Mr Dong Li


NameMr Dong Li
Job titleResearch Fellow in Biomedical Science Histology
Research institute
Primary appointmentNatural Sciences
Email addressD.Li@mdx.ac.uk
ORCIDhttps://orcid.org/0000-0001-9240-4173
Contact categoryAcademic staff

Research outputs

Identification of human papillomavirus from super resolution microscopic images generated using deep learning architectures

Gao, X., Wen, S., Li, D., Liu, W., Xiong, J., Xu, B., Liu, J., Zhang, H. and Liu, X. 2022. Identification of human papillomavirus from super resolution microscopic images generated using deep learning architectures. in: Wani, M. and Palade, V. (ed.) Deep Learning Applications, Volume 4 Springer.

Detection of human papillomavirus (HPV) from super resolution microscopic images applying an explainable deep learning network

Gao, X., Wen, S., Li, D., Liu, W., Xiong, J., Xu, B., Liu, J., Zhang, H. and Liu, X. 2022. Detection of human papillomavirus (HPV) from super resolution microscopic images applying an explainable deep learning network. SPIE Medical Imaging: Biomedical Applications in Molecular, Structural, and Functional Imaging. San Diego, USA 20 - 22 Feb 2022 Society of Photo-optical Instrumentation Engineers. https://doi.org/10.1117/12.2624423

Evaluation of GAN architectures for visualisation of HPV viruses from microscopic images

Gao, X., Wen, S., Li, D., Liu, W., Xiong, J., Xu, B., Liu, J., Zhang, H. and Liu, X. 2021. Evaluation of GAN architectures for visualisation of HPV viruses from microscopic images. 20th IEEE ICMLA 2021. Virtual online 13 - 16 Dec 2021 IEEE. pp. 829-833 https://doi.org/10.1109/ICMLA52953.2021.00137

Modelling and validating three-dimensional human breast and cancerous human breast tissues in vitro

Zuk, A., Burczynska, B., Li, D., Ghali, L., Dilworth, S. and Wen, S. 2020. Modelling and validating three-dimensional human breast and cancerous human breast tissues in vitro. Clinical Oncology and Research. 3 (4), pp. 1-9. https://doi.org/10.31487/j.COR.2020.04.05

Optimisation of folate-mediated liposomal encapsulated arsenic trioxide for treating HPV-positive cervical cancer cells in vitro

Akhtar, A., Ghali, L., Wang, S., Bell, C., Li, D. and Wen, S. 2019. Optimisation of folate-mediated liposomal encapsulated arsenic trioxide for treating HPV-positive cervical cancer cells in vitro. International Journal of Molecular Sciences. 20 (9), pp. 1-20. https://doi.org/10.3390/ijms20092156

Modelling and validating three dimensional human normal cervix and cervical cancer tissues in vitro

Zuk, A., Wen, S., Dilworth, S., Li, D. and Ghali, L. 2017. Modelling and validating three dimensional human normal cervix and cervical cancer tissues in vitro. Journal of Biomedical Research. 31 (3), pp. 240-247. https://doi.org/10.7555/JBR.31.20160150

Therapeutic potential of delivering arsenic trioxide into HPV-infected cervical cancer cells using liposomal nanotechnology

Wang, X., Li, D., Ghali, L., Xia, R., Pantoja Munoz, L., Garelick, H., Bell, C. and Wen, S. 2016. Therapeutic potential of delivering arsenic trioxide into HPV-infected cervical cancer cells using liposomal nanotechnology. Nanoscale Research Letters. 11 (1), pp. 1-8. https://doi.org/10.1186/s11671-016-1307-y

The role of ectopic human chorionic gonadotropin beta subunit in inducing epithelial mesenchymal transition in human keratinocytes and its possible pathways

Wen, S., Li, D., Farshori, Z., Wang, X. and Ghali, L. 2015. The role of ectopic human chorionic gonadotropin beta subunit in inducing epithelial mesenchymal transition in human keratinocytes and its possible pathways. British Pharmacological Society Winder Conference 2014. Queen Elizabeth II Conference Centre London 14 - 17 Dec 2014

Solution-processed anthracene-based molecular glasses as stable blue-light-emission laser gain media

Niu, Q., Zhang, Q., Xu, W., Jiang, Y., Xia, R., Bradley, D., Li, D. and Wen, S. 2015. Solution-processed anthracene-based molecular glasses as stable blue-light-emission laser gain media. Organic Electronics. 18, pp. 95-100. https://doi.org/10.1016/j.orgel.2015.01.012

Ectopic HCG beta may induce epithelialmensenchymal transition on human kera tinocytes in vitro and this could promote tumour progression and invasion.

Wen, S., Li, D., Ghali, L. and Iles, R. 2010. Ectopic HCG beta may induce epithelialmensenchymal transition on human kera tinocytes in vitro and this could promote tumour progression and invasion. Tumour Biology. 31 (S44).

Estradiol, progesterone, testosterone profiles in human follicular fluid and cultured granulosa cells from luteinized pre-ovulatory follicles

Wen, S., Li, D., Tozer, A., Docherty, S. and Iles, R. 2010. Estradiol, progesterone, testosterone profiles in human follicular fluid and cultured granulosa cells from luteinized pre-ovulatory follicles. Reproductive Biology and Endocrinology. 8 (117). https://doi.org/10.1186/1477-7827-8-117

hCGβ expression by cervical squamous carcinoma: in vivo histological association with tumour invasion and apoptosis

Li, D., Wen, S., Ghali, L., Al-Shalabi, F., Docherty, S., Purkis, P. and Iles, R. 2008. hCGβ expression by cervical squamous carcinoma: in vivo histological association with tumour invasion and apoptosis. Histopathology. 53 (2), pp. 147-155. https://doi.org/10.1111/j.1365-2559.2008.03082.x

Human granulosa-lutein cell in vitro production of progesterone, inhibin A, inhibin B, and activin A are dependent on follicular size and not the presence of the oocyte

Wen, S., Tozer, A., Li, D., Docherty, S., Al-Shawaf, T. and Iles, R. 2008. Human granulosa-lutein cell in vitro production of progesterone, inhibin A, inhibin B, and activin A are dependent on follicular size and not the presence of the oocyte. Fertility and Sterility. 89 (5), pp. 1406-1413. https://doi.org/10.1016/j.fertnstert.2007.03.086

hCGβ expression by cervical squamous carcinoma - in vivohistological association with tumour invasion and apoptosis

Li, D., Wen, S., Ghali, L., Al-Shalabi, F., Docherty, S., Purkis, P. and Iles, R. 2008. hCGβ expression by cervical squamous carcinoma - in vivohistological association with tumour invasion and apoptosis. Histopathology. 53 (2), pp. 147-155. https://doi.org/10.1111/j.1365-2559.2008.03082.x
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