Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

Kozak, M. (1987) · Nucleic Acids Research · doi:10.1093/nar/15.20.8125 · Cited by 5,090

Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility

VALE, R., REESE, T., & SHEETZ, M. (1985) · Cell · doi:10.1016/s0092-8674(85)80099-4 · Cited by 1,993

Kinesin and Dynein Superfamily Proteins and the Mechanism of Organelle Transport

Hirokawa, N. (1998) · Science · doi:10.1126/science.279.5350.519 · Cited by 1,689

Characterization of a cis-Golgi matrix protein, GM130.

Nakamura, N., Rabouille, C., Watson, R., Nilsson, T., Hui, N., Slusarewicz, P., Kreis, T. E., & Warren, W. G. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.6.1715 · Cited by 818

Altered microtubule organization in small-calibre axons of mice lacking tau protein

Harada, A., Oguchi, K., Okabe, S., Kuno, J., Terada, S., Ohshima, T., Sato-Yoshitake, R., Takei, Y., Noda, T., & Hirokawa, N. (1994) · Nature · doi:10.1038/369488a0 · Cited by 802

The neuron-specific kinesin superfamily protein KIF1A is a uniqye monomeric motor for anterograde axonal transport of synaptic vesicle precursors

Okada, Y., Yamazaki, H., Sekine‐Aizawa, Y., & Hirokawa, N. (1995) · Cell · doi:10.1016/0092-8674(95)90538-3 · Cited by 679

Microtubules and the endoplasmic reticulum are highly interdependent structures.

Terasaki, M. R., Chen, L. B., & Fujiwara, K. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.103.4.1557 · Cited by 650

A novel brain ATPase with properties expected for the fast axonal transport motor

Brady, S. T. (1985) · Nature · doi:10.1038/317073a0 · Cited by 618

KIF1B, a novel microtubule plus end-directed monomeric motor protein for transport of mitochondria

Nangaku, M., Sato-Yoshitake, R., Okada, Y., Noda, Y., Takemura, R., Yamazaki, H., & Hirokawa, N. (1994) · Cell · doi:10.1016/0092-8674(94)90012-4 · Cited by 608

Golgi dispersal during microtubule disruption: regeneration of Golgi stacks at peripheral endoplasmic reticulum exit sites.

Cole, N. B., Sciaky, N., Marotta, A., Song, J. L., & Lippincott‐Schwartz, J. (1996) · Molecular Biology of the Cell · doi:10.1091/mbc.7.4.631 · Cited by 502

Mitochondrial dynamics in Parkinson's disease: a role for α-synuclein?

Devoto, V. M. P., & Falzone, T. L. (2017) · Disease Models & Mechanisms · doi:10.1242/dmm.026294 · Cited by 184

Association of hepatitis B virus X protein with mitochondria causes mitochondrial aggregation at the nuclear periphery, leading to cell death

Takada, S., Shirakata, Y., Kaneniwa, N., & Koike, K. (1999) · Oncogene · doi:10.1038/sj.onc.1203188 · Cited by 178

Heterotrimeric Kinesin II Is the Microtubule Motor Protein Responsible for Pigment Dispersion in Xenopus Melanophores

Tuma, M. C., Zill, A. T., Bot, N. L., Vernos, I., & Gelfand, V. I. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.6.1547 · Cited by 179

Dynein and kinesin regulate stress-granule and P-body dynamics

Loschi, M., Leishman, C. C., Berardone, N., & Boccaccio, G. L. (2009) · Journal of Cell Science · doi:10.1242/jcs.051383 · Cited by 186

Loss of Dendritic Complexity Precedes Neurodegeneration in a Mouse Model with Disrupted Mitochondrial Distribution in Mature Dendrites

López‐Doménech, G., Higgs, N., Vaccaro, V., Roš, H., Arancibia‐Cárcamo, I. L., MacAskill, A. F., & Kittler, J. T. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.09.004 · Cited by 176

Molecular Motor KIF5A Is Essential for GABAA Receptor Transport, and KIF5A Deletion Causes Epilepsy

Nakajima, K., Yin, X., Takei, Y., Seog, D., Homma, N., & Hirokawa, N. (2012) · Neuron · doi:10.1016/j.neuron.2012.10.012 · Cited by 172

Miro1-mediated mitochondrial positioning shapes intracellular energy gradients required for cell migration

Schuler, M.-H., Lewandowska, A., Caprio, G. D., Skillern, W., Upadhyayula, S., Kirchhausen, T. L., Shaw, J. M., & Cunniff, B. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-10-0741 · Cited by 177

GTPase dependent recruitment of Grif-1 by Miro1 regulates mitochondrial trafficking in hippocampal neurons

MacAskill, A. F., Brickley, K., Stephenson, F. A., & Kittler, J. T. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.10.016 · Cited by 171

MAP7 family proteins regulate kinesin-1 recruitment and activation

Hooikaas, P. J., Martin, M., Mühlethaler, T., Kuijntjes, G.-J., Peeters, C. A. E., Katrukha, E. A., Ferrari, L., Stucchi, R., Verhagen, D. G. F., van Riel, W. E., et al. (2019) · Journal of Cell Biology · doi:10.1083/jcb.201808065 · Cited by 166

The role of lysosomes in cancer development and progression

Tang, T., Yang, Z., Wang, D., Yang, X., Wang, J., Li, L., Wen, Q., Gao, L., Bian, X., & Yu, S. (2020) · Cell & Bioscience · doi:10.1186/s13578-020-00489-x · Cited by 173

Live Cell Imaging of Mitochondrial Movement along Actin Cables in Budding Yeast

Fehrenbacher, K. L., Yang, H., Gay, A. C., Huckaba, T. M., & Pon, L. A. (2004) · Current Biology · doi:10.1016/j.cub.2004.11.004 · Cited by 170

Morpho-dynamic changes of mitochondria during ageing of human endothelial cells

Jendrach, M., Pohl, S., Vöth, M., Kowald, A., Hammerstein, P., & Bereiter‐Hahn, J. (2005) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2005.03.002 · Cited by 170

Inter and Intracellular mitochondrial trafficking in health and disease

Shanmughapriya, S., Langford, D., & Natarajaseenivasan, K. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101128 · Cited by 171

Kinesin 1 Drives Autolysosome Tubulation

Du, W., Su, Q. P., Chen, Y., Zhu, Y., Jiang, D., Rong, Y., Zhang, S., Zhang, Y., Ren, H., Zhang, C., et al. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.04.014 · Cited by 167

Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias: Table 1

Reid, E. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.2.81 · Cited by 166

Biology of Mitochondria in Neurodegenerative Diseases

Martin, L. J. (2012) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-385883-2.00005-9 · Cited by 164

A neuronal network of mitochondrial dynamics regulates metastasis

Caino, M. C., Seo, J. H., Aguinaldo, A., Wait, E. C., Bryant, K. G., Kossenkov, A. V., Hayden, J. E., Vaira, V., Morotti, A., Ferrero, S., et al. (2016) · Nature Communications · doi:10.1038/ncomms13730 · Cited by 162

Conventional kinesin KIF5B mediates insulin‐stimulated GLUT4 movements on microtubules

Semiz, S., Park, J. G., Nicoloro, S. M. C., Furcinitti, P. S., Zhang, C., Chawla, A., Leszyk, J., & Czech, M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg237 · Cited by 162

Mitochondria and Ca2+ signaling: old guests, new functions

Graier, W. F., Frieden, M., & Malli, R. (2007) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-007-0296-1 · Cited by 164

Extramitochondrial localization of mortalin/mthsp70/PBP74/GRP75

Ran, Q., Wadhwa, R., Kawai, R., Kaul, S. C., Sifers, R. N., Bick, R. J., Smith, J. R., & Pereira-Smith, O. M. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3237 · Cited by 182

Tight Functional Coupling of Kinesin-1A and Dynein Motors in the Bidirectional Transport of Neurofilaments

Uchida, A., Alami, N. H., & Brown, A. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-04-0304 · Cited by 153

Regulation of motor proteins, axonal transport deficits and adult-onset neurodegenerative diseases

Brady, S. T., & Morfini, G. A. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.04.010 · Cited by 150

Morphogenesis of the Endoplasmic Reticulum: Beyond Active Membrane Expansion

Vedrenne, C., & Hauri, H. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00419.x · Cited by 151

Mitochondria make a come back

Scheffler, I. E. (2001) · Advanced Drug Delivery Reviews · doi:10.1016/s0169-409x(01)00123-5 · Cited by 154

Syntabulin–Kinesin-1 Family Member 5B-Mediated Axonal Transport Contributes to Activity-Dependent Presynaptic Assembly

Cai, Q., Pan, P., & Sheng, Z. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0731-07.2007 · Cited by 152

The Genetics of Axonal Transport and Axonal Transport Disorders

Duncan, J. E., & Goldstein, L. S. B. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020124 · Cited by 158

Nonapoptotic cell death associated with S-phase arrest of prostate cancer cells via the peroxisome proliferator-activated receptor gamma ligand, 15-deoxy-delta12,14-prostaglandin J2.

Butler, R., Mitchell, S. H., Tindall, D. J., & Young, C. Y. (2000) · PubMed · Cited by 147

Disruption of Mitochondrial Networks by the Human Cytomegalovirus UL37 Gene Product Viral Mitochondrion-Localized Inhibitor of Apoptosis

McCormick, A. L., Smith, V. L., Chow, D. C., & Mocarski, E. S. (2002) · Journal of Virology · doi:10.1128/jvi.77.1.631-641.2003 · Cited by 147

Involvement of conventional kinesin in glucose-stimulated secretory granule movements and exocytosis in clonal pancreatic β-cells

Varadi, A., Ainscow, E. K., Allan, V. J., & Rutter, G. A. (2002) · Journal of Cell Science · doi:10.1242/jcs.00083 · Cited by 156

Effect of oxidative stress during repeated ovulation on the structure and functions of the ovary, oocytes, and their mitochondria

Miyamoto, K., Sato, E. F., Kasahara, E., Jikumaru, M., Hiramoto, K., Tabata, H., Katsuragi, M., Odo, S., Utsumi, K., & Inoue, M. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.05.025 · Cited by 152

An Emerging Role for Tubulin Isotypes in Modulating Cancer Biology and Chemotherapy Resistance

Parker, A. L., Teo, W. S., McCarroll, J. A., & Kavallaris, M. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071434 · Cited by 146

CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins

Gao, J., Schatton, D., Martinelli, P., Hansen, H., Pla‐Martín, D., Barth, E., Becker, C., Altmueller, J., Frommolt, P., Sardiello, M., et al. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201403129 · Cited by 147

Regulation of mitochondrial dynamics in astrocytes: Mechanisms, consequences, and unknowns

Jackson, J. G., & Robinson, M. B. (2017) · Glia · doi:10.1002/glia.23252 · Cited by 153

The role of kinesin family proteins in tumorigenesis and progression

Yu, Y., & Feng, Y. (2010) · Cancer · doi:10.1002/cncr.25461 · Cited by 148

Different microtubule motors move early and late endocytic compartments

Loubéry, S., Wilhelm, C., Hurbain, I., Neveu, S., Louvard, D., & Coudrier, E. (2008) · Traffic · doi:10.1111/j.1600-0854.2008.00704.x · Cited by 143

Kinesin-2 is a motor for late endosomes and lysosomes

Brown, C. L., Maier, K. C., Stauber, T., Ginkel, L. M., Wordeman, L., Vernos, I., & Schroer, T. A. (2005) · Traffic · doi:10.1111/j.1600-0854.2005.00347.x · Cited by 140

Amyotrophic lateral sclerosis-associated mutant VAPBP56S perturbs calcium homeostasis to disrupt axonal transport of mitochondria

Mórotz, G. M., Vos, K. J. D., Vagnoni, A., Ackerley, S., Shaw, C. E., & Miller, C. C. J. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds011 · Cited by 139

Differences in mitochondrial movement and morphology in young and mature primary cortical neurons in culture

Chang, D. T. W., & Reynolds, I. J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.01.034 · Cited by 139

Role of kinesin-1 and cytoplasmic dynein in endoplasmic reticulum movement in VERO cells

Wozniak, M. J., Bola, B. M., Brownhill, K., Yang, Y.-C., Levakova, V., & Allan, V. (2009) · Journal of Cell Science · doi:10.1242/jcs.041962 · Cited by 136

The remote ischemic preconditioning stimulus modifies gene expression in mouse myocardium

Konstantinov, I. E., Arab, S., Li, J., Coles, J. G., Boscarino, C., Mori, A., Cukerman, E., Dawood, F., Cheung, M. M. H., Shimizu, M., et al. (2005) · Journal of Thoracic and Cardiovascular Surgery · doi:10.1016/j.jtcvs.2005.03.050 · Cited by 135

Dynamic tubulation of mitochondria drives mitochondrial network formation

Wang, C., Du, W., Su, Q. P., Zhu, M., Feng, P., Li, Y., Zhou, Y., Mi, N., Zhu, Y., Jiang, D., et al. (2015) · Cell Research · doi:10.1038/cr.2015.89 · Cited by 133

Rab7 and Arl8 GTPases are Necessary for Lysosome Tubulation in Macrophages

Mrakovic, A., Kay, J. G., Furuya, W., Brumell, J. H., & Botelho, R. J. (2012) · Traffic · doi:10.1111/tra.12003 · Cited by 131

Nuclear-Mitochondrial Interactions

Walker, B. R., & Moraes, C. T. (2022) · Biomolecules · doi:10.3390/biom12030427 · Cited by 143

Automatic Morphological Subtyping Reveals New Roles of Caspases in Mitochondrial Dynamics

Peng, J.-Y., Lin, C., Chen, Y.-J., Kao, L., Liu, Y., Chou, C.-C., Huang, Y.-H., Chang, F., Wu, Y., Tsai, Y., et al. (2011) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002212 · Cited by 129

ROS Control Mitochondrial Motility through p38 and the Motor Adaptor Miro/Trak

Debattisti, V., Gerencser, A. A., Saotome, M., Das, S., & Hajnóczky, G. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.060 · Cited by 132

Association of the Kinesin‐Binding Domain of RanBP2 to KIF5B and KIF5C Determines Mitochondria Localization and Function

Cho, K., Cai, Y., Yi, H., Yeh, A., Aslanukov, A., & Ferreira, P. A. (2007) · Traffic · doi:10.1111/j.1600-0854.2007.00647.x · Cited by 130

Mitochondrial Function, Morphology, and Axonal Transport in Amyotrophic Lateral Sclerosis

Magrané, J., & Manfredi, G. (2009) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.2604 · Cited by 127

Depletion of Kinesin 5B Affects Lysosomal Distribution and Stability and Induces Peri-Nuclear Accumulation of Autophagosomes in Cancer Cells

Cardoso, C. M. P., Groth‐Pedersen, L., Høyer-Hansen, M. H., Kirkegaard, T., Corcelle, E., Andersen, J., Jäättelä, M., & Nylandsted, J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004424 · Cited by 125

Perinuclear Localization and Insulin Responsiveness of GLUT4 Requires Cytoskeletal Integrity in 3T3-L1 Adipocytes

Guilherme, A., Emoto, M., Buxton, J. M., Bose, S., Sabini, R. C., Theurkauf, W. E., Leszyk, J., & Czech, M. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m003432200 · Cited by 125

Mitochondria are transported along microtubules in membrane nanotubes to rescue distressed cardiomyocytes from apoptosis

Shen, J., Zhang, J., Xiao, H., Wu, J., He, K., Lv, Z.-Z., Li, Z., Xu, M., & Zhang, Y. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0145-x · Cited by 124

Mitochondrial morphology is dynamic and varied

Rube, D. A., & van der Bliek, A. M. (2003) · Molecular and Cellular Biochemistry · doi:10.1023/b:mcbi.0000009879.01256.f6 · Cited by 123

Kinesin and dynein mutants provide novel insights into the roles of vesicle traffic during cell morphogenesis in Neurospora

Seiler, S., Plamann, M. D., & Schliwa, M. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80360-1 · Cited by 123

Motor proteins at the mitochondria–cytoskeleton interface

Kruppa, A. J., & Buß, F. (2021) · Journal of Cell Science · doi:10.1242/jcs.226084 · Cited by 127

Polarization-Dependent Selective Transport to the Apical Membrane by KIF5B in MDCK Cells

Jaulin, F., Xue, X., Rodriguez-Boulan, E. J., & Kreitzer, G. E. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.08.001 · Cited by 118

Regulation of long-distance transport of mitochondria along microtubules

Melkov, A., & Abdu, U. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2590-1 · Cited by 129

Mitochondrial morphology and distribution in mammalian cells

Frazier, A. E., Kiu, C., Stojanovski, D., Hoogenraad, N. J., & Ryan, M. T. (2006) · Biological Chemistry · doi:10.1515/bc.2006.193 · Cited by 118

Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia

Score, J., Curtis, C., Waghorn, K., Stalder, M., Jotterand, M., Grand, F., & Cross, N. C. P. (2006) · Leukemia · doi:10.1038/sj.leu.2404154 · Cited by 117

TheCaenorhabditis elegansDopaminergic System: Opportunities for Insights into Dopamine Transport and Neurodegeneration

Nass, R., & Blakely, R. (2003) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.43.100901.135934 · Cited by 117

Tumor Necrosis Factor Induces Hyperphosphorylation of Kinesin Light Chain and Inhibits Kinesin-Mediated Transport of Mitochondria

Vos, K. J. D., Severin, F. F., Herreweghe, F. V., Vancompernolle, K., Goossens, V., Hyman, A. A., & Grooten, J. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.149.6.1207 · Cited by 117

Unique Function of Kinesin Kif5A in Localization of Mitochondria in Axons

Campbell, P. D., Shen, K., Sapio, M. R., Glenn, T. D., Talbot, W. S., & Marlow, F. L. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2770-14.2014 · Cited by 121

KIF16B/Rab14 Molecular Motor Complex Is Critical for Early Embryonic Development by Transporting FGF Receptor

Ueno, H., Huang, X., Tanaka, Y., & Hirokawa, N. (2011) · Developmental Cell · doi:10.1016/j.devcel.2010.11.008 · Cited by 116

Leukocyte transmigration requires kinesin-mediated microtubule-dependent membrane trafficking from the lateral border recycling compartment

Mamdouh, Z., Kreitzer, G. E., & Müller, W. A. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20072328 · Cited by 115

Mitochondrial trafficking in neurons and the role of the Miro family of GTPase proteins

Birsa, N., Norkett, R., Higgs, N., López‐Doménech, G., & Kittler, J. T. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130234 · Cited by 116

Opposite effects of microtubule-stabilizing and microtubule-destabilizing drugs on biogenesis of mitochondria in mammalian cells

Karbowski, M., Spodnik, J. H., Teranishi, M., Woźniak, M., Nishizawa, Y., Usukura, J., & Wakabayashi, T. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.2.281 · Cited by 113

Identification of Miro1 and Miro2 as mitochondrial receptors for myosin XIX

Oeding, S. J., Majstrowicz, K., Hu, X.-P., Schwarz, V., Freitag, A., Honnert, U., Nikolaus, P., & Bähler, M. (2018) · Journal of Cell Science · doi:10.1242/jcs.219469 · Cited by 118

Microtubule Actin Crosslinking Factor 1 Regulates the Balbiani Body and Animal-Vegetal Polarity of the Zebrafish Oocyte

Gupta, T., Marlow, F. L., Ferriola, D., Mackiewicz, K., Dapprich, J., Monos, D. S., & Mullins, M. C. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001073 · Cited by 109

MIRO-1 Determines Mitochondrial Shape Transition upon GPCR Activation and Ca2+ Stress

Nemani, N., Carvalho, E., Tomar, D., Dong, Z., Ketschek, A., Breves, S. L., Jaña, F., Worth, A. M., Heffler, J., Palaniappan, P., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.098 · Cited by 111

Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate

Charng, W., Karaca, E., Coban‐Akdemir, Z., Gambin, T., Atik, M. M., Gu, S., Posey, J. E., Jhangiani, S. N., Muzny, D. M., Doddapaneni, H., et al. (2016) · BMC Medical Genomics · doi:10.1186/s12920-016-0208-3 · Cited by 114

A Rab3a-dependent complex essential for lysosome positioning and plasma membrane repair

Encarnação, M., Espada, L., Escrevente, C., Mateus, D. D., Ramalho, J. S., Michelet, X., Santarino, I. B., Hsu, V. W., Brenner, M. B., Barral, D. C., et al. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201511093 · Cited by 112

SKIP, the Host Target of the Salmonella Virulence Factor SifA, Promotes Kinesin-1-Dependent Vacuolar Membrane Exchanges

Dumont, A., Boucrot, E., Drevensek, S., Daire, V., Gorvel, J., Poüs, C., Holden, D. W., & Méresse, S. (2010) · Traffic · doi:10.1111/j.1600-0854.2010.01069.x · Cited by 107

Transport of African Swine Fever Virus from Assembly Sites to the Plasma Membrane Is Dependent on Microtubules and Conventional Kinesin

Jouvenet, N., Monaghan, P., Way, M., & Wileman, T. E. (2004) · Journal of Virology · doi:10.1128/jvi.78.15.7990-8001.2004 · Cited by 107

Regulation of mitochondria distribution by RhoA and formins

Minin, A. A., Kulik, A. V., Gyoeva, F. K., Li, Y., Goshima, G., & Gelfand, V. I. (2006) · Journal of Cell Science · doi:10.1242/jcs.02762 · Cited by 102

Mitochondrial transport and docking in axons

Cai, Q., & Sheng, Z. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.03.024 · Cited by 105

Structure and Function of Mitochondria‐Associated Endoplasmic Reticulum Membranes (MAMs) and Their Role in Cardiovascular Diseases

Luan, Y., Luan, Y., Yuan, R., Feng, Q., Chen, X., & Yang, Y. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/4578809 · Cited by 115

Peroxisomes move by hitchhiking on early endosomes using the novel linker protein PxdA

Salogiannis, J., Egan, M. J., & Reck‐Peterson, S. L. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201512020 · Cited by 104

β‐Tubulin mutations that cause severe neuropathies disrupt axonal transport

Niwa, S., Takahashi, H., & Hirokawa, N. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.59 · Cited by 104

Molecular responses of human dermal fibroblasts to dual cues: Contact guidance and mechanical load

Mudera, V., Pleass, R., Eastwood, M., Tarnuzzer, R. W., Schultz, G., Khaw, P. T., McGrouther, D. A., & Brown, R. A. (2000) · Cell Motility and the Cytoskeleton · doi:10.1002/(sici)1097-0169(200001)45:1 · Cited by 135

Defective kinesin heavy chain behavior in mouse kinesin light chain mutants

Rahman, A., Kamal, A., Roberts, E. A., & Goldstein, L. S. B. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.146.6.1277 · Cited by 102

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function

Willemsen, M. H., Ba, W., Wissink-Lindhout, W. M., de Brouwer, A. P. M., Haas, S. A., Bienek, M., Hu, H., Vissers, L. E. L. M., van Bokhoven, H., Kalscheuer, V. M., et al. (2014) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2013-102182 · Cited by 99

A Role for Kinesin in Insulin-stimulated GLUT4 Glucose Transporter Translocation in 3T3-L1 Adipocytes

Emoto, M., Langille, S. E., & Czech, M. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010785200 · Cited by 101

KIF5B Motor Adaptor Syntabulin Maintains Synaptic Transmission in Sympathetic Neurons

Ma, H., Cai, Q., Lu, W., Sheng, Z., & Mochida, S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2517-09.2009 · Cited by 101

Brain-derived Neurotrophic Factor (BDNF)-induced Mitochondrial Motility Arrest and Presynaptic Docking Contribute to BDNF-enhanced Synaptic Transmission

Su, B., Ji, Y.-S., Sun, X., Liu, X., & Chen, Z.-Y. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.526129 · Cited by 99

Desmosomal cadherins utilize distinct kinesins for assembly into desmosomes

Nekrasova, O. E., Amargo, E. V., Smith, W. O., Chen, J., Kreitzer, G. E., & Green, K. J. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201106057 · Cited by 99

The Miro GTPases: At the heart of the mitochondrial transport machinery

Reis, K., Fransson, Å., & Aspenström, P. (2009) · FEBS Letters · doi:10.1016/j.febslet.2009.04.015 · Cited by 100

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Fast Axonal Transport Misregulation and Alzheimer's Disease

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Membrane motors

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Microtubule-based Endoplasmic Reticulum Motility inXenopus laevis: Activation of Membrane-associated Kinesin during Development

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AMP‐activated protein kinase mediates activity‐dependent axon branching by recruiting mitochondria to axon

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Synaptic Vesicle Precursors and Lysosomes Are Transported by Different Mechanisms in the Axon of Mammalian Neurons

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KBP is essential for axonal structure, outgrowth and maintenance in zebrafish, providing insight into the cellular basis of Goldberg-Shprintzen syndrome

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Motor and cargo interactions

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The Molecular Motor KIF1A Transports the TrkA Neurotrophin Receptor and Is Essential for Sensory Neuron Survival and Function

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E1 ∧ E4 Protein of Human Papillomavirus Type 16 Associates with Mitochondria

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VMP1 Establishes ER-Microdomains that Regulate Membrane Contact Sites and Autophagy

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Dynein Light Chain LC8 Regulates Syntaphilin-Mediated Mitochondrial Docking in Axons

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A) Mitochondrial perinuclear clustering (a consequence of defective trafficking) results from siRNA-mediated knockdown of KIF5B, but not of KIF11

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田中, 庸. (1999) · doi:10.11501/3190895

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Defective kinesin heavy chain behavior in mouse kinesin light chain mutants

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