X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (145) 145
humans (116) 116
peroxisomal multifunctional protein-2 (101) 101
animals (73) 73
biochemistry & molecular biology (47) 47
17-hydroxysteroid dehydrogenases - genetics (46) 46
male (45) 45
female (43) 43
mice (42) 42
enoyl-coa hydratase (41) 41
beta-oxidation (34) 34
hydro-lyases - genetics (34) 34
peroxisomes (32) 32
peroxisomes - metabolism (32) 32
17-hydroxysteroid dehydrogenases (30) 30
genetics & heredity (28) 28
fatty acids (26) 26
hydro-lyases - metabolism (24) 24
multienzyme complexes - genetics (24) 24
multienzyme complexes - metabolism (24) 24
mutation (24) 24
17-hydroxysteroid dehydrogenases - metabolism (23) 23
hydro-lyases - deficiency (23) 23
multienzyme complexes - deficiency (23) 23
oxidation-reduction (23) 23
zellweger-syndrome (23) 23
acyl-coa oxidase (22) 22
amino acid sequence (21) 21
cell biology (21) 21
mice, knockout (21) 21
molecular sequence data (21) 21
multifunctional protein-2 (21) 21
peroxisomal multifunctional protein-2 - genetics (21) 21
3-hydroxyacyl coa dehydrogenases - metabolism (20) 20
proteins (20) 20
enzymes (19) 19
fatty acids - metabolism (19) 19
endocrinology & metabolism (18) 18
peroxisomes - enzymology (18) 18
chain fatty-acids (17) 17
hydro-lyases (17) 17
peroxisomal disorders - genetics (17) 17
cells, cultured (16) 16
enoyl-coa hydratase - metabolism (16) 16
3-hydroxyacyl coa dehydrogenases - deficiency (15) 15
analysis (15) 15
enoyl-coa hydratase - genetics (15) 15
multienzyme complexes (15) 15
neurosciences (15) 15
rats (15) 15
17-hydroxysteroid dehydrogenases - deficiency (14) 14
d-bifunctional protein (14) 14
infant (14) 14
peroxisomal multifunctional protein-2 - deficiency (14) 14
physiological aspects (14) 14
rat-liver (14) 14
lipid metabolism (13) 13
peroxisomal multifunctional protein-2 - metabolism (13) 13
rhizomelic chondrodysplasia punctata (13) 13
x-linked adrenoleukodystrophy (13) 13
3-hydroxyacyl coa dehydrogenases - genetics (12) 12
adult (12) 12
d-3-hydroxyacyl-coa dehydratase (12) 12
disease models, animal (12) 12
fatty-acids (12) 12
fibroblasts (12) 12
genetics (12) 12
hsd17b4 (12) 12
liver - enzymology (12) 12
metabolism (12) 12
peroxisomal disorders - metabolism (12) 12
peroxisome (12) 12
rat-liver peroxisomes (12) 12
17-hydroxysteroid dehydrogenases - chemistry (11) 11
base sequence (11) 11
bifunctional protein-deficiency (11) 11
brain - pathology (11) 11
d-bifunctional protein deficiency (11) 11
enoyl-coa hydratase - deficiency (11) 11
expression (11) 11
gene (11) 11
lipids (11) 11
spectrum (11) 11
β-oxidation (11) 11
article (10) 10
biosynthesis (10) 10
brain (10) 10
hearing loss, sensorineural - genetics (10) 10
immunohistochemistry (10) 10
molecular-cloning (10) 10
multienzyme complexes - chemistry (10) 10
mutations (10) 10
neurology (10) 10
peroxisomal disorders - diagnosis (10) 10
rna, messenger - genetics (10) 10
17-beta-estradiol dehydrogenase (9) 9
bifunctional protein (9) 9
cancer (9) 9
carrier proteins - metabolism (9) 9
deficiency (9) 9
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain Pathology, ISSN 1015-6305, 09/2018, Volume 28, Issue 5, pp. 631 - 643
Peroxisomes play a crucial role in normal neurodevelopment and in the maintenance of the adult brain. This depends largely on intact peroxisomal beta-oxidation... 
peroxisomes | multifunctional protein‐2 | Purkinje cell | β‐oxidation | ataxia | axonal swellings | β-oxidation | multifunctional protein-2 | NERVOUS-SYSTEM | C DISEASE | DEATH | AUTOPHAGY | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | beta-oxidation | MOUSE MODEL | MICE | MUTANT MOUSE | MUTATIONS | EXPRESSION | Neurodegenerative Diseases - pathology | Peroxisomal Multifunctional Protein-2 - deficiency | Peroxisomal Multifunctional Protein-2 - genetics | Astrocytes - pathology | Cerebellar Ataxia - etiology | Mice, Transgenic | Axons - physiology | Gliosis - physiopathology | Cerebellar Ataxia - pathology | Purkinje Cells - physiology | Gliosis - pathology | Cerebellar Ataxia - physiopathology | Astrocytes - physiology | Animals | Microglia - physiology | Neurodegenerative Diseases - physiopathology | Peroxisomal Disorders - pathology | Axons - pathology | Aging | Microglia - pathology | Peroxisomal Disorders - physiopathology | Purkinje Cells - pathology | Disease Models, Animal | Enzymes | Ataxia | Neurons | Analysis | Cerebellum | Brain | Gene deletion | Neuronal-glial interactions | Mimicry | Atrophy | Proteins | Mouse devices | Clonal deletion | Neurodegeneration | Purkinje cells | Deletion | Evolution | Oxidation | Degeneration | Phenotypes | Cerebellar ataxia | Protein deficiency | Patients | Axons | Peroxisomes | Mutation | Dystrophy
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2013, Volume 58, pp. 258 - 269
Journal Article
The American Journal of Pathology, ISSN 0002-9440, 2006, Volume 168, Issue 4, pp. 1321 - 1334
In humans, mutations inactivating multifunctional protein-2 (MFP-2), and thus peroxisomal β-oxidation, cause neuronal heterotopia and demyelination, which is... 
BETA-OXIDATION | ALPHA-OXIDATION | IMMUNOCYTOCHEMICAL LOCALIZATION | NEURONAL SURVIVAL | DOCOSAHEXAENOIC ACID SYNTHESIS | ZELLWEGER-SYNDROME | D-BIFUNCTIONAL PROTEIN | POLYUNSATURATED FATTY-ACIDS | LIPID EXTRACTS | PATHOLOGY | RHIZOMELIC CHONDRODYSPLASIA PUNCTATA | Enoyl-CoA Hydratase - genetics | Up-Regulation | Ependyma - pathology | Central Nervous System - metabolism | Spinal Cord - metabolism | Neuroglia - pathology | Astrocytes - pathology | Central Nervous System - pathology | Multienzyme Complexes - metabolism | Muscle, Skeletal - metabolism | Motor Activity | Brain - metabolism | Multienzyme Complexes - deficiency | Spinal Cord - pathology | Enoyl-CoA Hydratase - deficiency | Enoyl-CoA Hydratase - metabolism | Axons - metabolism | Peroxisomal Disorders - metabolism | Ependyma - metabolism | Multienzyme Complexes - genetics | Peroxisomes - metabolism | Mice, Knockout | Catalase - metabolism | Peroxisomal Multifunctional Protein-2 | Animals | 17-Hydroxysteroid Dehydrogenases - deficiency | Peroxisomal Disorders - pathology | Peroxisomal Disorders - genetics | 17-Hydroxysteroid Dehydrogenases - genetics | Axons - pathology | Brain - pathology | Neuroglia - metabolism | Mice | Lipids - analysis | Muscle, Skeletal - pathology | 17-Hydroxysteroid Dehydrogenases - metabolism | Astrocytes - metabolism | Index Medicus | Abridged Index Medicus | Original Research Paper
Journal Article
Molecular Imaging and Biology, ISSN 1536-1632, 2/2018, Volume 20, Issue 1, pp. 94 - 102
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2010, Volume 87, Issue 2, pp. 282 - 288
Journal Article
Molecular and Cellular Neuroscience, ISSN 1044-7431, 04/2017, Volume 80, pp. 123 - 133
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 10/2015, Volume 5, Issue 1, pp. 15136 - 15136
SQAP is a novel and promising anticancer agent that was obtained by structural modifications from a natural compound. SQAP inhibits angiogenesis in vivo... 
LUNG-CANCER | PAXILLIN | TYROSINE PHOSPHORYLATION | TARGETING ANGIOGENESIS | MULTIDISCIPLINARY SCIENCES | ALPHA-SULFOQUINOVOSYLMONOACYLGLYCEROL | ENDOTHELIAL-CELLS | PHAGE DISPLAY | POTENT RADIOSENSITIZER | TUMOR ANGIOGENESIS | EXPRESSION | Human Umbilical Vein Endothelial Cells | Focal Adhesion Kinase 1 - genetics | Lung Neoplasms - drug therapy | Carcinoma, Small Cell - genetics | Membrane Glycoproteins - metabolism | Antineoplastic Agents - chemical synthesis | Humans | Membrane Glycoproteins - chemistry | Peroxisomal Multifunctional Protein-2 - chemistry | Peroxisomal Multifunctional Protein-2 - genetics | DNA Repair Enzymes - genetics | Molecular Sequence Data | Glycolipids - chemical synthesis | Lung Neoplasms - pathology | Peptide Library | Carcinoma, Small Cell - enzymology | DNA-Binding Proteins - metabolism | DNA Repair Enzymes - metabolism | Carrier Proteins - chemistry | Antineoplastic Agents - pharmacology | Phosphorylation - drug effects | Binding Sites | Focal Adhesion Kinase 1 - metabolism | DNA Repair Enzymes - chemistry | Lung Neoplasms - genetics | Amino Acid Sequence | Lung Neoplasms - enzymology | Carcinoma, Small Cell - drug therapy | Glycolipids - pharmacology | DNA-Binding Proteins - genetics | DNA-Binding Proteins - chemistry | Peroxisomal Multifunctional Protein-2 - metabolism | Membrane Glycoproteins - genetics | Xenograft Model Antitumor Assays | Carrier Proteins - genetics | Cell Movement - drug effects | Animals | Carrier Proteins - metabolism | Mice, Nude | Cell Line, Tumor | Protein Binding | Mice | Molecular Docking Simulation | Carcinoma, Small Cell - pathology | Focal Adhesion Kinase 1 - antagonists & inhibitors | Focal Adhesion Kinase 1 - chemistry | Ubiquitin | Phosphorylation | Leukocyte migration | Kinases | Endothelial cells | Cell adhesion & migration | Angiogenesis | Phage display | Proteasomes | Hypoxia | Surface plasmon resonance | Focal adhesion kinase | Umbilical vein | Cell migration | Cancer | Index Medicus
Journal Article