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Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 01/2019, Volume 27, Issue 1, pp. 224 - 229
Protein arginine methyltransferases (PRMTs) are a family of mammalian enzymes catalyzing the symmetric dimethylation (Type I), asymmetric dimethylation (Type... 
Chemical probe | Arginine | Protein arginine methyltransferase | Activity based probe | ABPP | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISTINCT | CHEMISTRY, ORGANIC | FAMILY | SUBSTRATE-SPECIFICITY | GENE | METHYLTRANSFERASES | PROTEIN ARGININE METHYLATION | BINDING | Methyltransferases | Isoenzymes | Investigations | Index Medicus
Journal Article
ISSN 1477-0520, 7/2015, Volume 13, Issue 31, pp. 855 - 8555
Protein AMPylation is a posttranslational modification (PTM) defined as the transfer of an adenosine monophosphate (AMP) from adenosine triphosphate (ATP) to a... 
Journal Article
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 238 - 238
Journal Article
Bioorganic & medicinal chemistry, 12/2018
Protein arginine methyltransferases (PRMTs) are a family of mammalian enzymes catalyzing the symmetric dimethylation (Type I), asymmetric dimethylation (Type... 
Journal Article
Journal of Immunology, ISSN 0022-1767, 04/2011, Volume 186, Issue 7, pp. 4396 - 4404
Journal Article
American Journal of Physiology - Gastrointestinal and Liver Physiology, ISSN 0193-1857, 06/2011, Volume 300, Issue 6, pp. 929 - 938
Inflammatory bowel diseases (IBDs), mainly Crohn's disease and ulcerative colitis, are dynamic, chronic inflammatory conditions that are associated with an... 
Citrullination | Inflammation | Apoptosis | PROTEIN ARGININE DEIMINASE-4 | RHEUMATOID-ARTHRITIS | PHYSIOLOGY | citrullination | ULCERATIVE-COLITIS | apoptosis | COLON-CANCER | INFLAMMATORY-BOWEL-DISEASE | MULTIPLE-SCLEROSIS | inflammation | GASTROENTEROLOGY & HEPATOLOGY | SPHINGOSINE KINASE | EXPRESSION | ASSOCIATION | Dextran Sulfate | Up-Regulation | Colon - enzymology | Apoptosis - drug effects | Humans | Citrulline - metabolism | Colon - drug effects | Gastrointestinal Agents - administration & dosage | Ornithine - analogs & derivatives | Colitis - pathology | Dose-Response Relationship, Drug | Enzyme Inhibitors - administration & dosage | Protein Processing, Post-Translational - drug effects | Colitis - chemically induced | Enzyme Inhibitors - toxicity | Anti-Inflammatory Agents - administration & dosage | Gastrointestinal Agents - toxicity | Disease Models, Animal | Hydrolases - metabolism | Administration, Oral | Anti-Inflammatory Agents - pharmacology | Colon - pathology | Anti-Inflammatory Agents - toxicity | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Ornithine - pharmacology | HT29 Cells | Gastrointestinal Agents - pharmacology | Animals | Colitis - enzymology | Ornithine - administration & dosage | Mice | Ornithine - toxicity | Colitis - prevention & control | Arginine - metabolism | Protein-Arginine Deiminases | Hydrolases - antagonists & inhibitors | Physiological aspects | Amidines | Colitis | Research | Inflammatory bowel disease | Side effects | Cytokines | Risk assessment | Rodents | Crohns disease | Index Medicus | Mediators | Immunity
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 2/2011, Volume 68, Issue 4, pp. 709 - 720
The recent approvals of anticancer therapeutic agents targeting the histone deacetylases and DNA methyltransferases have highlighted the important role that... 
Life Sciences | Biochemistry, general | Life Sciences, general | Epigenetics | Haloacetamidine | HL-60 | Inhibition | Citrulline | Protein arginine deiminase | Biomedicine general | Cell Biology | HISTONE DEACETYLASE INHIBITOR | PROTEIN-ARGININE-DEIMINASE-4 PAD4 | SUBEROYLANILIDE HYDROXAMIC ACID | BIOCHEMISTRY & MOLECULAR BIOLOGY | PEPTIDYLARGININE DEIMINASE | HL-60 CELLS | TUMOR-CELLS | ANTITUMOR-ACTIVITY | CELL BIOLOGY | IN-VITRO | DIFFERENTIATION | EXPRESSION | Hydrolases - metabolism | Cell Survival - drug effects | Hydrolases - genetics | Epigenomics | ADP-ribosyl Cyclase 1 - genetics | Antibiotics, Antineoplastic - pharmacology | Humans | Enzyme Inhibitors - pharmacology | Neoplasms - enzymology | Antineoplastic Agents - chemistry | Amidines - chemistry | Neoplasms - drug therapy | Drug Synergism | Animals | Cyclin-Dependent Kinase Inhibitor p21 - genetics | Neoplasms - genetics | Cell Differentiation - drug effects | Enzyme Inhibitors - chemistry | Cell Line, Tumor | Amidines - pharmacology | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Doxorubicin - pharmacology | Protein-Arginine Deiminases | Anthracyclines | Care and treatment | Arginine | Methyltransferases | Gene expression | Health aspects | Cancer | Proteins | Cellular biology | Gene therapy | Index Medicus | inhibition | citrulline | epigenetics | Protein Arginine Deiminase | haloacetamidine
Journal Article
PLoS Genetics, ISSN 1553-7390, 06/2011, Volume 7, Issue 6
  Peptidylarginine deiminase IV (PADI4) catalyzes the conversion of positively charged arginine and methylarginine residues to neutrally charged citrulline,... 
Proteins | Medical research | Epidermal growth factor | Rodents | Breast cancer | Kinases | Gene expression
Journal Article
Journal Article
Journal Article
Langmuir, ISSN 0743-7463, 07/2014, Volume 30, Issue 25, pp. 7447 - 7455
Journal Article
Journal of Physical Chemistry C, ISSN 1932-7447, 06/2015, Volume 119, Issue 22, pp. 12455 - 12463
Numerous strategies have been devised to register organosilane monolayers for applications ranging from lubricants to semiconductor surface resists. Of these... 
ALKYLSILOXANE MONOLAYERS | SELF-ASSEMBLED MONOLAYERS | LIQUID INTERFACE | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSCIENCE & NANOTECHNOLOGY | SURFACE-STRUCTURES | SILICA SURFACES | SILANE MONOLAYERS | ATOMIC-FORCE MICROSCOPY | CONSTRUCTIVE NANOLITHOGRAPHY | DIP-PEN NANOLITHOGRAPHY | MIXED MONOLAYERS
Journal Article
Developmental Biology, ISSN 0012-1606, 07/2011, Volume 355, Issue 2, pp. 205 - 214
Spinal cord regenerative ability is lost with development, but the mechanisms underlying this loss are still poorly understood. In chick embryos, effective... 
Development | Regeneration | Spinal cord | Peptidyl arginine deiminase | Deimination/citrullination | Apoptosis | MOUSE-BRAIN | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | CITRULLINATED PROTEINS | PEPTIDYLARGININE DEIMINASE | DEVELOPMENTAL BIOLOGY | FUNCTIONAL REPAIR | CELL-DEATH | MULTIPLE-SCLEROSIS | SPINAL-CORD-INJURY | GENETIC INFLUENCES | ARGININE METHYLATION | Hydrolases - metabolism | Immunohistochemistry | In Situ Nick-End Labeling | Age Factors | Oligonucleotide Array Sequence Analysis | Spinal Cord Injuries - metabolism | Apoptosis - drug effects | Calcium - metabolism | Humans | Ornithine - pharmacology | Ornithine - analogs & derivatives | DNA Primers - genetics | RNA, Messenger - metabolism | Chick Embryo | Blotting, Western | Spinal Cord Regeneration - physiology | Animals | Mass Spectrometry | Spinal Cord Injuries - embryology | Spinal Cord Injuries - physiopathology | Apoptosis - physiology | Protein-Arginine Deiminases | Gene Expression Regulation, Developmental - physiology | Hydrolases - antagonists & inhibitors | Post-translational modification | Proteins | Gene expression | Analysis | Enzymes | Calcium | Spinal cord injury | Substantia alba | Cavitation | Arginine | Developmental stages | Protein-arginine deiminase | Post-translation | Chelating agents | citrulline | Index Medicus | development | regeneration | citrullination | apoptosis | deimination | peptidyl arginine deiminase | spinal cord
Journal Article
ACS Chemical Biology, ISSN 1554-8929, 01/2012, Volume 7, Issue 1, pp. 160 - 165
Journal Article