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Andrew Curtis

Research Profile

Chemicals & Drugs

Concepts & Ideas

Genes & Molecular Sequences

Living Beings

Mouse

Disorders

Devices

Yeast Artificial Chromosomes

Anatomy

Physiology

Point Mutation

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Publications

TOP 3
Helen M Phillips; Glenn L Renforth; Cosma Spalluto; Tom Hearn; Andrew R J Curtis; Lyndsey Craven; Beatrice Havarani; Mark Clement-Jones; Carol English; Oliver Stumper; Tony Salmon; Susie Hutchinson; Michael S Jackson; David I Wilson
Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis.
Thuan Dinh Bui; Majlinda Lako; S Lejeune; Andrew R J Curtis; Tom Strachan; S Lindsay; Adrian L Harris
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25.
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.

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All Publications

2002: Helen M Phillips; Glenn L Renforth; Cosma Spalluto; Tom Hearn; Andrew R J Curtis; Lyndsey Craven; Beatrice Havarani; Mark Clement-Jones; Carol English; Oliver Stumper; Tony Salmon; Susie Hutchinson; Michael S Jackson; David I Wilson
Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis.
Genomics 2002;79(4):475-8.
1997: Thuan Dinh Bui; Majlinda Lako; S Lejeune; Andrew R J Curtis; Tom Strachan; S Lindsay; Adrian L Harris
Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25.
Gene 1997;189(1):25-9.
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.

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