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.
120 related articles for article (PubMed ID: 8503923)
41. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Verkerk AJ; Pieretti M; Sutcliffe JS; Fu YH; Kuhl DP; Pizzuti A; Reiner O; Richards S; Victoria MF; Zhang FP Cell; 1991 May; 65(5):905-14. PubMed ID: 1710175 [TBL] [Abstract][Full Text] [Related]
42. No mental retardation in a man with 40% abnormal methylation at the FMR-1 locus and transmission of sperm cell mutations as premutations. Rousseau F; Robb LJ; Rouillard P; Der Kaloustian VM Hum Mol Genet; 1994 Jun; 3(6):927-30. PubMed ID: 7951239 [TBL] [Abstract][Full Text] [Related]
43. Prenatal diagnosis of fragile X syndrome: (CGG)n expansion and methylation of chorionic villus samples. Castellví-Bel S; Milà M; Soler A; Carrió A; Sánchez A; Villa M; Jiménez MD; Estivill X Prenat Diagn; 1995 Sep; 15(9):801-7. PubMed ID: 8559749 [TBL] [Abstract][Full Text] [Related]
44. Absence of FMR-1 gene expression can be detected with RNA extracted from dried blood specimens. Pai JT; Tsai SF; Horng CJ; Chiu PC; Cheng MY; Hsiao KJ; Wuu KD Hum Genet; 1994 May; 93(5):488-93. PubMed ID: 7513295 [TBL] [Abstract][Full Text] [Related]
45. Hypermethylation of telomere-like foldbacks at codon 12 of the human c-Ha-ras gene and the trinucleotide repeat of the FMR-1 gene of fragile X. Smith SS; Laayoun A; Lingeman RG; Baker DJ; Riley J J Mol Biol; 1994 Oct; 243(2):143-51. PubMed ID: 7932745 [TBL] [Abstract][Full Text] [Related]
46. Mental status and fragile X expression in relation to FMR-1 gene mutation. de Vries BB; Wiegers AM; de Graaff E; Verkerk AJ; Van Hemel JO; Halley DJ; Fryns JP; Curfs LM; Niermeijer MF; Oostra BA Eur J Hum Genet; 1993; 1(1):72-9. PubMed ID: 8069653 [TBL] [Abstract][Full Text] [Related]
47. A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. Wöhrle D; Kotzot D; Hirst MC; Manca A; Korn B; Schmidt A; Barbi G; Rott HD; Poustka A; Davies KE Am J Hum Genet; 1992 Aug; 51(2):299-306. PubMed ID: 1642231 [TBL] [Abstract][Full Text] [Related]
49. Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome. McConkie-Rosell A; Lachiewicz AM; Spiridigliozzi GA; Tarleton J; Schoenwald S; Phelan MC; Goonewardena P; Ding X; Brown WT Am J Hum Genet; 1993 Oct; 53(4):800-9. PubMed ID: 8213810 [TBL] [Abstract][Full Text] [Related]
51. Occupancy and synergistic activation of the FMR1 promoter by Nrf-1 and Sp1 in vivo. Smith KT; Coffee B; Reines D Hum Mol Genet; 2004 Aug; 13(15):1611-21. PubMed ID: 15175277 [TBL] [Abstract][Full Text] [Related]
52. Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets. Chen X; Mariappan SV; Moyzis RK; Bradbury EM; Gupta G J Biomol Struct Dyn; 1998 Feb; 15(4):745-56. PubMed ID: 9514250 [TBL] [Abstract][Full Text] [Related]
53. Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins. Kruyer H; Milà M; Glover G; Carbonell P; Ballesta F; Estivill X Am J Hum Genet; 1994 Mar; 54(3):437-42. PubMed ID: 8116613 [TBL] [Abstract][Full Text] [Related]
54. DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation. Luo S; Robinson JC; Reiss AL; Migeon BR Somat Cell Mol Genet; 1993 Jul; 19(4):393-404. PubMed ID: 8211380 [TBL] [Abstract][Full Text] [Related]
55. Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region. Drouin R; Angers M; Dallaire N; Rose TM; Khandjian EW; Rousseau F Hum Mol Genet; 1997 Nov; 6(12):2051-60. PubMed ID: 9328468 [TBL] [Abstract][Full Text] [Related]
56. A distinct DNA-methylation boundary in the 5'- upstream sequence of the FMR1 promoter binds nuclear proteins and is lost in fragile X syndrome. Naumann A; Hochstein N; Weber S; Fanning E; Doerfler W Am J Hum Genet; 2009 Nov; 85(5):606-16. PubMed ID: 19853235 [TBL] [Abstract][Full Text] [Related]
57. A recombination-based assay demonstrates that the fragile X sequence is transcribed widely during development. Hanzlik AJ; Osemlak-Hanzlik MM; Hauser MA; Kurnit DM Nat Genet; 1993 Jan; 3(1):44-8. PubMed ID: 8490653 [TBL] [Abstract][Full Text] [Related]
58. Asymmetry of methylation with FMR-1 full mutation in two 45,X/46,XX mosaic females associated with normal intellect. Shapiro LR; Simensen RJ; Wilmot PL; Fisch GS; Vibert BK; Fenwick RG; Tarleton J; Phelan MC Am J Med Genet; 1994 Jul; 51(4):507-8. PubMed ID: 7943030 [TBL] [Abstract][Full Text] [Related]
59. [Age dependent and tissue specific FMR-1 gene expression in human organs]. Ito M; Sugie H Nihon Rinsho; 1999 Apr; 57(4):950-4. PubMed ID: 10222795 [TBL] [Abstract][Full Text] [Related]
60. The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation. Oostra BA; Verkerk AJ Chromosoma; 1992 Apr; 101(7):381-7. PubMed ID: 1618021 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]