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Title:	Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
Source:	Science [0036-8075] Oberle, I yr:1991

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description	1.	Kremer, E. "Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n." Science 252.5013 (1991): 1711-1714.
description	2.	Xu, E L. "Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene." Nature 402.6758 (1999): 187-91.
description	3.	Verkerk, M F J. "Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome." Cell 65.5 (1991): 905-14.
description	4.	Fu, Y H H. "Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox." Cell 67.6 (1992): 1047-58.
description	5.	GARBER, K. "Transcription, translation and fragile X syndrome." Current opinion in genetics & development 16.3 (2006): 270-275.
description	6.	Hayes, Eriel W. "Fragile X Syndrome." Pediatrics 124.2 (2009): 790-792.
description	7.	Heitz, D. "Isolation of sequences that span the fragile X and identification of a fragile x-related CpG island." Science 251.4998 (1991): 1236-1239.
description	8.	Tassone, F. "FMRP expression as a potential prognostic indicator in fragile X syndrome." American journal of human genetics 61.4 (1997).
description	9.	Pieretti, M. "Absence of expression of the FMR-1 gene in fragile X syndrome." Cell 66.4 (1991): 817-822.
description	10.	Oostra, B A C. "Prenatal diagnosis of fragile X syndrome." Lancet, The 348.9032 (1996): 967-8.
description	11.	Huber, Kimberly M M. "The fragile X-cerebellum connection." Trends in Neurosciences 29.4 (2006): 183-5.
description	12.	ASHLEY, C. "FMR1 PROTEIN - CONSERVED RNP FAMILY DOMAINS AND SELECTIVE RNA-BINDING." Science 262.5133 (1993): 563-566.
description	13.	Robertson, Keith D D. "DNA methylation and human disease." Nature reviews. Genetics 6.8: 597-610.
description	14.	Eichler, E E E. "Length of uninterrupted CGG repeats determines instability in the FMR1 gene." Nature genetics 8.1 (1994): 88-94.
description	15.	Nosyreva, Elena D. "Metabotropic Receptor-Dependent Long-Term Depression Persists in the Absence of Protein Synthesis in the Mouse Model of Fragile X Syndrome." Journal of neurophysiology 95.5 (2006): 3291-3295.
description	16.	Ueda Y, Okano M, Williams C, Chen T, Georgopoulos, Y. "Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome." Development 133.6: 1183-1192.
description	17.	Rangwala, Eric H. "The value-added genome: building and maintaining genomic cytosine methylation landscapes." Current opinion in genetics & development 14.6 (2004): 686-691.
description	18.	Herman, Paul J J. "Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population." JAMA 291.4 (2003): 460-9.
description	19.	Bourc'his, D. "Dnmt3L and the Establishment of Maternal Genomic Imprints." Science 294.5551 (2001): 2536-2539.
description	20.	McLennan, Y. "Fragile X Syndrome." Current genomics 12.3 (2011): 216-224.