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 *

182 related articles for article (PubMed ID: 33115980)

  • 1. A Database of
    Chung KW; Kim JS; Lee KS
    Mol Cells; 2020 Oct; 43(10):880-888. PubMed ID: 33115980
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Disruption of genes associated with Charcot-Marie-Tooth type 2 lead to common behavioural, cellular and molecular defects in Caenorhabditis elegans.
    Soh MS; Cheng X; Vijayaraghavan T; Vernon A; Liu J; Neumann B
    PLoS One; 2020; 15(4):e0231600. PubMed ID: 32294113
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy.
    Almutawa W; Smith C; Sabouny R; Smit RB; Zhao T; Wong R; Lee-Glover L; Desrochers-Goyette J; Ilamathi HS; ; Suchowersky O; Germain M; Mains PE; Parboosingh JS; Pfeffer G; Innes AM; Shutt TE
    EBioMedicine; 2019 Jul; 45():379-392. PubMed ID: 31231018
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A C. elegans stretch receptor neuron revealed by a mechanosensitive TRP channel homologue.
    Li W; Feng Z; Sternberg PW; Xu XZ
    Nature; 2006 Mar; 440(7084):684-7. PubMed ID: 16572173
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Serotonin deficiency shortens the duration of forward movement in Caenorhabditis elegans.
    Wakabayashi T; Osada T; Shingai R
    Biosci Biotechnol Biochem; 2005 Sep; 69(9):1767-70. PubMed ID: 16195598
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of function mutations in HARS cause a spectrum of inherited peripheral neuropathies.
    Safka Brozkova D; Deconinck T; Griffin LB; Ferbert A; Haberlova J; Mazanec R; Lassuthova P; Roth C; Pilunthanakul T; Rautenstrauss B; Janecke AR; Zavadakova P; Chrast R; Rivolta C; Zuchner S; Antonellis A; Beg AA; De Jonghe P; Senderek J; Seeman P; Baets J
    Brain; 2015 Aug; 138(Pt 8):2161-72. PubMed ID: 26072516
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Worms on the spectrum - C. elegans models in autism research.
    Schmeisser K; Parker JA
    Exp Neurol; 2018 Jan; 299(Pt A):199-206. PubMed ID: 28434869
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The small heat shock proteins of the nematode Caenorhabditis elegans: structure, regulation and biology.
    Candido EP
    Prog Mol Subcell Biol; 2002; 28():61-78. PubMed ID: 11908066
    [No Abstract]   [Full Text] [Related]  

  • 9. Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms.
    Warner LE; Garcia CA; Lupski JR
    Annu Rev Med; 1999; 50():263-75. PubMed ID: 10073277
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Locomotion Behavior Is Affected by the Gα
    Gottschling DC; Döring F; Lüersen K
    Genetics; 2017 May; 206(1):283-297. PubMed ID: 28341653
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dopamine signaling is essential for precise rates of locomotion by C. elegans.
    Omura DT; Clark DA; Samuel AD; Horvitz HR
    PLoS One; 2012; 7(6):e38649. PubMed ID: 22719914
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Overexpression of mutant HSP27 causes axonal neuropathy in mice.
    Lee J; Jung SC; Joo J; Choi YR; Moon HW; Kwak G; Yeo HK; Lee JS; Ahn HJ; Jung N; Hwang S; Rheey J; Woo SY; Kim JY; Hong YB; Choi BO
    J Biomed Sci; 2015 Jun; 22(1):43. PubMed ID: 26141737
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy.
    Tufano M; Cappuccio G; Terrone G; Manganelli F; Pisciotta C; Geroldi A; Capponi S; Del Giudice E
    J Peripher Nerv Syst; 2015 Dec; 20(4):415-8. PubMed ID: 26307494
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Precision mouse models of Yars/dominant intermediate Charcot-Marie-Tooth disease type C and Sptlc1/hereditary sensory and autonomic neuropathy type 1.
    Hines TJ; Tadenev ALD; Lone MA; Hatton CL; Bagasrawala I; Stum MG; Miers KE; Hornemann T; Burgess RW
    J Anat; 2022 Nov; 241(5):1169-1185. PubMed ID: 34875719
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Caenorhabditis elegans locomotion phenotype caused by transgenic repeats of the hlh-17 promoter sequence.
    Stout RF; Grubišić V; Parpura V
    PLoS One; 2013; 8(11):e81771. PubMed ID: 24312354
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Caenorhabditis elegans neprilysin NEP-1: an effector of locomotion and pharyngeal pumping.
    Spanier B; Stürzenbaum SR; Holden-Dye LM; Baumeister R
    J Mol Biol; 2005 Sep; 352(2):429-37. PubMed ID: 16081104
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
    Montecchiani C; Pedace L; Lo Giudice T; Casella A; Mearini M; Gaudiello F; Pedroso JL; Terracciano C; Caltagirone C; Massa R; St George-Hyslop PH; Barsottini OG; Kawarai T; Orlacchio A
    Brain; 2016 Jan; 139(Pt 1):73-85. PubMed ID: 26556829
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sorting nexin 3 mutation impairs development and neuronal function in Caenorhabditis elegans.
    Vieira N; Bessa C; Rodrigues AJ; Marques P; Chan FY; de Carvalho AX; Correia-Neves M; Sousa N
    Cell Mol Life Sci; 2018 Jun; 75(11):2027-2044. PubMed ID: 29196797
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Caenorhabditis elegans model of the myosin heavy chain IIa E706K [corrected] mutation.
    Tajsharghi H; Pilon M; Oldfors A
    Ann Neurol; 2005 Sep; 58(3):442-8. PubMed ID: 16130113
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.