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 *

434 related articles for article (PubMed ID: 16122633)

  • 1. Classic Rett syndrome in a boy with R133C mutation of MECP2.
    Masuyama T; Matsuo M; Jing JJ; Tabara Y; Kitsuki K; Yamagata H; Kan Y; Miki T; Ishii K; Kondo I
    Brain Dev; 2005 Sep; 27(6):439-42. PubMed ID: 16122633
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.
    Fukuda T; Yamashita Y; Nagamitsu S; Miyamoto K; Jin JJ; Ohmori I; Ohtsuka Y; Kuwajima K; Endo S; Iwai T; Yamagata H; Tabara Y; Miki T; Matsuishi T; Kondo I
    Brain Dev; 2005 Apr; 27(3):211-7. PubMed ID: 15737703
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy.
    Topçu M; Akyerli C; Sayi A; Törüner GA; Koçoğlu SR; Cimbiş M; Ozçelik T
    Eur J Hum Genet; 2002 Jan; 10(1):77-81. PubMed ID: 11896459
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Another patient with MECP2 mutation without classic Rett syndrome phenotype.
    Milani D; Pantaleoni C; D'Arrigo S; Selicorni A; Riva D
    Pediatr Neurol; 2005 May; 32(5):355-7. PubMed ID: 15866439
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.
    Schwartzman JS; Bernardino A; Nishimura A; Gomes RR; Zatz M
    Neuropediatrics; 2001 Jun; 32(3):162-4. PubMed ID: 11521215
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MeCP2 in neurons: closing in on the causes of Rett syndrome.
    Caballero IM; Hendrich B
    Hum Mol Genet; 2005 Apr; 14 Spec No 1():R19-26. PubMed ID: 15809268
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics.
    Kleefstra T; Yntema HG; Nillesen WM; Oudakker AR; Mullaart RA; Geerdink N; van Bokhoven H; de Vries BB; Sistermans EA; Hamel BC
    Eur J Hum Genet; 2004 Jan; 12(1):24-8. PubMed ID: 14560307
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preserved speech variant is allelic of classic Rett syndrome.
    De Bona C; Zappella M; Hayek G; Meloni I; Vitelli F; Bruttini M; Cusano R; Loffredo P; Longo I; Renieri A
    Eur J Hum Genet; 2000 May; 8(5):325-30. PubMed ID: 10854091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation.
    Kaufmann WE; Jarrar MH; Wang JS; Lee YJ; Reddy S; Bibat G; Naidu S
    Brain Dev; 2005 Aug; 27(5):331-9. PubMed ID: 16023547
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Mutational analysis of MECP2 gene in Rett syndrome].
    Pan H; Wang Y; Meng H; Bao X; Zhang Y; Shen Y; Wu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):276-80. PubMed ID: 12170461
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Developmental disorder in girls due to Rett syndrome].
    Pruissen DM; Sinke RJ; Terhal PA; Beemer FA; Peters AC
    Ned Tijdschr Geneeskd; 2003 Aug; 147(32):1560-3. PubMed ID: 12942847
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation.
    Yamada Y; Miura K; Kumagai T; Hayakawa C; Miyazaki S; Matsumoto A; Kurosawa K; Nomura N; Taniguchi H; Sonta SI; Yamanaka T; Wakamatsu N
    Hum Mutat; 2001 Sep; 18(3):253. PubMed ID: 11524741
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
    Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.
    Moretti P; Bouwknecht JA; Teague R; Paylor R; Zoghbi HY
    Hum Mol Genet; 2005 Jan; 14(2):205-20. PubMed ID: 15548546
    [TBL] [Abstract][Full Text] [Related]  

  • 15. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
    Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
    Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings.
    Geerdink N; Rotteveel JJ; Lammens M; Sistermans EA; Heikens GT; Gabreëls FJ; Mullaart RA; Hamel BC
    Neuropediatrics; 2002 Feb; 33(1):33-6. PubMed ID: 11930274
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Closely related Swedish Rett Syndrome females - none with MECP2 mutation revealed.
    Xiang F; Stenbom Y; Anvret M; Hagberg B
    Neuropediatrics; 2001 Aug; 32(4):217-8. PubMed ID: 11571704
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG
    Ment Retard Dev Disabil Res Rev; 2004; 10(2):154-8. PubMed ID: 15362175
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome.
    Yaron Y; Ben Zeev B; Shomrat R; Bercovich D; Naiman T; Orr-Urtreger A
    Hum Mutat; 2002 Oct; 20(4):323-4. PubMed ID: 12325033
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy.
    Bienvenu T; Souville I; Poirier K; Aquaviva C; Burglen L; Amiel J; Héron B; Kaminska A; Couvert P; Beldjord C; Chelly J
    Hum Mutat; 2001 Sep; 18(3):251-2. PubMed ID: 11524737
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.