Christopher F. Graham

Affiliations: 
University of Oxford, Oxford, United Kingdom 
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"Christopher Graham"
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Royer C, Leonavicius K, Kip A, et al. (2020) Establishment of a relationship between blastomere geometry and YAP localisation during compaction. Development (Cambridge, England)
Graham CF, Solter D, Gearhart JD, et al. (2016) Honoring the work and life of Leroy C. Stevens. A symposium as part of the International Stem Cell Initiative Workshop. The International Journal of Developmental Biology. 60: 327-336
Haley VL, Barnes DJ, Sandovici I, et al. (2012) Igf2 pathway dependency of the Trp53 developmental and tumour phenotypes. Embo Molecular Medicine. 4: 705-18
Charalambous M, Cowley M, Geoghegan F, et al. (2010) Maternally-inherited Grb10 reduces placental size and efficiency. Developmental Biology. 337: 1-8
Shipley RJ, Bonsall MB, Allwright DJ, et al. (2009) Theoretical exploration of blastocyst morphogenesis. The International Journal of Developmental Biology. 53: 447-457
Lahiri D, Dutton JR, Duarte A, et al. (2007) Nephropathy and defective spermatogenesis in mice transgenic for a single isoform of the Wilms' tumour suppressor protein, WT1-KTS, together with one disrupted Wt1 allele. Molecular Reproduction and Development. 74: 300-11
Hill DJ, Strutt B, Arany E, et al. (2000) Increased and persistent circulating insulin-like growth factor II in neonatal transgenic mice suppresses developmental apoptosis in the pancreatic islets. Endocrinology. 141: 1151-1157
Gardner RL, Squire S, Zaina S, et al. (1999) Insulin-like growth factor-2 regulation of conceptus composition: Effects of the trophectoderm and inner cell mass genotypes in the mouse Biology of Reproduction. 60: 190-195
Zaina S, Newton RV, Paul MR, et al. (1998) Local reduction of organ size in transgenic mice expressing a soluble insulin-like growth factor II/mannose-6-phosphate receptor. Endocrinology. 139: 3886-95
Duarte A, Caricasole AA, Graham CF, et al. (1998) Wilms' tumour-suppressor protein isoforms have opposite effects on Igf2 expression in primary embryonic cells, independently of p53 genotype British Journal of Cancer. 77: 253-259
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