J. Bond

发表

Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings.

C. Woods, W. Enard, J. Bond, 2005, American journal of human genetics.

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.

Mustaq Ahmed, F Lucy Raymond, Martin McKibbin, 2006, American journal of human genetics.

High-Content, High-Throughput Screening for the Identification of Cytotoxic Compounds Based on Cell Morphology and Cell Proliferation Markers

J. Bond, S. Bell, S. Warriner, 2014, PloS one.

A MAPK/c-Jun-mediated switch regulates the initial adaptive and cell death responses to mitochondrial damage in a neuronal cell model.

J. Bond, S. Bell, S. Sweeney, 2018, The international journal of biochemistry & cell biology.

Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice

Colin A. Johnson, S. Jacobson, Rebecca K. Chance, 2009, American journal of human genetics.

Receptor tyrosine kinase inhibitors negatively impact on pro-reparative characteristics of human cardiac progenitor cells

J. Bond, F. Lewis-McDougall, Andrew J Smith, 2022, Scientific Reports.

Apolipoprotein(a) acts as a chemorepellent to human vascular smooth muscle cells via integrin αVβ3 and RhoA/ROCK-mediated mechanisms☆

S. Ball, A. Maqbool, M. Koschinsky, 2013, The international journal of biochemistry & cell biology.

Polymorphism and Divergence in the (cid:98) -Globin Replication Origin Initiation Region

S. Fullerton, J. Bond, R. Harding, 1999 .

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Colin A. Johnson, Teunis J. P. van Dam, J. Shendure, 2015, Nature Cell Biology.

Expression analysis of the MCPH1/BRIT1 and BRCA1 tumor suppressor genes and telomerase splice variants in epithelial ovarian cancer.

J. Bond, S. Burchill, S. Bell, 2018, Gene.

Bluetongue virus infection induces aberrant mitosis in mammalian cells

J. Bond, P. Mertens, P. Monaghan, 2013, Virology Journal.

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response

Jonathan C. Fuller, D. Bonthron, E. Bertini, 2009, Nature Genetics.

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

Hussain Jafri, Emma Roberts, Sheila Scott, 2005, Nature Genetics.

Archaic African and Asian lineages in the genetic ancestry of modern humans.

R. Griffiths, S. Fullerton, J. Bond, 1997, American journal of human genetics.

A high-content screen profiles cytotoxic microRNAs in pediatric and adult glioblastoma cells and identifies miR-1300 as a potent inducer of cytokinesis failure

J. Bond, M. Boissinot, S. Lawler, 2019, bioRxiv.

Deregulation of Microcephalin and ASPM Expression Are Correlated with Epithelial Ovarian Cancer Progression

Anke Brüning-Richardson, J. Bond, S. Bell, 2014, PloS one.

What primary microcephaly can tell us about brain growth.

C. Woods, J. Bond, J. Cox, 2006, Trends in molecular medicine.

ASPM is a major determinant of cerebral cortical size

Alexander F. Markham, Emma Roberts, Christopher A. Walsh, 2002, Nature Genetics.

Differential Proteome Analysis of Replicative Senescence in Rat Embryo Fibroblasts*S

A. Burlingame, M. Zvelebil, S. Hockfield, 2002, Molecular & Cellular Proteomics.

Cytoskeletal genes regulating brain size.

C. Woods, J. Bond, C. G. Woods, 2006, Current opinion in cell biology.

MCPH , a disorder of neurogenic mitosis affecting foetal brain growth

C. Woods, J. Bond, 2006 .

Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36

C. Woods, A. Mubaidin, Y. Crow, 2001, Journal of medical genetics.

Polymorphism and Divergence in the β-Globin Replication Origin Initiation Region

S. Fullerton, J. Bond, R. Harding, 2000 .

Human ASPM participates in spindle organisation, spindle orientation and cytokinesis

C. Woods, J. Bond, C. Midgley, 2010, BMC Cell Biology.

Measles virus causes immunogenic cell death in human melanoma

J. Bond, A. Melcher, R. Vile, 2011, Gene Therapy.

MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34

C. Woods, J. Bond, K. Springell, 2006, European Journal of Human Genetics.

Protein-truncating mutations in ASPM cause variable reduction in brain size.

C. Walsh, R. Hennekam, C. Woods, 2003, American journal of human genetics.

Drug and siRNA screens identify ROCK2 as a therapeutic target for ciliopathies

Colin A. Johnson, S. Grellscheid, J. Bond, 2020 .

A High-Throughput Assay to Identify Modifiers of Premature Chromosome Condensation

Darren C. Tomlinson, J. Bond, S. Bell, 2014, Journal of biomolecular screening.

Minisatellite mutational processes reduce Fst estimates

L. Excoffier, M. Beaumont, J. Flint, 1999, Human Genetics.

Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation

C. Woods, Y. Crow, J. Bond, 2002, Journal of medical genetics.

Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

C. Woods, Y. Crow, J. Bond, 2003, Journal of medical genetics.

The molecular landscape of ASPM mutations in primary microcephaly

M. Fichera, C. Romano, C. Woods, 2008, Journal of Medical Genetics.

Conditional immortalization of freshly isolated human mammary fibroblasts and endothelial cells.

J. Bond, Y. Takeuchi, A. Neville, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.

S. Mundlos, C. Woods, J. Bond, 2006, American journal of human genetics.

Telomerase repressor sequences on chromosome 3 and induction of permanent growth arrest in human breast cancer cells.

C. Cooper, J. Bond, E. K. Parkinson, 1999, Journal of the National Cancer Institute.

Polymorphism and divergence in the beta-globin replication origin initiation region.

S. Fullerton, J. Bond, R. Harding, 2000, Molecular biology and evolution.

Autosomal recessive primary microcephaly: an analysis of locus heterogeneity and phenotypic variation

C. Woods, Y. Crow, J. Bond, 2002, Journal of medical genetics.

ASPM and microcephalin expression in epithelial ovarian cancer correlates with tumour grade and survival

G. Hall, J. Bond, P. Burns, 2011, British Journal of Cancer.

Racgap1 knockdown results in cells with multiple cilia due to cytokinesis failure

J. Bond, G. Wheway, K. Szymanska, 2023, Annals of human genetics.

Affimer-mediated locking of p21-activated kinase 5 in an intermediate activation state results in kinase inhibition.

J. Bond, C. Hurst, H. Martin, 2023, Cell reports.