Buckle VJ - Search Results

1

Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domains.

Oudelaar AM, Davies JOJ, Hanssen LLP, Telenius JM, Schwessinger R, Liu Y, Brown JM, Downes DJ, Chiariello AM, Bianco S, Nicodemi M, Buckle VJ, Dekker J, Higgs DR, Hughes JR. Oudelaar AM, et al. Among authors: buckle vj. Nat Genet. 2018 Dec;50(12):1744-1751. doi: 10.1038/s41588-018-0253-2. Epub 2018 Oct 29. Nat Genet. 2018. PMID: 30374068 Free PMC article.

2

Targeted breakage of a human chromosome mediated by cloned human telomeric DNA.

Itzhaki JE, Barnett MA, MacCarthy AB, Buckle VJ, Brown WR, Porter AC. Itzhaki JE, et al. Among authors: buckle vj. Nat Genet. 1992 Dec;2(4):283-7. doi: 10.1038/ng1292-283. Nat Genet. 1992. PMID: 1303280

3

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Gibbons RJ, Suthers GK, Wilkie AO, Buckle VJ, Higgs DR. Gibbons RJ, et al. Among authors: buckle vj. Am J Hum Genet. 1992 Nov;51(5):1136-49. Am J Hum Genet. 1992. PMID: 1415255 Free PMC article.

4

Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.

Wilkie AO, Higgs DR, Rack KA, Buckle VJ, Spurr NK, Fischel-Ghodsian N, Ceccherini I, Brown WR, Harris PC. Wilkie AO, et al. Among authors: buckle vj. Cell. 1991 Feb 8;64(3):595-606. doi: 10.1016/0092-8674(91)90243-r. Cell. 1991. PMID: 1991321

5

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

Wilkie AO, Zeitlin HC, Lindenbaum RH, Buckle VJ, Fischel-Ghodsian N, Chui DH, Gardner-Medwin D, MacGillivray MH, Weatherall DJ, Higgs DR. Wilkie AO, et al. Among authors: buckle vj. Am J Hum Genet. 1990 Jun;46(6):1127-40. Am J Hum Genet. 1990. PMID: 2339705 Free PMC article.

6

Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.

Hatton CS, Wilkie AO, Drysdale HC, Wood WG, Vickers MA, Sharpe J, Ayyub H, Pretorius IM, Buckle VJ, Higgs DR. Hatton CS, et al. Among authors: buckle vj. Blood. 1990 Jul 1;76(1):221-7. Blood. 1990. PMID: 2364173 Free article.

7

Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic disease.

Lamb J, Wilkie AO, Harris PC, Buckle VJ, Lindenbaum RH, Barton NJ, Reeders ST, Weatherall DJ, Higgs DR. Lamb J, et al. Among authors: buckle vj. Lancet. 1989 Oct 7;2(8667):819-24. doi: 10.1016/s0140-6736(89)92995-4. Lancet. 1989. PMID: 2477654

8

Localisation of human alpha globin to 16p13.3----pter.

Buckle VJ, Higgs DR, Wilkie AO, Super M, Weatherall DJ. Buckle VJ, et al. J Med Genet. 1988 Dec;25(12):847-9. doi: 10.1136/jmg.25.12.847. J Med Genet. 1988. PMID: 3236367 Free PMC article.

9

Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elements.

Flint J, Rochette J, Craddock CF, Dodé C, Vignes B, Horsley SW, Kearney L, Buckle VJ, Ayyub H, Higgs DR. Flint J, et al. Among authors: buckle vj. Hum Mol Genet. 1996 Aug;5(8):1163-9. doi: 10.1093/hmg/5.8.1163. Hum Mol Genet. 1996. PMID: 8842736

10

Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16.

Daniels RJ, Peden JF, Lloyd C, Horsley SW, Clark K, Tufarelli C, Kearney L, Buckle VJ, Doggett NA, Flint J, Higgs DR. Daniels RJ, et al. Among authors: buckle vj. Hum Mol Genet. 2001 Feb 15;10(4):339-52. doi: 10.1093/hmg/10.4.339. Hum Mol Genet. 2001. PMID: 11157797

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