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Journal of Cell Biology, ISSN 0021-9525, 12/2018, Volume 217, Issue 12, pp. 4164 - 4183
Kinesin-1, the founding member of the kinesin superfamily of proteins, is known to use only a subset of microtubules for transport in living cells. This biased... 
SLOWLY HYDROLYZABLE ANALOG | VISUALIZATION | PURIFICATION | X-RAY | MOLECULAR MOTORS | AXONAL-TRANSPORT | DYNAMIC INSTABILITY | TUBULIN | STRUCTURES REVEAL | GTP HYDROLYSIS | CELL BIOLOGY | Binding | Second harmonic generation | GTP | Fluorescence | Proteins | GDP | Diffraction | Microscopy | Microtubules | Affinity | Transport | Axonal transport | Adenosine triphosphate | Kinesin | Conformation
Journal Article
Journal Article
Journal Article
Bioscience Reports, ISSN 0144-8463, 2013, Volume 33, Issue 2, pp. 217 - 227
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 10/2012, Volume 40, Issue 19, pp. 9717 - 9737
Journal Article
Cardiovascular Research, ISSN 0008-6363, 08/2017, Volume 113, Issue 10, pp. 1173 - 1185
Aims Mitochondria are important organelles, dedicated to energy production. Mitochondrial p32/C1qbp, which functions as an RNA and protein chaperone, interacts... 
Integrated stress response | Cardiomyopathy | Mitokine | p32/C1qbp | MYOCARDIUM | OXIDATIVE-PHOSPHORYLATION | CARDIAC & CARDIOVASCULAR SYSTEMS | P-32 PROTEIN | BIOMARKER | DISORDERS | BINDING PROTEIN | UNFOLDED PROTEIN RESPONSE | METABOLISM | DISEASE | ENDOPLASMIC-RETICULUM
Journal Article
Journal Article
Journal Article
Bioscience Reports, ISSN 0144-8463, 12/2012, Volume 32, Issue 6, pp. 631 - 639
Miller syndrome is a recessive inherited disorder characterized by postaxial acrofacial dysostosis. It is caused by dysfunction of the DHODH (dihydroorotate... 
Mitochondrion | Miller syndrome | Protein stability | Dihydro-orotate dehydrogenase (DHODH) | Missense mutation | MITOCHONDRIAL-DNA MUTATIONS | METHOTREXATE | protein stability | missense mutation | mitochondrion | CELL BIOLOGY | SYNTHASE | GENE | BIOSYNTHESIS | DISEASE | dihydro-orotate dehydrogenase (DHODH) | NEURAL CREST | INHIBITOR | LEFLUNOMIDE | Abnormalities, Multiple - metabolism | Limb Deformities, Congenital - enzymology | Limb Deformities, Congenital - genetics | Mitochondria - enzymology | Electron Transport Complex III - metabolism | Humans | Micrognathism - genetics | Limb Deformities, Congenital - metabolism | Micrognathism - enzymology | Ubiquinone - metabolism | Mitochondria - metabolism | Mutation, Missense | Oxidoreductases Acting on CH-CH Group Donors - metabolism | Micrognathism - metabolism | Mandibulofacial Dysostosis - genetics | Oxidoreductases Acting on CH-CH Group Donors - analysis | Mandibulofacial Dysostosis - enzymology | Abnormalities, Multiple - enzymology | Oxidoreductases Acting on CH-CH Group Donors - genetics | Succinate Dehydrogenase - metabolism | HeLa Cells | Mandibulofacial Dysostosis - metabolism | Protein Stability | Abnormalities, Multiple - genetics | anti-HA, anti-haemagglutinin | DCPIP, dichlorophenolindophenol | LFN, leflunomide | UMPS, UMP synthase | CHX, cycloheximide | DHODH-HA, DHODH with a C-terminal HA tag | FBS, fetal bovine serum | Original Paper | DHFR, dihydrofolate reductase | DHO, dihydroorotate