9
results
for author:"Buckle V.J."
in Literature Citations
| A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter. De Gobbi M., Viprakasit V., Hughes J.R., Fisher C., Buckle V.J., Ayyub H., Gibbons R.J., Vernimmen D., Yoshinaga Y., de Jong P. et al. Science 312:1215-1217(2006) · UniProtKB (7) |
| Coregulated human globin genes are frequently in spatial proximity when active. Brown J.M., Leach J., Reittie J.E., Atzberger A., Lee-Prudhoe J., Wood W.G., Higgs D.R., Iborra F.J., Buckle V.J. J. Cell Biol. 172:177-187(2006) · Mapped (39) |
| Sequence, structure and pathology of the fully annotated terminal 2 Mb of the short arm of human chromosome 16. Daniels R.J., Peden J.F., Lloyd C., Horsley S.W., Clark K., Tufarelli C., Kearney L., Buckle V.J., Doggett N.A., Flint J. et al. Hum. Mol. Genet. 10:339-352(2001) · UniProtKB (91) |
| Relationship between novel isoforms, functionally important domains, and subcellular distribution of CD164/endolyn. Chan J.Y.-H., Lee-Prudhoe J.E., Jorgensen B., Ihrke G., Doyonnas R., Zannettino A.C.W., Buckle V.J., Ward C.J., Simmons P.J., Watt S.M. J. Biol. Chem. 276:2139-2152(2001) · UniProtKB (2) |
| Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes. McDowell T.L., Gibbons R.J., Sutherland H., O'Rourke D.M., Bickmore W.A., Pombo A., Turley H., Gatter K., Picketts D.J., Buckle V.J. et al. Proc. Natl. Acad. Sci. U.S.A. 96:13983-13988(1999) · UniProtKB (2) |
| No title Ward C.J., Peral B., Hughes J., Thomas S., Gamble V., Maccarthy A.B., Sloane-Stanley J., Buckle V.J., Kearney L., Higgs D.R. et al. Cell 78:725-725(1994) |
| The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. Ward C.J., Peral B., Hughes J., Thomas S., Gamble V., Maccarthy A.B., Sloane-Stanley J., Buckle V.J., Kearney L., Higgs D.R. et al. Cell 77:881-894(1994) · UniProtKB (2) |
| Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease. Buckle V.J., Fujita N., Ryder-Cook A.S., Derry J.M., Barnard P.J., Lebo R.V., Schofield P.R., Seeburg P.H., Bateson A.N., Darlison M.G. Neuron 3:647-654(1989) · Mapped (24) |
| Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus. Buckle V.J., Guenet J.L., Simon-Chazottes D., Love D.R., Davies K.E. Hum. Genet. 85:324-326(1990) · Mapped (38) |
