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2000, Taylor & Francis series in pharmaceutical sciences, ISBN 0748408045, 189
Introduction - Structure and Function of the ß3-Adrenoreceptor, A.D. Strosberg and C.C. Gerhardt Regulation of the ß3-Adrenoreceptor Signalling Efficacy, M.... 
Adrenergic beta agonists | Beta adrenoceptors
eBook
1996, Current topics in microbiology and immunology, ISBN 3540593446, Volume 205., x, 182
Book
Journal of Biotechnology, ISSN 0168-1656, 10/2012, Volume 161, Issue 3, pp. 294 - 301
This study focuses on the cloning, expression, and characterization of recombinant ginsenoside hydrolyzing glycosidase from Sanguibacter keddieii in order to... 
Bioconversion | β-Glucosidase | Rg1 | Ginsenoside | Sanguibacter keddieii | Ginsenoside C-O | Ginsenoside Rg | Ginsenoside F | Ginsenoside Rd | Ginsenoside Rb | Ginsenoside Rc | Ginsenoside C-K | S | Gypenoside LXXV | Ginsenoside C-Mc | Gypenoside XVII | Ginsenoside Rh | Ginsenoside C-Y | p-Nitrophenyl- beta -D-glucopyranoside | Escherichia coli | Homology | glycoside hydrolase | Ginsenoside C-Mc 20-O-[ alpha -l-arabinofuranosyl-(1-6)- beta -d-glucopyranosyl]- 20(S)-protopanaxadiol | Ginsenoside C-Y 20-O-[ alpha -l-arabinopyranosyl-(1-6)- beta -d-glucopyranosyl]- 20(S)-protopanaxadiol | Ginsenoside Rd 3-O-[ beta -d-glucopyranosyl-(1-2)- beta -d-glucopyranosyl]-20- O- beta -d-glucopyranosyl-20(S)-protopanaxadiol | Ginsenoside F2 3-O- beta -d-glucopyranosyl-20-O- beta -d-glucopyranosyl-20(S)- protopanaxadiol | Resins | Enzymes | Ginsenoside Rh2(S) 3-O- beta -d-glucopyranosyl-20(S)-protopanaxadiol | Ginsenoside C-O 3-O- beta -d-glucopyranosyl-20-O-[ alpha -l-arabinopyranosyl-(1- 6)- beta -d-glucopyranosyl]-20(S)-protopanaxadiol | bioconversion | beta -Glucosidase | Ginsenoside Rb2 3-O-[ beta -d-glucopyranosyl-(1-2)- beta -d-glucopyranosyl]-20- O-[ alpha -l-arabinopyranosyl-(1-6)- beta -d-glucopyranosyl]-20(S )-protopanaxadiol | F1 | Ginsenoside Rb1 3-O-[ beta -d-glucopyranosyl-(1-2)- beta -d-glucopyranosyl]-20- O-[ beta -d-glucopyranosyl-(1-6)- beta -d-glucopyranosyl]-20(S)- protopanaxadiol | Ginsenoside C-K 20-O- beta -d-glucopyranosyl-20(S)-protopanaxadiol | Gypenoside LXXV 20-O-[ beta -d-glucopyranosyl-(1-6)- beta -d-glucopyranosyl]-20 (S)-protopanaxadiol | ginsenosides | Kinetics | Ginsenoside Rc 3-O-[ beta -d-glucopyranosyl-(1-2)- beta -d-glucopyranosyl]-20- O-[ alpha -l-arabinofuranosyl-(1-6)- beta -d-glucopyranosyl]-20(S )-protopanaxadiol | Gypenoside XVII 3-O- beta -d-glucopyranosyl-20-O-[ beta -d-glucopyranosyl-(1-6) - beta -d-glucopyranosyl]-20(S)-protopanaxadiol | Ginsenoside Rg3(S) 3-O-[ beta -d-glucopyranosyl-(1-2)- beta -d-glucopyranosyl]-20( S)-protopanaxadiol | Ginsenoside C-Mc1 3-O- beta -d-glucopyranosyl-20-O-[ alpha -l-arabinofuranosyl-(1- 6)- beta -d-glucopyranosyl]-20(S)-protopanaxadiol | Biotechnology | Genes | Mathematical analysis | Glycosides | Recombinant | Glycosidases | Vectors (mathematics) | Recombinant Proteins - metabolism | Temperature | Electrophoresis, Polyacrylamide Gel | Glycoside Hydrolases - genetics | Enzyme Stability | Substrate Specificity | Ions | Ginsenosides - metabolism | Recombinant Proteins - genetics | Chromatography, High Pressure Liquid | Chromatography, Thin Layer | Actinomycetales - enzymology | Hydrolysis | Recombinant Proteins - isolation & purification | Biotransformation | Cloning, Molecular | Glycoside Hydrolases - metabolism | Ginsenosides - chemistry | Hydrogen-Ion Concentration | Index Medicus
Journal Article
1997, Lung biology in health and disease, ISBN 9780824794965, Volume 106, xvi, 443
Book
Antimicrobial Agents and Chemotherapy, ISSN 0066-4804, 04/2017, Volume 61, Issue 4
Lactamase- mediated resistance is a growing threat to the continued use of beta- lactam antibiotics. The use of the beta-lactam-based serine-beta-lactamase (... 
Inhibitors | Beta-lactams | Antibiotic resistance | Beta-lactamases | Boronate | Carbapenemase | Metalloenzymes | CLASS-A | inhibitors | beta-lactamases | MICROBIOLOGY | carbapenemase | COMBINATION | AVIBACTAM | boronate | GRAM-NEGATIVE PATHOGENS | beta-lactams | antibiotic resistance | STRUCTURAL BASIS | PSEUDOMONAS-AERUGINOSA | metalloenzymes | PENICILLIN-BINDING PROTEINS | RESISTANCE | PHARMACOLOGY & PHARMACY | BROAD-SPECTRUM INHIBITOR | THIOMANDELIC ACID | Enzymes | Clavulanic acid | Conservation | Clinical isolates | Antimicrobial agents | Mimicry | Intermediates | Infection | Hydrolysis | beta -Lactamase | Chemotherapy | Tazobactam | Pseudomonas aeruginosa | Serine- beta -lactamases | Catalysis | Metallo- beta -lactamase | Sulbactam | beta -Lactam antibiotics | Crystal structure | Enterobacteriaceae - enzymology | Bacterial Proteins - chemistry | Substrate Specificity | Crystallography, X-Ray | Thermodynamics | beta-Lactamases - genetics | Cloning, Molecular | Escherichia coli - metabolism | Protein Interaction Domains and Motifs | beta-Lactamases - metabolism | Binding Sites | Boronic Acids - chemical synthesis | Enterobacteriaceae - growth & development | Recombinant Proteins - metabolism | Bacterial Proteins - antagonists & inhibitors | Gene Expression | Protein Structure, Secondary | Bacterial Proteins - genetics | Enterobacteriaceae - genetics | Models, Molecular | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | beta-Lactamase Inhibitors - pharmacology | Amino Acid Motifs | Anti-Bacterial Agents - chemical synthesis | beta-Lactamases - chemistry | beta-Lactams - pharmacology | Cyclization | Escherichia coli - genetics | Enterobacteriaceae - drug effects | beta-Lactamase Inhibitors - chemical synthesis | Protein Binding | Bacterial Proteins - metabolism | Anti-Bacterial Agents - pharmacology | beta-Lactam Resistance - genetics | Kinetics | Boronic Acids - pharmacology | beta-Lactam Resistance - drug effects | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2015, Volume 10, Issue 3, pp. e0120045 - e0120045
Cervical cancer is the major cause of cancer related deaths in women, especially in developing countries and Human Papilloma Virus infection in conjunction... 
EPITHELIAL-MESENCHYMAL TRANSITION | BREAST-CANCER | GROWTH-FACTOR-BETA | INVASION | MULTIDISCIPLINARY SCIENCES | TRANSFORMING GROWTH-FACTOR-BETA-1 | PANCREATIC-CANCER | GENE-EXPRESSION | MECHANISMS | HUMAN-PAPILLOMAVIRUS | TRANSCRIPTION FACTOR | Downstream effects | Migration | Crosstalk | Biochemistry | Metastasis | Pin1 protein | Cancer therapies | Smad4 protein | Proteins | Signal transduction | TGF-beta signaling cascade | Tumorigenesis | Inhibition | Membrane potential | Medical research | Gene expression | Signalling | India | Chemotherapy | Phytochemicals | Ligands | Cell migration | Cervical cancer | Biotechnology | Deregulation | Wnt protein | Mesenchyme | Developing countries | Signal inhibition | Viruses | Smad3 protein | Kinases | Developing nations | Carcinogenesis | Developing countries--LDCs | Cell adhesion & migration | Mitochondrial membrane | β-catenin | Carcinogens | Pathways | Cell cycle | HeLa cells | Curcumin | Downstream | Luciferase | Breast cancer | Tumor cell lines | Cervix | Emodin | Cell lines | Cell cycle and cell division | Cancer | Apoptosis | CTNNB1 protein, human | SNAI1 protein, human | Antineoplastic Agents, Phytogenic | Cell Proliferation | Humans | Protein-Serine-Threonine Kinases | Gene Expression Regulation, Neoplastic | Wnt Proteins | Cyclin D1 | Peptidylprolyl Isomerase | matrigel | Laminin | Epithelial-Mesenchymal Transition | Female | Snail Family Transcription Factors | SMAD4 protein, human | Transforming Growth Factor beta | Proteoglycans | Signal Transduction | beta Catenin | Cyclin-Dependent Kinase Inhibitor p21 | NIMA-Interacting Peptidylprolyl Isomerase | Smad4 Protein | CCND1 protein, human | Index Medicus | Drug Synergism | SMAD3 protein, human | Smad3 Protein | transforming growth factor-beta type II receptor | Collagen | Cell Line, Tumor | Receptors, Transforming Growth Factor beta | Transcription Factors | HeLa Cells | Drug Combinations | Cell Movement | PIN1 protein, human | Receptors, Transforming Growth Factor beta - genetics | Collagen - chemistry | Epithelial-Mesenchymal Transition - drug effects | Wnt Proteins - metabolism | Smad4 Protein - genetics | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Peptidylprolyl Isomerase - metabolism | Peptidylprolyl Isomerase - genetics | Protein-Serine-Threonine Kinases - metabolism | Emodin - pharmacology | Curcumin - pharmacology | Cyclin-Dependent Kinase Inhibitor p21 - antagonists & inhibitors | Smad3 Protein - antagonists & inhibitors | beta Catenin - metabolism | Cell Movement - drug effects | Receptors, Transforming Growth Factor beta - antagonists & inhibitors | Cyclin D1 - genetics | Signal Transduction - drug effects | Laminin - chemistry | Cyclin D1 - metabolism | Smad4 Protein - antagonists & inhibitors | Smad3 Protein - metabolism | Proteoglycans - chemistry | Smad3 Protein - genetics | Cyclin D1 - antagonists & inhibitors | Cyclin-Dependent Kinase Inhibitor p21 - genetics | Wnt Proteins - genetics | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Transforming Growth Factor beta - antagonists & inhibitors | Protein-Serine-Threonine Kinases - genetics | Transcription Factors - antagonists & inhibitors | Transcription Factors - genetics | Smad4 Protein - metabolism | beta Catenin - genetics | Transcription Factors - metabolism | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | beta Catenin - antagonists & inhibitors | Cell Proliferation - drug effects | Antineoplastic Agents, Phytogenic - pharmacology | Transforming Growth Factor beta - metabolism | LDCs
Journal Article
Journal Article
BIOCHEMICAL JOURNAL, ISSN 0264-6021, 06/2005, Volume 388, Issue 2, pp. 515 - 525
XylT (beta 1,2-xylosyltransferase) is a unique Golgi-bound glycosyl-transferase that is involved in the biosynthesis of glycoproteinbound N-glycans in plants.... 
ACETYLGLUCOSAMINYLTRANSFERASE I | SUBSTRATE SPECIFICITIES | Arabidopsis | BIOCHEMISTRY & MOLECULAR BIOLOGY | proteolytic processing | INSECT CELLS | GLYCANS | GOLGI-APPARATUS | ASPARAGINE-LINKED OLIGOSACCHARIDES | Golgi apparatus | N-glycan biosynthesis | glycosyltransferase | AMINO-ACIDS | MEDIAL-GOLGI | xylosyltransferase | PROTEINS | EXPRESSION | oligosaccharides | glycopeptide | endo H | GnT I | Xyl beta 1-2[Man alpha 1-6(Man alpha 1-3)]Man beta 1-O-octyl | Arabidopsis thaliana | matrix-assisted laser-desorption ionization-time-of-flight MS | Man alpha 1-6(Man alpha 1-3)Man alpha 1-6(GlcNAc beta 1-2Man alpha 1-3)Man beta 1-4GlcNAc beta 1-4GlcNAc | trans-epoxysuccinyl- L -leucylamido-(4-guanidino)butane | peptide N-glycosidase F | GlcNAc beta 1-2Man alpha 1-6(GlcNAc beta 1-2Man alpha 1-3)Man beta 1-4GlcNAc beta 1-4GlcNAc | core alpha 1,3-fucosyltransferase | Xyl beta 1-2[GlcNAc beta 1-2Man alpha 1-6(GlcNAc beta 1-2Man alpha 1-3)]Man beta 1-4GlcNAc beta 1- 4GlcNAc | Enzymes | FucT | GnGnF | GlcNAc beta 1-2Man alpha 1-6(GlcNAc beta 1-2Man alpha 1-3)Man beta 1-4 GlcNAc beta 1-4(Fuc alpha 1 -3)GlcNAc | Ions | Glycosylation | beta 1,2-N-acetylglucosaminyltransferase I | beta 1,2-xylosyltransferase | MGn-octyl | Insect cells | Man alpha 1-6(Gal beta 1-4GlcNAc beta 1-2Man alpha 1-3) | GlcNAc beta 1-2Man alpha 1-6 (GlcNAc beta 1-2Man alpha 1-3)Man beta 1-O-octyl | Glycosyltransferase | Metals | GnGn-octyl | PNGase F | Amino acids | MM-octyl | Man alpha 1-6(Man alpha 1-3)Man beta 1-O-octyl | Deletion mutant | GnGnX | (rough) endoplasmic reticulum | endoglycosidase H | Substrate specificity | MMX-octyl | Man alpha 1-6(GlcNAc beta 1-2Man alpha 1-3)Man beta 1-O-octyl | XylT | MALDI-TOF-MS | cytoplasmic and transmembrane domain | (r)ER | E-64 | MGnX-octyl | N-glycans | Man5Gn | xylosyltransferase Abbreviations: CT domain | GnGn | Xyl beta 1-2[Man alpha 1-6(GlcNAc beta 1-2Man alpha 1-3)]Man beta 1-O-octyl | MA-octyl
Journal Article
Cancer Letters, ISSN 0304-3835, 2016, Volume 379, Issue 1, pp. 143 - 153
Highlights • PDACs with an angiogenic gene signature are enriched in lymphangiogenic genes. • Tumors from the KRC PDAC model harbor LECs and have a... 
Hematology, Oncology and Palliative Medicine | TGF-β | Mouse model | Lymphangiogenesis | Pancreatic cancer | TCGA | ENDOTHELIAL-GROWTH-FACTOR | FACTOR-C | DUCTAL ADENOCARCINOMA | PRIMARY TUMOR | VEGF-C | LYMPH-NODE METASTASES | TGF-beta | PHASE-II TRIAL | ONCOLOGY | EXPRESSION | CARCINOMA | Carcinoma, Pancreatic Ductal - secondary | Receptor, Epidermal Growth Factor - genetics | Receptor, ErbB-2 - genetics | Apoptosis - drug effects | Proto-Oncogene Proteins p21(ras) - genetics | Humans | Neovascularization, Pathologic | Receptor, ErbB-2 - metabolism | Male | Molecular Targeted Therapy | Cell Movement - genetics | Quinolines - pharmacology | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Carcinoma, Pancreatic Ductal - genetics | Pancreatic Neoplasms - drug therapy | Receptor, Epidermal Growth Factor - metabolism | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Transforming Growth Factor beta - antagonists & inhibitors | Female | Receptor, ErbB-2 - antagonists & inhibitors | Protein-Serine-Threonine Kinases - metabolism | Pyrazoles - pharmacology | Genetic Predisposition to Disease | Neoplasm Invasiveness | Genes, Retinoblastoma | Pancreatic Neoplasms - pathology | Pancreatic Neoplasms - enzymology | Angiogenesis Inhibitors - pharmacology | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Gene Expression Profiling - methods | Mice, Transgenic | Pancreatic Neoplasms - genetics | Carcinoma, Pancreatic Ductal - enzymology | Lymphangiogenesis - drug effects | Carcinoma, Pancreatic Ductal - drug therapy | Cell Movement - drug effects | Phenotype | Animals | Receptors, Transforming Growth Factor beta - antagonists & inhibitors | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | Signal Transduction - drug effects | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Mutation | Quinazolines - pharmacology | Lymphangiogenesis - genetics | Transforming Growth Factor beta - metabolism | Index Medicus
Journal Article
FEBS Letters, ISSN 0014-5793, 10/2015, Volume 589, Issue 20, pp. 3098 - 3106
The β‐xylosidase B from Bifidobacterium adolescentis ATCC15703 belongs to the newly characterized family 120 of glycoside hydrolases. In order to investigate... 
Bifidobacterium adolescentis | Catalytic residue | β-Xylosidase | Retaining mechanism | Glycoside hydrolase family 120 | Site-directed mutagenesis | 4-methylumbelliferone | ATCC15703 | xylopyranosyl | transition state | XylC | glycoside hydrolase | 2-NP-β | 3,4-dinitrophenyl-β | 3,4-dinitrophenol | xylopyranoside | 4-methylumbelliferyl β | xylooligosaccharides | leaving group | 4-MU-β | xylosyl azide | XylB | 2-nitrophenol | 4-NP | Thermoanaerobacterium saccharolyticum | 4-nitrophenol | β-xylosidase B from | 4-nitrophenyl β | Xyl | 2-NP | 2-nitrophenyl β | 3,4-dNP-β | 3,4-dNP | β-xylosidase C from | JW/SL-YS485 | 4-MU | 4-NP-β | XOS | beta;-Xylosidase | MECHANISM | METAGENOME | BIOCHEMISTRY & MOLECULAR BIOLOGY | MICROBIOTA | CELL BIOLOGY | BIOPHYSICS | GLUCOSIDASE | beta-Xylosidase | ACID/BASE CATALYST | ASSOCIATION | SULFATE-REDUCING BACTERIA | Humans | Substrate Specificity | Xylosidases | Molecular Structure | Binding Sites | Protein Structure, Tertiary | Catalytic Domain | Intestines | Bifidobacterium | Magnetic Resonance Spectroscopy | Models, Molecular | Oligosaccharides | Glucuronates | Bacterial Proteins | exo-1,4-beta-D-xylosidase | Index Medicus | Hydrolysis | xylooligosaccharide | Kinetics | Mutation | Hydrogen-Ion Concentration | 3,4-dNP- beta -d-Xylp 3,4-dinitrophenyl- beta -d-xylopyranoside | Catalysts | 4-MU- beta -d-Xylp 4-methylumbelliferyl beta -d-xylopyranoside | pH effects | glycosides | 4-NP 4-nitrophenol | beta -Xylosidase | XOS xylooligosaccharides | Bacteria | 4-MU 4-methylumbelliferone | N3- beta -d-Xylp beta -d-xylosyl azide | Nucleophiles | 3,4-dNP 3,4-dinitrophenol | Digestive tract | 4-NP- beta -d-Xylp 4-nitrophenyl beta -d-xylopyranoside | LG leaving group | Enzymes | BaXylB beta -xylosidase B from Bifidobacterium adolescentis ATCC15703 | TsXylC beta -xylosidase C from Thermoanaerobacterium saccharolyticum JW/SL-YS485 | N.M.R | 2-NP- beta -d-Xylp 2-nitrophenyl beta -d-xylopyranoside | 2-NP 2-nitrophenol | d-Xylp d-xylopyranosyl | TS transition state | GH glycoside hydrolase | Bacterial Proteins - chemistry | Glucuronates - metabolism | Oligosaccharides - chemistry | Bifidobacterium - metabolism | Glucuronates - chemistry | Bifidobacterium - genetics | Bacterial Proteins - genetics | Xylosidases - chemistry | Binding Sites - genetics | Oligosaccharides - metabolism | Intestines - microbiology | Xylosidases - metabolism | Xylosidases - genetics | Bacterial Proteins - metabolism | Life Sciences | Microbiology and Parasitology | Protistology
Journal Article