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Items: 1 to 20 of 132

1.

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 2;300(5620):808-12.

2.

Defects in dynein linked to motor neuron degeneration in mice.

Andersen J.

Sci Aging Knowledge Environ. 2003 May 7;2003(18):PE10.

PMID:
12844533
3.

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.

PMID:
13129801
4.
5.

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. doi: 10.1016/j.expneurol.2008.09.019. Epub 2008 Oct 8.

PMID:
18952079
6.

Reduction of the size of the Golgi apparatus of spinal anterior horn cells in patients with X-linked spinal and bulbar muscular atrophy.

Yaguchi M, Hashizume Y, Yoshida M, K Gonatas N, Okamoto K.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Apr;4(1):17-21.

PMID:
12745613
7.

[Motor neuron diseases: a type of programmed cell death?].

Ferrer I.

Neurologia. 1996 Dec;11 Suppl 5:7-13. Review. Spanish.

PMID:
9044576
8.

Progressive motor neuronopathy: a critical role of the tubulin chaperone TBCE in axonal tubulin routing from the Golgi apparatus.

Schaefer MK, Schmalbruch H, Buhler E, Lopez C, Martin N, Guénet JL, Haase G.

J Neurosci. 2007 Aug 15;27(33):8779-89.

9.

Motor neuron diseases in man and animals.

Duchen LW.

Invest Cell Pathol. 1978 Jul-Sep;1(3):249-62.

PMID:
93105
10.

Mice, the motor system, and human motor neuron pathology.

Nicholson SJ, Witherden AS, Hafezparast M, Martin JE, Fisher EM.

Mamm Genome. 2000 Dec;11(12):1041-52. Review.

PMID:
11130970
11.

Progressive degeneration of motor nerve terminals in GAD mutant mouse with hereditary sensory axonopathy.

Miura H, Oda K, Endo C, Yamazaki K, Shibasaki H, Kikuchi T.

Neuropathol Appl Neurobiol. 1993 Feb;19(1):41-51.

PMID:
8474599
12.

Sensory neuropathy in progressive motor neuronopathy (pmn) mice is associated with defects in microtubule polymerization and axonal transport.

Schäfer MK, Bellouze S, Jacquier A, Schaller S, Richard L, Mathis S, Vallat JM, Haase G.

Brain Pathol. 2017 Jul;27(4):459-471. doi: 10.1111/bpa.12422. Epub 2016 Oct 18.

PMID:
27488538
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. doi: 10.1111/j.1471-4159.2008.05393.x. Epub 2008 Apr 1. Review.

14.

Androgen receptor YAC transgenic mice recapitulate SBMA motor neuronopathy and implicate VEGF164 in the motor neuron degeneration.

Sopher BL, Thomas PS Jr, LaFevre-Bernt MA, Holm IE, Wilke SA, Ware CB, Jin LW, Libby RT, Ellerby LM, La Spada AR.

Neuron. 2004 Mar 4;41(5):687-99.

15.
16.

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 30;34(5):715-27.

17.

Polyglutamine tract-binding protein-1 dysfunction induces cell death of neurons through mitochondrial stress.

Marubuchi S, Wada Y, Okuda T, Hara Y, Qi ML, Hoshino M, Nakagawa M, Kanazawa I, Okazawa H.

J Neurochem. 2005 Nov;95(3):858-70. Epub 2005 Aug 16.

19.

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M.

Hum Mol Genet. 2004 Sep 15;13(18):2031-42. Epub 2004 Jul 21.

PMID:
15269181
20.

An early onset progressive motor neuron disorder in Scyl1-deficient mice is associated with mislocalization of TDP-43.

Pelletier S, Gingras S, Howell S, Vogel P, Ihle JN.

J Neurosci. 2012 Nov 21;32(47):16560-73. doi: 10.1523/JNEUROSCI.1787-12.2012.

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