Buckle VJ - Search Results

1

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

Scott C, Downes DJ, Brown JM, Beagrie R, Olijnik AA, Gosden M, Schwessinger R, Fisher CA, Rose A, Ferguson DJP, Johnson E, Hill QA, Okoli S, Renella R, Ryan K, Brand M, Hughes J, Roy NBA, Higgs DR, Babbs C, Buckle VJ. Scott C, et al. Among authors: buckle vj. Haematologica. 2021 Nov 1;106(11):2960-2970. doi: 10.3324/haematol.2020.260158. Haematologica. 2021. PMID: 33121234 Free PMC article.

2

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.

3

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

4

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.

5

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.

6

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

7

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.

8

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

9

Expression of alpha- and beta-globin genes occurs within different nuclear domains in haemopoietic cells.

Brown KE, Amoils S, Horn JM, Buckle VJ, Higgs DR, Merkenschlager M, Fisher AG. Brown KE, et al. Among authors: buckle vj. Nat Cell Biol. 2001 Jun;3(6):602-6. doi: 10.1038/35078577. Nat Cell Biol. 2001. PMID: 11389446

10

Coregulated human globin genes are frequently in spatial proximity when active.

Brown JM, Leach J, Reittie JE, Atzberger A, Lee-Prudhoe J, Wood WG, Higgs DR, Iborra FJ, Buckle VJ. Brown JM, et al. Among authors: buckle vj. J Cell Biol. 2006 Jan 16;172(2):177-87. doi: 10.1083/jcb.200507073. J Cell Biol. 2006. PMID: 16418531 Free PMC article.

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