BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

387 related articles for article (PubMed ID: 18321864)

  • 1. A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome.
    Samaco RC; Fryer JD; Ren J; Fyffe S; Chao HT; Sun Y; Greer JJ; Zoghbi HY; Neul JL
    Hum Mol Genet; 2008 Jun; 17(12):1718-27. PubMed ID: 18321864
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
    Chao HT; Chen H; Samaco RC; Xue M; Chahrour M; Yoo J; Neul JL; Gong S; Lu HC; Heintz N; Ekker M; Rubenstein JL; Noebels JL; Rosenmund C; Zoghbi HY
    Nature; 2010 Nov; 468(7321):263-9. PubMed ID: 21068835
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome.
    Moretti P; Levenson JM; Battaglia F; Atkinson R; Teague R; Antalffy B; Armstrong D; Arancio O; Sweatt JD; Zoghbi HY
    J Neurosci; 2006 Jan; 26(1):319-27. PubMed ID: 16399702
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice.
    Gemelli T; Berton O; Nelson ED; Perrotti LI; Jaenisch R; Monteggia LM
    Biol Psychiatry; 2006 Mar; 59(5):468-76. PubMed ID: 16199017
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The role of MeCP2 in brain development and neurodevelopmental disorders.
    Gonzales ML; LaSalle JM
    Curr Psychiatry Rep; 2010 Apr; 12(2):127-34. PubMed ID: 20425298
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice.
    Kerr B; Alvarez-Saavedra M; Sáez MA; Saona A; Young JI
    Hum Mol Genet; 2008 Jun; 17(12):1707-17. PubMed ID: 18321865
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Selective preservation of MeCP2 in catecholaminergic cells is sufficient to improve the behavioral phenotype of male and female Mecp2-deficient mice.
    Lang M; Wither RG; Brotchie JM; Wu C; Zhang L; Eubanks JH
    Hum Mol Genet; 2013 Jan; 22(2):358-71. PubMed ID: 23077217
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome.
    Adachi M; Autry AE; Covington HE; Monteggia LM
    J Neurosci; 2009 Apr; 29(13):4218-27. PubMed ID: 19339616
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome.
    Ren J; Ding X; Funk GD; Greer JJ
    J Neurosci; 2012 Nov; 32(48):17230-40. PubMed ID: 23197715
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MeCP2-mediated alterations of striatal features accompany psychomotor deficits in a mouse model of Rett syndrome.
    Kao FC; Su SH; Carlson GC; Liao W
    Brain Struct Funct; 2015 Jan; 220(1):419-34. PubMed ID: 24218106
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.
    Stearns NA; Schaevitz LR; Bowling H; Nag N; Berger UV; Berger-Sweeney J
    Neuroscience; 2007 May; 146(3):907-21. PubMed ID: 17383101
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progressive Changes in a Distributed Neural Circuit Underlie Breathing Abnormalities in Mice Lacking MeCP2.
    Huang TW; Kochukov MY; Ward CS; Merritt J; Thomas K; Nguyen T; Arenkiel BR; Neul JL
    J Neurosci; 2016 May; 36(20):5572-86. PubMed ID: 27194336
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
    Samaco RC; Hogart A; LaSalle JM
    Hum Mol Genet; 2005 Feb; 14(4):483-92. PubMed ID: 15615769
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MeCP2 dysfunction in humans and mice.
    Zoghbi HY
    J Child Neurol; 2005 Sep; 20(9):736-40. PubMed ID: 16225828
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Wild-type microglia arrest pathology in a mouse model of Rett syndrome.
    Derecki NC; Cronk JC; Lu Z; Xu E; Abbott SB; Guyenet PG; Kipnis J
    Nature; 2012 Mar; 484(7392):105-9. PubMed ID: 22425995
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Fluoxetine rescues rotarod motor deficits in Mecp2 heterozygous mouse model of Rett syndrome via brain serotonin.
    Villani C; Sacchetti G; Carli M; Invernizzi RW
    Neuropharmacology; 2020 Oct; 176():108221. PubMed ID: 32652084
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The relationship of Rett syndrome and MECP2 disorders to autism.
    Neul JL
    Dialogues Clin Neurosci; 2012 Sep; 14(3):253-62. PubMed ID: 23226951
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.
    Robinson L; Guy J; McKay L; Brockett E; Spike RC; Selfridge J; De Sousa D; Merusi C; Riedel G; Bird A; Cobb SR
    Brain; 2012 Sep; 135(Pt 9):2699-710. PubMed ID: 22525157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rescue of behavioral and EEG deficits in male and female Mecp2-deficient mice by delayed Mecp2 gene reactivation.
    Lang M; Wither RG; Colic S; Wu C; Monnier PP; Bardakjian BL; Zhang L; Eubanks JH
    Hum Mol Genet; 2014 Jan; 23(2):303-18. PubMed ID: 24009314
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.