X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (666) 666
Publication (88) 88
Book Chapter (22) 22
Newsletter (5) 5
Book / eBook (4) 4
Book Review (4) 4
Dissertation (2) 2
Newspaper Article (2) 2
Data Set (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (404) 404
index medicus (336) 336
mitochondrial trifunctional protein (252) 252
animals (240) 240
male (178) 178
female (159) 159
mitochondria (158) 158
fatty acids (152) 152
biochemistry & molecular biology (144) 144
fatty acids - metabolism (144) 144
oxidation-reduction (121) 121
metabolism (112) 112
mutation (107) 107
genetics & heredity (106) 106
enzymes (104) 104
mice (104) 104
mitochondria - metabolism (100) 100
multienzyme complexes - genetics (95) 95
pediatrics (95) 95
beta-oxidation (92) 92
mitochondrial dna (92) 92
proteins (85) 85
fatty-acid oxidation (84) 84
endocrinology & metabolism (80) 80
multienzyme complexes - metabolism (78) 78
infant, newborn (76) 76
physiological aspects (76) 76
pregnancy (74) 74
rats (72) 72
analysis (71) 71
medicine, research & experimental (70) 70
3-hydroxyacyl coa dehydrogenases - deficiency (69) 69
medicine & public health (62) 62
article (59) 59
oxidation (59) 59
disease (57) 57
fatty acid oxidation (57) 57
oxidative stress (57) 57
lipid metabolism, inborn errors - genetics (56) 56
liver (56) 56
adult (55) 55
internal medicine (55) 55
multienzyme complexes - deficiency (53) 53
biochemistry, general (52) 52
molecular sequence data (52) 52
proteomics (51) 51
alpha-subunit (50) 50
infant (50) 50
deficiency (49) 49
expression (49) 49
cell biology (48) 48
3-hydroxyacyl coa dehydrogenases - genetics (47) 47
research (47) 47
child (46) 46
gene expression (46) 46
amino acid sequence (45) 45
phenotype (45) 45
diagnosis (44) 44
disorders (44) 44
lipid metabolism, inborn errors - diagnosis (44) 44
3-hydroxyacyl-coa dehydrogenase-deficiency (42) 42
mitochondrial trifunctional protein - deficiency (42) 42
trifunctional protein (42) 42
metabolic diseases (41) 41
medicine (40) 40
mitochondria - enzymology (40) 40
human genetics (39) 39
lipids (39) 39
cardiomyopathy (38) 38
carnitine (38) 38
mitochondrial (38) 38
acyl-coa dehydrogenase (37) 37
biology (37) 37
child, preschool (37) 37
mass spectrometry (37) 37
multidisciplinary sciences (37) 37
adolescent (36) 36
defects (36) 36
genes (36) 36
mitochondrial proteins - metabolism (36) 36
neurosciences (36) 36
research article (36) 36
3-hydroxyacyl coa dehydrogenases - metabolism (35) 35
carnitine - analogs & derivatives (35) 35
cells, cultured (35) 35
energy metabolism (35) 35
insulin-resistance (35) 35
chain 3-hydroxyacyl-coa dehydrogenase (34) 34
long-chain-3-hydroxyacyl-coa dehydrogenase (34) 34
mitochondrial diseases - genetics (34) 34
base sequence (33) 33
heart (33) 33
disease models, animal (32) 32
genotype (32) 32
health aspects (32) 32
oxidation-reduction reaction (32) 32
apoptosis (31) 31
biophysics (31) 31
oxidative phosphorylation (31) 31
physiology (31) 31
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (672) 672
Japanese (18) 18
Chinese (6) 6
French (4) 4
German (4) 4
Spanish (2) 2
Czech (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2019, Volume 116, Issue 13, pp. 6069 - 6074
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 07/2018, Volume 115, Issue 27, pp. 7039 - 7044
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, 07/2018, Volume 115, Issue 27, p. 7039
The mitochondrial trifunctional protein (TFP) catalyzes three reactions in the fatty acid β-oxidation process. Mutations in the two TFP subunits cause... 
Cryoelectron Microscopy | Mitochondrial Trifunctional Protein - ultrastructure | Protein Structure, Secondary | Mitochondrial Trifunctional Protein - metabolism | Humans | Protein Structure, Quaternary
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, p. e48628
Cardiolipin (CL) is a mitochondrial membrane phospholipid which plays a key role in apoptosis and supports mitochondrial respiratory chain complexes involved... 
PHOSPHATIDYLGLYCEROL | HEART MITOCHONDRIA | METABOLISM | FATTY-ACID OXIDATION | BIOSYNTHESIS | MULTIDISCIPLINARY SCIENCES | BARTH-SYNDROME PATIENTS | RAT-LIVER MITOCHONDRIA | ACYLTRANSFERASE CONTROLS | ENDOTHELIAL LINEAGES | DEFICIENCY | Lysophospholipids - metabolism | Mitochondrial Trifunctional Protein | Humans | Molecular Sequence Data | Multienzyme Complexes - metabolism | Substrate Specificity | Male | Acyltransferases - metabolism | Acyltransferases - genetics | Recombinant Fusion Proteins - metabolism | RNA Interference | Acyl Coenzyme A - metabolism | Fatty Acids - metabolism | Amino Acid Sequence | Cell Line | Gene Expression | Oxidation-Reduction | Palmitoyl Coenzyme A - metabolism | Rats | Cardiolipins - metabolism | Multienzyme Complexes - genetics | Recombinant Fusion Proteins - chemistry | Multienzyme Complexes - chemistry | Gene Expression Regulation - drug effects | Sequence Alignment | Animals | Protein Binding | Acyltransferases - chemistry | Enzyme Activation | Thyroxine - pharmacology | Enzymes | Membrane lipids | Amino acids | Oxidation-reduction reaction | Cardiolipin | Fatty acids | Acylation | Dehydrogenases | Childrens health | Lipids | Biochemistry | Phospholipids | Remodeling | Palmitic acid | Proteins | Mitochondria | Atherosclerosis | Oxidation | Trends | Recombinant | Lymphoblasts | Pharmacology | Acyltransferase | Substrates | Mutation | Electron transport | Apoptosis
Journal Article
Ophthalmology, ISSN 0161-6420, 10/2016, Volume 123, Issue 10, pp. 2183 - 2195
Purpose To assess long-term effects of genotype on chorioretinopathy severity in patients with mitochondrial trifunctional protein (MTP) disorders. Design... 
AMPLITUDE-DECORRELATION ANGIOGRAPHY | COA DEHYDROGENASE | OPTICAL COHERENCE TOMOGRAPHY | FATTY-ACID OXIDATION | STRATEGY | OPTIMAL DIETARY THERAPY | OPHTHALMOLOGY | RETINOPATHY | G1528C MUTATION | SPECTRUM | 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY | Lipid Metabolism, Inborn Errors - genetics | Prognosis | Follow-Up Studies | Humans | Child, Preschool | Rhabdomyolysis - complications | Infant | Male | Nervous System Diseases - genetics | Nervous System Diseases - diagnosis | Young Adult | Cardiomyopathies - genetics | Rhabdomyolysis - diagnosis | Visual Fields | Cardiomyopathies - diagnosis | Adult | Female | Retrospective Studies | Mitochondrial Myopathies - diagnosis | Child | Choroid Diseases - genetics | Fluorescein Angiography | Electroretinography | Mitochondrial Trifunctional Protein - genetics | Mitochondrial Myopathies - complications | Tomography, Optical Coherence | Lipid Metabolism, Inborn Errors - diagnosis | Genotype | Choroid Diseases - etiology | Visual Acuity | Forecasting | Nervous System Diseases - complications | Mitochondrial Myopathies - genetics | Mitochondrial Trifunctional Protein - metabolism | Rhabdomyolysis - genetics | Adolescent | Cardiomyopathies - complications | Lipid Metabolism, Inborn Errors - complications | Choroid Diseases - diagnosis | Fundus Oculi | Mitochondrial Trifunctional Protein - deficiency
Journal Article
Journal Article