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 *

475 related articles for article (PubMed ID: 20225023)

  • 1. The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth disease.
    Palau F; Estela A; Pla-Martín D; Sánchez-Piris M
    Adv Exp Med Biol; 2009; 652():129-37. PubMed ID: 20225023
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial dynamics and inherited peripheral nerve diseases.
    Pareyson D; Saveri P; Sagnelli A; Piscosquito G
    Neurosci Lett; 2015 Jun; 596():66-77. PubMed ID: 25847151
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial fusion/fission dynamics in neurodegeneration and neuronal plasticity.
    Bertholet AM; Delerue T; Millet AM; Moulis MF; David C; Daloyau M; Arnauné-Pelloquin L; Davezac N; Mils V; Miquel MC; Rojo M; Belenguer P
    Neurobiol Dis; 2016 Jun; 90():3-19. PubMed ID: 26494254
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. Calcium Deregulation and Mitochondrial Bioenergetics in GDAP1-Related CMT Disease.
    González-Sánchez P; Satrústegui J; Palau F; Del Arco A
    Int J Mol Sci; 2019 Jan; 20(2):. PubMed ID: 30669311
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mfn2
    Zhang Y; Ma L; Wang Z; Gao C; Yang L; Li M; Tang X; Yuan H; Pang D; Ouyang H
    Int J Biol Macromol; 2024 Oct; 278(Pt 1):134673. PubMed ID: 39142491
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial diseases of the brain.
    Chaturvedi RK; Flint Beal M
    Free Radic Biol Med; 2013 Oct; 63():1-29. PubMed ID: 23567191
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dysregulation of mitochondrial fusion and fission: an emerging concept in neurodegeneration.
    Frank S
    Acta Neuropathol; 2006 Feb; 111(2):93-100. PubMed ID: 16468021
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations.
    Cassereau J; Chevrollier A; Gueguen N; Desquiret V; Verny C; Nicolas G; Dubas F; Amati-Bonneau P; Reynier P; Bonneau D; Procaccio V
    Exp Neurol; 2011 Jan; 227(1):31-41. PubMed ID: 20849849
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The role of mitochondrial dynamics in neurodegeneration].
    Li WW; Zhu M; Lv CZ
    Sheng Li Ke Xue Jin Zhan; 2011 Oct; 42(5):347-52. PubMed ID: 22242401
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial dynamics in cell death and neurodegeneration.
    Cho DH; Nakamura T; Lipton SA
    Cell Mol Life Sci; 2010 Oct; 67(20):3435-47. PubMed ID: 20577776
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial dynamics: to be in good shape to survive.
    Herzig S; Martinou JC
    Curr Mol Med; 2008 Mar; 8(2):131-7. PubMed ID: 18336293
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations.
    Baloh RH; Schmidt RE; Pestronk A; Milbrandt J
    J Neurosci; 2007 Jan; 27(2):422-30. PubMed ID: 17215403
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.
    Stuppia G; Rizzo F; Riboldi G; Del Bo R; Nizzardo M; Simone C; Comi GP; Bresolin N; Corti S
    J Neurol Sci; 2015 Sep; 356(1-2):7-18. PubMed ID: 26143526
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease.
    Niemann A; Ruegg M; La Padula V; Schenone A; Suter U
    J Cell Biol; 2005 Sep; 170(7):1067-78. PubMed ID: 16172208
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders.
    Carelli V; La Morgia C; Valentino ML; Barboni P; Ross-Cisneros FN; Sadun AA
    Biochim Biophys Acta; 2009 May; 1787(5):518-28. PubMed ID: 19268652
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
    Abrams AJ; Hufnagel RB; Rebelo A; Zanna C; Patel N; Gonzalez MA; Campeanu IJ; Griffin LB; Groenewald S; Strickland AV; Tao F; Speziani F; Abreu L; Schüle R; Caporali L; La Morgia C; Maresca A; Liguori R; Lodi R; Ahmed ZM; Sund KL; Wang X; Krueger LA; Peng Y; Prada CE; Prows CA; Schorry EK; Antonellis A; Zimmerman HH; Abdul-Rahman OA; Yang Y; Downes SM; Prince J; Fontanesi F; Barrientos A; Németh AH; Carelli V; Huang T; Zuchner S; Dallman JE
    Nat Genet; 2015 Aug; 47(8):926-32. PubMed ID: 26168012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease).
    Berger P; Niemann A; Suter U
    Glia; 2006 Sep; 54(4):243-57. PubMed ID: 16856148
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Review of the recent literature on hereditary neuropathies].
    Birouk N
    Rev Neurol (Paris); 2014 Dec; 170(12):846-9. PubMed ID: 25459128
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A.
    Cartoni R; Martinou JC
    Exp Neurol; 2009 Aug; 218(2):268-73. PubMed ID: 19427854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.