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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.
Cell. 1993 Jul 16;74(1):127-34
PMID: 8334699
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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.
Nature. 1993 Jun 24;363(6431):722-4
PMID: 8515814
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Molecular and thermodynamic properties of d(A(+)-G)10, a single-stranded nucleic acid helix without paired or stacked bases.
Biochemistry. 1993 Sep 28;32(38):10263-70
PMID: 8399154
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Human genetic diseases due to codon reiteration: relationship to an evolutionary mechanism.
Cell. 1993 Sep 24;74(6):955-6
PMID: 8104707
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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;2(9):1429-35
PMID: 8242066
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Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p.
Nat Genet. 1994 Jan;6(1):14-8
PMID: 8136826
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Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
Nat Genet. 1994 Jan;6(1):9-13
PMID: 8136840
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The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.
Proc Natl Acad Sci U S A. 1994 May 24;91(11):4950-4
PMID: 8197163
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Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene.
Science. 1994 Jul 29;265(5172):669-71
PMID: 8036515
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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;243(2):143-51
PMID: 7932745
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Transcriptional block caused by a negative supercoiling induced structural change in an alternating CG sequence.
Cell. 1985 Jan;40(1):129-37
PMID: 2981624
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Facile cruciform formation by an (A-T)34 sequence from a Xenopus globin gene.
J Mol Biol. 1985 Oct 5;185(3):461-78
PMID: 2997451
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(A-T)n tracts embedded in random sequence DNA--formation of a structure which is chemically reactive and torsionally deformable.
Nucleic Acids Res. 1986 Dec 9;14(23):9291-309
PMID: 3797241
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Stabilization of translationally active mRNA by prokaryotic REP sequences.
Cell. 1987 Jan 30;48(2):297-310
PMID: 2433046
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A two-state conformational equilibrium for alternating (A-T)n sequences in negatively supercoiled DNA.
J Mol Biol. 1987 Oct 20;197(4):707-21
PMID: 3430599
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Monovalent cation-induced structure of telomeric DNA: the G-quartet model.
Cell. 1989 Dec 1;59(5):871-80
PMID: 2590943
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Genomic imprinting and genetic disorders in man.
Trends Genet. 1989 Oct;5(10):331-6
PMID: 2692240
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Superhelical torsion in cellular DNA responds directly to environmental and genetic factors.
Proc Natl Acad Sci U S A. 1990 Nov;87(21):8373-7
PMID: 2172986
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Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome.
Cell. 1991 Feb 22;64(4):861-6
PMID: 1997211
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Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island.
Science. 1991 Mar 8;251(4998):1236-9
PMID: 2006411
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Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.
Science. 1991 May 24;252(5009):1097-102
PMID: 2031184
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Fragile X genotype characterized by an unstable region of DNA.
Science. 1991 May 24;252(5009):1179-81
PMID: 2031189
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Structural alteration in alternating adenine-thymine sequences in positively supercoiled DNA.
J Mol Biol. 1991 May 20;219(2):145-9
PMID: 2038050
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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
Cell. 1991 May 31;65(5):905-14
PMID: 1710175
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Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.
Nature. 1991 Jul 4;352(6330):77-9
PMID: 2062380
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Absence of expression of the FMR-1 gene in fragile X syndrome.
Cell. 1991 Aug 23;66(4):817-22
PMID: 1878973
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Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Cell. 1991 Dec 20;67(6):1047-58
PMID: 1760838
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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.
Cell. 1992 Feb 21;68(4):799-808
PMID: 1310900
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An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
Science. 1992 Mar 6;255(5049):1256-8
PMID: 1546326
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Triplet repeat mutations in human disease.
Science. 1992 May 8;256(5058):784-9
PMID: 1589758
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The puzzle of the triple repeats.
Science. 1993 Jun 4;260(5113):1422-3
PMID: 8502986
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A tetrameric DNA structure with protonated cytosine.cytosine base pairs.
Nature. 1993 Jun 10;363(6429):561-5
PMID: 8389423
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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
Nat Genet. 1993 Jul;4(3):221-6
PMID: 8358429