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1. Full Text Growth differentiation factor 15 is a myomitokine governing systemic energy homeostasis
by Chung, Hyo Kyun and Ryu, Dongryeol and Kim, Koon Soon and Chang, Joon Young and Kim, Yong Kyung and Yi, Hyon-Seung and Kang, Seul Gi and Choi, Min Jeong and Lee, Seong Eun and Jung, Saet-Byel and Ryu, Min Jeong and Kim, Soung Jung and Kweon, Gi Ryang and Kim, Hail and Hwang, Jung Hwan and Lee, Chul-Ho and Lee, Se-Jin and Wall, Christopher E and Downes, Michael and Evans, Ronald M and Auwerx, Johan and Shong, Minho
Journal of Cell Biology, ISSN 0021-9525, 2017, Volume 216, Issue 1, pp. 149 - 165
Reduced mitochondria! electron transport chain activity promotes longevity and improves energy homeostasis via cell-autonomous and non-autonomous factors in... 
SKELETAL-MUSCLE | OXIDATIVE-PHOSPHORYLATION | UNFOLDED PROTEIN RESPONSE | INSULIN-RESISTANCE | GENE-EXPRESSION | TGF-BETA SUPERFAMILY | TYPE-2 DIABETES-MELLITUS | MAMMALIAN MITOCHONDRIAL RIBOSOME | ELECTRON-TRANSPORT | MTDNA MUTATOR MICE | CELL BIOLOGY | Transcription Factor CHOP - genetics | Mitochondria, Liver - metabolism | Mitochondria, Muscle - metabolism | Homeostasis | Male | Muscle, Skeletal - metabolism | Obesity - genetics | Growth Differentiation Factor 15 - genetics | Adipose Tissue - metabolism | Transfection | Liver - drug effects | RNA Interference | Time Factors | Muscle, Skeletal - drug effects | Cell Cycle Proteins - genetics | Weight Gain | Genetic Predisposition to Disease | Oxidation-Reduction | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Insulin Resistance | Oxidative Phosphorylation | Cell Cycle Proteins - deficiency | Leptin - genetics | Growth Differentiation Factor 15 - deficiency | Recombinant Proteins - pharmacology | 3T3-L1 Cells | Unfolded Protein Response | Lipolysis | Mice, Knockout | Obesity - metabolism | Phenotype | Animals | Obesity - prevention & control | Mice, Obese | Growth Differentiation Factor 15 - pharmacology | Mice | Growth Differentiation Factor 15 - metabolism | Leptin - deficiency | Transcription Factor CHOP - metabolism | Adipose Tissue - drug effects | Energy Metabolism - drug effects | Muscles | Physiological aspects | Insulin resistance | Growth | Proteins | Mitochondria | Cellular biology | Bioenergetics | Stress response
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2. Full Text GFRAL is the receptor for GDF15 and the ligand promotes weight loss in mice and nonhuman primates
by Mullican, Shannon E and Lin-Schmidt, Xiefan and Chin, Chen-Ni and Chavez, Jose A and Furman, Jennifer L and Armstrong, Anthony A and Beck, Stephen C and South, Victoria J and Dinh, Thai Q and Cash-Mason, Tanesha D and Cavanaugh, Cassandre R and Nelson, Serena and Huang, Chichi and Hunter, Michael J and Rangwala, Shamina M
Nature Medicine, ISSN 1078-8956, 10/2017, Volume 23, Issue 10, pp. 1150 - 1157
Growth differentiation factor 15 (GDF15), a distant member of the transforming growth factor (TGF)-beta family, is a secreted protein that circulates as a... 
RET | MEDICINE, RESEARCH & EXPERIMENTAL | GDNF FAMILY | BIOCHEMISTRY & MOLECULAR BIOLOGY | BRAIN-STEM | CELL BIOLOGY | OBESITY | CYTOKINE MIC-1 | DIFFERENTIATION FACTOR 15 | BETA SUPERFAMILY MEMBER | SIGNALING PATHWAY | BINDING | ASSOCIATION | Humans | Glial Cell Line-Derived Neurotrophic Factor Receptors - metabolism | Macaca fascicularis | Weight Loss - drug effects | Eating - genetics | Glial Cell Line-Derived Neurotrophic Factor Receptors - genetics | Growth Differentiation Factor 15 - genetics | Mice, Knockout | Obesity - metabolism | Eating - drug effects | Animals | Diet, High-Fat | Growth Differentiation Factor 15 - pharmacology | Mice | Growth Differentiation Factor 15 - metabolism | Weight Loss - genetics | Obesity | Development and progression | Cell receptors | Care and treatment | Genetic aspects | Health aspects | Transforming growth factor | Body weight | Solitary tract nucleus | Body weight loss | High fat diet | Receptors | Area postrema | Clonal deletion | Rodents | Primates | Deletion | Recombinant | Glial cell line-derived neurotrophic factor | Neurons | Weight loss | Pharmacology | Metabolism | Insulin | Signaling | Weight control | Food intake | Weight reduction | Ligands
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3. Full Text The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice
by Guillem Casanovas and Maja Vujić Spasić and Carla Casu and Stefano Rivella and Jens Strelau and Klaus Unsicker and Martina U. Muckenthaler
Haematologica, ISSN 0390-6078, 03/2013, Volume 98, Issue 3, pp. 444 - 447
In conditions of increased erythropoiesis, expression of hepcidin, the master regulator of systemic iron homeostasis, is decreased to allow for the release of... 
HEPATOCYTES | PROTEIN | METABOLISM | CYTOKINE-1 GDF-15/MIC-1 | GDF15 | INEFFECTIVE ERYTHROPOIESIS | FERROPORTIN | THALASSEMIA | TGF-BETA SUPERFAMILY | HEPCIDIN EXPRESSION | HEMATOLOGY | Hepcidins - metabolism | Liver - metabolism | RNA, Messenger - genetics | Phlebotomy | Homeostasis | Erythrocyte Indices | Male | RNA, Messenger - metabolism | Iron - metabolism | Growth Differentiation Factor 15 - genetics | Mice, Knockout | Animals | Spleen - metabolism | Bone Marrow - metabolism | Hepcidins - genetics | Female | Mice | Growth Differentiation Factor 15 - metabolism | Iron - blood
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4. Full Text Growth Differentiation Factor 15 Maturation Requires Proteolytic Cleavage by PCSK3, -5, and -6
by Li, Jing Jing and Li, Jing Jing and Liu, Jian and Liu, Jian and Lupino, Katherine and Lupino, Katherine and Liu, Xueyuan and Zhang, Lili and Pei, Liming and Peia, Liming
Molecular and cellular biology, ISSN 0270-7306, 11/2018, Volume 38, Issue 21
Growth differentiation factor 15 (GDF15) is a secreted protein with pleotropic functions from the transforming growth factor beta (TGF-beta) family. GDF15 is... 
cardiomyocytes | cardiac endocrinology | GDF15 | heart disease | PCSK | BONE MORPHOGENETIC PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | WEIGHT-LOSS | TGF-BETA SUPERFAMILY | RECEPTOR | CYTOKINE | MEMBER | CELL BIOLOGY | PROPROTEIN CONVERTASES | METABOLISM | ERR-GAMMA | Cell Line | Humans | Mice, Inbred C57BL | Proprotein Convertases - metabolism | Mice, Knockout | Animals | Proteolysis | HEK293 Cells | Myocytes, Cardiac - metabolism | Signal Transduction - physiology | Mice | Serine Endopeptidases - metabolism | Subtilisins - metabolism | Growth Differentiation Factor 15 - metabolism | Transforming Growth Factor beta - metabolism
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5. Full Text Prognostic Value of N-Terminal Pro-B-Type Natriuretic Peptide, Troponin-T, and Growth-Differentiation Factor 15 in Adult Congenital Heart Disease
by Baggen, Vivan J.M and van den Bosch, Annemien E and Eindhoven, Jannet A and Schut, Anne-Rose W and Cuypers, Judith A.A.E and Witsenburg, Maarten and de Waart, Monique and van Schaik, Ron H.N and Zijlstra, Felix and Boersma, Eric and Roos-Hesselink, Jolien W
Circulation, ISSN 0009-7322, 01/2017, Volume 135, Issue 3, pp. 264 - 279
BACKGROUND:The number of patients with adult congenital heart disease (ACHD) is rapidly increasing. To optimize patient management, there is a great need to... 
congenital heart disease | intercellular signaling peptides and proteins | troponin | biomarkers | pro-brain natriuretic peptide (1-76) | CARDIAC-FUNCTION | MORTALITY | VENTRICLE | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | RISK STRATIFICATION | FOLLOW-UP | FAILURE | TASK-FORCE | PERIPHERAL VASCULAR DISEASE | ASSOCIATION | Peptide Fragments - metabolism | Prognosis | Prospective Studies | Humans | Natriuretic Peptide, Brain - metabolism | Echocardiography - methods | Male | Troponin T - metabolism | Adult | Female | Growth Differentiation Factor 15 - metabolism | Cohort Studies | Heart Defects, Congenital - blood | Congenital heart disease | Adults | Research | Biological markers | Health aspects
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6. Full Text Growth Differentiation Factor 15 Mediates Systemic Glucose Regulatory Action of T-Helper Type 2 Cytokines
by Lee, Seong Eun and Kang, Seul Gi and Choi, Min Jeong and Jung, Saet-Byel and Ryu, Min Jeong and Chung, Hyo Kyun and Chang, Joon Young and Kim, Yong Kyung and Lee, Ju Hee and Kim, Koon Soon and Kim, Hyun Jin and Lee, Heung Kyu and Yi, Hyon-Seung and Shong, Minho
Diabetes, ISSN 0012-1797, 11/2017, Volume 66, Issue 11, pp. 2774 - 2788
T-helper type 2 (Th2) cytokines, including interleukin (IL)-13 and IL-4, produced in adipose tissue, are critical regulators of intra-adipose and systemic... 
B-CELLS | ALTERNATIVELY ACTIVATED MACROPHAGES | SIGNALING PATHWAYS | OBESITY | IMMUNE CELLS | RNA-SEQ | INSULIN-RESISTANCE | ADIPOSE-TISSUE INFLAMMATION | ENDOCRINOLOGY & METABOLISM | IL-4 RECEPTOR | EXPRESSION | Blood Glucose - physiology | Interleukin-13 - physiology | Th2 Cells - physiology | Interleukin-33 - pharmacology | Janus Kinases - metabolism | STAT6 Transcription Factor - genetics | Glucose Intolerance | Growth Differentiation Factor 15 - genetics | Interleukin-13 - genetics | RNA Interference | Diet, High-Fat | Interleukin-4 - genetics | Interleukin-4 - physiology | Janus Kinases - genetics | Interleukin-4 - metabolism | Receptors, Cell Surface - metabolism | Recombinant Proteins - pharmacology | STAT6 Transcription Factor - metabolism | 3T3-L1 Cells | Interleukin-13 - metabolism | Protein Disulfide Reductase (Glutathione) | Mice, Knockout | Animals | Glucose - metabolism | Mice | Mice, Inbred BALB C | Growth Differentiation Factor 15 - metabolism | Interleukin-33 - administration & dosage | Receptors, Cell Surface - genetics | Medical research | Obesity | Data analysis | Animal models | Adipose tissue | Cytokines | Homeostasis | Data processing | Lymphocytes T | Interleukin 13 | Glucose | Adipocytes | Ribonucleic acid--RNA | Insulin | High fat diet | Glucose tolerance | Glucose metabolism | Intolerance | Interleukin 4 | Stat6 protein | Janus kinase | Lipid metabolism | Galactosylceramide
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7. Full Text Growth differentiation factor 15 in erythroid health and disease
by Tanno, Toshihiko and Noel, Pierre and Miller, Jeffery L
Current Opinion in Hematology, ISSN 1065-6251, 05/2010, Volume 17, Issue 3, pp. 184 - 190
PURPOSE OF REVIEWGrowth differentiation factor 15 (GDF15) was identified as a hepcidin-suppression factor that is expressed at high levels in patients with... 
GDF15 | Iron regulation | Ineffective erythropoiesis | WEIGHT-LOSS | ineffective erythropoiesis | TGF-BETA SUPERFAMILY | IRON-METABOLISM | ANEMIA TYPE-I | MACROPHAGE-INHIBITORY CYTOKINE-1 | PROSTATE-CANCER | PYRUVATE-KINASE DEFICIENCY | HEMATOLOGY | UP-REGULATION | iron regulation | TRANSGENIC MICE | Anemia - metabolism | Animals | Iron Overload - metabolism | Humans | Thalassemia - metabolism | Anemia - pathology | Thalassemia - pathology | Growth Differentiation Factor 15 - metabolism | Iron Overload - pathology | Erythropoiesis - physiology
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8. Full Text Divergent molecular mechanisms underlying the pleiotropic functions of macrophage inhibitory cytokine‐1 in cancer
by Mimeault, Murielle and Batra, Surinder K
Journal of Cellular Physiology, ISSN 0021-9541, 09/2010, Volume 224, Issue 3, pp. 626 - 635
Multifunctional macrophage inhibitory cytokine‐1, MIC‐1, is a member of the transforming growth factor‐β (TGF‐β) superfamily that plays key roles in the... 
GROWTH-FACTOR-BETA | SIGNALING PATHWAYS | PHYSIOLOGY | ACTIVATED GENE NAG-1 | PROTEIN | DIFFERENTIATION FACTOR 15 | DEPENDENT REGULATION | DNA-DAMAGE | TGF-BETA SUPERFAMILY | UP-REGULATION | EXPRESSION | CELL BIOLOGY | Neoplasms - metabolism | Prognosis | Humans | Gene Expression Regulation, Neoplastic | Neoplasms - diagnosis | Disease Progression | Growth Differentiation Factor 15 - chemistry | Growth Differentiation Factor 15 - genetics | Pregnancy | Animals | Transforming Growth Factor beta - genetics | Neoplasms - genetics | Biomarkers, Tumor - metabolism | Female | Signal Transduction - physiology | Biomarkers, Tumor - genetics | Growth Differentiation Factor 15 - metabolism | Neoplasms - pathology | Transforming Growth Factor beta - metabolism | Index Medicus
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9. Full Text Sex-specific differences in the modulation of Growth Differentiation Factor 15 (GDF15) by hyperoxia in vivo and in vitro: Role of Hif-1α
by Zhang, Yuhao and Jiang, Weiwu and Wang, Lihua and Lingappan, Krithika
Toxicology and Applied Pharmacology, ISSN 0041-008X, 10/2017, Volume 332, pp. 8 - 14
Male premature neonates are more susceptible than females to the development of bronchopulmonary dysplasia (BPD). The reasons underlying sexually dimorphic... 
HIF-1alpha | Bronchopulmonary dysplasia | GDF15 | Hyperoxia | Sex-specific | ANGIOGENESIS | LUNG INJURY | OXYGEN-TOXICITY | RAT LUNG | RESPIRATORY-DISTRESS-SYNDROME | HYPOXIA-INDUCIBLE FACTORS | ENDOTHELIAL-CELLS | INFANTS | GENE-EXPRESSION | PHARMACOLOGY & PHARMACY | TOXICOLOGY | Animals, Newborn | Human Umbilical Vein Endothelial Cells | Lung Injury - pathology | Cell Proliferation | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Humans | Mice, Inbred C57BL | RNA, Messenger - genetics | Gene Expression Regulation | Male | RNA, Messenger - metabolism | Hyperoxia - diagnosis | Growth Differentiation Factor 15 - genetics | Lung Injury - genetics | Animals | Hyperoxia - genetics | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Sex Factors | Female | Mice | Growth Differentiation Factor 15 - metabolism | Apoptosis | Index Medicus | Bronchopulmonary Dysplasia
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10. Full Text Concise Review: Growth Differentiation Factor 15 in Pathology: A Clinical Role?
by Corre, Jill and Hébraud, Benjamin and Bourin, Philippe
STEM CELLS Translational Medicine, ISSN 2157-6564, 12/2013, Volume 2, Issue 12, pp. 946 - 952
Increased blood concentration of GDF15 is associated with numerous pathological conditions, but the biological significance underlying these observations is... 
Clinical translation | Drug target | Malignancy | Cancer | MULTIPLE-MYELOMA | HUMAN BREAST | RISK STRATIFICATION | MACROPHAGE INHIBITORY CYTOKINE-1 | HEART-FAILURE | TGF-BETA SUPERFAMILY | PANCREATIC ADENOCARCINOMA | MESENCHYMAL STEM-CELLS | CELL & TISSUE ENGINEERING | ACTIVATED GENE NAG-1 | PROSTATE-CANCER CELLS | Erythropoiesis | Neoplasms - metabolism | Prognosis | Cardiovascular Diseases - metabolism | Signal Transduction | Humans | Gene Expression Regulation | Growth Differentiation Factor 15 - genetics | Animals | Neoplasms - genetics | Erythrocytes - metabolism | Biomarkers, Tumor - metabolism | Growth Differentiation Factor 15 - metabolism | Neoplasms - pathology | Proteins | Pathology | Cell growth | Disease | Cytokines | Mortality | Multiple myeloma | Growth factors | Blood levels | Tumors | Tissue-Specific Progenitor and Stem Cells
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