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 *

675 related articles for article (PubMed ID: 19234456)

  • 1. Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology.
    Ballas N; Lioy DT; Grunseich C; Mandel G
    Nat Neurosci; 2009 Mar; 12(3):311-7. PubMed ID: 19234456
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate.
    Maezawa I; Jin LW
    J Neurosci; 2010 Apr; 30(15):5346-56. PubMed ID: 20392956
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A role for glia in the progression of Rett's syndrome.
    Lioy DT; Garg SK; Monaghan CE; Raber J; Foust KD; Kaspar BK; Hirrlinger PG; Kirchhoff F; Bissonnette JM; Ballas N; Mandel G
    Nature; 2011 Jun; 475(7357):497-500. PubMed ID: 21716289
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions.
    Maezawa I; Swanberg S; Harvey D; LaSalle JM; Jin LW
    J Neurosci; 2009 Apr; 29(16):5051-61. PubMed ID: 19386901
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MeCP2 deficiency is associated with impaired microtubule stability.
    Delépine C; Nectoux J; Bahi-Buisson N; Chelly J; Bienvenu T
    FEBS Lett; 2013 Jan; 587(2):245-53. PubMed ID: 23238081
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation.
    Wang IT; Reyes AR; Zhou Z
    Neurobiol Dis; 2013 Oct; 58():3-12. PubMed ID: 23659895
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.
    Jentarra GM; Olfers SL; Rice SG; Srivastava N; Homanics GE; Blue M; Naidu S; Narayanan V
    BMC Neurosci; 2010 Feb; 11():19. PubMed ID: 20163734
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations.
    Chapleau CA; Calfa GD; Lane MC; Albertson AJ; Larimore JL; Kudo S; Armstrong DL; Percy AK; Pozzo-Miller L
    Neurobiol Dis; 2009 Aug; 35(2):219-33. PubMed ID: 19442733
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Graded and pan-neural disease phenotypes of Rett Syndrome linked with dosage of functional MeCP2.
    Chen X; Han X; Blanchi B; Guan W; Ge W; Yu YC; Sun YE
    Protein Cell; 2021 Aug; 12(8):639-652. PubMed ID: 32851591
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling.
    Vacca M; Tripathi KP; Speranza L; Aiese Cigliano R; Scalabrì F; Marracino F; Madonna M; Sanseverino W; Perrone-Capano C; Guarracino MR; D'Esposito M
    BMC Bioinformatics; 2016 Jan; 17 Suppl 2(Suppl 2):14. PubMed ID: 26821710
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neural development of methyl-CpG-binding protein 2 null embryonic stem cells: a system for studying Rett syndrome.
    Okabe Y; Kusaga A; Takahashi T; Mitsumasu C; Murai Y; Tanaka E; Higashi H; Matsuishi T; Kosai K
    Brain Res; 2010 Nov; 1360():17-27. PubMed ID: 20816763
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Astrocyte Transcriptome from the Mecp2(308)-Truncated Mouse Model of Rett Syndrome.
    Delépine C; Nectoux J; Letourneur F; Baud V; Chelly J; Billuart P; Bienvenu T
    Neuromolecular Med; 2015 Dec; 17(4):353-63. PubMed ID: 26208914
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome.
    Ehinger Y; Matagne V; Cunin V; Borloz E; Seve M; Bourgoin-Voillard S; Borges-Correia A; Villard L; Roux JC
    Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33919253
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deciphering Rett syndrome with mouse genetics, epigenomics, and human neurons.
    Tao J; Wu H; Sun YE
    Int Rev Neurobiol; 2009; 89():147-60. PubMed ID: 19900619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hippocampal CA1 pyramidal neurons of Mecp2 mutant mice show a dendritic spine phenotype only in the presymptomatic stage.
    Chapleau CA; Boggio EM; Calfa G; Percy AK; Giustetto M; Pozzo-Miller L
    Neural Plast; 2012; 2012():976164. PubMed ID: 22919518
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rett syndrome induced pluripotent stem cell-derived neurons reveal novel neurophysiological alterations.
    Farra N; Zhang WB; Pasceri P; Eubanks JH; Salter MW; Ellis J
    Mol Psychiatry; 2012 Dec; 17(12):1261-71. PubMed ID: 22230884
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural and functional differences in the barrel cortex of Mecp2 null mice.
    Lee LJ; Tsytsarev V; Erzurumlu RS
    J Comp Neurol; 2017 Dec; 525(18):3951-3961. PubMed ID: 28857161
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MeCP2 Deficiency Leads to Loss of Glial Kir4.1.
    Kahanovitch U; Cuddapah VA; Pacheco NL; Holt LM; Mulkey DK; Percy AK; Olsen ML
    eNeuro; 2018; 5(1):. PubMed ID: 29464197
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome.
    Kahanovitch U; Patterson KC; Hernandez R; Olsen ML
    Int J Mol Sci; 2019 Aug; 20(15):. PubMed ID: 31387202
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations.
    Larimore JL; Chapleau CA; Kudo S; Theibert A; Percy AK; Pozzo-Miller L
    Neurobiol Dis; 2009 May; 34(2):199-211. PubMed ID: 19217433
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.