BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 21965300)

  • 1. Charcot-Marie-Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential.
    Noack R; Frede S; Albrecht P; Henke N; Pfeiffer A; Knoll K; Dehmel T; Meyer Zu Hörste G; Stettner M; Kieseier BC; Summer H; Golz S; Kochanski A; Wiedau-Pazos M; Arnold S; Lewerenz J; Methner A
    Hum Mol Genet; 2012 Jan; 21(1):150-62. PubMed ID: 21965300
    [TBL] [Abstract][Full Text] [Related]  

  • 2. GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance.
    Niemann A; Wagner KM; Ruegg M; Suter U
    Neurobiol Dis; 2009 Dec; 36(3):509-20. PubMed ID: 19782751
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria.
    Pedrola L; Espert A; Wu X; Claramunt R; Shy ME; Palau F
    Hum Mol Genet; 2005 Apr; 14(8):1087-94. PubMed ID: 15772096
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Evolutionary and structural analyses of GDAP1, involved in Charcot-Marie-Tooth disease, characterize a novel class of glutathione transferase-related genes.
    Marco A; Cuesta A; Pedrola L; Palau F; Marín I
    Mol Biol Evol; 2004 Jan; 21(1):176-87. PubMed ID: 14595091
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease.
    Niemann A; Huber N; Wagner KM; Somandin C; Horn M; Lebrun-Julien F; Angst B; Pereira JA; Halfter H; Welzl H; Feltri ML; Wrabetz L; Young P; Wessig C; Toyka KV; Suter U
    Brain; 2014 Mar; 137(Pt 3):668-82. PubMed ID: 24480485
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy.
    Barneo-Muñoz M; Juárez P; Civera-Tregón A; Yndriago L; Pla-Martin D; Zenker J; Cuevas-Martín C; Estela A; Sánchez-Aragó M; Forteza-Vila J; Cuezva JM; Chrast R; Palau F
    PLoS Genet; 2015 Apr; 11(4):e1005115. PubMed ID: 25860513
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondria-lysosome membrane contacts are defective in GDAP1-related Charcot-Marie-Tooth disease.
    Cantarero L; Juárez-Escoto E; Civera-Tregón A; Rodríguez-Sanz M; Roldán M; Benítez R; Hoenicka J; Palau F
    Hum Mol Genet; 2021 Jan; 29(22):3589-3605. PubMed ID: 33372681
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

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

  • 11. Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease.
    Sivera R; Espinós C; Vílchez JJ; Mas F; Martínez-Rubio D; Chumillas MJ; Mayordomo F; Muelas N; Bataller L; Palau F; Sevilla T
    J Peripher Nerv Syst; 2010 Dec; 15(4):334-44. PubMed ID: 21199105
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A novel mutation in the GDAP1 gene is associated with autosomal recessive Charcot-Marie-Tooth disease in an Amish family.
    Xin B; Puffenberger E; Nye L; Wiznitzer M; Wang H
    Clin Genet; 2008 Sep; 74(3):274-8. PubMed ID: 18492089
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structural and functional divergence of GDAP1 from the glutathione S-transferase superfamily.
    Googins MR; Woghiren-Afegbua AO; Calderon M; St Croix CM; Kiselyov KI; VanDemark AP
    FASEB J; 2020 May; 34(5):7192-7207. PubMed ID: 32274853
    [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. The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2K.
    Crimella C; Tonelli A; Airoldi G; Baschirotto C; D'Angelo MG; Bonato S; Losito L; Trabacca A; Bresolin N; Bassi MT
    J Med Genet; 2010 Oct; 47(10):712-6. PubMed ID: 20685671
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T; Cuesta A; Chumillas MJ; Mayordomo F; Pedrola L; Palau F; Vílchez JJ
    Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease.
    Pedrola L; Espert A; Valdés-Sánchez T; Sánchez-Piris M; Sirkowski EE; Scherer SS; Fariñas I; Palau F
    J Cell Mol Med; 2008 Apr; 12(2):679-89. PubMed ID: 18021315
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Charcot-Marie-Tooth-related gene GDAP1 complements cell cycle delay at G2/M phase in Saccharomyces cerevisiae fis1 gene-defective cells.
    Estela A; Pla-Martín D; Sánchez-Piris M; Sesaki H; Palau F
    J Biol Chem; 2011 Oct; 286(42):36777-86. PubMed ID: 21890626
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.