BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 13129801)

  • 1. 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]  

  • 2. The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease.
    El-Kadi AM; Bros-Facer V; Deng W; Philpott A; Stoddart E; Banks G; Jackson GS; Fisher EM; Duchen MR; Greensmith L; Moore AL; Hafezparast M
    J Biol Chem; 2010 Jun; 285(24):18627-39. PubMed ID: 20382740
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders.
    Parkinson NJ; Baumer D; Rose-Morris A; Talbot K
    Neuromuscul Disord; 2008 May; 18(5):394-7. PubMed ID: 18395445
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.
    Münch C; Sedlmeier R; Meyer T; Homberg V; Sperfeld AD; Kurt A; Prudlo J; Peraus G; Hanemann CO; Stumm G; Ludolph AC
    Neurology; 2004 Aug; 63(4):724-6. PubMed ID: 15326253
    [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. Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex.
    Zhang F; Ström AL; Fukada K; Lee S; Hayward LJ; Zhu H
    J Biol Chem; 2007 Jun; 282(22):16691-9. PubMed ID: 17403682
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1.
    Strickland AV; Schabhüttl M; Offenbacher H; Synofzik M; Hauser NS; Brunner-Krainz M; Gruber-Sedlmayr U; Moore SA; Windhager R; Bender B; Harms M; Klebe S; Young P; Kennerson M; Garcia AS; Gonzalez MA; Züchner S; Schule R; Shy ME; Auer-Grumbach M
    J Neurol; 2015 Sep; 262(9):2124-34. PubMed ID: 26100331
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Disruption of axonal transport in motor neuron diseases.
    Ikenaka K; Katsuno M; Kawai K; Ishigaki S; Tanaka F; Sobue G
    Int J Mol Sci; 2012; 13(1):1225-1238. PubMed ID: 22312314
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutations.
    Sprute R; Jergas H; Ölmez A; Alawbathani S; Karasoy H; Dafsari HS; Becker K; Daimagüler HS; Nürnberg P; Muntoni F; Topaloglu H; Uyanik G; Cirak S
    Am J Med Genet A; 2021 Feb; 185(2):344-354. PubMed ID: 33155358
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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; 32(47):16560-73. PubMed ID: 23175812
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approach.
    Shah PR; Ahmad-Annuar A; Ahmadi KR; Russ C; Sapp PC; Horvitz HR; Brown RH; Goldstein DB; Fisher EM
    Amyotroph Lateral Scler; 2006 Mar; 7(1):46-56. PubMed ID: 16546759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases.
    Hübers A; Marroquin N; Schmoll B; Vielhaber S; Just M; Mayer B; Högel J; Dorst J; Mertens T; Just W; Aulitzky A; Wais V; Ludolph AC; Kubisch C; Weishaupt JH; Volk AE
    Neurobiol Aging; 2014 May; 35(5):1214.e1-6. PubMed ID: 24378086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.