BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 31439839)

  • 1. Sp1-regulated expression of p11 contributes to motor neuron degeneration by membrane insertion of TASK1.
    García-Morales V; Rodríguez-Bey G; Gómez-Pérez L; Domínguez-Vías G; González-Forero D; Portillo F; Campos-Caro A; Gento-Caro Á; Issaoui N; Soler RM; Garcera A; Moreno-López B
    Nat Commun; 2019 Aug; 10(1):3784. PubMed ID: 31439839
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.
    Hossaini M; Cardona Cano S; van Dis V; Haasdijk ED; Hoogenraad CC; Holstege JC; Jaarsma D
    J Neuropathol Exp Neurol; 2011 Aug; 70(8):662-77. PubMed ID: 21760539
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression of p11 and Heteromeric TASK Channels in Rat Carotid Body Glomus Cells and Nerve Growth Factor-differentiated PC12 Cells.
    Matsuoka H; Pokorski M; Harada K; Yoshimura R; Inoue M
    J Histochem Cytochem; 2020 Oct; 68(10):679-690. PubMed ID: 32886017
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Guanabenz delays the onset of disease symptoms, extends lifespan, improves motor performance and attenuates motor neuron loss in the SOD1 G93A mouse model of amyotrophic lateral sclerosis.
    Jiang HQ; Ren M; Jiang HZ; Wang J; Zhang J; Yin X; Wang SY; Qi Y; Wang XD; Feng HL
    Neuroscience; 2014 Sep; 277():132-8. PubMed ID: 24699224
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Early signs of motoneuron vulnerability in a disease model system: Characterization of transverse slice cultures of spinal cord isolated from embryonic ALS mice.
    Avossa D; Grandolfo M; Mazzarol F; Zatta M; Ballerini L
    Neuroscience; 2006; 138(4):1179-94. PubMed ID: 16442737
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of p11 expression facilitates acidity-sensing function of TASK1 channels in mouse adrenal medullary cells.
    Inoue M; Matsuoka H; Lesage F; Harada K
    FASEB J; 2019 Jan; 33(1):455-468. PubMed ID: 30001168
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The retention factor p11 confers an endoplasmic reticulum-localization signal to the potassium channel TASK-1.
    Renigunta V; Yuan H; Zuzarte M; Rinné S; Koch A; Wischmeyer E; Schlichthörl G; Gao Y; Karschin A; Jacob R; Schwappach B; Daut J; Preisig-Müller R
    Traffic; 2006 Feb; 7(2):168-81. PubMed ID: 16420525
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neurons.
    Lasiene J; Komine O; Fujimori-Tonou N; Powers B; Endo F; Watanabe S; Shijie J; Ravits J; Horner P; Misawa H; Yamanaka K
    Acta Neuropathol Commun; 2016 Feb; 4():15. PubMed ID: 26891847
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disruption of the astrocytic TNFR1-GDNF axis accelerates motor neuron degeneration and disease progression in amyotrophic lateral sclerosis.
    Brambilla L; Guidotti G; Martorana F; Iyer AM; Aronica E; Valori CF; Rossi D
    Hum Mol Genet; 2016 Jul; 25(14):3080-3095. PubMed ID: 27288458
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ablation of proliferating microglia does not affect motor neuron degeneration in amyotrophic lateral sclerosis caused by mutant superoxide dismutase.
    Gowing G; Philips T; Van Wijmeersch B; Audet JN; Dewil M; Van Den Bosch L; Billiau AD; Robberecht W; Julien JP
    J Neurosci; 2008 Oct; 28(41):10234-44. PubMed ID: 18842883
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expression of heat shock transcription factor 1 and its downstream target protein T-cell death associated gene 51 in the spinal cord of a mouse model of amyotrophic lateral sclerosis.
    Mimoto T; Morimoto N; Miyazaki K; Kurata T; Sato K; Ikeda Y; Abe K
    Brain Res; 2012 Dec; 1488():123-31. PubMed ID: 23063459
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transgenic mice with human mutant genes causing Parkinson's disease and amyotrophic lateral sclerosis provide common insight into mechanisms of motor neuron selective vulnerability to degeneration.
    Martin LJ
    Rev Neurosci; 2007; 18(2):115-36. PubMed ID: 17593875
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TASK1 modulates inflammation and neurodegeneration in autoimmune inflammation of the central nervous system.
    Bittner S; Meuth SG; Göbel K; Melzer N; Herrmann AM; Simon OJ; Weishaupt A; Budde T; Bayliss DA; Bendszus M; Wiendl H
    Brain; 2009 Sep; 132(Pt 9):2501-16. PubMed ID: 19570851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Degeneration of respiratory motor neurons in the SOD1 G93A transgenic rat model of ALS.
    Lladó J; Haenggeli C; Pardo A; Wong V; Benson L; Coccia C; Rothstein JD; Shefner JM; Maragakis NJ
    Neurobiol Dis; 2006 Jan; 21(1):110-8. PubMed ID: 16084734
    [TBL] [Abstract][Full Text] [Related]  

  • 15. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient.
    Niessen HG; Angenstein F; Sander K; Kunz WS; Teuchert M; Ludolph AC; Heinze HJ; Scheich H; Vielhaber S
    Exp Neurol; 2006 Oct; 201(2):293-300. PubMed ID: 16740261
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A potential role for the p75 low-affinity neurotrophin receptor in spinal motor neuron degeneration in murine and human amyotrophic lateral sclerosis.
    Lowry KS; Murray SS; McLean CA; Talman P; Mathers S; Lopes EC; Cheema SS
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Sep; 2(3):127-34. PubMed ID: 11771768
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Calcitonin gene-related peptide expression levels predict motor neuron vulnerability in the superoxide dismutase 1-G93A mouse model of amyotrophic lateral sclerosis.
    Ringer C; Weihe E; Schütz B
    Neurobiol Dis; 2012 Jan; 45(1):547-54. PubMed ID: 21964254
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Increased ER stress during motor neuron degeneration in a transgenic mouse model of amyotrophic lateral sclerosis.
    Nagata T; Ilieva H; Murakami T; Shiote M; Narai H; Ohta Y; Hayashi T; Shoji M; Abe K
    Neurol Res; 2007 Dec; 29(8):767-71. PubMed ID: 17672929
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Depletion of reduced glutathione enhances motor neuron degeneration in vitro and in vivo.
    Chi L; Ke Y; Luo C; Gozal D; Liu R
    Neuroscience; 2007 Feb; 144(3):991-1003. PubMed ID: 17150307
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Overexpression of TDP-43 Protein in the Neuron and Oligodendrocyte Cells Causes the Progressive Motor Neuron Degeneration in the SOD1 G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis.
    Lu Y; Tang C; Zhu L; Li J; Liang H; Zhang J; Xu R
    Int J Biol Sci; 2016; 12(9):1140-9. PubMed ID: 27570488
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.