts - metabolism | Proto-Oncogene Proteins - blood | Homeostasis - genetics | Osteogenesis | Osteoporosis | Exercise | RNA | Analysis | Genes | Homeostasis | Physiological aspects
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2011, Volume 305, Issue 1, pp. 28 - 33
Abstract Background Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by an irreversible cognitive decline and neuronal loss...
Neurology | Alzheimer's disease (AD) | Biomarker | Lipocalin 2 (LCN2) | Inflammation | Mild cognitive impairment (MCI) | ELISA | PROTEIN | NEUTROPHIL GELATINASE | CSF BIOMARKERS | GELATINASE-ASSOCIATED LIPOCALIN | PROINFLAMMATORY CYTOKINES | OVARIAN-CANCER | CEREBROSPINAL-FLUID | NEUROSCIENCES | CLINICAL NEUROLOGY | INFLAMMATORY MARKERS | PRECLINICAL ALZHEIMERS-DISEASE | EXPRESSION | Lipocalins - biosynthesis | Predictive Value of Tests | Encephalitis - diagnosis | Cognition Disorders - blood | Humans | Middle Aged | Male | Acute-Phase Proteins - genetics | Proto-Oncogene Proteins - biosynthesis | Alzheimer Disease - pathology | Lipocalins - blood | Lipocalins - genetics | Female | Encephalitis - genetics | Cognition Disorders - pathology | Proto-Oncogene Proteins - genetics | Cognition Disorders - genetics | Disease Progression | Lipocalin-2 | Aged | Alzheimer Disease - genetics | Proto-Oncogene Proteins - blood | Acute-Phase Proteins - biosynthesis | Encephalitis - blood | Alzheimer Disease - blood | Alzheimer's disease | Nervous system diseases | Amyloid beta-protein
Neurology | Alzheimer's disease (AD) | Biomarker | Lipocalin 2 (LCN2) | Inflammation | Mild cognitive impairment (MCI) | ELISA | PROTEIN | NEUTROPHIL GELATINASE | CSF BIOMARKERS | GELATINASE-ASSOCIATED LIPOCALIN | PROINFLAMMATORY CYTOKINES | OVARIAN-CANCER | CEREBROSPINAL-FLUID | NEUROSCIENCES | CLINICAL NEUROLOGY | INFLAMMATORY MARKERS | PRECLINICAL ALZHEIMERS-DISEASE | EXPRESSION | Lipocalins - biosynthesis | Predictive Value of Tests | Encephalitis - diagnosis | Cognition Disorders - blood | Humans | Middle Aged | Male | Acute-Phase Proteins - genetics | Proto-Oncogene Proteins - biosynthesis | Alzheimer Disease - pathology | Lipocalins - blood | Lipocalins - genetics | Female | Encephalitis - genetics | Cognition Disorders - pathology | Proto-Oncogene Proteins - genetics | Cognition Disorders - genetics | Disease Progression | Lipocalin-2 | Aged | Alzheimer Disease - genetics | Proto-Oncogene Proteins - blood | Acute-Phase Proteins - biosynthesis | Encephalitis - blood | Alzheimer Disease - blood | Alzheimer's disease | Nervous system diseases | Amyloid beta-protein
Journal Article
CANCERS, ISSN 2072-6694, 03/2019, Volume 11, Issue 3, p. 385
Hepatocellular carcinoma (HCC) is one of the most prevalent and deadly cancers worldwide. Therefore, current global research focuses on molecular tools for...
NGAL | PROTEIN | TUMOR-MARKERS | liver | HCC | HEPATIC PROGENITOR CELLS | PROLIFERATION | AFP | OVEREXPRESSION | LIVER-INJURY | ONCOLOGY | ROLES | LCN2 | cancer | PLIN5 | ALPHA-FETOPROTEIN
NGAL | PROTEIN | TUMOR-MARKERS | liver | HCC | HEPATIC PROGENITOR CELLS | PROLIFERATION | AFP | OVEREXPRESSION | LIVER-INJURY | ONCOLOGY | ROLES | LCN2 | cancer | PLIN5 | ALPHA-FETOPROTEIN
Journal Article
Investigative ophthalmology & visual science, ISSN 0146-0404, 12/2018, Volume 59, Issue 15, pp. 6014 - 6025
PURPOSE. Lipocalin 2 ( LCN2) is reported to be one of the key regulators of cell survival and death; however, its effect on retinal degeneration is unclear....
LCN2 | Retinal degeneration | Oxidative stress | Photoreceptor | Apoptosis | PROTEIN FAMILY | retinal degeneration | ACTIVATION | photoreceptor | INJURY | apoptosis | MACULAR DEGENERATION | RECEPTOR | 24P3 PROTEIN | DEATH | PREVALENCE | OPHTHALMOLOGY | BCL-2 FAMILY | EXPRESSION | oxidative stress
LCN2 | Retinal degeneration | Oxidative stress | Photoreceptor | Apoptosis | PROTEIN FAMILY | retinal degeneration | ACTIVATION | photoreceptor | INJURY | apoptosis | MACULAR DEGENERATION | RECEPTOR | 24P3 PROTEIN | DEATH | PREVALENCE | OPHTHALMOLOGY | BCL-2 FAMILY | EXPRESSION | oxidative stress
Journal Article
The Prostate, ISSN 0270-4137, 06/2015, Volume 75, Issue 9, pp. 957 - 968
BACKGROUND Metastasis is the primary cause of prostate cancer (PCa) lethality and poses a huge clinical obstacle. Lipocalin 2 (LCN2), a member of the lipocalin...
LCN2 | prostate cancer | SLUG | EMT | ERK | CARCINOMA-CELLS | NEUTROPHIL GELATINASE | GELATINASE-ASSOCIATED LIPOCALIN | EPITHELIAL-MESENCHYMAL TRANSITIONS | E-CADHERIN | BREAST-CANCER | TUMOR-METASTASIS | ENDOCRINOLOGY & METABOLISM | UROLOGY & NEPHROLOGY | UP-REGULATION | PROGRESSION | SNAIL | Lipocalins - biosynthesis | Nitriles - pharmacology | Humans | Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors | Male | Acute-Phase Proteins - genetics | Extracellular Signal-Regulated MAP Kinases - metabolism | Proto-Oncogene Proteins - biosynthesis | Cell Movement - physiology | MAP Kinase Signaling System | RNA - genetics | Heterografts | Prostatic Neoplasms - genetics | Lipocalins - blood | Lipocalins - genetics | Epithelial-Mesenchymal Transition | Prostatic Neoplasms - blood | Snail Family Transcription Factors | Prostatic Neoplasms - pathology | Butadienes - pharmacology | Neoplasm Invasiveness | Enzyme Inhibitors - pharmacology | Proto-Oncogene Proteins - genetics | Transcription Factors - biosynthesis | Transcription Factors - genetics | RNA - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Animals | Lipocalin-2 | Mice, Nude | Histocytochemistry | Cell Line, Tumor | Mice | Proto-Oncogene Proteins - blood | Acute-Phase Proteins - biosynthesis | Development and progression | Prostate cancer
LCN2 | prostate cancer | SLUG | EMT | ERK | CARCINOMA-CELLS | NEUTROPHIL GELATINASE | GELATINASE-ASSOCIATED LIPOCALIN | EPITHELIAL-MESENCHYMAL TRANSITIONS | E-CADHERIN | BREAST-CANCER | TUMOR-METASTASIS | ENDOCRINOLOGY & METABOLISM | UROLOGY & NEPHROLOGY | UP-REGULATION | PROGRESSION | SNAIL | Lipocalins - biosynthesis | Nitriles - pharmacology | Humans | Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors | Male | Acute-Phase Proteins - genetics | Extracellular Signal-Regulated MAP Kinases - metabolism | Proto-Oncogene Proteins - biosynthesis | Cell Movement - physiology | MAP Kinase Signaling System | RNA - genetics | Heterografts | Prostatic Neoplasms - genetics | Lipocalins - blood | Lipocalins - genetics | Epithelial-Mesenchymal Transition | Prostatic Neoplasms - blood | Snail Family Transcription Factors | Prostatic Neoplasms - pathology | Butadienes - pharmacology | Neoplasm Invasiveness | Enzyme Inhibitors - pharmacology | Proto-Oncogene Proteins - genetics | Transcription Factors - biosynthesis | Transcription Factors - genetics | RNA - chemistry | Reverse Transcriptase Polymerase Chain Reaction | Animals | Lipocalin-2 | Mice, Nude | Histocytochemistry | Cell Line, Tumor | Mice | Proto-Oncogene Proteins - blood | Acute-Phase Proteins - biosynthesis | Development and progression | Prostate cancer
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 06/2018, Volume 33, Issue 6, pp. 1141 - 1153
ABSTRACT Lipocalin 2 (Lcn2) is an adipokine that carries out a variety of functions in diverse organs. We investigated the bone phenotype and the energy...
NGAL | LCN2 | OSTEOBLAST | GLUT1 | ENERGY METABOLISM | BONE METABOLISM | HOMEOSTASIS | HYPERINSULINEMIA | EXPENDITURE | OBESITY | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | WEIGHT | Glucose metabolism | Phosphatases | Body weight | Physiological aspects | Glucose | Insulin | Dextrose | Hyperinsulinemia | Alkaline phosphatase | Energy metabolism | Bone (trabecular) | Osteoblasts | Bone growth | Mineralization | Rodents | Bone marrow | Protein transport | Osteopenia | Hyperphagia | Glucose transporter | Phenotypes | Lipocalin | Bone turnover | Metabolism | Glucose tolerance | Calvaria | Stromal cells | Polyuria | Renal cortex | Osteogenesis | Proteinuria
NGAL | LCN2 | OSTEOBLAST | GLUT1 | ENERGY METABOLISM | BONE METABOLISM | HOMEOSTASIS | HYPERINSULINEMIA | EXPENDITURE | OBESITY | INSULIN-RESISTANCE | ENDOCRINOLOGY & METABOLISM | WEIGHT | Glucose metabolism | Phosphatases | Body weight | Physiological aspects | Glucose | Insulin | Dextrose | Hyperinsulinemia | Alkaline phosphatase | Energy metabolism | Bone (trabecular) | Osteoblasts | Bone growth | Mineralization | Rodents | Bone marrow | Protein transport | Osteopenia | Hyperphagia | Glucose transporter | Phenotypes | Lipocalin | Bone turnover | Metabolism | Glucose tolerance | Calvaria | Stromal cells | Polyuria | Renal cortex | Osteogenesis | Proteinuria
Journal Article
Cellular Physiology and Biochemistry, ISSN 1015-8987, 05/2015, Volume 36, Issue 2, pp. 753 - 762
Background: Lipocalin 2 (LCN2), a protein primarily produced by hepatocytes, is highly upregulated under various conditions that induce cellular stress, such...
Original Paper | LCN2 | Hepatocytes | TNF-α | IL-1β | IL-6 | ACTIVATION | PHYSIOLOGY | TNF-alpha | MACROPHAGES | NEUTROPHIL GELATINASE | IL-1 beta | GELATINASE-ASSOCIATED LIPOCALIN | INDUCTION | CELL BIOLOGY | INHIBITION | LIVER-INJURY | INFLAMMATION | GENE-EXPRESSION | INFECTION | Cell Line | RNA, Small Interfering - genetics | Up-Regulation | Interleukin-6 - genetics | Humans | RNA, Messenger - genetics | Tumor Necrosis Factor-alpha - genetics | Gene Expression Regulation | Interleukin-1beta - immunology | Proto-Oncogene Proteins - genetics | Acute-Phase Proteins - genetics | Hepatocytes - metabolism | Hepatocytes - immunology | RNA Interference | Lipocalin-2 | Lipocalins - genetics | Lipocalins - immunology | Proto-Oncogene Proteins - immunology | Acute-Phase Proteins - immunology
Original Paper | LCN2 | Hepatocytes | TNF-α | IL-1β | IL-6 | ACTIVATION | PHYSIOLOGY | TNF-alpha | MACROPHAGES | NEUTROPHIL GELATINASE | IL-1 beta | GELATINASE-ASSOCIATED LIPOCALIN | INDUCTION | CELL BIOLOGY | INHIBITION | LIVER-INJURY | INFLAMMATION | GENE-EXPRESSION | INFECTION | Cell Line | RNA, Small Interfering - genetics | Up-Regulation | Interleukin-6 - genetics | Humans | RNA, Messenger - genetics | Tumor Necrosis Factor-alpha - genetics | Gene Expression Regulation | Interleukin-1beta - immunology | Proto-Oncogene Proteins - genetics | Acute-Phase Proteins - genetics | Hepatocytes - metabolism | Hepatocytes - immunology | RNA Interference | Lipocalin-2 | Lipocalins - genetics | Lipocalins - immunology | Proto-Oncogene Proteins - immunology | Acute-Phase Proteins - immunology
Journal Article
The Journal of Infectious Diseases, ISSN 0022-1899, 3/2010, Volume 201, Issue 5, pp. 783 - 792
Iron is an essential nutrient for microbes, and many pathogenic bacteria depend on siderophores to obtain iron. The mammalian innate immunity protein lipocalin...
Transferrins | Mycobacterium tuberculosis | Neutrophils | Lysosomes | Phagosomes | Bacteria | Infections | Iron | Macrophages | Endosomes | INFECTIOUS DISEASES | RAB5 | MACROPHAGES | MICROBIOLOGY | GELATINASE-ASSOCIATED LIPOCALIN | IMMUNOLOGY | MATURATION | MEDIATED IRON ACQUISITION | TUBERCULOSIS PHAGOSOME | INHIBITION | GROWTH | EARLY ENDOSOMES | PROTEINS | Oncogene Proteins - blood | Lysosomes - chemistry | Liver - microbiology | Tuberculosis - microbiology | Blood - microbiology | Colony Count, Microbial | Spleen - microbiology | Lysosomes - metabolism | Lipocalins - blood | Mycobacterium avium - pathogenicity | Oncogene Proteins - immunology | Macrophages - immunology | Macrophages - microbiology | Lipocalins - metabolism | rab GTP-Binding Proteins - metabolism | Acute-Phase Proteins - metabolism | Mice, Inbred C57BL | Oncogene Proteins - metabolism | Mycobacterium avium - immunology | Mycobacterium avium - metabolism | Tuberculosis - immunology | Animals | Lysosomes - microbiology | Lipocalin-2 | Lipocalins - immunology | Mice | Transferrin - metabolism | Mycobacterium avium - growth & development | Acute-Phase Proteins - immunology | Transferrin | Growth | Physiological aspects | Mycobacterium avium | Genetic aspects | Research | mouse | infection | Rab11 | Mycobacteria | transferrin | iron | Lcn2
Transferrins | Mycobacterium tuberculosis | Neutrophils | Lysosomes | Phagosomes | Bacteria | Infections | Iron | Macrophages | Endosomes | INFECTIOUS DISEASES | RAB5 | MACROPHAGES | MICROBIOLOGY | GELATINASE-ASSOCIATED LIPOCALIN | IMMUNOLOGY | MATURATION | MEDIATED IRON ACQUISITION | TUBERCULOSIS PHAGOSOME | INHIBITION | GROWTH | EARLY ENDOSOMES | PROTEINS | Oncogene Proteins - blood | Lysosomes - chemistry | Liver - microbiology | Tuberculosis - microbiology | Blood - microbiology | Colony Count, Microbial | Spleen - microbiology | Lysosomes - metabolism | Lipocalins - blood | Mycobacterium avium - pathogenicity | Oncogene Proteins - immunology | Macrophages - immunology | Macrophages - microbiology | Lipocalins - metabolism | rab GTP-Binding Proteins - metabolism | Acute-Phase Proteins - metabolism | Mice, Inbred C57BL | Oncogene Proteins - metabolism | Mycobacterium avium - immunology | Mycobacterium avium - metabolism | Tuberculosis - immunology | Animals | Lysosomes - microbiology | Lipocalin-2 | Lipocalins - immunology | Mice | Transferrin - metabolism | Mycobacterium avium - growth & development | Acute-Phase Proteins - immunology | Transferrin | Growth | Physiological aspects | Mycobacterium avium | Genetic aspects | Research | mouse | infection | Rab11 | Mycobacteria | transferrin | iron | Lcn2
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 11/2015, Volume 30, Issue 11, pp. 2078 - 2085
Lipocalin 2 (LCN2) or neutrophil gelatinase–associated lipocalin (NGAL) is expressed in a wide range of cells and pathological states. Mounting evidence...
NGAL | LCN2 | PHYSICAL ACTIVITY | OSTEOPOROSIS | FRACTURE RISK | ELDERLY WOMEN | GELATINASE-ASSOCIATED LIPOCALIN | OBESE WOMEN | DECLINE | INFLAMMATION | ENDOCRINOLOGY & METABOLISM | RESISTANCE | OLDER WOMEN | PHYSICAL-ACTIVITY | BONE MASS | POSTMENOPAUSAL WOMEN | Body Mass Index | Bone Density | Glomerular Filtration Rate | Prospective Studies | Acute-Phase Proteins | Humans | Osteoporotic Fractures - diagnostic imaging | Risk Factors | Linear Models | Hospitalization | Motor Activity | Heel - diagnostic imaging | Lipocalin-2 | Lipocalins - blood | Ultrasonography | Female | Aged | Osteoporotic Fractures - blood | Hip Fractures - complications | Osteoporotic Fractures - physiopathology | Proto-Oncogene Proteins - blood | Accidental Falls | Women | Osteoporosis | Analysis | Bones | Density | Health aspects
NGAL | LCN2 | PHYSICAL ACTIVITY | OSTEOPOROSIS | FRACTURE RISK | ELDERLY WOMEN | GELATINASE-ASSOCIATED LIPOCALIN | OBESE WOMEN | DECLINE | INFLAMMATION | ENDOCRINOLOGY & METABOLISM | RESISTANCE | OLDER WOMEN | PHYSICAL-ACTIVITY | BONE MASS | POSTMENOPAUSAL WOMEN | Body Mass Index | Bone Density | Glomerular Filtration Rate | Prospective Studies | Acute-Phase Proteins | Humans | Osteoporotic Fractures - diagnostic imaging | Risk Factors | Linear Models | Hospitalization | Motor Activity | Heel - diagnostic imaging | Lipocalin-2 | Lipocalins - blood | Ultrasonography | Female | Aged | Osteoporotic Fractures - blood | Hip Fractures - complications | Osteoporotic Fractures - physiopathology | Proto-Oncogene Proteins - blood | Accidental Falls | Women | Osteoporosis | Analysis | Bones | Density | Health aspects
Journal Article
Liver International, ISSN 1478-3223, 04/2015, Volume 35, Issue 4, pp. 1195 - 1202
Background & Aims Various immune mediators such as interleukin‐6 (IL‐6) have been implicated in the process of liver regeneration. Lipocalin‐2 (LCN2) has been...
partial hepatectomy | LCN2 | hepatic proliferation | lipocalin‐2 | biomarker | liver regeneration | Biomarker | Hepatic proliferation | Partial hepatectomy | Lipocalin-2 | Liver regeneration | PARTIAL-HEPATECTOMY | CYTOKINES | ACUTE-PHASE PROTEIN | MOUSE | INJURY | GELATINASE-ASSOCIATED LIPOCALIN | EPITHELIAL-CELLS | MICE | lipocalin-2 | KIDNEY | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | Oncogene Proteins - genetics | Up-Regulation | Humans | Middle Aged | Male | Acute-Phase Proteins - genetics | Liver - physiopathology | Time Factors | Interleukin-6 - blood | Lipocalins - blood | Lipocalins - genetics | Adult | Female | Acute-Phase Proteins - deficiency | Liver - surgery | Lipocalins - metabolism | Liver Regeneration | Hepatectomy - methods | Signal Transduction | Acute-Phase Proteins - metabolism | Liver - metabolism | Oncogene Proteins - metabolism | Biomarkers - blood | Mice, Knockout | Homozygote | Phenotype | Animals | Heterozygote | Oncogene Proteins - deficiency | Aged | Proto-Oncogene Proteins - blood | Liver | Analysis
partial hepatectomy | LCN2 | hepatic proliferation | lipocalin‐2 | biomarker | liver regeneration | Biomarker | Hepatic proliferation | Partial hepatectomy | Lipocalin-2 | Liver regeneration | PARTIAL-HEPATECTOMY | CYTOKINES | ACUTE-PHASE PROTEIN | MOUSE | INJURY | GELATINASE-ASSOCIATED LIPOCALIN | EPITHELIAL-CELLS | MICE | lipocalin-2 | KIDNEY | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | Oncogene Proteins - genetics | Up-Regulation | Humans | Middle Aged | Male | Acute-Phase Proteins - genetics | Liver - physiopathology | Time Factors | Interleukin-6 - blood | Lipocalins - blood | Lipocalins - genetics | Adult | Female | Acute-Phase Proteins - deficiency | Liver - surgery | Lipocalins - metabolism | Liver Regeneration | Hepatectomy - methods | Signal Transduction | Acute-Phase Proteins - metabolism | Liver - metabolism | Oncogene Proteins - metabolism | Biomarkers - blood | Mice, Knockout | Homozygote | Phenotype | Animals | Heterozygote | Oncogene Proteins - deficiency | Aged | Proto-Oncogene Proteins - blood | Liver | Analysis
Journal Article
Development (Cambridge), ISSN 0950-1991, 2014, Volume 141, Issue 10, pp. 2157 - 2164
Mammalian sperm undergo multiple maturation steps after leaving the testis in order to become competent for fertilization, but the molecular mechanisms...
Lipid raft | Phosphatidylethanolamine | Mouse | Sperm | PKA | LCN2 | Oviduct | CONTACT | PROTEIN | FUSION | MOUSE SPERMATOZOA | MAMMALIAN FERTILIZATION | IRON | DEVELOPMENTAL BIOLOGY | INFECTION | MOLECULAR-BASIS | CAPACITATION | ACROSOME REACTION | Oncogene Proteins - genetics | Cricetulus | Membrane Fluidity - genetics | Male | Acute-Phase Proteins - genetics | Fertility - genetics | Lipocalins - genetics | Sperm Maturation - genetics | Female | CHO Cells | Lipocalins - metabolism | Cricetinae | Movement | Acute-Phase Proteins - metabolism | Mice, Inbred C57BL | Oncogene Proteins - metabolism | Membrane Microdomains - chemistry | Mice, Transgenic | Cholesterol - metabolism | Pregnancy | Cyclic AMP-Dependent Protein Kinases - physiology | Animals | Lipocalin-2 | Membrane Microdomains - physiology | Mice | Phosphatidylethanolamines - metabolism | Protein Binding - physiology
Lipid raft | Phosphatidylethanolamine | Mouse | Sperm | PKA | LCN2 | Oviduct | CONTACT | PROTEIN | FUSION | MOUSE SPERMATOZOA | MAMMALIAN FERTILIZATION | IRON | DEVELOPMENTAL BIOLOGY | INFECTION | MOLECULAR-BASIS | CAPACITATION | ACROSOME REACTION | Oncogene Proteins - genetics | Cricetulus | Membrane Fluidity - genetics | Male | Acute-Phase Proteins - genetics | Fertility - genetics | Lipocalins - genetics | Sperm Maturation - genetics | Female | CHO Cells | Lipocalins - metabolism | Cricetinae | Movement | Acute-Phase Proteins - metabolism | Mice, Inbred C57BL | Oncogene Proteins - metabolism | Membrane Microdomains - chemistry | Mice, Transgenic | Cholesterol - metabolism | Pregnancy | Cyclic AMP-Dependent Protein Kinases - physiology | Animals | Lipocalin-2 | Membrane Microdomains - physiology | Mice | Phosphatidylethanolamines - metabolism | Protein Binding - physiology
Journal Article
Journal of Orthopaedic Research, ISSN 0736-0266, 07/2013, Volume 31, Issue 7, pp. 1046 - 1052
Lipocalin 2 (LCN2) has recently emerged as a novel adipokine involved in different processes including arthritis and chondrocyte inflammatory response....
LCN2 | nitric oxide | adipokines | chondrocyte | inflammation | TLR4 | APOPTOSIS | ACTIVATION | GELATINASE-ASSOCIATED LIPOCALIN | INDUCTION | GENE | PATHWAY | TOLL-LIKE RECEPTORS | ARTICULAR CHONDROCYTES | OSTEOARTHRITIS | ORTHOPEDICS | Chondrocytes - cytology | Guanidines - pharmacology | Nitroprusside - pharmacology | Chondrocytes - drug effects | Matrix Metalloproteinase 9 - metabolism | Nitric Oxide Donors - pharmacology | Chondrocytes - metabolism | Lipocalins - metabolism | Cell Line | Cell Survival - drug effects | Lipocalins - pharmacology | Acute-Phase Proteins - metabolism | Cells, Cultured | Oncogene Proteins - metabolism | Oncogene Proteins - pharmacology | Macrophages - cytology | Toll-Like Receptor 4 - metabolism | Macrophages - metabolism | Animals | Lipocalin-2 | Lipopolysaccharides - pharmacology | Macrophages - drug effects | Mice | Nitric Oxide - metabolism | Acute-Phase Proteins - pharmacology | Periodical publishing | Genetic research | Gene expression | Analysis | Nitric oxide
LCN2 | nitric oxide | adipokines | chondrocyte | inflammation | TLR4 | APOPTOSIS | ACTIVATION | GELATINASE-ASSOCIATED LIPOCALIN | INDUCTION | GENE | PATHWAY | TOLL-LIKE RECEPTORS | ARTICULAR CHONDROCYTES | OSTEOARTHRITIS | ORTHOPEDICS | Chondrocytes - cytology | Guanidines - pharmacology | Nitroprusside - pharmacology | Chondrocytes - drug effects | Matrix Metalloproteinase 9 - metabolism | Nitric Oxide Donors - pharmacology | Chondrocytes - metabolism | Lipocalins - metabolism | Cell Line | Cell Survival - drug effects | Lipocalins - pharmacology | Acute-Phase Proteins - metabolism | Cells, Cultured | Oncogene Proteins - metabolism | Oncogene Proteins - pharmacology | Macrophages - cytology | Toll-Like Receptor 4 - metabolism | Macrophages - metabolism | Animals | Lipocalin-2 | Lipopolysaccharides - pharmacology | Macrophages - drug effects | Mice | Nitric Oxide - metabolism | Acute-Phase Proteins - pharmacology | Periodical publishing | Genetic research | Gene expression | Analysis | Nitric oxide
Journal Article
Oncotarget, ISSN 1949-2553, 2015, Volume 6, Issue 17, pp. 15050 - 15064
Journal Article
Oncogene, ISSN 0950-9232, 04/2010, Volume 29, Issue 15, pp. 2292 - 2301
NFAT1 and NFAT5 act as pro-invasive and promigratory transcription factors in breast carcinoma, contributing to the formation of metastases. We report that...
Breast | LCN2 | Estrogen receptor a | Motility | NFAT3 | NGAL | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | estrogen receptor alpha | PANCREATIC-CANCER | GELATINASE-ASSOCIATED LIPOCALIN | IDENTIFICATION | CELL BIOLOGY | INVASION | ONCOLOGY | ESTROGEN-RECEPTOR-ALPHA | GENETICS & HEREDITY | motility | NUCLEAR FACTOR | breast | EXPRESSION | T-CELLS | Neoplasm Invasiveness | Humans | NFATC Transcription Factors - metabolism | Actins - metabolism | Gene Expression Regulation, Neoplastic | Proto-Oncogene Proteins - genetics | Acute-Phase Proteins - genetics | Proto-Oncogene Proteins - deficiency | Breast Neoplasms - metabolism | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Lipocalin-2 | Lipocalins - genetics | Cell Line, Tumor | Protein Binding | Estrogen Receptor alpha - metabolism | Acute-Phase Proteins - deficiency | Cell Movement | NFATC Transcription Factors - genetics | Cellular proteins | Transcription factors | Physiological aspects | Development and progression | Breast cancer | Genetic aspects | Research | Cells | Signal transduction | Gene expression | Estrogen | Cell adhesion & migration | Acute-Phase Proteins | Actins | NFATC Transcription Factors | Breast Neoplasms | Life Sciences | Estrogen Receptor alpha | Lipocalins | Proto-Oncogene Proteins | Cancer
Breast | LCN2 | Estrogen receptor a | Motility | NFAT3 | NGAL | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | estrogen receptor alpha | PANCREATIC-CANCER | GELATINASE-ASSOCIATED LIPOCALIN | IDENTIFICATION | CELL BIOLOGY | INVASION | ONCOLOGY | ESTROGEN-RECEPTOR-ALPHA | GENETICS & HEREDITY | motility | NUCLEAR FACTOR | breast | EXPRESSION | T-CELLS | Neoplasm Invasiveness | Humans | NFATC Transcription Factors - metabolism | Actins - metabolism | Gene Expression Regulation, Neoplastic | Proto-Oncogene Proteins - genetics | Acute-Phase Proteins - genetics | Proto-Oncogene Proteins - deficiency | Breast Neoplasms - metabolism | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Lipocalin-2 | Lipocalins - genetics | Cell Line, Tumor | Protein Binding | Estrogen Receptor alpha - metabolism | Acute-Phase Proteins - deficiency | Cell Movement | NFATC Transcription Factors - genetics | Cellular proteins | Transcription factors | Physiological aspects | Development and progression | Breast cancer | Genetic aspects | Research | Cells | Signal transduction | Gene expression | Estrogen | Cell adhesion & migration | Acute-Phase Proteins | Actins | NFATC Transcription Factors | Breast Neoplasms | Life Sciences | Estrogen Receptor alpha | Lipocalins | Proto-Oncogene Proteins | Cancer
Journal Article