ZFIN ID: ZDB-PERS-980518-1
Hoyle, Jacqueline
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Affiliation:
Address: Molecular and Medical Genetics Group Department of Medical and Molecular Genetics Division of Genetics and Molecular Medicine Kings College School of Medicine Guy's Campus 7th Floor Guy's Tower London, SE1 9RT United Kingdom
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Phone: 44-207-188-9307
Fax: 44-207-188-2585
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BIOGRAPHY AND RESEARCH INTERESTS


PUBLICATIONS
Turner, K.J., Hoyle, J., Valdivia, L.E., Cerveny, K.L., Hart, W., Mangoli, M., Geisler, R., Rees, M., Houart, C., Poole, R.J., Wilson, S.W., Gestri, G. (2019) Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficits. PLoS One. 14:e0211073
Denais, C., Dent, C.L., Southgate, L., Hoyle, J., Dafou, D., Trembath, R.C., and Machado, R.D. (2011) Dymeclin, the gene underlying Dyggve-Melchior-Clausen syndrome, encodes a protein integral to extracellular matrix and golgi organization and is associated with protein secretion pathways critical in bone development. Human Mutation. 32(2):231-239
Southgate, L., Dafou, D., Hoyle, J., Li, N., Kinning, E., Critchley, P., Nemeth, A.H., Talbot, K., Bindu, P.S., Sinha, S., Taly, A.B., Raghavendra, S., Muller, F., Maher, E.R., and Trembath, R.C. (2010) Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish. Neurogenetics. 11(4):379-389

NON-ZEBRAFISH PUBLICATIONS