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JA Terrett

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P Hayes; Helen J Meadows; Martin Gunthorpe; Mark H Harries; DM Duckworth; William Cairns; David C Harrison; Catherine E Clarke; K Ellington; Rab Prinjha; A J Barton; Andrew D Medhurst; G D Smith; S Topp; Paul R Murdock; GJ Sanger; JA Terrett; O Jenkins; Christopher D Benham; Andrew D Randall; IS Gloger; John B Davis
Cloning and functional expression of a human orthologue of rat vanilloid receptor-1.
J Evans; H Herdon; William Cairns; E O'Brien; C Chapman; JA Terrett; IS Gloger
Cloning, functional characterisation and population analysis of a variant form of the human glycine type 2 transporter.
CH Yi; JA Terrett; Quanyi Li; K Ellington; Elizabeth A Packham; L Armstrong-Buisseret; P McClure; T Slingsby; J David Brook
Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19.

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All Publications

2000: P Hayes; Helen J Meadows; Martin Gunthorpe; Mark H Harries; DM Duckworth; William Cairns; David C Harrison; Catherine E Clarke; K Ellington; Rab Prinjha; A J Barton; Andrew D Medhurst; G D Smith; S Topp; Paul R Murdock; GJ Sanger; JA Terrett; O Jenkins; Christopher D Benham; Andrew D Randall; IS Gloger; John B Davis
Cloning and functional expression of a human orthologue of rat vanilloid receptor-1.
Pain 2000;88(2):205-15.
1999: J Evans; H Herdon; William Cairns; E O'Brien; C Chapman; JA Terrett; IS Gloger
Cloning, functional characterisation and population analysis of a variant form of the human glycine type 2 transporter.
FEBS letters 1999;463(3):301-6.
1999: CH Yi; JA Terrett; Quanyi Li; K Ellington; Elizabeth A Packham; L Armstrong-Buisseret; P McClure; T Slingsby; J David Brook
Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19.
Genomics 1999;55(1):10-20.
1998: SQ Rice; Christopher Southan; Helen F Boyd; JA Terrett; Colin H Macphee; Kitty E Moores; IS Gloger; David Tew
Expression, purification and characterization of a human serine-dependent phospholipase A2 with high specificity for oxidized phospholipids and platelet activating factor.
The Biochemical journal 1998;330 ( Pt 3)():1309-15.
1997: Quanyi Li; Ruth Newbury-Ecob; JA Terrett; David I Wilson; Andrew R J Curtis; CH Yi; TC Gebuhr; PJ Bullen; Steve C Robson; Tom Strachan; Damien Bonnet; Stanislas LYONNET; I D Young; J A Raeburn; A J Buckler; David J Law; J David Brook
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
Nature genetics 1997;15(1):21-9.
1996: JA Terrett; R Newbury-Ecob; N M Smith; Quanyi Li; C Garrett; P Cox; D Bonnet; Stanislas LYONNET; A Munnich; AJ Buckler; J David Brook
A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene.
American journal of human genetics 1996;59(6):1337-41.
1996: JA Terrett; S Miles; R H Thomas
Complete DNA sequence of the mitochondrial genome of Cepaea nemoralis (Gastropoda: Pulmonata).
Journal of molecular evolution 1996;42(2):160-8.
1994: JA Terrett; R Newbury-Ecob; G S Cross; Iain Fenton; J A Raeburn; I D Young; J David Brook
Holt-Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q.
Nature genetics 1994;6(4):401-4.