BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 33395696)

  • 1. Loss of FEZ1, a gene deleted in Jacobsen syndrome, causes locomotion defects and early mortality by impairing motor neuron development.
    Gunaseelan S; Wang Z; Tong VKJ; Ming SWS; Razar RBBA; Srimasorn S; Ong WY; Lim KL; Chua JJE
    Hum Mol Genet; 2021 Mar; 30(1):5-20. PubMed ID: 33395696
    [TBL] [Abstract][Full Text] [Related]  

  • 2. FEZ2 has acquired additional protein interaction partners relative to FEZ1: functional and evolutionary implications.
    Alborghetti MR; Furlan AS; Kobarg J
    PLoS One; 2011 Mar; 6(3):e17426. PubMed ID: 21408165
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FEZ1 Forms Complexes with CRMP1 and DCC to Regulate Axon and Dendrite Development.
    Chua JY; Ng SJ; Yagensky O; Wanker EE; Chua JJE
    eNeuro; 2021; 8(2):. PubMed ID: 33771901
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The kinesin-associated protein UNC-76 is required for axonal transport in the Drosophila nervous system.
    Gindhart JG; Chen J; Faulkner M; Gandhi R; Doerner K; Wisniewski T; Nandlestadt A
    Mol Biol Cell; 2003 Aug; 14(8):3356-65. PubMed ID: 12925768
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of fasciculation and elongation protein zeta-1 (FEZ1) in the developing rat brain.
    Honda A; Miyoshi K; Baba K; Taniguchi M; Koyama Y; Kuroda S; Katayama T; Tohyama M
    Brain Res Mol Brain Res; 2004 Mar; 122(1):89-92. PubMed ID: 14992819
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Interstitial deletion of 11q-implicating the KIRREL3 gene in the neurocognitive delay associated with Jacobsen syndrome.
    Guerin A; Stavropoulos DJ; Diab Y; Chénier S; Christensen H; Kahr WH; Babul-Hirji R; Chitayat D
    Am J Med Genet A; 2012 Oct; 158A(10):2551-6. PubMed ID: 22965935
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Periventricular nodular heterotopia and transverse limb reduction defect in a woman with interstitial 11q24 deletion in the Jacobsen syndrome region.
    So J; Stockley T; Stavropoulos DJ
    Am J Med Genet A; 2014 Feb; 164A(2):511-5. PubMed ID: 24311471
    [TBL] [Abstract][Full Text] [Related]  

  • 8. UNC-51/ATG1 kinase regulates axonal transport by mediating motor-cargo assembly.
    Toda H; Mochizuki H; Flores R; Josowitz R; Krasieva TB; Lamorte VJ; Suzuki E; Gindhart JG; Furukubo-Tokunaga K; Tomoda T
    Genes Dev; 2008 Dec; 22(23):3292-307. PubMed ID: 19056884
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Functions of fasciculation and elongation protein zeta-1 (FEZ1) in the brain.
    Maturana AD; Fujita T; Kuroda S
    ScientificWorldJournal; 2010 Aug; 10():1646-54. PubMed ID: 20730382
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).
    Coldren CD; Lai Z; Shragg P; Rossi E; Glidewell SC; Zuffardi O; Mattina T; Ivy DD; Curfs LM; Mattson SN; Riley EP; Treier M; Grossfeld PD
    Neurogenetics; 2009 Apr; 10(2):89-95. PubMed ID: 18855024
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural analysis of intermolecular interactions in the kinesin adaptor complex fasciculation and elongation protein zeta 1/ short coiled-coil protein (FEZ1/SCOCO).
    Alborghetti MR; Furlan Ada S; da Silva JC; Sforça ML; Honorato RV; Granato DC; dos Santos Migueleti DL; Neves JL; de Oliveira PS; Paes-Leme AF; Zeri AC; de Torriani IC; Kobarg J
    PLoS One; 2013; 8(10):e76602. PubMed ID: 24116125
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Axonal guidance protein FEZ1 associates with tubulin and kinesin motor protein to transport mitochondria in neurites of NGF-stimulated PC12 cells.
    Fujita T; Maturana AD; Ikuta J; Hamada J; Walchli S; Suzuki T; Sawa H; Wooten MW; Okajima T; Tatematsu K; Tanizawa K; Kuroda S
    Biochem Biophys Res Commun; 2007 Sep; 361(3):605-10. PubMed ID: 17669366
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Unc-51/ATG1 controls axonal and dendritic development via kinesin-mediated vesicle transport in the Drosophila brain.
    Mochizuki H; Toda H; Ando M; Kurusu M; Tomoda T; Furukubo-Tokunaga K
    PLoS One; 2011 May; 6(5):e19632. PubMed ID: 21589871
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Human FEZ1 protein forms a disulfide bond mediated dimer: implications for cargo transport.
    Alborghetti MR; Furlan AS; Silva JC; Paes Leme AF; Torriani IC; Kobarg J
    J Proteome Res; 2010 Sep; 9(9):4595-603. PubMed ID: 20812761
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synaptic exocytosis and nervous system development impaired in Caenorhabditis elegans unc-13 mutants.
    Maruyama H; Rakow TL; Maruyama IN
    Neuroscience; 2001; 104(2):287-97. PubMed ID: 11377834
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Morphological and genetic abnormalities in a Jacobsen syndrome.
    Jurcă AD; Kozma K; Ioana M; Streaţă I; Petcheşi CD; Bembea M; Jurcă MC; Cuc EA; Vesa CM; Buhaş CL
    Rom J Morphol Embryol; 2017; 58(4):1531-1534. PubMed ID: 29556653
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FEZ1 participates in human embryonic brain development by modulating neuronal progenitor subpopulation specification and migrations.
    Qu Y; Lim JJ; An O; Yang H; Toh YC; Chua JJE
    iScience; 2023 Dec; 26(12):108497. PubMed ID: 38213789
    [TBL] [Abstract][Full Text] [Related]  

  • 18. FEZ1 dimerization and interaction with transcription regulatory proteins involves its coiled-coil region.
    Assmann EM; Alborghetti MR; Camargo ME; Kobarg J
    J Biol Chem; 2006 Apr; 281(15):9869-81. PubMed ID: 16484223
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Restoration of Motor Defects Caused by Loss of
    Lembke KM; Scudder C; Morton DB
    J Neurosci; 2017 Sep; 37(39):9486-9497. PubMed ID: 28847811
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Knockdown of the Drosophila FIG4 induces deficient locomotive behavior, shortening of motor neuron, axonal targeting aberration, reduction of life span and defects in eye development.
    Kyotani A; Azuma Y; Yamamoto I; Yoshida H; Mizuta I; Mizuno T; Nakagawa M; Tokuda T; Yamaguchi M
    Exp Neurol; 2016 Mar; 277():86-95. PubMed ID: 26708557
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.