These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 26791407)

  • 41. Dimerization is required for GARS-mediated neurotoxicity in dominant CMT disease.
    Malissovas N; Griffin LB; Antonellis A; Beis D
    Hum Mol Genet; 2016 Apr; 25(8):1528-42. PubMed ID: 27008886
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mutations in the neurofilament light gene linked to Charcot-Marie-Tooth disease cause defects in transport.
    Pérez-Ollé R; López-Toledano MA; Goryunov D; Cabrera-Poch N; Stefanis L; Brown K; Liem RK
    J Neurochem; 2005 May; 93(4):861-74. PubMed ID: 15857389
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Structural basis for recruitment of RILP by small GTPase Rab7.
    Wu M; Wang T; Loh E; Hong W; Song H
    EMBO J; 2005 Apr; 24(8):1491-501. PubMed ID: 15933719
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Zebrafish as a Model to Investigate Dynamin 2-Related Diseases.
    Bragato C; Gaudenzi G; Blasevich F; Pavesi G; Maggi L; Giunta M; Cotelli F; Mora M
    Sci Rep; 2016 Feb; 6():20466. PubMed ID: 26842864
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Phenotype of Charcot-Marie-Tooth disease Type 2.
    Bienfait HM; Baas F; Koelman JH; de Haan RJ; van Engelen BG; Gabreëls-Festen AA; Ongerboer de Visser BW; Meggouh F; Weterman MA; De Jonghe P; Timmerman V; de Visser M
    Neurology; 2007 May; 68(20):1658-67. PubMed ID: 17502546
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations.
    Sancho P; Bartesaghi L; Miossec O; García-García F; Ramírez-Jiménez L; Siddell A; Åkesson E; Hedlund E; Laššuthová P; Pascual-Pascual SI; Sevilla T; Kennerson M; Lupo V; Chrast R; Espinós C
    Hum Mol Genet; 2019 May; 28(10):1629-1644. PubMed ID: 30624633
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Neuropathy-associated histidyl-tRNA synthetase variants attenuate protein synthesis in vitro and disrupt axon outgrowth in developing zebrafish.
    Mullen P; Abbott JA; Wellman T; Aktar M; Fjeld C; Demeler B; Ebert AM; Francklyn CS
    FEBS J; 2021 Jan; 288(1):142-159. PubMed ID: 32543048
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice.
    Klein D; Patzkó Á; Schreiber D; van Hauwermeiren A; Baier M; Groh J; West BL; Martini R
    Brain; 2015 Nov; 138(Pt 11):3193-205. PubMed ID: 26297559
    [TBL] [Abstract][Full Text] [Related]  

  • 49. An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.
    Achilli F; Bros-Facer V; Williams HP; Banks GT; AlQatari M; Chia R; Tucci V; Groves M; Nickols CD; Seburn KL; Kendall R; Cader MZ; Talbot K; van Minnen J; Burgess RW; Brandner S; Martin JE; Koltzenburg M; Greensmith L; Nolan PM; Fisher EM
    Dis Model Mech; 2009; 2(7-8):359-73. PubMed ID: 19470612
    [TBL] [Abstract][Full Text] [Related]  

  • 50. In vivo imaging of cell behaviors and F-actin reveals LIM-HD transcription factor regulation of peripheral versus central sensory axon development.
    Andersen EF; Asuri NS; Halloran MC
    Neural Dev; 2011 May; 6():27. PubMed ID: 21619654
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Axon degeneration and PGC-1α-mediated protection in a zebrafish model of α-synuclein toxicity.
    O'Donnell KC; Lulla A; Stahl MC; Wheat ND; Bronstein JM; Sagasti A
    Dis Model Mech; 2014 May; 7(5):571-82. PubMed ID: 24626988
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Membrane Targeting and GTPase Activity of Rab7 Are Required for Its Ubiquitination by RNF167.
    Ghilarducci K; Cabana VC; Harake A; Cappadocia L; Lussier MP
    Int J Mol Sci; 2022 Jul; 23(14):. PubMed ID: 35887194
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Islet1 selectively promotes peripheral axon outgrowth in Rohon-Beard primary sensory neurons.
    Tanaka H; Nojima Y; Shoji W; Sato M; Nakayama R; Ohshima T; Okamoto H
    Dev Dyn; 2011 Jan; 240(1):9-22. PubMed ID: 21108318
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by
    Sleigh JN; Dawes JM; West SJ; Wei N; Spaulding EL; Gómez-Martín A; Zhang Q; Burgess RW; Cader MZ; Talbot K; Yang XL; Bennett DL; Schiavo G
    Proc Natl Acad Sci U S A; 2017 Apr; 114(16):E3324-E3333. PubMed ID: 28351971
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons.
    Cioni JM; Lin JQ; Holtermann AV; Koppers M; Jakobs MAH; Azizi A; Turner-Bridger B; Shigeoka T; Franze K; Harris WA; Holt CE
    Cell; 2019 Jan; 176(1-2):56-72.e15. PubMed ID: 30612743
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Knockdown of Pnpla6 protein results in motor neuron defects in zebrafish.
    Song Y; Wang M; Mao F; Shao M; Zhao B; Song Z; Shao C; Gong Y
    Dis Model Mech; 2013 Mar; 6(2):404-13. PubMed ID: 22996643
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Identification of possible downstream genes required for the extension of peripheral axons in primary sensory neurons.
    Aoki M; Segawa H; Naito M; Okamoto H
    Biochem Biophys Res Commun; 2014 Mar; 445(2):357-62. PubMed ID: 24513284
    [TBL] [Abstract][Full Text] [Related]  

  • 58. WldS and PGC-1α regulate mitochondrial transport and oxidation state after axonal injury.
    O'Donnell KC; Vargas ME; Sagasti A
    J Neurosci; 2013 Sep; 33(37):14778-90. PubMed ID: 24027278
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Charcot-Marie-Tooth disease: emerging mechanisms and therapies.
    d'Ydewalle C; Benoy V; Van Den Bosch L
    Int J Biochem Cell Biol; 2012 Aug; 44(8):1299-304. PubMed ID: 22575637
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 12.