Items where authors include "Bond, J."

Article

Smith, C. E. L., Streets, A. J., Lake, A. V. R. et al. (14 more authors) (2025) Drug and siRNA screens identify ROCK2 as a therapeutic target for ciliopathies. Communications Medicine, 5. 129. ISSN 2730-664X

Smith, C.E.L., Streets, A.J. orcid.org/0000-0002-4328-044X, Lake, A.V.R. orcid.org/0000-0002-6341-8661 et al. (14 more authors) (2025) Drug and siRNA screens identify ROCK2 as a therapeutic target for ciliopathies. Communications Medicine, 5. 129. ISSN 2730-664X

Ashi, A., Awaji, A.A., Bond, J. orcid.org/0000-0001-5390-5688 et al. (3 more authors) (2025) Threonine and tyrosine kinase (TTK) mRNA and protein expression in breast cancer; prognostic significance in the neoadjuvant setting. Histopathology. ISSN 0309-0167

Tsikandelova, R., Galo, E., Cerniauskas, E. et al. (18 more authors) (2024) Retinal cells derived from patients with DRAM2-dependent CORD21 dystrophy exhibit key lysosomal enzyme deficiency and lysosomal content accumulation. Stem Cell Reports, 19 (8). pp. 1107-1121. ISSN 2213-6711

Martin, H.L., Turner, A.L., Higgins, J. et al. (14 more authors) (2023) Affimer-mediated locking of p21-activated kinase 5 in an intermediate activation state results in kinase inhibition. Cell Reports, 42 (10). 113184. ISSN 2211-1247

Basu, B. orcid.org/0000-0002-5434-5202, Lake, A.V.R. orcid.org/0000-0002-6341-8661, China, B. et al. (6 more authors) (2023) Racgap1 knockdown results in cells with multiple cilia due to cytokinesis failure. Annals of Human Genetics. ISSN 0003-4800

Richards, J.D. orcid.org/0000-0003-3938-899X, Beswick, P., Bond, J. et al. (4 more authors) (2004) Excavations at the Viking Barrow Cemetery at Heath Wood, Ingleby, Derbyshire. The Antiquaries Journal. pp. 23-116. ISSN 1758-5309

Roberts, E., Hampshire, D.J., Pattison, L. et al. (8 more authors) (2002) Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation. Journal of Medical Genetics, 39 (10). pp. 718-721. ISSN 0022-2593

Hampshire, D.J., Roberts, E., Crow, Y. et al. (5 more authors) (2001) Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36. Journal of Medical Genetics, 38 (10). pp. 680-682. ISSN 0022-2593

Proceedings Paper

Poulter, J., Nadat, F., O'Callaghan, E. et al. (13 more authors) (2024) P13.018.D Biallelic mutation of CWF19L2, encoding a core spliceosome subunit, causes a combined neurodevelopmental and immunodeficiency disorder. In: European Journal of Human Genetics. 57th European Society of Human Genetics (ESHG) Conference, 01-04 Jun 2024, Berlin, Germany. .