BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 18295506)

  • 21. Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome.
    De Filippis B; Ricceri L; Laviola G
    Genes Brain Behav; 2010 Mar; 9(2):213-23. PubMed ID: 19958389
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders.
    Wong VC; Li SY
    J Child Neurol; 2007 Dec; 22(12):1397-400. PubMed ID: 18174559
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A segment of the Mecp2 promoter is sufficient to drive expression in neurons.
    Adachi M; Keefer EW; Jones FS
    Hum Mol Genet; 2005 Dec; 14(23):3709-22. PubMed ID: 16251199
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation.
    Tejada MI; Peñagarikano O; Rodriguez-Revenga L; Martinez-Bouzas C; García B; Bádenas C; Guitart M; Minguez M; García-Alegría E; Sanz-Parra A; Beristain E; Milá M
    Clin Genet; 2006 Aug; 70(2):140-4. PubMed ID: 16879196
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The ups and downs of BDNF in Rett syndrome.
    Sun YE; Wu H
    Neuron; 2006 Feb; 49(3):321-3. PubMed ID: 16446133
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MECP2 mutations in Serbian Rett syndrome patients.
    Djarmati A; Dobricić V; Kecmanović M; Marsh P; Jancić-Stefanović J; Klein C; Djurić M; Romac S
    Acta Neurol Scand; 2007 Dec; 116(6):413-9. PubMed ID: 17986102
    [TBL] [Abstract][Full Text] [Related]  

  • 27. MeCP2 involvement in the regulation of neuronal alpha-tubulin production.
    Abuhatzira L; Shemer R; Razin A
    Hum Mol Genet; 2009 Apr; 18(8):1415-23. PubMed ID: 19174478
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A case report: bone marrow mesenchymal stem cells from a Rett syndrome patient are prone to senescence and show a lower degree of apoptosis.
    Squillaro T; Hayek G; Farina E; Cipollaro M; Renieri A; Galderisi U
    J Cell Biochem; 2008 Apr; 103(6):1877-85. PubMed ID: 18059018
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Environmental enrichment alters locomotor behaviour and ventricular volume in Mecp2 1lox mice.
    Nag N; Moriuchi JM; Peitzman CG; Ward BC; Kolodny NH; Berger-Sweeney JE
    Behav Brain Res; 2009 Jan; 196(1):44-8. PubMed ID: 18687363
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Evidence for abnormal early development in a mouse model of Rett syndrome.
    Santos M; Silva-Fernandes A; Oliveira P; Sousa N; Maciel P
    Genes Brain Behav; 2007 Apr; 6(3):277-86. PubMed ID: 16848781
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Rett syndrome: clinical and molecular aspects].
    Záhoráková D; Zeman J; Martásek P
    Cas Lek Cesk; 2007; 146(8):647-52. PubMed ID: 17874730
    [TBL] [Abstract][Full Text] [Related]  

  • 32. MeCP2 mutant protein is expressed in astrocytes as well as in neurons and localizes in the nucleus.
    Kifayathullah LA; Arunachalam JP; Bodda C; Agbemenyah HY; Laccone FA; Mannan AU
    Cytogenet Genome Res; 2010; 129(4):290-7. PubMed ID: 20625242
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse.
    Panayotis N; Pratte M; Borges-Correia A; Ghata A; Villard L; Roux JC
    Neurobiol Dis; 2011 Feb; 41(2):385-97. PubMed ID: 20951208
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
    Temudo T; Oliveira P; Santos M; Dias K; Vieira J; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Barbot C; Fonseca M; Cabral A; Dias A; Cabral P; Monteiro J; Borges L; Gomes R; Barbosa C; Mira G; Eusébio F; Santos M; Sequeiros J; Maciel P
    Neurology; 2007 Apr; 68(15):1183-7. PubMed ID: 17420401
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Effects of postnatal dietary choline supplementation on motor regional brain volume and growth factor expression in a mouse model of Rett syndrome.
    Nag N; Mellott TJ; Berger-Sweeney JE
    Brain Res; 2008 Oct; 1237():101-9. PubMed ID: 18778693
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The MECP2 gene mutation screening in Rett syndrome patients from Croatia.
    Matijević T; Knezević J; Barisić I; Resić B; Culić V; Pavelić J
    Ann N Y Acad Sci; 2006 Dec; 1091():225-32. PubMed ID: 17341617
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome--Mecp2 gene dosage effects and BDNF expression.
    Kondo M; Gray LJ; Pelka GJ; Christodoulou J; Tam PP; Hannan AJ
    Eur J Neurosci; 2008 Jun; 27(12):3342-50. PubMed ID: 18557922
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.
    Santos M; Temudo T; Kay T; Carrilho I; Medeira A; Cabral H; Gomes R; Lourenço MT; Venâncio M; Calado E; Moreira A; Oliveira G; Maciel P
    J Child Neurol; 2009 Jan; 24(1):49-55. PubMed ID: 19168818
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
    Buoni S; Zannolli R; Felice CD; Saponari S; Strambi M; Dotti MT; Castrucci E; Corbini L; Orsi A; Hayek J
    Clin Neurophysiol; 2008 Nov; 119(11):2455-8. PubMed ID: 18842453
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice.
    Pelka GJ; Watson CM; Radziewic T; Hayward M; Lahooti H; Christodoulou J; Tam PP
    Brain; 2006 Apr; 129(Pt 4):887-98. PubMed ID: 16467389
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.