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 *

136 related articles for article (PubMed ID: 15967618)

  • 1. Mutation analysis of methyl-CpG binding protein family genes in autistic patients.
    Li H; Yamagata T; Mori M; Yasuhara A; Momoi MY
    Brain Dev; 2005 Aug; 27(5):321-5. PubMed ID: 15967618
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis of the coding sequence of the MECP2 gene in infantile autism.
    Beyer KS; Blasi F; Bacchelli E; Klauck SM; Maestrini E; Poustka A;
    Hum Genet; 2002 Oct; 111(4-5):305-9. PubMed ID: 12384770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. MeCP2 gene mutation analysis in autistic boys with developmental regression.
    Xi CY; Ma HW; Lu Y; Zhao YJ; Hua TY; Zhao Y; Ji YH
    Psychiatr Genet; 2007 Apr; 17(2):113-6. PubMed ID: 17413451
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A MECP2 missense mutation within the MBD domain in a Brazilian male with autistic disorder.
    Campos M; Pestana CP; dos Santos AV; Ponchel F; Churchman S; Abdalla-Carvalho CB; dos Santos JM; dos Santos FL; Gikovate CG; Santos-Rebouças CB; Pimentel MM
    Brain Dev; 2011 Nov; 33(10):807-9. PubMed ID: 21600714
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Methyl-CpG binding domain proteins and their involvement in the regulation of the MAGE-A1, MAGE-A2, MAGE-A3, and MAGE-A12 gene promoters.
    Wischnewski F; Friese O; Pantel K; Schwarzenbach H
    Mol Cancer Res; 2007 Jul; 5(7):749-59. PubMed ID: 17634428
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Methyl CpG-binding proteins and transcriptional repression.
    Wade PA
    Bioessays; 2001 Dec; 23(12):1131-7. PubMed ID: 11746232
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome.
    Laccone F; Jünemann I; Whatley S; Morgan R; Butler R; Huppke P; Ravine D
    Hum Mutat; 2004 Mar; 23(3):234-44. PubMed ID: 14974082
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.
    Parmeggiani A; Tedde MR; Arbizzani A; Posar A; Scaduto MC; Santucci M; Sangiorgi S
    J Child Neurol; 2009 Jun; 24(6):772-4. PubMed ID: 19189931
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Low frequency of MECP2 mutations in mentally retarded males.
    Yntema HG; Kleefstra T; Oudakker AR; Romein T; de Vries BB; Nillesen W; Sistermans EA; Brunner HG; Hamel BC; van Bokhoven H
    Eur J Hum Genet; 2002 Aug; 10(8):487-90. PubMed ID: 12111644
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dynamic changes in the localization of five members of the methyl binding domain (MBD) gene family during murine and bovine preimplantation embryo development.
    Ruddock-D'Cruz NT; Xue J; Wilson KJ; Heffernan C; Prashadkumar S; Cooney MA; Sanchez-Partida LG; French AJ; Holland MK
    Mol Reprod Dev; 2008 Jan; 75(1):48-59. PubMed ID: 17546630
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.
    Li H; Yamagata T; Mori M; Momoi MY
    Brain Dev; 2005 Apr; 27(3):207-10. PubMed ID: 15737702
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.
    Cukier HN; Rabionet R; Konidari I; Rayner-Evans MY; Baltos ML; Wright HH; Abramson RK; Martin ER; Cuccaro ML; Pericak-Vance MA; Gilbert JR
    Neurogenetics; 2010 Jul; 11(3):291-303. PubMed ID: 19921286
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Silencing of MBD1 and MeCP2 in prostate-cancer-derived PC3 cells produces differential gene expression profiles and cellular phenotypes.
    Yaqinuddin A; Abbas F; Naqvi SZ; Bashir MU; Qazi R; Qureshi SA
    Biosci Rep; 2008 Dec; 28(6):319-26. PubMed ID: 18666890
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region.
    Bonora E; Bacchelli E; Levy ER; Blasi F; Marlow A; Monaco AP; Maestrini E;
    Mol Psychiatry; 2002; 7(3):289-301. PubMed ID: 11920156
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Methyl-CpG binding proteins in the nervous system.
    Fan G; Hutnick L
    Cell Res; 2005 Apr; 15(4):255-61. PubMed ID: 15857580
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of MECP2 gene copy number in boys with autism.
    Xi CY; Lu Y; Tan YH; Hua TY; Zhao YJ; Liu XM; Gao H
    J Child Neurol; 2011 May; 26(5):570-3. PubMed ID: 21531908
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Point mutation analysis of the FMR-1 gene in autism.
    Vincent JB; Konecki DS; Munstermann E; Bolton P; Poustka A; Poustka F; Gurling HM
    Mol Psychiatry; 1996 Jul; 1(3):227-31. PubMed ID: 9118347
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation.
    Lesca G; Bernard V; Bozon M; Touraine R; Gérard D; Edery P; Calender A
    Eur J Med Genet; 2007; 50(3):200-8. PubMed ID: 17383248
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.