227 related articles for article (PubMed ID: 18952079)
1. 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]
2. 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]
3. Mutations in dynein link motor neuron degeneration to defects in retrograde transport.
Hafezparast M; Klocke R; Ruhrberg C; Marquardt A; Ahmad-Annuar A; Bowen S; Lalli G; Witherden AS; Hummerich H; Nicholson S; Morgan PJ; Oozageer R; Priestley JV; Averill S; King VR; Ball S; Peters J; Toda T; Yamamoto A; Hiraoka Y; Augustin M; Korthaus D; Wattler S; Wabnitz P; Dickneite C; Lampel S; Boehme F; Peraus G; Popp A; Rudelius M; Schlegel J; Fuchs H; Hrabe de Angelis M; Schiavo G; Shima DT; Russ AP; Stumm G; Martin JE; Fisher EM
Science; 2003 May; 300(5620):808-12. PubMed ID: 12730604
[TBL] [Abstract][Full Text] [Related]
4. Defects in dynein linked to motor neuron degeneration in mice.
Andersen J
Sci Aging Knowledge Environ; 2003 May; 2003(18):PE10. PubMed ID: 12844533
[TBL] [Abstract][Full Text] [Related]
5. Mutant superoxide dismutase disrupts cytoplasmic dynein in motor neurons.
Ligon LA; LaMonte BH; Wallace KE; Weber N; Kalb RG; Holzbaur EL
Neuroreport; 2005 Apr; 16(6):533-6. PubMed ID: 15812301
[TBL] [Abstract][Full Text] [Related]
6. A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice.
Teuling E; van Dis V; Wulf PS; Haasdijk ED; Akhmanova A; Hoogenraad CC; Jaarsma D
Hum Mol Genet; 2008 Sep; 17(18):2849-62. PubMed ID: 18579581
[TBL] [Abstract][Full Text] [Related]
7. The neuroprotective factor Wlds does not attenuate mutant SOD1-mediated motor neuron disease.
Vande Velde C; Garcia ML; Yin X; Trapp BD; Cleveland DW
Neuromolecular Med; 2004; 5(3):193-203. PubMed ID: 15626820
[TBL] [Abstract][Full Text] [Related]
8. Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice.
Banks GT; Bros-Facer V; Williams HP; Chia R; Achilli F; Bryson JB; Greensmith L; Fisher EM
PLoS One; 2009 Jul; 4(7):e6218. PubMed ID: 19593442
[TBL] [Abstract][Full Text] [Related]
9. Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration.
LaMonte BH; Wallace KE; Holloway BA; Shelly SS; Ascaño J; Tokito M; Van Winkle T; Howland DS; Holzbaur EL
Neuron; 2002 May; 34(5):715-27. PubMed ID: 12062019
[TBL] [Abstract][Full Text] [Related]
10. Mutant dynein (Loa) triggers proprioceptive axon loss that extends survival only in the SOD1 ALS model with highest motor neuron death.
Ilieva HS; Yamanaka K; Malkmus S; Kakinohana O; Yaksh T; Marsala M; Cleveland DW
Proc Natl Acad Sci U S A; 2008 Aug; 105(34):12599-604. PubMed ID: 18719118
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The expression of the chemorepellent Semaphorin 3A is selectively induced in terminal Schwann cells of a subset of neuromuscular synapses that display limited anatomical plasticity and enhanced vulnerability in motor neuron disease.
De Winter F; Vo T; Stam FJ; Wisman LA; Bär PR; Niclou SP; van Muiswinkel FL; Verhaagen J
Mol Cell Neurosci; 2006; 32(1-2):102-17. PubMed ID: 16677822
[TBL] [Abstract][Full Text] [Related]
13. Retrograde axonal transport and motor neuron disease.
Ström AL; Gal J; Shi P; Kasarskis EJ; Hayward LJ; Zhu H
J Neurochem; 2008 Jul; 106(2):495-505. PubMed ID: 18384644
[TBL] [Abstract][Full Text] [Related]
14. Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age.
Eschbach J; Sinniger J; Bouitbir J; Fergani A; Schlagowski AI; Zoll J; Geny B; René F; Larmet Y; Marion V; Baloh RH; Harms MB; Shy ME; Messadeq N; Weydt P; Loeffler JP; Ludolph AC; Dupuis L
Neurobiol Dis; 2013 Oct; 58():220-30. PubMed ID: 23742762
[TBL] [Abstract][Full Text] [Related]
15. Neuromuscular junction destruction during amyotrophic lateral sclerosis: insights from transgenic models.
Dupuis L; Loeffler JP
Curr Opin Pharmacol; 2009 Jun; 9(3):341-6. PubMed ID: 19386549
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic mice.
Wong M; Martin LJ
Hum Mol Genet; 2010 Jun; 19(11):2284-302. PubMed ID: 20223753
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA.
Wang J; Xu G; Slunt HH; Gonzales V; Coonfield M; Fromholt D; Copeland NG; Jenkins NA; Borchelt DR
Neurobiol Dis; 2005 Dec; 20(3):943-52. PubMed ID: 16046140
[TBL] [Abstract][Full Text] [Related]
20. Synaptic sprouting increases the uptake capacities of motoneurons in amyotrophic lateral sclerosis mice.
Millecamps S; Nicolle D; Ceballos-Picot I; Mallet J; Barkats M
Proc Natl Acad Sci U S A; 2001 Jun; 98(13):7582-7. PubMed ID: 11404466
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
