Colin Johnson
Affiliations: | University of Leeds | University of Leeds, Leeds, England, United Kingdom |
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"Colin Johnson"
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| Abdelhamed ZA, Natarajan S, Wheway G, et al. (2015) The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway. Disease Models & Mechanisms. 8: 527-41 |
| Hartill V, Logan C, Parry D, et al. (2015) Investigation into the Importance of genes encoding ciliary proteins in congenital heart disease using whole exome sequencing Cilia. 4: 9 |
| Shoaib E, Abdelhamed Z, Szymanska K, et al. (2015) Biochemical characterization of transmembrane proteins (TMEMs) in the ciliary transition zone Cilia. 4: 75 |
| Abdelhamed Z, Natarajan S, Inglehearn C, et al. (2015) The Meckel-Gruber Syndrome protein TMEM67 (meckelin) regulates basal body planar polarization and non-canonical Wnt signalling via Wnt5a and ROR2 Cilia. 4 |
| Frank V, Habbig S, Bartram MP, et al. (2013) Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression. Human Molecular Genetics. 22: 2177-85 |
| Travaglini L, Brancati F, Silhavy J, et al. (2013) Phenotypic spectrum and prevalence of INPP5E mutations in Joubert syndrome and related disorders. European Journal of Human Genetics : Ejhg. 21: 1074-8 |
| Adams M, Dawe H, Wheway G, et al. (2009) 16-P005 Mutations in the lethal ciliopathy Meckel–Gruber syndrome alter the subcellular distribution of actin-binding proteins and disrupt the actin cytoskeleton Mechanisms of Development. 126 |
| Beales PL, Bland E, Tobin JL, et al. (2007) IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy. Nature Genetics. 39: 727-9 |