serw-MX  [xml]  
 


    
 DeCS Categories

A18 Plant Structures .
A18.024 Plant Components, Aerial .
A18.024.875 Plant Shoots .
A18.024.875.875 Meristem .
A18.024.937 Plant Stems .
A18.024.937.500 Meristem .
A18.400 Plant Roots .
A18.400.500 Meristem .
B01 Eukaryota .
B01.050 Animals .
B01.050.150 Chordata .
B01.050.150.900 Vertebrates .
B01.050.150.900.649 Mammals .
B01.050.150.900.649.313 Eutheria .
B01.050.150.900.649.313.992 Rodentia .
B01.050.150.900.649.313.992.635 Muridae .
B01.050.150.900.649.313.992.635.300 Gerbillinae .
C05 Musculoskeletal Diseases .
C05.651 Muscular Diseases .
C05.651.460 Mitochondrial Myopathies .
C05.651.460.620 Mitochondrial Encephalomyopathies .
C05.651.460.620.530 MERRF Syndrome .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.545 MERRF Syndrome .
C10.228.140.490 Epilepsy .
C10.228.140.490.375 Epilepsy, Generalized .
C10.228.140.490.375.130 Epilepsies, Myoclonic .
C10.228.140.490.375.130.650 Myoclonic Epilepsies, Progressive .
C10.228.140.490.375.130.650.700 MERRF Syndrome .
C10.228.140.490.493 Epileptic Syndromes .
C10.228.140.490.493.063 Epilepsies, Myoclonic .
C10.228.140.490.493.063.650 Myoclonic Epilepsies, Progressive .
C10.228.140.490.493.063.650.700 MERRF Syndrome .
C10.668 Neuromuscular Diseases .
C10.668.491 Muscular Diseases .
C10.668.491.500 Mitochondrial Myopathies .
C10.668.491.500.500 Mitochondrial Encephalomyopathies .
C10.668.491.500.500.550 MERRF Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.545 MERRF Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.545 MERRF Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.545 MERRF Syndrome .
C18.452.660 Mitochondrial Diseases .
C18.452.660.560 Mitochondrial Myopathies .
C18.452.660.560.620 Mitochondrial Encephalomyopathies .
C18.452.660.560.620.530 MERRF Syndrome .
D02 Organic Chemicals .
D02.065 Amides .
D02.065.277 Benzamides .
D02.065.277.866 Sulpiride .
D02.241 Carboxylic Acids .
D02.241.223 Acids, Carbocyclic .
D02.241.223.100 Benzoates .
D02.241.223.100.100 Benzamides .
D02.241.223.100.100.866 Sulpiride .
D02.455 Hydrocarbons .
D02.455.426 Hydrocarbons, Cyclic .
D02.455.426.559 Hydrocarbons, Aromatic .
D02.455.426.559.389 Benzene Derivatives .
D02.455.426.559.389.127 Benzoates .
D02.455.426.559.389.127.085 Benzamides .
D02.455.426.559.389.127.085.866 Sulpiride .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.725 Pyridines .
D03.383.725.762 Pyridinium Compounds .
D03.383.725.762.232 Cetylpyridinium .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.100 Heterocyclic Compounds, 2-Ring .
D03.633.100.531 Isoquinolines .
D03.633.100.531.535 Nomifensine .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.913 Transferases .
D08.811.913.696 Phosphotransferases .
D08.811.913.696.620 Phosphotransferases (Alcohol Group Acceptor) .
D08.811.913.696.620.682 Protein Kinases .
D08.811.913.696.620.682.725 Protein-Tyrosine Kinases .
D08.811.913.696.620.682.725.400 Receptor Protein-Tyrosine Kinases .
D08.811.913.696.620.682.725.400.003 c-Mer Tyrosine Kinase .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.395 Glycoproteins .
D12.776.395.550 Membrane Glycoproteins .
D12.776.395.550.530 Laminin .
D12.776.543 Membrane Proteins .
D12.776.543.550 Membrane Glycoproteins .
D12.776.543.550.500 Laminin .
D12.776.543.685 Neurofibromin 2 .
D12.776.543.750 Receptors, Cell Surface .
D12.776.543.750.630 Receptor Protein-Tyrosine Kinases .
D12.776.543.750.630.003 c-Mer Tyrosine Kinase .
D12.776.624 Neoplasm Proteins .
D12.776.624.664 Oncogene Proteins .
D12.776.624.664.700 Proto-Oncogene Proteins .
D12.776.624.664.700.037 c-Mer Tyrosine Kinase .
D12.776.624.776 Tumor Suppressor Proteins .
D12.776.624.776.612 Neurofibromin 2 .
D12.776.860 Scleroproteins .
D12.776.860.300 Extracellular Matrix Proteins .
D12.776.860.300.675 Laminin .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Cetylpyridinium .
Angifonil .
Biosept .
Catamium .
Ceepryn Chloride .
Cetamium .
Cetylpyridinium Chloride .
Cetylpyridinium Chloride Anhydrous .
Cetylpyridium .
Cetylyre .
Dobendan .
Hexadecylpyridinium .
Merocets .
Pristacin .
Pyrisept .
Sterogenol .
Anhydrous, Cetylpyridinium Chloride .
Chloride Anhydrous, Cetylpyridinium .
Chloride, Ceepryn .
Chloride, Cetylpyridinium .
Cationic bactericidal surfactant used as a topical antiseptic for skin, wounds, mucous membranes, instruments, etc.; and also as a component in mouthwash and lozenges. .
1.00
43859
 
Laminin .
Glycoprotein GP-2 .
Laminin M .
Laminin M Chain .
Chain, Laminin M .
Glycoprotein GP 2 .
M Chain, Laminin .
Merosin .
Large, noncollagenous glycoprotein with antigenic properties. It is localized in the basement membrane lamina lucida and functions to bind epithelial cells to the basement membrane. Evidence suggests that the protein plays a role in tumor invasion. .
0.63
9513687
 
Gerbillinae .
Gerbil .
Jirds .
Merione .
Rat, Sand .
Sand Rat .
Sand Rats .
Gerbils .
Jird 17684 .
Meriones .
Psammomys .
Rats, Sand .
A subfamily of the Muridae consisting of several genera including Gerbillus, Rhombomys, Tatera, Meriones, and Psammomys. .
0.55
489782
 
Sulpiride .
Aiglonyl .
Arminol .
Deponerton .
Desisulpid .
Digton .
Dogmatil .
Dolmatil .
Eglonyl .
Ekilid .
Guastil .
Lebopride .
Meresa .
Pontiride .
Psicocen .
Sulp 10277 .
Sulperide .
Sulpitil .
Sulpivert .
Sulpor .
Synédil .
Tepavil .
Vertigo-Meresa .
neogama .
vertigo-neogama .
Vertigo Meresa .
vertigo neogama .
A dopamine D2-receptor antagonist. It has been used therapeutically as an antidepressant, antipsychotic, and as a digestive aid. (From Merck Index, 11th ed) .
0.55
473830
 
Nomifensine .
Hoe-984 .
Linamiphen .
Merital .
Nomifensin .
Nomifensine Maleate .
Nomifensine Maleate (1:1) .
Hoe 984 .
Hoe984 .
Maleate, Nomifensine .
An isoquinoline derivative that prevents dopamine reuptake into synaptosomes. The maleate was formerly used in the treatment of depression. It was withdrawn worldwide in 1986 due to the risk of acute hemolytic anemia with intravascular hemolysis resulting from its use. In some cases, renal failure also developed. (From Martindale, The Extra Pharmacopoeia, 30th ed, p266) .
0.54
91067
 
Neurofibromin 2 .
Merlin .
Moesin-Ezrin-Radixin-Like Protein .
NF2 Gene Product .
Neurofibromatosis 2 Gene Product .
Schwannomin Protein .
Gene Product, NF2 .
Moesin Ezrin Radixin Like Protein .
Protein, Schwannomin .
Neurofibromatosis Type 2 Protein .
Schwannomin .
A membrane protein homologous to the ERM (Ezrin-Radixin-Moesin) family of cytoskeleton-associated proteins which regulate physical properties of membranes. Alterations in neurofibromin 2 are the cause of NEUROFIBROMATOSIS 2. .
0.53
1616
 
c-Mer Tyrosine Kinase .
MERTK .
c-Mer Proto-Oncogene Tyrosine Kinase .
Kinase, c-Mer Tyrosine .
Tyrosine Kinase, c-Mer .
c Mer Proto Oncogene Tyrosine Kinase .
c Mer Tyrosine Kinase .
A receptor tyrosine kinase that transduces signals from EXTRACELLULAR MATRIX to the CYTOPLASM by binding ligands such as GALECTIN 3. It regulates many physiologic processes that include cell survival, migration, differentiation, and PHAGOCYTOSIS of apoptotic cells and ROD PHOTORECEPTORS in the RETINAL PIGMENT EPITHELIUM. Mutations in the MERTK gene are associated with type 38 RETINITIS PIGMENTOSA; it also plays a critical role as an inhibitor of TOLL-LIKE RECEPTORS signaling. .
0.53
0355
 
MERRF Syndrome .
Fukuhara Syndrome .
MERRF .
Myoclonic Epilepsy Associated with Ragged-Red Fibers .
Myoclonic Epilepsy and Ragged Red Fibers .
Myoclonic Epilepsy with Ragged-Red Fibers .
Myoclonus with Epilepsy with Ragged Red Fibers .
Myoencephalopathy Ragged-Red Fiber Disease .
Myoclonic Epilepsy Associated with Ragged Red Fibers .
Myoencephalopathy Ragged Red Fiber Disease .
Syndrome, Fukuhara .
Syndrome, MERRF .
Fukuhara Disease .
Myoclonic Epilepsy with Ragged Red Fibers .
A mitochondrial encephalomyopathy characterized clinically by a mixed seizure disorder, myoclonus, progressive ataxia, spasticity, and a mild myopathy. Dysarthria, optic atrophy, growth retardation, deafness, and dementia may also occur. This condition tends to present in childhood and to be transmitted via maternal lineage. Muscle biopsies reveal ragged-red fibers and respiratory chain enzymatic defects. (From Adams et al., Principles of Neurology, 6th ed, p986) .
0.52
2333
 
Meristem .
Meristems .
Root Tips .
Tip, Root .
Tips, Root .
Root Tip .
A group of plant cells that are capable of dividing infinitely and whose main function is the production of new growth at the growing tip of a root or stem. (From Concise Dictionary of Biology, 1990) .
0.51
203432