fragile X messenger ribonucleoprotein 1 ; Homo sapiens






421 Article(s)
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1 1301165 Methylation analysis of CGG sites in the CpG island of the human FMR1 gene. Hum Mol Genet 1992 Nov 1
2 1424438 Molecular analysis of the fragile X syndrome. Dis Markers 1992 Jan-Feb 1
3 1605197 Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site. Am J Med Genet 1992 Apr 15-May 1 2
4 7485265 Fragile X syndrome: discordant levels of CGG repeat mosaicism in two brothers. Am J Med Genet 1995 Aug 14 1
5 7581460 Contribution of the FMR1 gene mutation to human intellectual dysfunction. Nat Genet 1995 Nov 1
6 7633450 Characterization of FMR1 proteins isolated from different tissues. Hum Mol Genet 1995 May 1
7 7670500 Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome. Nat Genet 1995 Aug 1
8 7692601 FMR1 protein: conserved RNP family domains and selective RNA binding. Science 1993 Oct 22 1
9 7732383 Translational suppression by trinucleotide repeat expansion at FMR1. Science 1995 May 5 2
10 7825604 Two new cases of FMR1 deletion associated with mental impairment. Am J Hum Genet 1995 Jan 3
11 7833910 Precursor arrays for triplet repeat expansion at the fragile X locus. Hum Mol Genet 1994 Sep 1
12 7901988 Direct DNA testing for fragile X syndrome. Am J Dis Child 1993 Nov 3
13 7927336 Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families. Hum Genet 1994 Oct 1
14 7932745 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. J Mol Biol 1994 Oct 21 1
15 7935515 A simple fragile X PCR assay with 7-deazaguanine-substituted DNA visualized by ethidium bromide. Mol Cell Probes 1994 Apr 3
16 7959688 Apparent regression of the CGG repeat in FMR1 to an allele of normal size. Hum Genet 1994 Nov 1
17 7977358 Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families. Am J Hum Genet 1994 Nov 2
18 7987398 Length of uninterrupted CGG repeats determines instability in the FMR1 gene. Nat Genet 1994 Sep 1
19 8012350 Frequency and stability of the fragile X premutation. Hum Mol Genet 1994 Mar 1
20 8156595 Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome. Cell 1994 Apr 8 1
21 8187801 The fragile X syndrome: implications of molecular genetics for the clinical syndrome. Eur J Clin Invest 1994 Jan 1
22 8197163 The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure. Proc Natl Acad Sci U S A 1994 May 24 1
23 8219287 [X-linked mental retardation: variations in the fragile X mutations and genetic counseling]. Nihon Koshu Eisei Zasshi 1993 Aug 1
24 8237919 A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome. Am J Dis Child 1993 Nov 1
25 8239933 Molecular pathology of the fragile X syndrome. Arch Pathol Lab Med 1993 Nov 1
26 8242066 Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins. Hum Mol Genet 1993 Sep 1
27 8268919 High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome. Hum Mol Genet 1993 Oct 6
28 8275570 Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome. Clin Genet 1993 Sep 1
29 8301764 Molecular predictors of cognitive involvement in female carriers of fragile X syndrome. JAMA 1994 Feb 16 2
30 8322740 Molecular-clinical correlations in children and adults with fragile X syndrome. Am J Dis Child 1993 Jul 4
31 8358432 Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat. Nat Genet 1993 Jul 1
32 8411050 Origins of the fragile X syndrome mutation. J Med Genet 1993 Aug 1
33 8526888 A fragile gene. Bioessays 1995 Nov 1
34 8539651 [Fragile X syndrome: clinical and molecular genetics correlations]. Ther Umsch 1995 Dec 1
35 8552426 Complex behavior of simple repeats: the fragile X syndrome. Pediatr Res 1995 Nov 1
36 8552427 Reduced cyclic AMP production in fragile X syndrome: cytogenetic and molecular correlations. Pediatr Res 1995 Nov 5
37 8559749 Prenatal diagnosis of fragile X syndrome: (CGG)n expansion and methylation of chorionic villus samples. Prenat Diagn 1995 Sep 1
38 8659532 On the formation of nucleosomes within the FMR1 trinucleotide repeat. Am J Hum Genet 1996 Jul 1
39 8746743 Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome. J Intellect Disabil Res 1995 Dec 1
40 8750357 Screening for CGG trinucleotide repeat expansion in the fragile X mental retardation 1 gene in schizophrenic patients. Psychiatr Genet 1995 Winter 3
41 8751854 Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission. Am J Hum Genet 1996 Sep 1
42 8808273 The chicken FMR1 gene is highly conserved with a CCT 5'-untranslated repeat and encodes an RNA-binding protein. Genomics 1996 Jan 1 2
43 8834253 Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome. Hum Genet 1996 Apr 1
44 8842725 The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals. Hum Mol Genet 1996 Aug 5
45 8998538 [Molecular biology of fragile X syndrome: recent data and diagnostic applications]. Arch Pediatr 1996 Aug 3
46 9131013 Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus. Somat Cell Mol Genet 1996 Nov 1
47 9138377 [Molecular and genetic features of fragile X syndrome]. Rev Med Chil 1996 Jul 1
48 9208564 [Detection of FMR-1 gene expression by RT-PCR]. Zhongguo Yi Xue Ke Xue Yuan Xue Bao 1995 Dec 1
49 9293305 Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects. Ann Clin Biochem 1997 Sep 1
50 9302255 Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1. Hum Mol Genet 1997 Oct 1