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

Intact Lysosome Transport and Phagosome Function Despite Kinectin Deficiency

Plitz, T., & Pfeffer, K. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.17.6044-6055.2001 · Cited by 25

Kinesin-1 Regulates Extrasynaptic Targeting of NMDARs and Neuronal Vulnerability Toward Excitotoxicity

Lin, R., Duan, Z., Sun, H., Fung, M.-L., Chen, H., Wang, J., Lau, C. G., Yang, D., Liu, Y., Ni, Y., et al. (2019) · iScience · doi:10.1016/j.isci.2019.02.009 · Cited by 23

Structural studies of human fission protein FIS1 reveal a dynamic region important for GTPase DRP1 recruitment and mitochondrial fission

Egner, J. M., Nolden, K. A., Harwig, M. C., Bonate, R., de Anda, J., Tessmer, M. H., Noey, E. L., Ihenacho, U. K., Liu, Z., Peterson, F. C., et al. (2022) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2022.102620 · Cited by 25

Creatine kinase B deficient neurons exhibit an increased fraction of motile mitochondria

Kuiper, J. W., Oerlemans, F. T. J. J., Fransen, J. A. M., & Wieringa, B. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-73 · Cited by 23

A two‐dimensional electrophoretic map of human mitochondrial proteins from immortalized lymphoblastoid cell lines: A prerequisite to study mitochondrial disorders in patients

Xie, J., Techritz, S., Haebel, S., Horn, A., Neitzel, H., Klose, J., & Schuelke, M. (2005) · PROTEOMICS · doi:10.1002/pmic.200401191 · Cited by 24

Receptor‐mediated regulation of peroxisomal motility in CHO and endothelial cells

Huber, C. M., Saffrich, R., Ansorge, W. J., & Just, W. W. (1999) · The EMBO Journal · doi:10.1093/emboj/18.20.5476 · Cited by 23

Clonal Tests of Conventional Kinesin Function during Cell Proliferation and Differentiation

Brendza, R. P., Sheehan, K. B., Turner, F. R., & Saxton, W. M. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.4.1329 · Cited by 23

The BH3 domain is required for caspase-independent cell death induced by Bax and oligomycin

Fitch, M., Chang, C.-M., & Parslow, T. G. (2000) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400659 · Cited by 23

Sarcopenia‐related changes in serum GLP‐1 level affect myogenic differentiation

Huang, H., Wang, Y., Jiang, H., Yu, H. W., Chen, Y., Chiou, A., & Kuo, J. (2024) · Journal of Cachexia, Sarcopenia and Muscle · doi:10.1002/jcsm.13524 · Cited by 22

Armadillo repeat-containing kinesin represents the versatile plus-end-directed transporter in Physcomitrella

Yoshida, M. W., Hakozaki, M., & Goshima, G. (2023) · Nature Plants · doi:10.1038/s41477-023-01397-x · Cited by 20

Cellular Motors for Molecular Manufacturing

Dinu, C. Z., Chrisey, D. B., Diez, S., & Howard, J. (2007) · The Anatomical Record · doi:10.1002/ar.20599 · Cited by 22

Monitoring the Mitochondrial Dynamics in Mammalian Cells

Simula, L., & Campello, S. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7831-1_15 · Cited by 22

CLASP regulates mitochondrial distribution in Schizosaccharomyces pombe

Chiron, S., Bobkova, A., Zhou, H., & Yaffe, M. P. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200712147 · Cited by 22

Positively charged residues within the MYO19 MyMOMA domain are essential for proper localization of MYO19 to the mitochondrial outer membrane

Hawthorne, J. L., Mehta, P. R., Singh, P. P., Wong, N. Q., & Quintero, O. A. (2016) · Cytoskeleton · doi:10.1002/cm.21305 · Cited by 21

Kinesin-II recruits Armadillo and Dishevelled for Wingless signaling in Drosophila

Vuong, L. T., Mukhopadhyay, B., & Choi, K.-W. (2014) · Development · doi:10.1242/dev.106229 · Cited by 21

Kinesins in Mammalian Spermatogenesis and Germ Cell Transport

Yao, M., Qu, H., Han, Y., Cheng, C. Y., & Xiao, X. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.837542 · Cited by 20

New approach to capture and characterize synaptic proteome

Liu, X.-A., Kadakkuzha, B. M., Pascal, B. D., Steckler, C., Akhmedov, K., Yan, L., Chalmers, M. J., & Puthanveettil, S. V. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1401483111 · Cited by 19

Control of mitochondrial integrity in Parkinson’s disease

Vives-Bauzá, C., Tocilescu, M. A., deVries, R. L. A., Wolken, D. M. A., Jackson-Lewis, V. R., & Przedborski, S. (2010) · Progress in brain research · doi:10.1016/s0079-6123(10)83006-7 · Cited by 20

Zinc finger E‐box binding homeobox‐1 (Zeb1) drives anterograde lysosome trafficking and tumor cell invasion via upregulation of Na+/H+ Exchanger‐1 (NHE1)

Dykes, S. S., Gao, C., Songock, W. K., Bigelow, R. L. H., Woude, G. V., Bodily, J. M., & Cardelli, J. A. (2016) · Molecular Carcinogenesis · doi:10.1002/mc.22528 · Cited by 21

Asymmetric inheritance of mitochondria in yeast

Klecker, T., & Westermann, B. (2020) · Biological Chemistry · doi:10.1515/hsz-2019-0439 · Cited by 23

Mitoptosis, Twenty Years After

Lyamzaev, K. G., Кнорре, Д. А., & Chernyak, B. V. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920120020 · Cited by 21

RUSC2 and WDR47 oppositely regulate kinesin–1-dependent distribution of ATG9A to the cell periphery

Guardia, C. M. A., Jain, A., Mattera, R., Friefeld, A., Li, Y., & Bonifacino, J. S. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e21-06-0295 · Cited by 23

From electron microscopy to molecular cell biology, molecular genetics and structural biology: intracellular transport and kinesin superfamily proteins, KIFs: genes, structure, dynamics and functions

Hirokawa, N. (2011) · Microscopy · doi:10.1093/jmicro/dfr051 · Cited by 23

UXT (Ubiquitously Expressed Transcript) causes mitochondrial aggregation

Moss, T. N., Vo, A., McKeehan, W. L., & Liu, L. (2007) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-007-9016-6 · Cited by 21

Neuronal KIF 5b deletion induces striatum‐dependent locomotor impairments and defects in membrane presentation of dopamine D2 receptors

Cromberg, L. E., Saez, T. M. M., Otero, M. G., Tomasella, E., Alloatti, M., Damianich, A., Devoto, V. M. P., Ferrario, J. E., Gelman, D. M., Rubinstein, M., et al. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14665 · Cited by 20

14-3-3γ meditated transport of plakoglobin to the cell border is required for the initiation of desmosome assembly in vitro and in vivo

Sehgal, L., Mukhopadhyay, A., Rajan, A., Khapare, N., Sawant, M., Vishal, S. S., Bhatt, K., Ambatipudi, S., Antao, N. V., Alam, H., et al. (2014) · Journal of Cell Science · doi:10.1242/jcs.125807 · Cited by 20

Regulation of adrenocortical steroid hormone production by RhoA–diaphanous 1 signaling and the cytoskeleton

Sewer, M. B., & Li, D. (2012) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2012.11.014 · Cited by 19

Silkworm Coatomers and Their Role in Tube Expansion of Posterior Silkgland

Wang, Q., Shen, B., Zheng, P., Feng, H., Chen, L., Zhang, J., Zhang, C., Zhang, G., Teng, J., & Chen, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013252 · Cited by 20

cAMP-stimulated phosphorylation of diaphanous 1 regulates protein stability and interaction with binding partners in adrenocortical cells

Li, D., Dammer, E. B., Lucki, N. C., & Sewer, M. B. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-08-0597 · Cited by 20

Hypertrophy induced KIF5B controls mitochondrial localization and function in neonatal rat cardiomyocytes

Tigchelaar, W., de Jong, A. M., Bloks, V. W., van Gilst, W. H., de Boer, R. A., & Silljé, H. H. W. (2016) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2016.04.005 · Cited by 20

Hypoxia-induced mitochondrial and nuclear DNA damage in the rat brain

Englander, E. W., Greeley, G. H., Wang, G., Perez-Polo, J. R., & Lee, H.-M. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19991015)58:2 · Cited by 51

Kinesins in the nervous system

Martin, M., Hurd, D. D., & Saxton, W. M. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050422 · Cited by 20

cRel induces mitochondrial alterations in correlation with proliferation arrest

Bernard, D., Slomianny, C., Vandenbunder, B., & Abbadie, C. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00668-2 · Cited by 20

Matrix mechanics regulates muscle regeneration by modulating kinesin-1 activity

Chiang, W.-Y., Yu, H. W., Wu, M.-C., Huang, Y.-M., Chen, Y., Lin, J., Liu, Y.-W., You, L., Chiou, A., & Kuo, J. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.122551 · Cited by 20

Roles of developmentally regulated KIF2A alternative isoforms in cortical neuron migration and differentiation

Akkaya, C., Atak, D., Kamacıoğlu, A., Akarlar, B. A., Güner, G., Bayam, E., Taşkın, A. C., Özlü, N., & Ince-Dunn, G. (2021) · Development · doi:10.1242/dev.192674 · Cited by 19

Tau phosphorylation and PAD exposure in regulation of axonal growth

Morris, S. L., & Brady, S. T. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.1023418 · Cited by 19

Gigaxonin is required for intermediate filament transport

Renganathan, B., Zewe, J. P., Cheng, Y., Paumier, J., Kittisopikul, M., Ridge, K. M., Opal, P., & Gelfand, V. I. (2023) · The FASEB Journal · doi:10.1096/fj.202202119r · Cited by 18

Spaced training activates Miro/Milton-dependent mitochondrial dynamics in neuronal axons to sustain long-term memory

Pavlowsky, A., Comyn, T., Minatchy, J., Gény, D., Bun, P., Danglot, L., Préat, T., & Plaçais, P.-Y. (2024) · Current Biology · doi:10.1016/j.cub.2024.03.050 · Cited by 19

Normal levels of KIF5 but reduced KLC1 levels in both Alzheimer disease and Alzheimer disease in Down syndrome: evidence suggesting defects in anterograde transport

Chen, X., Das, U., Park, G., & Mobley, W. C. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00796-6 · Cited by 20

Role of kinesin light chain‐2 of kinesin‐1 in the traffic of Na,K‐ATPase‐containing vesicles in alveolar epithelial cells

Bittar, H. E. T., Lecuona, E., Grillo, D., Szleifer, I. G., Nekrasova, O. E., Gelfand, V. I., & Sznajder, J. I. (2009) · The FASEB Journal · doi:10.1096/fj.09-137802 · Cited by 19

Kinesin-1 and mitochondrial motility control by discrimination of structurally equivalent but distinct subdomains in Ran-GTP-binding domains of Ran-binding protein 2

Patil, H., Cho, K., Lee, J., Yang, Y., Orry, A. J. W., & Ferreira, P. A. (2013) · Open Biology · doi:10.1098/rsob.120183 · Cited by 19

A Novel C-terminal Kinesin Is Essential for Maintaining Functional Acidocalcisomes in Trypanosoma brucei

Dutoya, S., Gibert, S., Lemercier, G., Santarelli, X., Baltz, D., Baltz, T., & Bakalara, N. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105962200 · Cited by 19

Nesprin-2 coordinates opposing microtubule motors during nuclear migration in neurons

Zhou, C., Wu, Y. K., Ishidate, F., Fujiwara, T. K., & Kengaku, M. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202405032 · Cited by 18

Unraveling the interplay of kinesin-1, tau, and microtubules in neurodegeneration associated with Alzheimer’s disease

Durairajan, S. S. K., Selvarasu, K., Singh, A. K., Patnaik, S., Iyaswamy, A., Jaiswal, Y., Williams, L. L., & Huang, J. (2024) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2024.1432002 · Cited by 18

CRMP/UNC-33 organizes microtubule bundles for KIF5-mediated mitochondrial distribution to axon

Chen, Y.-C., Huang, H.-R., Hsu, C., & Ou, C.-Y. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009360 · Cited by 19

Kinesin 5B (KIF5B) Is Required for Progression through Female Meiosis and Proper Chromosomal Segregation in Mitotic Cells

Kidane, D., Sakkas, D., Nottoli, T., McGrath, J. M., & Sweasy, J. B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058585 · Cited by 18

The Subcellular Dynamics of the Gs-Linked Receptor GPR3 Contribute to the Local Activation of PKA in Cerebellar Granular Neurons

Miyagi, T., Tanaka, S., Hide, I., Shirafuji, T., & Sakai, N. (2016) · PLoS ONE · doi:10.1371/journal.pone.0147466 · Cited by 18

Motor Proteins and Spermatogenesis

Wu, S., Li, H., Wang, L., Mak, N., Wu, X., Ge, R., Sun, F., & Cheng, C. Y. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-77779-1_7 · Cited by 18

Contributions of Bcl-xL to acute and long term changes in bioenergetics during neuronal plasticity

Jonas, E. A. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.11.007 · Cited by 18

Inefficient recruitment of kinesin-1 to melanosomes precludes it from facilitating their transport

Robinson, C. L., Evans, R. D., Briggs, D. A., Ramalho, J. S., & Hume, A. N. (2017) · Journal of Cell Science · doi:10.1242/jcs.186064 · Cited by 17

The microtubule motor protein KIF13A is involved in intracellular trafficking of the Lassa virus matrix protein Z

Fehling, S. K., Noda, T., Maisner, A., Lamp, B., Conzelmann, K., Kawaoka, Y., Klenk, H., Garten, W., & Strecker, T. (2012) · Cellular Microbiology · doi:10.1111/cmi.12095 · Cited by 17

Hippocampal to basal forebrain transport of Mn 2+ is impaired by deletion of KLC1, a subunit of the conventional kinesin microtubule-based motor

Medina, C. S., Biris, O., Falzone, T. L., Zhang, X., Zimmerman, A. J., & Bearer, E. L. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.09.035 · Cited by 16

Mitosomes in Parasitic Protists

Tachezy, J., & Šmíd, O. (2007) · Springer eBooks · doi:10.1007/7171_2007_113 · Cited by 17

Presynaptic Precursor Vesicles—Cargo, Biogenesis, and Kinesin-Based Transport across Species

Petzoldt, A. G. (2023) · Cells · doi:10.3390/cells12182248 · Cited by 18

Lysosome-associated membrane proteins (LAMPs) regulate intracellular positioning of mitochondria in MC3T3-E1 cells

Rajapakshe, A. R., Podyma‐Inoue, K. A., Terasawa, K., Hasegawa, K., Namba, T., Kumei, Y., Yanagishita, M., & Hara‐Yokoyama, M. (2014) · Experimental Cell Research · doi:10.1016/j.yexcr.2014.09.014 · Cited by 16

Mitochondria: transportation, distribution and function during spermiogenesis

Sun, X. Y., & Yang, W. (2010) · Advances in Bioscience and Biotechnology · doi:10.4236/abb.2010.12014 · Cited by 19

Lysosome trafficking is necessary for EGF-driven invasion and is regulated by p38 MAPK and Na+/H+ exchangers

Dykes, S. S., Steffan, J. J., & Cardelli, J. A. (2017) · BMC Cancer · doi:10.1186/s12885-017-3660-3 · Cited by 17

Kif1Bβ isoform is enriched in motor neurons but does not change in a mouse model of amyotrophic lateral sclerosis

Conforti, L., Dell’Agnello, C., Calvaresi, N., Tortarolo, M., Giorgini, A., Coleman, M. P., & Bendotti, C. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10517 · Cited by 16

Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics

Sharma, G., Pfeffer, G., & Shutt, T. E. (2021) · Biology · doi:10.3390/biology10040268 · Cited by 18

Axonal transport and neurodegenerative disease: vesicle-motor complex formation and their regulation

Gunawardena, S., Anderson, E. N., & White, J. (2014) · Degenerative Neurological and Neuromuscular Disease · doi:10.2147/dnnd.s57502 · Cited by 16

Dominantly acting KIF5B variants with pleiotropic cellular consequences cause variable clinical phenotypes

Flex, E., Albadri, S., Radio, F. C., Cecchetti, S., Lauri, A., Priolo, M., Kissopoulos, M., Carpentieri, G., Fasano, G., Venditti, M., et al. (2022) · Human Molecular Genetics · doi:10.1093/hmg/ddac213 · Cited by 17

KIF3B promotes a PI3K signaling gradient causing changes in a Shh protein gradient and suppressing polydactyly in mice

Wang, S., Tanaka, Y., Xu, Y., Takeda, S., & Hirokawa, N. (2022) · Developmental Cell · doi:10.1016/j.devcel.2022.09.007 · Cited by 13

Multimodal transport and dispersion of organelles in narrow tubular cells

Mogre, S. S., & Koslover, E. F. (2018) · Physical review. E · doi:10.1103/physreve.97.042402 · Cited by 15

Proteolytic regulation of mitochondrial dynamics

Dietz, J. V., Bohovych, I., Viana, M. P., & Khalimonchuk, O. (2019) · Mitochondrion · doi:10.1016/j.mito.2019.04.008 · Cited by 15

Hyperglycemia-induced mitochondrial abnormalities in autonomic neurons via the RAGE axis

Otero, M. G., Henao–Romero, N., Krysak, T. M., Vu-Lu, M. T., Morales, O. O. M., Momeni, Z., Yamamoto, Y., Falzone, T. L., & Campanucci, V. A. (2025) · Scientific Reports · doi:10.1038/s41598-025-10933-y · Cited by 14

Pathophysiology of Amyotrophic Lateral Sclerosis

Fabian, H., Clara, M., & Alvaro, G. (2013) · InTech eBooks · doi:10.5772/56562 · Cited by 17

Miro1 as a novel regulator of hypertrophy in neonatal rat cardiomyocytes

Conejeros, C., Parra, V., Sánchez, G., Pedrozo, Z., & Olmedo, I. (2020) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2020.03.014 · Cited by 14

Air Plasma-Activated Medium Evokes a Death-Associated Perinuclear Mitochondrial Clustering

Suzuki‐Karasaki, M., Ando, T., Ochiai, Y., Kawahara, K., Suzuki‐Karasaki, M., Nakayama, H., & Suzuki‐Karasaki, Y. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031124 · Cited by 15

KIF5A regulates axonal repair and time-dependent axonal transport of SFPQ granules and mitochondria in human motor neurons

Juan, I. G. S., Brunner, J., Eggan, K. C., Toonen, R. F. G., & Verhage, M. (2024) · Neurobiology of Disease · doi:10.1016/j.nbd.2024.106759 · Cited by 17

Dynactin suppresses the retrograde movement of apically localized mRNA in Drosophila blastoderm embryos

Vendra, G., Hamilton, R. S., & Davis, I. (2007) · RNA · doi:10.1261/rna.509007 · Cited by 14

Kinesin Light Chain 1 Suppression Impairs Human Embryonic Stem Cell Neural Differentiation and Amyloid Precursor Protein Metabolism

Killian, R. L., Flippin, J. D., Herrera, C. M., Almenar‐Queralt, A., & Goldstein, L. S. B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029755 · Cited by 14

A signal transduction pathway involved in microtubule‐mediated cell polarization

Liao, G., Kreitzer, G. E., Cook, T. A., & Gundersen, G. G. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.9002.s257 · Cited by 14

Neurons dispose of hyperactive kinesin into glial cells for clearance

Xie, C., Chen, G., Li, M., Huang, P., Chen, Z., Lei, K., Li, D., Wang, Y., Cleetus, A., Mohamed, M. A., et al. (2024) · The EMBO Journal · doi:10.1038/s44318-024-00118-0 · Cited by 14

KIF5C deficiency causes abnormal cortical neuronal migration, dendritic branching, and spine morphology in mice

Li, W., Cheng, T., Dong, X., Chen, H., Yang, L., Qiu, Z., & Zhou, W. (2021) · Pediatric Research · doi:10.1038/s41390-021-01922-8 · Cited by 14

Mitochondrial Dynamics

Scott, I., & Logan, D. C. (2010) · Springer eBooks · doi:10.1007/978-0-387-89781-3_2 · Cited by 14

Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling

Marom, R., Zhang, B., Washington, M. E., Song, I.-W., Burrage, L. C., Rossi, V. C., Berrier, A. S., Lindsey, A., Lesinski, J., Nonet, M. L., et al. (2023) · PLoS Genetics · doi:10.1371/journal.pgen.1011005 · Cited by 13

Axonal transport dysfunction of mitochondria in traumatic brain injury: A novel therapeutic target

Shin, S. S., Karlsson, M., Mazandi, V. M., Ranganathan, A., Hallowell, T., Delso, N., & Kilbaugh, T. J. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113311 · Cited by 13

Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants

Vergani, L., Malena, A., Sabatelli, P., Loro, E., Cavallini, L., Magalhães, P. M. R., Valente, L., Bragantini, F., Carrara, F., Léger, B., et al. (2007) · Brain · doi:10.1093/brain/awm151 · Cited by 13

Stretching the lung and programmed cell death

Chandel, N. S., & Sznajder, J. I. (2000) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2000.279.6.l1003 · Cited by 13

Mitochondrial Alterations in Neurons Derived from the Murine AppNL-F Knock-In Model of Alzheimer’s Disease

Dentoni, G., Naia, L., Portal, B., Leal, N. S., Nilsson, P., Lindskog, M., & Ankarcrona, M. (2022) · Journal of Alzheimer s Disease · doi:10.3233/jad-220383 · Cited by 13

Role of tubulin post-translational modifications in peripheral neuropathy

Pero, M. E., Chowdhury, F., & Bartolini, F. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114274 · Cited by 16

Autophagy core protein BECN1 is vital for spermatogenesis and male fertility in mice

Ke, L., Lin, X., Yuchuan, L., Tao, S., Chang, Y., He, Y., Wu, Y., Liu, N., & Qin, Y. (2023) · Biology of Reproduction · doi:10.1093/biolre/ioad160 · Cited by 13

Analysis of the function of KIF3A and KIF3B in the spermatogenesis in Boleophthalmus pectinirostris

Zhao, Y.-Q., Mu, D.-L., Wang, D., Han, Y., Hou, C.-C., & Zhu, J. (2018) · Fish Physiology and Biochemistry · doi:10.1007/s10695-017-0461-1 · Cited by 13

Mitochondrial dynamics and their intracellular traffic in porcine oocytes

Yamochi, T., Hashimoto, S., Amo, A., Goto, H., Yamanaka, M., Inoue, M., Nakaoka, Y., & Morimoto, Y. (2015) · Zygote · doi:10.1017/s0967199415000489 · Cited by 12

Keeping Neuronal Cargoes on the Right Track: New Insights into Regulators of Axonal Transport

Miller, K. G. (2016) · The Neuroscientist · doi:10.1177/1073858416648307 · Cited by 13

Impairments in age-dependent ubiquitin proteostasis and structural integrity of selective neurons by uncoupling Ran GTPase from the Ran-binding domain 3 of Ranbp2 and identification of novel mitochondrial isoforms of ubiquitin-conjugating enzyme E2I (ubc9) and Ranbp2

Patil, H., Yoon, D., Bhowmick, R., Cai, Y., Cho, K., & Ferreira, P. A. (2017) · Small GTPases · doi:10.1080/21541248.2017.1356432 · Cited by 12

Peroxisomes Exist in Growth Cones and Move Anterogradely and Retrogradely in Neurites of PC12D Cells

Ishikawa, T., Kawai, C., Sano, M., & Minatogawa, Y. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5226 · Cited by 12

Mechanical and functional properties of epothilone‐stabilized microtubules

Yu, D., Pessino, V., Kuei, S., & Valentine, M. T. (2012) · Cytoskeleton · doi:10.1002/cm.21091 · Cited by 12

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Parker, A. L., Teo, W. S., Brayford, S., Moorthi, U. K., Arumugam, S., Ferguson, C., Parton, R. G., McCarroll, J. A., & Kavallaris, M. (2022) · Cells · doi:10.3390/cells11050776 · Cited by 11

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Hamidizadeh, L., Abadi, R. H. H. B., Baigi, M. A. B., Dastsooz, H., Khazaei Nejhad, A., & Fardaei, M. (2015) · PubMed · Cited by 11

Regulation of Mitoflash Biogenesis and Signaling by Mitochondrial Dynamics

Li, W., Sun, T., Liu, B., Wu, D., Qi, W., Wang, X., Ma, Q., & Cheng, H. (2016) · Scientific Reports · doi:10.1038/srep32933 · Cited by 11

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Reignault, L. C., Alcantara, C. D. L., Barrias, E., & de Souza, W. (2019) · Journal of Structural Biology · doi:10.1016/j.jsb.2018.12.010 · Cited by 11

Dynamic microtubule organization and mitochondrial transport are regulated by distinct Kinesin-1 pathways

Melkov, A., Simchoni, Y., Alcalay, Y., & Abdu, U. (2015) · Biology Open · doi:10.1242/bio.015206 · Cited by 11

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Ringer, K., Riehl, J., Müller, M., Dewes, J., Hoff, F., & Jacob, R. (2018) · Traffic · doi:10.1111/tra.12616 · Cited by 10

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Huo, D., Yang, H., Huang, J., Cai, J., & Cui, J. (2021) · Oncology Reports · doi:10.3892/or.2021.8072 · Cited by 10

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Fang, Z., Fallet, M., Moest, T., Gorvel, J., & Méresse, S. (2021) · Journal of Cell Science · doi:10.1242/jcs.259183 · Cited by 10

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Perinuclear mitochondrial clustering for mesenchymal-to-epithelial transition in pluripotency induction

Xiang, G., Liu, Z., Yuan, Z., Ying, Z., Ding, Y., Lin, D., Qin, H., Dong, S., Zhou, S., Yuan, H., et al. (2025) · Stem Cell Reports · doi:10.1016/j.stemcr.2025.102474 · Cited by 9

Mitochondrial Dynamics: The Control of Mitochondrial Shape, Size, Number, Motility, and Cellular Inheritance

Scott, I., & Logan, D. C. (2007) · John Wiley & Sons, Inc. eBooks · doi:10.1002/9780470986592.ch1 · Cited by 9

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Wei Li, M. H. B. (2011) · Figshare · doi:10.6084/m9.figshare.68396

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田中, 庸. (1999) · doi:10.11501/3190895

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Pasolli, M. (2025) · doi:10.33540/3164

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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

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Mutants, C., & Kamal, A. R. A. (2013)