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107 related items for PubMed ID: 8325640

  • 1. mnd2: a new mouse model of inherited motor neuron disease.
    Jones JM, Albin RL, Feldman EL, Simin K, Schuster TG, Dunnick WA, Collins JT, Chrisp CE, Taylor BA, Meisler MH.
    Genomics; 1993 Jun; 16(3):669-77. PubMed ID: 8325640
    [Abstract] [Full Text] [Related]

  • 2. Genetic and physical delineation of the region overlapping the progressive motor neuropathy (pmn) locus on mouse chromosome 13.
    Martin N, Jaubert J, Glaser P, Szatanik M, Guénet JL.
    Genomics; 2001 Jul; 75(1-3):9-16. PubMed ID: 11472062
    [Abstract] [Full Text] [Related]

  • 3. Genetic transfer of the wobbler gene to a C57BL/6J x NZB hybrid stock: natural history of the motor neuron disease and response to CNTF and BDNF cotreatment.
    Ishiyama T, Klinkosz B, Pioro EP, Mitsumoto H.
    Exp Neurol; 1997 Nov; 148(1):247-55. PubMed ID: 9398466
    [Abstract] [Full Text] [Related]

  • 4. The mouse mutation muscle deficient (mdf) is characterized by a progressive motoneuron disease.
    Blot S, Poirier C, Dreyfus PA.
    J Neuropathol Exp Neurol; 1995 Nov; 54(6):812-25. PubMed ID: 7595654
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  • 5. Progressive loss of striatal neurons causes motor dysfunction in MND2 mutant mice and is not prevented by Bcl-2.
    Rathke-Hartlieb S, Schlomann U, Heimann P, Meisler MH, Jockusch H, Bartsch JW.
    Exp Neurol; 2002 May; 175(1):87-97. PubMed ID: 12009762
    [Abstract] [Full Text] [Related]

  • 6. High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6.
    Weber JS, Jang W, Simin K, Lu W, Yu J, Meisler MH.
    Genomics; 1998 Nov 15; 54(1):107-15. PubMed ID: 9806835
    [Abstract] [Full Text] [Related]

  • 7. Genetics of primary and timing effects in the mnd mouse.
    Messer A, Plummer J, MacMillen MC, Frankel WN.
    Am J Med Genet; 1995 Jun 05; 57(2):361-4. PubMed ID: 7668363
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  • 11. The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
    Brunialti AL, Poirier C, Schmalbruch H, Guénet JL.
    Genomics; 1995 Sep 01; 29(1):131-5. PubMed ID: 8530062
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  • 12. A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.
    Maystadt I, Zarhrate M, Leclair-Richard D, Estournet B, Barois A, Renault F, Routon MC, Durand MC, Lefebvre S, Munnich A, Verellen-Dumoulin C, Viollet L.
    Neurology; 2006 Jul 11; 67(1):120-4. PubMed ID: 16728649
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  • 13. Loss of the astrocyte glutamate transporter GLT1 modifies disease in SOD1(G93A) mice.
    Pardo AC, Wong V, Benson LM, Dykes M, Tanaka K, Rothstein JD, Maragakis NJ.
    Exp Neurol; 2006 Sep 11; 201(1):120-30. PubMed ID: 16753145
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  • 14. Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice.
    Jones JM, Datta P, Srinivasula SM, Ji W, Gupta S, Zhang Z, Davies E, Hajnóczky G, Saunders TL, Van Keuren ML, Fernandes-Alnemri T, Meisler MH, Alnemri ES.
    Nature; 2003 Oct 16; 425(6959):721-7. PubMed ID: 14534547
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  • 15. The effect of the nonpeptide neurotrophic compound SR 57746A on the progression of the disease state of the pmn mouse.
    Duong F, Fournier J, Keane PE, Guénet JL, Soubrié P, Warter JM, Borg J, Poindron P.
    Br J Pharmacol; 1998 Jun 16; 124(4):811-7. PubMed ID: 9690875
    [Abstract] [Full Text] [Related]

  • 16. Aberrant deltaPKC activation in the spinal cord of Wobbler mouse: a model of motor neuron disease.
    Dave KR, Raval AP, Purroy J, Kirkinezos IG, Moraes CT, Bradley WG, Pérez-Pinzón MA.
    Neurobiol Dis; 2005 Feb 16; 18(1):126-33. PubMed ID: 15649703
    [Abstract] [Full Text] [Related]

  • 17. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A, French Research Network on FTD/FTD-MND.
    Neurology; 2009 May 12; 72(19):1669-76. PubMed ID: 19433740
    [Abstract] [Full Text] [Related]

  • 18. Motor neuron degeneration after sciatic nerve avulsion in adult rat evolves with oxidative stress and is apoptosis.
    Martin LJ, Kaiser A, Price AC.
    J Neurobiol; 1999 Aug 12; 40(2):185-201. PubMed ID: 10413449
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  • 19. A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation.
    Blumen SC, Astord S, Robin V, Vignaud L, Toumi N, Cieslik A, Achiron A, Carasso RL, Gurevich M, Braverman I, Blumen N, Munich A, Barkats M, Viollet L.
    Ann Neurol; 2012 Apr 12; 71(4):509-19. PubMed ID: 22522442
    [Abstract] [Full Text] [Related]

  • 20. 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 02; 300(5620):808-12. PubMed ID: 12730604
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