157 related articles for article (PubMed ID: 9660961)
1. FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.
Hewett DR; Handt O; Hobson L; Mangelsdorf M; Eyre HJ; Baker E; Sutherland GR; Schuffenhauer S; Mao JI; Richards RI
Mol Cell; 1998 May; 1(6):773-81. PubMed ID: 9660961
[TBL] [Abstract][Full Text] [Related]
2. Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat.
Yu S; Mangelsdorf M; Hewett D; Hobson L; Baker E; Eyre HJ; Lapsys N; Le Paslier D; Doggett NA; Sutherland GR; Richards RI
Cell; 1997 Feb; 88(3):367-74. PubMed ID: 9039263
[TBL] [Abstract][Full Text] [Related]
3. Human chromosome fragility.
Lukusa T; Fryns JP
Biochim Biophys Acta; 2008 Jan; 1779(1):3-16. PubMed ID: 18078840
[TBL] [Abstract][Full Text] [Related]
4. Analysis of replication timing at the FRA10B and FRA16B fragile site loci.
Handt O; Baker E; Dayan S; Gartler SM; Woollatt E; Richards RI; Hansen RS
Chromosome Res; 2000; 8(8):677-88. PubMed ID: 11196131
[TBL] [Abstract][Full Text] [Related]
5. Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.
Nancarrow JK; Kremer E; Holman K; Eyre H; Doggett NA; Le Paslier D; Callen DF; Sutherland GR; Richards RI
Science; 1994 Jun; 264(5167):1938-41. PubMed ID: 8009225
[TBL] [Abstract][Full Text] [Related]
6. Molecular basis for expression of common and rare fragile sites.
Zlotorynski E; Rahat A; Skaug J; Ben-Porat N; Ozeri E; Hershberg R; Levi A; Scherer SW; Margalit H; Kerem B
Mol Cell Biol; 2003 Oct; 23(20):7143-51. PubMed ID: 14517285
[TBL] [Abstract][Full Text] [Related]
7. Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus.
Nancarrow JK; Holman K; Mangelsdorf M; Hori T; Denton M; Sutherland GR; Richards RI
Hum Mol Genet; 1995 Mar; 4(3):367-72. PubMed ID: 7795589
[TBL] [Abstract][Full Text] [Related]
8. Fragile sites, chromosomal lesions, tandem repeats, and disease.
Mirceta M; Shum N; Schmidt MHM; Pearson CE
Front Genet; 2022; 13():985975. PubMed ID: 36468036
[TBL] [Abstract][Full Text] [Related]
9. A novel minisatellite repeat expansion identified at FRA16B in a Japanese carrier.
Yamauchi M; Tsuji S; Mita K; Saito T; Morimyo M
Genes Genet Syst; 2000 Jun; 75(3):149-54. PubMed ID: 10984839
[TBL] [Abstract][Full Text] [Related]
10. Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.
Snow K; Tester DJ; Kruckeberg KE; Schaid DJ; Thibodeau SN
Hum Mol Genet; 1994 Sep; 3(9):1543-51. PubMed ID: 7833909
[TBL] [Abstract][Full Text] [Related]
11. Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.
Richards RI; Holman K; Kozman H; Kremer E; Lynch M; Pritchard M; Yu S; Mulley J; Sutherland GR
J Med Genet; 1991 Dec; 28(12):818-23. PubMed ID: 1757956
[TBL] [Abstract][Full Text] [Related]
12. Human fragile site FRA16B DNA excludes nucleosomes in the presence of distamycin.
Hsu YY; Wang YH
J Biol Chem; 2002 May; 277(19):17315-9. PubMed ID: 11880377
[TBL] [Abstract][Full Text] [Related]
13. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n.
Kremer EJ; Pritchard M; Lynch M; Yu S; Holman K; Baker E; Warren ST; Schlessinger D; Sutherland GR; Richards RI
Science; 1991 Jun; 252(5013):1711-4. PubMed ID: 1675488
[TBL] [Abstract][Full Text] [Related]
14. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; Baker E; Kokkinaki M; Talley P; Maltby EL; French L; Harder L; Hinzmann B; Nobile C; Richkind K; Finnis M; Deloukas P; Sutherland GR; Kutsche K; Moschonas NK; Siebert R; Gécz J;
Genomics; 2004 Jul; 84(1):69-81. PubMed ID: 15203205
[TBL] [Abstract][Full Text] [Related]
15. The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
Ritchie RJ; Knight SJ; Hirst MC; Grewal PK; Bobrow M; Cross GS; Davies KE
Hum Mol Genet; 1994 Dec; 3(12):2115-21. PubMed ID: 7881407
[TBL] [Abstract][Full Text] [Related]
16. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
Parrish JE; Oostra BA; Verkerk AJ; Richards CS; Reynolds J; Spikes AS; Shaffer LG; Nelson DL
Nat Genet; 1994 Nov; 8(3):229-35. PubMed ID: 7874164
[TBL] [Abstract][Full Text] [Related]
17. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.
Fu YH; Kuhl DP; Pizzuti A; Pieretti M; Sutcliffe JS; Richards S; Verkerk AJ; Holden JJ; Fenwick RG; Warren ST
Cell; 1991 Dec; 67(6):1047-58. PubMed ID: 1760838
[TBL] [Abstract][Full Text] [Related]
18. [Medical pathology due to trinucleotide repeats].
Arenas-Aranda D; Peñaloza R; Salamanca-Gómez F
Gac Med Mex; 1999; 135(1):53-65. PubMed ID: 10204311
[TBL] [Abstract][Full Text] [Related]
19. Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.
Jones C; Slijepcevic P; Marsh S; Baker E; Langdon WY; Richards RI; Tunnacliffe A
Hum Mol Genet; 1994 Dec; 3(12):2123-30. PubMed ID: 7881408
[TBL] [Abstract][Full Text] [Related]
20. New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines.
Banchs I; Bosch A; Guimerà J; Lázaro C; Puig A; Estivill X
Hum Mutat; 1994; 3(4):365-72. PubMed ID: 8081390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
