serw-MX  [xml]  
 


    
 DeCS Categories

A11 Cells .
A11.284 Cellular Structures .
A11.284.430 Intracellular Space .
A11.284.430.214 Cytoplasm .
A11.284.430.214.190 Cytoplasmic Structures .
A11.284.430.214.190.875 Organelles .
A11.284.430.214.190.875.393 Lipid Droplets .
C10 Nervous System Diseases .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.550 Neuronal Ceroid-Lipofuscinoses .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.600 Neuronal Ceroid-Lipofuscinoses .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.509 Neuronal Ceroid-Lipofuscinoses .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.509 Neuronal Ceroid-Lipofuscinoses .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.509 Neuronal Ceroid-Lipofuscinoses .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.157 Carrier Proteins .
D12.776.157.464 Lipid Droplet Associated Proteins .
D12.776.157.464.500 Perilipins .
D12.776.157.464.500.937 Perilipin-5 .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Lipid Droplets .
Adiposomes .
Lipid Bodies .
Lipid Storage Bodies .
Oil Bodies .
Oleosomes .
Spherosomes .
Adiposome .
Droplet, Lipid .
Droplets, Lipid .
Lipid Body .
Lipid Droplet .
Lipid Storage Body .
Oil Body .
Oleosome .
Spherosome .
Storage Bodies, Lipid .
Storage Body, Lipid .
Dynamic cytoplasmic organelles found in almost all cells. They consist of a central core of LIPIDS surrounded by a phospholipid monolayer studded with surface proteins, and are involved in LIPID METABOLISM and storage. .
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5666
 
Perilipin-5 .
LSDP5 Protein .
Lipid Storage Droplet Protein 5 .
OXPAT Protein .
PLIN5 Protein .
Perilipin 5 Protein .
Perilipin 5 .
Protein, LSDP5 .
Protein, OXPAT .
Protein, PLIN5 .
Protein, Perilipin 5 .
A perilipin that functions in LIPOGENESIS; LIPOLYSIS; and fatty acid oxidation in BROWN ADIPOSE TISSUE; heart, liver, and skeletal muscle. It recruits MITOCHONDRIA to the surface of LIPID DROPLETS where it functions in both the storage of fatty acids as TRIGLYCERIDES, and their release for mitochondrial fatty acid oxidation in response to metabolic needs. .
0.53
044
 
Neuronal Ceroid-Lipofuscinoses .
Adult Neuronal Ceroid Lipofuscinosis .
Amaurotic Idiocy, Adult Type .
Batten-Mayou Disease .
Batten-Spielmeyer-Vogt Disease .
CLN3-Related Neuronal Ceroid-Lipofuscinosis .
CLN4A .
CLN4B .
Ceroid Lipofuscinosis, Neuronal 3, Juvenile .
Ceroid Lipofuscinosis, Neuronal 4 .
Ceroid Lipofuscinosis, Neuronal, 3 .
Ceroid Lipofuscinosis, Neuronal, 4A, Autosomal Recessive .
Ceroid Lipofuscinosis, Neuronal, 4B, Autosomal Dominant .
Ceroid Lipofuscinosis, Neuronal, Parry Type .
Ceroid Storage Disease .
Infantile Neuronal Ceroid Lipofuscinosis .
Juvenile Batten Disease .
Juvenile Cerebroretinal Degeneration .
Juvenile Neuronal Ceroid Lipofuscinosis .
Kuf's Disease .
Kufs Disease Autosomal Recessive .
Kufs Disease, Autosomal Dominant .
Kufs Disease, Autosomal Recessive .
Kufs Type Neuronal Ceroid Lipofuscinosis .
Late-Infantile Neuronal Ceroid Lipofuscinosis .
Lipofuscin Storage Disease .
Lipofuscinosis, Neuronal Ceroid .
Neuronal Ceroid Lipofuscinosis .
Neuronal Ceroid Lipofuscinosis Juvenile Type .
Neuronal Ceroid Lipofuscinosis, Adult .
Neuronal Ceroid Lipofuscinosis, Adult Type .
Neuronal Ceroid Lipofuscinosis, Infantile .
Neuronal Ceroid Lipofuscinosis, Juvenile .
Neuronal Ceroid Lipofuscinosis, Late Infantile .
Neuronal Ceroid Lipofuscinosis, Late-Infantile .
Neuronal Ceroid-Lipofuscinosis .
Spielmeyer-Sjogren Disease .
Vogt Spielmeyer Disease .
Vogt-Spielmeyer Disease .
Batten Disease, Juvenile .
Batten Diseases, Juvenile .
Batten Mayou Disease .
Batten Spielmeyer Vogt Disease .
CLN3 Related Neuronal Ceroid Lipofuscinosis .
CLN3-Related Neuronal Ceroid-Lipofuscinoses .
CLN4As .
Cerebroretinal Degeneration, Juvenile .
Cerebroretinal Degenerations, Juvenile .
Ceroid Lipofuscinosis, Neuronal .
Ceroid Storage Diseases .
Ceroid-Lipofuscinoses, CLN3-Related Neuronal .
Ceroid-Lipofuscinosis, CLN3-Related Neuronal .
Disease, Ceroid Storage .
Disease, Juvenile Batten .
Disease, Kuf's .
Disease, Lipofuscin Storage .
Disease, Spielmeyer-Sjogren .
Disease, Vogt Spielmeyer .
Disease, Vogt-Spielmeyer .
Diseases, Ceroid Storage .
Diseases, Juvenile Batten .
Diseases, Lipofuscin Storage .
Jansky Bielschowsky Disease .
Juvenile Batten Diseases .
Juvenile Cerebroretinal Degenerations .
Kuf Disease .
Lipofuscin Storage Diseases .
Neuronal Ceroid Lipofuscinoses .
Neuronal Ceroid-Lipofuscinoses, CLN3-Related .
Neuronal Ceroid-Lipofuscinosis, CLN3-Related .
Santavuori Haltia Disease .
Spielmeyer Disease, Vogt .
Spielmeyer Sjogren Disease .
Spielmeyer Vogt Disease .
Storage Disease, Ceroid .
Storage Disease, Lipofuscin .
Storage Diseases, Ceroid .
Storage Diseases, Lipofuscin .
Batten Disease .
Ceroid-Lipofuscinosis, Neuronal .
Jansky-Bielschowsky Disease .
Kufs Disease .
Santavuori-Haltia Disease .
Spielmeyer-Vogt Disease .
Neuronal Ceroid-Lipofuscinosis .
CEROID-LIPOFUSCINOSIS .
BATTEN-SPIELMEYER-VOGT DISEASE .
LIPOFUSCINOSIS, NEURONAL CEROID .
A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure. .
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