144 related articles for article (PubMed ID: 21346813)
1. Neuromuscular junction defects in mice with mutation of dynein heavy chain 1.
Courchesne SL; Pazyra-Murphy MF; Lee DJ; Segal RA
PLoS One; 2011 Feb; 6(2):e16753. PubMed ID: 21346813
[TBL] [Abstract][Full Text] [Related]
2. Neurodegenerative mutation in cytoplasmic dynein alters its organization and dynein-dynactin and dynein-kinesin interactions.
Deng W; Garrett C; Dombert B; Soura V; Banks G; Fisher EM; van der Brug MP; Hafezparast M
J Biol Chem; 2010 Dec; 285(51):39922-34. PubMed ID: 20889981
[TBL] [Abstract][Full Text] [Related]
3. A cytoplasmic dynein tail mutation impairs motor processivity.
Ori-McKenney KM; Xu J; Gross SP; Vallee RB
Nat Cell Biol; 2010 Dec; 12(12):1228-34. PubMed ID: 21102439
[TBL] [Abstract][Full Text] [Related]
4. Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease.
Dupuis L; Fergani A; Braunstein KE; Eschbach J; Holl N; Rene F; Gonzalez De Aguilar JL; Zoerner B; Schwalenstocker B; Ludolph AC; Loeffler JP
Exp Neurol; 2009 Jan; 215(1):146-52. PubMed ID: 18952079
[TBL] [Abstract][Full Text] [Related]
5. Changes in kinesin expression in the CNS of mice with dynein heavy chain 1 mutation.
Kuźma-Kozakiewicz M; Kaźmierczak B; Usarek E; Barańczyk-Kuźma A
Acta Biochim Pol; 2013; 60(1):51-5. PubMed ID: 23460941
[TBL] [Abstract][Full Text] [Related]
6. Dync1h1 Mutation Causes Proprioceptive Sensory Neuron Loss and Impaired Retrograde Axonal Transport of Dorsal Root Ganglion Neurons.
Zhao J; Wang Y; Xu H; Fu Y; Qian T; Bo D; Lu YX; Xiong Y; Wan J; Zhang X; Dong Q; Chen XJ
CNS Neurosci Ther; 2016 Jul; 22(7):593-601. PubMed ID: 27080913
[TBL] [Abstract][Full Text] [Related]
7. Mice with mutation in dynein heavy chain 1 do not share the same tau expression pattern with mice with SOD1-related motor neuron disease.
Kuźma-Kozakiewicz M; Usarek E; Ludolph AC; Barańczyk-Kuźma A
Neurochem Res; 2011 Jun; 36(6):978-85. PubMed ID: 21380844
[TBL] [Abstract][Full Text] [Related]
8. A novel phenotype for the dynein heavy chain mutation Loa: altered dendritic morphology, organelle density, and reduced numbers of trigeminal motoneurons.
Wiggins LM; Kuta A; Stevens JC; Fisher EM; von Bartheld CS
J Comp Neurol; 2012 Aug; 520(12):2757-73. PubMed ID: 22684941
[TBL] [Abstract][Full Text] [Related]
9. A dynein mutation attenuates motor neuron degeneration in SOD1(G93A) mice.
Teuchert M; Fischer D; Schwalenstoecker B; Habisch HJ; Böckers TM; Ludolph AC
Exp Neurol; 2006 Mar; 198(1):271-4. PubMed ID: 16427626
[TBL] [Abstract][Full Text] [Related]
10. Cytoplasmic dynein heavy chain: the servant of many masters.
Schiavo G; Greensmith L; Hafezparast M; Fisher EM
Trends Neurosci; 2013 Nov; 36(11):641-51. PubMed ID: 24035135
[TBL] [Abstract][Full Text] [Related]
11. Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene.
Chen XJ; Levedakou EN; Millen KJ; Wollmann RL; Soliven B; Popko B
J Neurosci; 2007 Dec; 27(52):14515-24. PubMed ID: 18160659
[TBL] [Abstract][Full Text] [Related]
12. No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.
Ahmad-Annuar A; Shah P; Hafezparast M; Hummerich H; Witherden AS; Morrison KE; Shaw PJ; Kirby J; Warner TT; Crosby A; Proukakis C; Wilkinson P; Orrell RW; Bradley L; Martin JE; Fisher EM
Amyotroph Lateral Scler Other Motor Neuron Disord; 2003 Sep; 4(3):150-7. PubMed ID: 13129801
[TBL] [Abstract][Full Text] [Related]
13. A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease.
Sabblah TT; Nandini S; Ledray AP; Pasos J; Calderon JLC; Love R; King LE; King SJ
Sci Rep; 2018 Jan; 8(1):1739. PubMed ID: 29379136
[TBL] [Abstract][Full Text] [Related]
14. Differences in glutathione S-transferase pi expression in transgenic mice with symptoms of neurodegeneration.
Kaźmierczak B; Kuźma-Kozakiewicz M; Usarek E; Barańczyk-Kuźma A
Acta Biochim Pol; 2011; 58(4):621-6. PubMed ID: 22132373
[TBL] [Abstract][Full Text] [Related]
15. TMEM184b Promotes Axon Degeneration and Neuromuscular Junction Maintenance.
Bhattacharya MR; Geisler S; Pittman SK; Doan RA; Weihl CC; Milbrandt J; DiAntonio A
J Neurosci; 2016 Apr; 36(17):4681-9. PubMed ID: 27122027
[TBL] [Abstract][Full Text] [Related]
16. Mutations in cytoplasmic dynein and its regulators cause malformations of cortical development and neurodegenerative diseases.
Lipka J; Kuijpers M; Jaworski J; Hoogenraad CC
Biochem Soc Trans; 2013 Dec; 41(6):1605-12. PubMed ID: 24256262
[TBL] [Abstract][Full Text] [Related]
17. Proteomic Analysis of Dynein-Interacting Proteins in Amyotrophic Lateral Sclerosis Synaptosomes Reveals Alterations in the RNA-Binding Protein Staufen1.
Gershoni-Emek N; Mazza A; Chein M; Gradus-Pery T; Xiang X; Li KW; Sharan R; Perlson E
Mol Cell Proteomics; 2016 Feb; 15(2):506-22. PubMed ID: 26598648
[TBL] [Abstract][Full Text] [Related]
18. Cytoplasmic dynein in neurodegeneration.
Eschbach J; Dupuis L
Pharmacol Ther; 2011 Jun; 130(3):348-63. PubMed ID: 21420428
[TBL] [Abstract][Full Text] [Related]
19. Cytoplasmic dynein, the dynactin complex, and kinesin are interdependent and essential for fast axonal transport.
Martin M; Iyadurai SJ; Gassman A; Gindhart JG; Hays TS; Saxton WM
Mol Biol Cell; 1999 Nov; 10(11):3717-28. PubMed ID: 10564267
[TBL] [Abstract][Full Text] [Related]
20. CNS myelination requires cytoplasmic dynein function.
Yang ML; Shin J; Kearns CA; Langworthy MM; Snell H; Walker MB; Appel B
Dev Dyn; 2015 Feb; 244(2):134-45. PubMed ID: 25488883
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
