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oxidoreductases acting on ch-nh group donors - metabolism (4) 4
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1. Full Text PURIFICATION AND CHARACTERIZATION OF AKR1B10 FROM HUMAN LIVER: ROLE IN CARBONYL REDUCTION OF XENOBIOTICS
by Hans-Jörg Martin and Ursula Breyer-Pfaff and Vladimir Wsol and Simone Venz and Simone Block and Edmund Maser
Drug Metabolism and Disposition, ISSN 0090-9556, 03/2006, Volume 34, Issue 3, pp. 464 - 470
Members of the aldo-keto reductase (AKR) superfamily have a broad substrate specificity in catalyzing the reduction of carbonyl group-containing xenobiotics.... 
Inactivation, Metabolic | Aldehyde Reductase - genetics | Liver - enzymology | Oxidation-Reduction | Electrophoresis, Polyacrylamide Gel | Humans | Molecular Sequence Data | Immunoblotting | Recombinant Proteins - genetics | Xenobiotics - pharmacokinetics | Xenobiotics - chemistry | Aldehyde Reductase - physiology | Recombinant Proteins - isolation & purification | Aldehyde Reductase - isolation & purification | Spectrometry, Mass, Electrospray Ionization | Escherichia coli - genetics | Base Sequence
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2. Full Text Nicotinamide N-Methyltransferase and Its Precursor Substrate Methionine Directly and Indirectly Control Malignant Metabolism During Progression of Renal Cell Carcinoma
by HOLSTEIN, SINA and VENZ, SIMONE and JUNKER, HEIKE and WALTHER, REINHARD and STOPE, MATTHIAS B and ZIMMERMANN, UWE
Anticancer Research, ISSN 0250-7005, 10/2019, Volume 39, Issue 10, pp. 5427 - 5436
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3. Full Text Stage-related alterations in renal cell carcinoma - comprehensive quantitative analysis by 2D-DIGE and Protein Network Analysis
by Junker, Heike and Venz, Simone and Zimmermann, Uwe and Thiele, Andrea and Scharf, Christian and Walther, Reinhard
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 7, p. e21867
Renal cell carcinoma accounts for about 3% of adult malignancies and 85% of neoplasms arising from the kidney. To identify potential progression markers for... 
CANCER-CELLS | BREAST-CANCER | IN-VITRO | PROHIBITIN GENE | PEROXIREDOXIN-III | BIOLOGY | CANDIDATE BIOMARKERS | COMPARATIVE GENOMIC HYBRIDIZATION | PROTEOMIC ANALYSIS | EXPRESSION | MASS-SPECTROMETRY | Immunohistochemistry | Humans | Middle Aged | Male | Kidney Neoplasms - metabolism | Neoplasm Proteins - metabolism | Two-Dimensional Difference Gel Electrophoresis - methods | Mass Spectrometry | Aged, 80 and over | Adult | Female | Principal Component Analysis | Reproducibility of Results | Neoplasm Proteins - classification | Signal Transduction | Carcinoma, Renal Cell - pathology | Neoplasm Proteins - chemistry | Blotting, Western | Carcinoma, Renal Cell - metabolism | Proteomics | Kidney Neoplasms - pathology | Aged | Neoplasm Staging | Proteome - metabolism | Cluster Analysis | Carcinoma, Renal cell | Viral proteins | Proteases | Quality control | Genomics | Lung cancer | Statistical methods | Biochemistry | Metastasis | Cancer therapies | Neoplasms | Proteins | Mitochondria | Lipid metabolism | Labeling | Two dimensional analysis | Quantitative analysis | Evaluation | Cytokines | Gene expression | Metabolism | Studies | Robust control | Peptidases | Correlation analysis | Kidney cancer | Biomarkers | Cytoskeleton | Scientific imaging | Mass spectrometry | Transporter | Clear cell-type renal cell carcinoma | Kidney transplantation | Fluorescence | Otolaryngology | Kinases | Urology | Ethics | Network analysis | Spots | Cell cycle | Endoscopy | Statistical analysis | Gel electrophoresis | Principal components analysis | Clustering | Biopsy | Diagnostic systems | Molecular biology | Cancer
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4. Full Text The marine triterpene glycoside frondoside A exhibits activity in vitro and in vivo in prostate cancer
by Dyshlovoy, Sergey A and Menchinskaya, Ekaterina S and Venz, Simone and Rast, Stefanie and Amann, Kerstin and Hauschild, Jessica and Otte, Katharina and Kalinin, Vladimir I and Silchenko, Alexandra S and Avilov, Sergey A and Alsdorf, Winfried and Madanchi, Ramin and Bokemeyer, Carsten and Schumacher, Udo and Walther, Reinhard and Aminin, Dmitry L and Fedorov, Sergey N and Shubina, Larisa K and Stonik, Valentin A and Balabanov, Stefan and Honecker, Friedemann and von Amsberg, Gunhild
International Journal of Cancer, ISSN 0020-7136, 05/2016, Volume 138, Issue 10, pp. 2450 - 2465
Despite recent advances in the treatment of metastatic castration‐resistant prostate cancer (CRPC), outcome of patients remains poor due to the development of... 
castration‐resistant prostate cancer | anti‐metastatic activity | apoptosis | frondoside A | autophagy | anti-metastatic activity | castration-resistant prostate cancer | CELLS | DOCETAXEL | SEA | INHIBITION | ANTICANCER | ONCOLOGY | ENZALUTAMIDE RESISTANCE | EXPRESSION | AAPTAMINE | Triterpenes - pharmacology | Apoptosis - drug effects | Humans | Drug Resistance, Neoplasm | Male | Autophagy - drug effects | Prostatic Neoplasms, Castration-Resistant - genetics | Prostatic Neoplasms, Castration-Resistant - pathology | Apoptosis Regulatory Proteins - genetics | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Disease Models, Animal | Cell Survival - drug effects | Tumor Stem Cell Assay | Reproducibility of Results | Prostatic Neoplasms, Castration-Resistant - drug therapy | Glycosides - pharmacology | Prostatic Neoplasms, Castration-Resistant - metabolism | Apoptosis Regulatory Proteins - metabolism | Xenograft Model Antitumor Assays | Animals | Cell Cycle Checkpoints - drug effects | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Proteins | Keratin | Drug resistance | Prostate cancer | Analysis | Rodents | Medical prognosis | Cell cycle | Metastasis | Autophagy | Apoptosis | Cell proliferation | Drugs | Alternative splicing | Bax protein | Bcl-2 protein | Toxicity | Drug development | Caspase-3 | Immunosuppressive agents | Metastases | Castration | Down-regulation | Interleukin 1 | Cathepsin B | Cleavage | Inhibition | Cell survival | Immunomodulation | Tumor cells | Caspase | Poly(ADP-ribose) polymerase | Androgens | Lungs | Cell lines | Bcl protein | Phagocytosis | Cancer | Index Medicus
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5. Full Text Isoform 1 of TPD52 (PC-1) promotes neuroendocrine transdifferentiation in prostate cancer cells
by Moritz, Tom and Venz, Simone and Junker, Heike and Kreuz, Sarah and Walther, Reinhard and Zimmermann, Uwe
Tumor Biology, ISSN 1010-4283, 8/2016, Volume 37, Issue 8, pp. 10435 - 10446
The tumour protein D52 isoform 1 (PC-1), a member of the tumour protein D52 (TPD52) protein family, is androgen-regulated and prostate-specific expressed.... 
TPD52 | PC-1 | Biomedicine | LNCaP | PrLZ | Cancer Research | Neuroendocrine transdifferentiation | Prostate cancer | ACTIVATION | RECEPTOR | INTERLEUKIN-6 | GENE | ONCOLOGY | PROTEIN EXPRESSION | ACINAR-CELLS | DIFFERENTIATION | TUMOR-GROWTH | ANDROGEN DEPRIVATION THERAPY | Neuroendocrine Cells - chemistry | Adenocarcinoma - pathology | Humans | Neoplasm Proteins - physiology | Male | Recombinant Fusion Proteins - metabolism | Cell Transdifferentiation - physiology | Transfection | Receptors, Androgen - biosynthesis | Antineoplastic Agents, Hormonal - therapeutic use | Cell Transdifferentiation - drug effects | Protein Domains | Neoplasm Proteins - genetics | Prostatic Neoplasms - drug therapy | Prostatic Neoplasms - pathology | Interleukin-6 - therapeutic use | Neuroendocrine Cells - pathology | Protein Isoforms - physiology | Androgens | Interleukin-6 - pharmacology | Neoplasms, Hormone-Dependent - pathology | Androgen Antagonists - therapeutic use | Biomarkers | Cell Line, Tumor | Neoplasm Proteins - analysis | Neoplasms, Hormone-Dependent - drug therapy | Protein Isoforms - genetics | Development and progression | Interleukins | Tumor proteins | Proteins | Cellular biology
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6. Full Text Proteomic‐based investigations on the mode of action of the marine anticancer compound rhizochalinin
by Dyshlovoy, Sergey A and Otte, Katharina and Venz, Simone and Hauschild, Jessica and Junker, Heike and Makarieva, Tatyana N and Balabanov, Stefan and Alsdorf, Winfried H and Madanchi, Ramin and Honecker, Friedemann and Bokemeyer, Carsten and Stonik, Valentin A and Amsberg, Gunhild
PROTEOMICS, ISSN 1615-9853, 06/2017, Volume 17, Issue 11, pp. 1700048 - n/a
Rhizochalinin (Rhiz) is a novel marine natural sphingolipid‐like compound, which shows promising in vitro and in vivo activity in human castration‐resistant... 
Rhizochalinin | ERK1/2 | Ingenuity pathway analysis (IPA) | Prostate cancer | Antimigratory activity | GERM-CELL CANCER | MIGRATION | ALKALOID MONANCHOCIDIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | INDUCTION | INDUCED NEOPLASTIC TRANSFORMATION | IN-VITRO | INHIBITION | CYTOTOXIC PROPERTIES | PROSTATE-CANCER | CASTRATION-RESISTANT | Prostatic Neoplasms - metabolism | Keratins, Type II - metabolism | Humans | Male | LIM Domain Proteins - metabolism | Fatty Alcohols - pharmacology | Rhizoctonia - chemistry | Interleukin-1beta - metabolism | Cytoskeletal Proteins - metabolism | Antineoplastic Agents - pharmacology | Membrane Proteins - metabolism | Gene Expression Regulation, Neoplastic - drug effects | Proteomics - methods | Prostatic Neoplasms - drug therapy | Fibroblasts - metabolism | Prostatic Neoplasms - pathology | Cells, Cultured | Proteome - analysis | HSP70 Heat-Shock Proteins - metabolism | Cell Movement - drug effects | MAP Kinase Signaling System - drug effects | Fibroblasts - drug effects | Cell Proliferation - drug effects | Adaptor Proteins, Signal Transducing - metabolism | Keratins, Hair-Specific - metabolism | Stathmin - metabolism | Drug Screening Assays, Antitumor | Proteins | Keratin | Care and treatment | Analysis | Investigations | Cancer | Surgical implants | Leukocyte migration | Biochemistry | Western blotting | Cell adhesion & migration | Anticancer properties | Synergistic effects | Biomedical materials | Functional anatomy | Antitumor agents | Castration | Interleukin 1 | Biocompatibility | Activation analysis | Extracellular signal-regulated kinase | Data processing | Biological activity | Mode of action | Stathmin | Screening | Molecular modelling | Inhibitors | Proteomics | Isoforms | In vivo methods and tests | ATP | Prostate | In vitro methods and tests | Cell migration | Adenosine triphosphatase
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7. Full Text Prohibitin identified by proteomic analysis of prostate biopsies distinguishes hyperplasia and cancer
by Ummanni, Ramesh and Junker, Heike and Zimmermann, Uwe and Venz, Simone and Teller, Steffen and Giebel, Jürgen and Scharf, Christian and Woenckhaus, Christian and Dombrowski, Frank and Walther, Reinhard
Cancer Letters, ISSN 0304-3835, 2008, Volume 266, Issue 2, pp. 171 - 185
Abstract Prostate cancer (PCA) is the most common type of cancer found in men of western countries and is the leading cancer death next to lung cancer and... 
Hematology, Oncology and Palliative Medicine | Prostate biopsies | Hyperplasia | Prohibitin | Proteomics | Cancer | DIAGNOSIS | ANTIPROLIFERATIVE ACTIVITY | proteomics | prostate biopsies | PROGNOSIS | ADENOCARCINOMA | TISSUE | prohibitin | CELL-LINES | BIOMARKERS | ONCOLOGY | PROTEIN EXPRESSION | hyperplasia | cancer | NEEDLE-BIOPSY | ANTIGEN | Prostatic Neoplasms - metabolism | Prostatic Neoplasms - pathology | Prostatic Hyperplasia - pathology | Biomarkers, Tumor - analysis | Humans | Middle Aged | Repressor Proteins - genetics | Electrophoresis, Gel, Two-Dimensional | Male | Prostatic Hyperplasia - genetics | Repressor Proteins - analysis | Prostate - metabolism | Prostatic Hyperplasia - metabolism | Prostate - pathology | Prostatic Neoplasms - genetics | Biomarkers, Tumor - metabolism | Aged | Biomarkers, Tumor - genetics | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | Biopsy, Needle | Repressor Proteins - metabolism | Enzymes | Ethanol | Peptides | Colleges & universities | Gene expression | Patients | Proteins | Pathology | Mens health | Keratin | Men | Protein expression | Prostate cancer
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8. Full Text Exosomal particles secreted by prostate cancer cells are potent mRNA and protein vehicles for the interference of tumor and tumor environment
by Rauschenberger, Lisa and Staar, Doreen and Thom, Kathleen and Scharf, Christian and Venz, Simone and Homuth, Georg and Schlüter, Rabea and Brandenburg, Lars‐Ove and Ziegler, Patrick and Zimmermann, Uwe and Weitschies, Werner and Völker, Uwe and Lendeckel, Uwe and Walther, Reinhard and Burchardt, Martin and Stope, Matthias B
The Prostate, ISSN 0270-4137, 03/2016, Volume 76, Issue 4, pp. 409 - 424
BackgroundRemodeling of the tumor environment and the modulation of tumor associated non-malignant cells are essential events in tumor progression. Exosomes... 
microenvironment | prostate cancer | protein uptake | exosomes | APOPTOSIS | MICROVESICLES | RECEPTOR | RELEASE | BIOMARKERS | EXTRACELLULAR VESICLES | ENDOCRINOLOGY & METABOLISM | UROLOGY & NEPHROLOGY | ANTIGEN | Microscopy, Electron, Transmission | RNA Transport - physiology | Humans | RNA, Messenger - analysis | Tumor Microenvironment | Cell Communication - physiology | Male | Protein Transport - physiology | Proteins - analysis | RNA, Messenger - metabolism | Particle Size | Animals | Proteins - metabolism | Prostatic Neoplasms - ultrastructure | Exosomes - physiology | Dogs | HEK293 Cells | Madin Darby Canine Kidney Cells | Cell Line, Tumor | Dynamic Light Scattering | Exosomes - ultrastructure | Proteins | DNA microarrays | Messenger RNA | Analysis | Cancer cells | Physiological aspects | Development and progression | Prostate cancer | Mass spectrometry | Tumors
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9. Inhibition of calpain-1 stabilizes TCF11/Nrf1 but does not affect its activation in response to proteasome inhibition
by Karolin Nowak and Ramona M Taubert and Stefanie Haberecht and Simone Venz and Elke Krüger
Bioscience Reports, ISSN 0144-8463, 10/2018, Volume 38, Issue 5
Protein degradation is essential to compensate for the damaging effects of proteotoxic stress. To ensure protein and redox homeostasis in response to... 
Translocation | Transcription factors | Calcium | Homeostasis | Calpain | Activation | siRNA | Kinases | Nuclear transport | Proteins | Degradation | Organic chemistry | Proteasomes | Cleavage | Inhibition | Endoplasmic reticulum
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10. Full Text Altered expression of tumor protein D52 regulates apoptosis and migration of prostate cancer cells
by Ummanni, Ramesh and Teller, Steffen and Junker, Heike and Zimmermann, Uwe and Venz, Simone and Scharf, Christian and Giebel, Jürgen and Walther, Reinhard
FEBS Journal, ISSN 1742-464X, 11/2008, Volume 275, Issue 22, pp. 5703 - 5713
Tumor protein D52 (TPD52) is a protein found to be overexpressed in prostate and breast cancer due to gene amplification. However, its physiological function... 
Cell proliferation | TPD52 | Prostate carcinoma | Cell migration | Apoptosis | BREAST-CARCINOMA | cell proliferation | BIOCHEMISTRY & MOLECULAR BIOLOGY | BONE-MARROW | apoptosis | IDENTIFICATION | LINES | FAMILY | ADHESION | AMPLIFICATION | INTEGRINS | COPY NUMBER | cell migration | TPD52 GENE | prostate carcinoma | Prostatic Neoplasms - pathology | Cell Proliferation | Signal Transduction | Humans | Neoplasm Proteins - physiology | Gene Expression Regulation - physiology | Apoptosis - genetics | Male | Integrin alphaVbeta3 | Cell Movement - genetics | Proto-Oncogene Proteins c-akt | Prostatic Neoplasms - genetics | Cell Line, Tumor | Mitochondria - physiology | Neoplasm Proteins - genetics | RNA | Membrane potentials | Fluorescence | Analysis | Cancer cells | Physiological aspects | Genetic research | Health aspects | Prostate cancer | Protein kinases | Integrins | Tumors | Biochemistry | Cellular biology | Proteomics
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11. Full Text Cabazitaxel overcomes cisplatin resistance in germ cell tumour cells
by Gerwing, Mirjam and Jacobsen, Christine and Dyshlovoy, Sergey and Hauschild, Jessica and Rohlfing, Tina and Oing, Christoph and Venz, Simone and Oldenburg, Jan and Oechsle, Karin and Bokemeyer, Carsten and von Amsberg, Gunhild and Honecker, Friedemann
Journal of Cancer Research and Clinical Oncology, ISSN 0171-5216, 9/2016, Volume 142, Issue 9, pp. 1979 - 1994
Cisplatin-based chemotherapy is highly effective in metastasized germ cell tumours (GCT). However, 10–30 % of patients develop resistance to cisplatin,... 
Medicine & Public Health | Hematology | Oncology | Cancer Research | Internal Medicine | Germ cell tumour | Cisplatin resistance | Cabazitaxel | Apoptosis | PROTEIN | TESTICULAR CANCER | LINES | CHEMOTHERAPY | IN-VITRO | NUCLEOPHOSMIN | RETINOIC ACID | ONCOLOGY | TAXOL | DIFFERENTIATION | EXPRESSION | Paclitaxel - pharmacology | Taxoids - pharmacology | Apoptosis - drug effects | Humans | Male | Antineoplastic Agents - therapeutic use | Testicular Neoplasms - pathology | Cisplatin - therapeutic use | Testicular Neoplasms - drug therapy | Cell Line, Tumor | Neoplasms, Germ Cell and Embryonal - drug therapy | Antineoplastic Agents - pharmacology | Cell Cycle - drug effects | Neoplasms, Germ Cell and Embryonal - pathology | Drug Resistance, Neoplasm - drug effects | Antimitotic agents | Chemotherapy | Antineoplastic agents | Analysis | Tumors | Cancer
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12. Full Text Identification of clinically relevant protein targets in prostate cancer with 2D-DIGE coupled mass spectrometry and systems biology network platform
by Ummanni, Ramesh and Mundt, Frederike and Pospisil, Heike and Venz, Simone and Scharf, Christian and Barett, Christine and Fälth, Maria and Köllermann, Jens and Walther, Reinhard and Schlomm, Thorsten and Sauter, Guido and Bokemeyer, Carsten and Sültmann, Holger and Schuppert, A and Brümmendorf, Tim H and Balabanov, Stefan
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, p. e16833
Prostate cancer (PCa) is the most common type of cancer found in men and among the leading causes of cancer death in the western world. In the present study,... 
BIOMARKERS | ANDROGEN RECEPTOR | PEROXIREDOXINS | PROGNOSIS | STATISTICS | MULTIDISCIPLINARY SCIENCES | PRINCIPLE | PROTEOMIC ANALYSIS | EXPRESSION | PROGRESSION | ARGINASE-II | Proteins | Comparative analysis | Mass spectrometry | Prostate cancer | Communications software | Oxidative stress | Hydrogen peroxide | Genomics | Otolaryngology | Oncology | Genomes | Biochemistry | Thyroid gland | Biology | Polyamines | Cell growth | Spots | Bone marrow | Physiology | Bioindicators | Dissection | Spectroscopy | Hematology | Gel electrophoresis | Benign | Principal components analysis | Mass spectroscopy | Breast cancer | Gene expression | Patients | Studies | Pathology | Androgens | Hospitals | Proteomics | Biomarkers | Diagnostic systems | Molecular biology | Prostate | Cancer | Apoptosis
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13. Full Text Anti‐migratory activity of marine alkaloid monanchocidin A – proteomics‐based discovery and confirmation
by Dyshlovoy, Sergey A and Venz, Simone and Hauschild, Jessica and Tabakmakher, Ksenya M and Otte, Katharina and Madanchi, Ramin and Walther, Reinhard and Guzii, Alla G and Makarieva, Tatyana N and Shubina, Larisa K and Fedorov, Sergey N and Stonik, Valentin A and Bokemeyer, Carsten and Balabanov, Stefan and Honecker, Friedemann and v. Amsberg, Gunhild
PROTEOMICS, ISSN 1615-9853, 05/2016, Volume 16, Issue 10, pp. 1590 - 1603
Monanchocidin A (MonA) is a novel marine alkaloid with promising anti‐cancer properties. We recently demonstrated its high efficacy in human urogenital cancers... 
Monanchocidin A | Anti‐migratory activity | Biomedicine | Apolipoprotein E | Germ cell tumor cells | eIF5A | EIF5A | Anti-migratory activity | BIOCHEMISTRY & MOLECULAR BIOLOGY | BIOCHEMICAL RESEARCH METHODS | CELL-PROLIFERATION | AUTOPHAGY | APOLIPOPROTEIN-E | INHIBITION | HYPUSINE | INITIATION-FACTOR 5A | IN-VIVO | GROWTH | AAPTAMINE | Cell Survival - drug effects | Proteome - genetics | Gene Expression - drug effects | Guanidine - pharmacology | Humans | Guanidine - analogs & derivatives | Cell Movement - drug effects | Proteomics | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | Proteome - metabolism | Drug Screening Assays, Antitumor | Alkaloids | Analysis | Metastasis | Apolipoproteins | Intermediate filament proteins | Genetic translation | Vimentin | Transcription | Translation initiation | Cytotoxicity | Cisplatin | Biological activity | Molecular chains | Cell adhesion & migration | Mode of action | Proteins | Molecular modelling | Isoforms | Cell migration | Cancer | Tumors
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14. Full Text Inhibition of calpain-1 stabilizes TCF11/Nrf1 but does not affect its activation in response to proteasome inhibition
by Nowak, Karolin and Taubert, Ramona M and Haberecht, Stefanie and Venz, Simone and Krüger, Elke
Bioscience Reports, ISSN 0144-8463, 09/2018, Volume 38, Issue 5, pp. 1 - 11
Protein degradation is essential to compensate for the damaging effects of proteotoxic stress. To ensure protein and redox homeostasis in response to... 
SYSTEM | DEGRADATION | PROTEIN | NRF1 | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY
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15. Full Text The Angiotensin-(1–7)/Mas Axis Improves Pancreatic β-Cell Function in Vitro and in Vivo
by Sahr, Anika and Wolke, Carmen and Maczewsky, Jonas and Krippeit-Drews, Peter and Tetzner, Anja and Drews, Gisela and Venz, Simone and Gürtler, Sarah and van den Brandt, Jens and Berg, Sabine and Döring, Paula and Dombrowski, Frank and Walther, Thomas and Lendeckel, Uwe
Endocrinology, ISSN 0013-7227, 12/2016, Volume 157, Issue 12, pp. 4677 - 4690
The angiotensin-converting enzyme 2/angiotensin (Ang)-(1–7)/Mas axis of the renin-angiotensin system often opposes the detrimental effects of the... 
DIABETES-MELLITUS | SYSTEM | PHOSPHORYLATION | GLUCOSE | INSULIN-SECRETION | ENDOCRINOLOGY & METABOLISM | RATS | RECEPTOR | MICE | MAS | CAMP | Proto-Oncogene Proteins - metabolism |