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Associate Professor James Wells
Associate Professor

James Wells

Email: 
Phone: 
+61 7 344 36983

Overview

Background

Associate Professor James Wells is an innovative cancer immunologist who leads the Novel Cancer Therapeutics Group at the Frazer Institute and serves as Director of Immunology at the Dermatology Research Centre, University of Queensland. His research programme is focused on deciphering the fundamental mechanisms that govern immune responses within tumours and translating those discoveries into transformative new cancer therapies. He has a particular track record in skin cancer and an expanding portfolio of novel therapeutic approaches across oncology more generally.

A/Prof Wells has secured over $7.6 million in competitive funding as lead investigator from the NHMRC, ARC, US Department of Defense, Cancer Council Queensland, NFMRI, and international sources. His body of work spans 111 peer-reviewed publications cited over 3,115 times, with 5.8% ranking in the top 5% most cited globally (SciVal). His influence extends across 26 disciplines beyond medicine, including biochemistry, genetics, molecular biology, and neuroscience, and his research has been featured 42 times in leading media outlets including New Scientist, Forbes, MedicalXpress, and EurekAlert!. He holds two patents and has completed advanced commercialisation training through QUT's Bridge Program.

Biography

A/Prof Wells completed his PhD in cancer immunotherapy at King's College London, followed by postdoctoral training at Harvard Medical School, where he founded a new orthopaedic oncology research programme, secured independent grant funding, and was recognised with a Research Excellence Award and promotion to Faculty as Instructor of Orthopaedic Surgery within just two years. In 2011, he was recruited to the University of Queensland by Professor Ian Frazer AC, co-inventor of the human papillomavirus vaccine, to establish and lead an independent cancer immunology laboratory, supported by a prestigious five-year Perpetual Trustees Fellowship.

Key Discoveries

A hallmark achievement of A/Prof Wells’ laboratory is the discovery and patenting of Q-2361 — a world-first topical antagonist of the immunosuppressive drugs tacrolimus, sirolimus, and everolimus. Q-2361 is a first-in-class drug candidate designed to combat the huge issue of skin cancer development in immune suppressed solid organ transplant recipients through the reactivation of anti-tumour CD8 T cells locally in the skin without disturbing systemic immunosuppression or risking graft survival. Preclinical proof-of-concept studies demonstrated 100% tumour regression, and Q-2361 is now advancing through formulation towards IND-enabling studies and first-in-human clinical trials. This research programme was supported by an NHMRC Development Grant and an NFMRI grant. Building on this translational foundation, A/Prof Wells now leads multiple drug discovery programmes targeting cancer beyond the skin.

Research Training

A/Prof Wells has trained more than 55 students and trainees, including PhD graduates who have gone on to postdoctoral positions at the NIH, UCSF, The Scripps Research Institute, and the University of Cambridge. He serves as Vice President of the Molecular and Experimental Pathology Society of Australasia and regularly reviews grants for the NHMRC, ARC, MRC (UK), Wellcome Trust/DBT India Alliance, and Health Research Council of New Zealand.

Research Areas

  • Cancer immunology and immune-based cancer therapy
  • First-in-class drug discovery and translational oncology
  • T cell regulation in tumours and the immune microenvironment
  • Targeted therapy for immunosuppressed patients with skin cancer
  • Novel metabolic and immune targets for pan-cancer therapeutics

James would like to thank the granting bodies and philanthropic partnerships that make his goal of delivering new and effective cancer drugs possible.

Availability

Associate Professor James Wells is:
Available for supervision

Qualifications

  • Bachelor of Science, University of Edinburgh
  • Doctor of Philosophy, University College London

Research impacts

A/Prof Wells' research is driving a new paradigm in cancer treatment — one that harnesses, restores, and re-engineers the immune system to fight tumours across a range of cancer types and patient populations. His near-term translational focus is Q-2361, which addresses a critical unmet need for the ~50,000 Australians living as organ transplant recipients who face dramatically elevated skin cancer risk but cannot access existing immunotherapies without risking graft rejection. His longer-term pipeline targets fundamental vulnerabilities shared by many cancers, with the potential to benefit patients in the broader immune-competent population.

His work benefits patients and society by:

  • Delivering first-in-class therapeutics: advancing Q-2361 towards clinical trial, and developing novel drug candidates targeting cancer cell metabolism and T cell activation with broad oncological relevance.
  • Unlocking new therapeutic mechanisms: identifying previously unrecognised immune regulatory pathways, novel T cell subsets, and druggable targets applicable across multiple cancer types and treatment modalities.
  • Accelerating translation to the clinic: driving Q-2361 through formulation development with industry partner Formulytica Pty Ltd.
  • Generating foundational discoveries: producing 111 peer-reviewed publications cited across 88 countries and 160 leading institutions, including Harvard Medical School, Johns Hopkins, King's College London, and the Mayo Clinic.
  • Building Australia's research capacity: training the next generation of cancer immunologists, with mentees who have collectively attracted over 20 competitive grants and fellowships, including NIH Cancer Research Training Fellowships, MRFF awards, and ARC DECRAs.
  • Engaging the broader community: contributing to national and international conversations about cancer, immunotherapy, and transplant medicine through 42 media appearances in outlets reaching audiences worldwide.

Works

Search Professor James Wells’s works on UQ eSpace

115 works between 2004 and 2026

1 - 20 of 115 works

2026

Journal Article

Recurrence of keratinocyte cancers after superficial radiation therapy

Daley, Laura, Byrnes, Kurt, Caldwell, Peter J, Wells, James W, Dicks, Colin and Schaider, Helmut (2026). Recurrence of keratinocyte cancers after superficial radiation therapy. Skin Health and Disease vzag047. doi: 10.1093/skinhd/vzag047

Recurrence of keratinocyte cancers after superficial radiation therapy

2026

Journal Article

Using targeted therapy to promote a pro-inflammatory tumour microenvironment and anti-tumour immune response in high grade serous ovarian cancer

Zeng, Zhen, Gandini, Anastasia, Bhatt, Rituparna, Proctor, Martina, Goh, Nicole-Lisa Li-Ann, Vora, Shivam, Walsh, Thomas P., Wu, Sherry Y., Ferguson, Kaltin, Coward, Jermaine I., Kumari, Snehlata, Haass, Nikolas K., Wells, James W., Hardy, Janet, Perrin, Lewis, He, Yaowu, Hooper, John D., Ho, Gwo-Yaw, Gonzalez Cruz, Jazmina L. and Gabrielli, Brian (2026). Using targeted therapy to promote a pro-inflammatory tumour microenvironment and anti-tumour immune response in high grade serous ovarian cancer. British Journal of Cancer, 1-11. doi: 10.1038/s41416-026-03416-y

Using targeted therapy to promote a pro-inflammatory tumour microenvironment and anti-tumour immune response in high grade serous ovarian cancer

2026

Conference Publication

Q-2361, a treatment for skin cancer prevention in organ transplant recipients

Pouwer, Rebecca, Beaumont, Kimberley, Veitch, Margaret, Reyes, Maria Parra, Chintala, Bhanu, Chew, Hui Yi, Soyer, Peter, Campbell, Scott, Wells, James, Harvey, Andrew, Cock, Terrie-Anne and Dymock, Brian (2026). Q-2361, a treatment for skin cancer prevention in organ transplant recipients. AACR Annual Meeting 2026, San Diego, CA, United States, 17-22 April 2026. Philadelphia, PA, United States: American Association for Cancer Research. doi: 10.1158/1538-7445.AM2026-7106

Q-2361, a treatment for skin cancer prevention in organ transplant recipients

2026

Conference Publication

Q-2361 Reverses Tacrolimus-Induced Carcinogenic Transformation of Keratinocytes: A Novel Prevention Strategy for Squamous Cell Carcinoma in Transplant Recipients

Parra Reyes, M., Chintala, B., Anwaar, S., Soderholm, A., Dymock, B., Pouwer, R. and Wells, J. (2026). Q-2361 Reverses Tacrolimus-Induced Carcinogenic Transformation of Keratinocytes: A Novel Prevention Strategy for Squamous Cell Carcinoma in Transplant Recipients. 22nd EADO Congress 2026, Prague, Czech Republic, 23 - 25 April 2026. London, United Kingdom: Elsevier. doi: 10.1016/j.ejcskn.2026.101119

Q-2361 Reverses Tacrolimus-Induced Carcinogenic Transformation of Keratinocytes: A Novel Prevention Strategy for Squamous Cell Carcinoma in Transplant Recipients

2025

Journal Article

Immunomodulation of UVB-induced regulatory T cells prevents the establishment of squamous cell carcinoma

Anwaar, Shoaib, Ashraf, Amina, Jahfali, Sarah, Yunis, Joseph, Gonzalez Cruz, Jazmina L. and Wells, James W. (2025). Immunomodulation of UVB-induced regulatory T cells prevents the establishment of squamous cell carcinoma. Journal for ImmunoTherapy of Cancer, 13 (12) e013118. doi: 10.1136/jitc-2025-013118

Immunomodulation of UVB-induced regulatory T cells prevents the establishment of squamous cell carcinoma

2025

Journal Article

Sacrificial redox modulation by a secreted bacterial effector molecule mitigates oxidative stress and inflammation in vivo

Andersson, Tilde, Anwaar, Shoaib, Fuentes-Lemus, Eduardo, Allhorn, Maria, Happonen, Lotta, Veitch, Margaret, Chew, Hui Yi, Montes de Oca, Marcela, Tanner, Lloyd, Brüggemann, Holger, Nordenfelt, Pontus, Davies, Michael J, Wells, James W and Lood, Rolf (2025). Sacrificial redox modulation by a secreted bacterial effector molecule mitigates oxidative stress and inflammation in vivo. Free Radical Biology & Medicine, 240, 339-346. doi: 10.1016/j.freeradbiomed.2025.08.038

Sacrificial redox modulation by a secreted bacterial effector molecule mitigates oxidative stress and inflammation in vivo

2025

Conference Publication

Understanding the role of immature myeloid cells/myeloid-derived suppressor cells in early melanoma establishment

Wells, James W. and Hou, Xiaoyu (2025). Understanding the role of immature myeloid cells/myeloid-derived suppressor cells in early melanoma establishment. OXFORD: OXFORD UNIV PRESS. doi: 10.1093/jimmun/vkaf283.1175

Understanding the role of immature myeloid cells/myeloid-derived suppressor cells in early melanoma establishment

2025

Journal Article

TLR4 endocytosis and endosomal TLR4 signaling are distinct and independent outcomes of TLR4 activation

Schultz, Thomas E., Mathmann, Carmen D., Domínguez Cadena, Leslie C., Muusse, Timothy W., Kim, Hyoyoung, Wells, James W., Ulett, Glen C., Hamerman, Jessica A., Brooks, Andrew J., Kobe, Bostjan, Sweet, Matthew J., Stacey, Katryn J. and Blumenthal, Antje (2025). TLR4 endocytosis and endosomal TLR4 signaling are distinct and independent outcomes of TLR4 activation. EMBO Reports, 26 (10) 2250056, 2740-2766. doi: 10.1038/s44319-025-00444-2

TLR4 endocytosis and endosomal TLR4 signaling are distinct and independent outcomes of TLR4 activation

2025

Journal Article

Harnessing cytokine immunocomplexes and cytokine fusion proteins for cancer therapy: mechanisms and clinical potential

Kong, Wei Yang, Soderholm, Amelia, Brooks, Andrew J., Gonzalez Cruz, Jazmina L. and Wells, James W. (2025). Harnessing cytokine immunocomplexes and cytokine fusion proteins for cancer therapy: mechanisms and clinical potential. Cancer Treatment Reviews, 136 102937. doi: 10.1016/j.ctrv.2025.102937

Harnessing cytokine immunocomplexes and cytokine fusion proteins for cancer therapy: mechanisms and clinical potential

2025

Conference Publication

Targeting replication stress promotes anti-tumour immune responses that are suppressed by tumour-associated myeloid cells

Zeng, Zhen, Bhatt, Ritu, Gandini, Anastasia, Cruz, Jazmina Gonzalez, Proctor, Martina, Irvine, Katharine, Dolcetti, Riccardo, Wells, James and Gabrielli, Brian (2025). Targeting replication stress promotes anti-tumour immune responses that are suppressed by tumour-associated myeloid cells. AACR IO: Discovery and Innovation in Cancer Immunology: Revolutionizing Treatment through Immunotherapy, Los Angeles, CA USA, 23-26 February 2025. Washington, DC USA: American Association for Cancer Research. doi: 10.1158/2326-6074.io2025-a118

Targeting replication stress promotes anti-tumour immune responses that are suppressed by tumour-associated myeloid cells

2025

Journal Article

A synthetic cyclic peptide for promoting antigen presentation and immune activation

Zhang, Jiahui, Madge, Harrison Y. R., Mahmoud, Asmaa, Lu, Lantian, Wang, Wanyi, Huang, Wenbin, Koirala, Prashamsa, Gonzalez Cruz, Jazmina L., Kong, Wei Yang, Bashiri, Sahra, Shalash, Ahmed O., Hussein, Waleed M., Khalil, Zeinab G., Wells, James W., Toth, Istvan and Stephenson, Rachel J. (2025). A synthetic cyclic peptide for promoting antigen presentation and immune activation. NPJ Vaccines, 10 (1) 9, 9-1. doi: 10.1038/s41541-024-01050-4

A synthetic cyclic peptide for promoting antigen presentation and immune activation

2024

Conference Publication

Unravelling the biology of double-positive CD4/CD8αβ T cells in peripheral tissues

Kong, Wei Yang, Soderholm, Amelia, de Oca, Marcela Montes, Chew, Hui Yi, Brooks, Andrew, Cruz, Jazmina and Wells, James (2024). Unravelling the biology of double-positive CD4/CD8αβ T cells in peripheral tissues. Annual Meeting of the American-Association-of-Immunologists (IMMUNOLOGY), Chicago, IL USA, 3-7 May 2024. Cary, NC USA: Oxford University Press. doi: 10.4049/jimmunol.212.supp.1341.4154

Unravelling the biology of double-positive CD4/CD8αβ T cells in peripheral tissues

2024

Journal Article

Utilizing murine dendritic cell line DC2.4 to evaluate the immunogenicity of subunit vaccines in vitro

Lu, Lantian, Kong, Wei Yang, Zhang, Jiahui, Firdaus, Farrhana, Wells, James W., Stephenson, Rachel J., Toth, Istvan, Skwarczynski, Mariusz and Cruz, Jazmina L. Gonzalez (2024). Utilizing murine dendritic cell line DC2.4 to evaluate the immunogenicity of subunit vaccines in vitro. Frontiers in Immunology, 15 1298721, 1-13. doi: 10.3389/fimmu.2024.1298721

Utilizing murine dendritic cell line DC2.4 to evaluate the immunogenicity of subunit vaccines in vitro

2024

Journal Article

Arginase-induced cell death pathways and metabolic changes in cancer cells are not altered by insulin

Chew, Hui Yi, Cvetkovic, Goran, Tepic, Slobodan and Wells, James W. (2024). Arginase-induced cell death pathways and metabolic changes in cancer cells are not altered by insulin. Scientific Reports, 14 (1) 4112, 4112. doi: 10.1038/s41598-024-54520-z

Arginase-induced cell death pathways and metabolic changes in cancer cells are not altered by insulin

2024

Journal Article

Predicting tacrolimus concentrations in the skin of adult kidney transplant recipients: a feasibility study

Sartain, Felicity, Viecelli, Andrea K., Veitch, Margaret, Franklin, Michael E., Dymock, Brian W., Wells, James W. and Campbell, Scott B. (2024). Predicting tacrolimus concentrations in the skin of adult kidney transplant recipients: a feasibility study. Transplant International, 37 12019, 1-7. doi: 10.3389/ti.2024.12019

Predicting tacrolimus concentrations in the skin of adult kidney transplant recipients: a feasibility study

2024

Journal Article

Checkpoint kinase 1 inhibitor + low‐dose hydroxyurea efficiently kills BRAF inhibitor‐ and immune checkpoint inhibitor‐resistant melanomas

Zeng, Zhen, Ngo, Hung Long, Proctor, Martina, Rizos, Helen, Dolcetti, Riccardo, Cruz, Jazmina Gonzalez, Wells, James W. and Gabrielli, Brian (2024). Checkpoint kinase 1 inhibitor + low‐dose hydroxyurea efficiently kills BRAF inhibitor‐ and immune checkpoint inhibitor‐resistant melanomas. Pigment Cell and Melanoma Research, 37 (1), 45-50. doi: 10.1111/pcmr.13120

Checkpoint kinase 1 inhibitor + low‐dose hydroxyurea efficiently kills BRAF inhibitor‐ and immune checkpoint inhibitor‐resistant melanomas

2024

Journal Article

Peritumoral administration of immunomodulatory antibodies as a triple combination suppresses skin tumor growth without systemic toxicity

Wright, Quentin G., Sinha, Debottam, Wells, James W., Frazer, Ian H., Gonzalez Cruz, Jazmina L. and Leggatt, Graham Robert (2024). Peritumoral administration of immunomodulatory antibodies as a triple combination suppresses skin tumor growth without systemic toxicity. Journal for ImmunoTherapy of Cancer, 12 (1) e007960, e007960. doi: 10.1136/jitc-2023-007960

Peritumoral administration of immunomodulatory antibodies as a triple combination suppresses skin tumor growth without systemic toxicity

2023

Journal Article

Local blockade of tacrolimus promotes T-cell-mediated tumor regression in systemically immunosuppressed hosts

Veitch, Margaret, Beaumont, Kimberly, Pouwer, Rebecca, Chew, Hui Yi, Frazer, Ian H., Soyer, H. Peter, Campbell, Scott, Dymock, Brian W., Harvey, Andrew, Cock, Terrie-Anne and Wells, James W. (2023). Local blockade of tacrolimus promotes T-cell-mediated tumor regression in systemically immunosuppressed hosts. Journal for ImmunoTherapy of Cancer, 11 (9) e006783, 1-15. doi: 10.1136/jitc-2023-006783

Local blockade of tacrolimus promotes T-cell-mediated tumor regression in systemically immunosuppressed hosts

2023

Journal Article

Mono-phosphorylation at Ser4 of barrier-to-autointegration factor (Banf1) significantly reduces its DNA binding capability by inducing critical changes in its local conformation and DNA binding surface

Tang, Ming, Suraweera, Amila, Nie, Xuqiang, Li, Zilin, Lai, Pinglin, Wells, James W., O’Byrne, Kenneth J., Woods, Robert J, Bolderson, Emma and Richard, Derek J (2023). Mono-phosphorylation at Ser4 of barrier-to-autointegration factor (Banf1) significantly reduces its DNA binding capability by inducing critical changes in its local conformation and DNA binding surface. Physical Chemistry Chemical Physics, 25 (36), 24657-24677. doi: 10.1039/d3cp02302h

Mono-phosphorylation at Ser4 of barrier-to-autointegration factor (Banf1) significantly reduces its DNA binding capability by inducing critical changes in its local conformation and DNA binding surface

2023

Journal Article

Enhanced hydrophobicity of CeO2 thin films: role of the morphology, adsorbed species and crystallography

Mamedov, D., Asland, A. C., Cooil, S. P., Rost, H. I., Bakkelund, J., Allaniyazov, A., Wells, J. W. and Karazhanov, S. (2023). Enhanced hydrophobicity of CeO2 thin films: role of the morphology, adsorbed species and crystallography. Materials Today Communications, 35 106323, 1-8. doi: 10.1016/j.mtcomm.2023.106323

Enhanced hydrophobicity of CeO2 thin films: role of the morphology, adsorbed species and crystallography

Funding

Current funding

  • 2025 - 2030
    Drug discovery to eliminate high grade cancers
    Merchant Charitable Foundation
    Open grant
  • 2025 - 2026
    The development of Q2361 for skin cancer prevention and treatment in transplant patients
    National Foundation for Medical Research and Innovation
    Open grant
  • 2024 - 2026
    Preventing the cancer-promoting effects of tacrolimus on UV-treated keratinocytes
    Australasian College of Dermatologists Scientific Research Fund
    Open grant
  • 2020 - 2026
    Donation to support the research of James Wells
    Kyon Biotech AG
    Open grant

Past funding

  • 2024 - 2026
    Development of novel drugs targeting skin cancers in immunosuppressed organ transplant recipients (Externally administered by MSHHS)
    Metro South Hospital and Health Service
    Open grant
  • 2022 - 2025
    Understanding the Role of Immature Myeloid Cells in Early Melanoma Establishment
    United States Congressionally Directed Medical Research Programs - Melanoma Research Program
    Open grant
  • 2021 - 2024
    Enhancing tumour immune detection by targeting replication stress
    Established Investigator
    Open grant
  • 2021 - 2023
    Preclinical development of Q2361, a transforming new drug for skin cancer prevention in organ transplant recipients
    NHMRC Development Grant
    Open grant
  • 2021 - 2024
    The Ins and Outs of Endocytosis inhibition: Providing diverse opportunities for treatment of incurable cancers
    NHMRC IDEAS Grants
    Open grant
  • 2020
    Development of a preclinical skin tumour model
    Vaxxas Pty Ltd
    Open grant
  • 2020 - 2022
    Saving your skin: physiology of immune regulation in mammalian lymph nodes
    ARC Discovery Projects
    Open grant
  • 2019 - 2020
    Development of a novel drug to prevent skin cancer in solid organ transplant recipient
    Princess Alexandra Hospital R&D Foundation
    Open grant
  • 2019 - 2025
    Drug discovery to eliminate skin cancers in transplant patients
    Merchant Charitable Foundation
    Open grant
  • 2018 - 2019
    Immune signatures as diagnostic tools for suspicious skin rashes
    F & E Bauer Foundation Scholarship
    Open grant
  • 2018 - 2020
    Towards clinical diagnosis of inflammatory skin rashes using minimally-invasive microsampling techniques
    TRI Spore Grants
    Open grant
  • 2018 - 2020
    Development of a human skin model to assess topical pharmaceutical and complementary and alternative medicine (CAM) toxicity and effects (SCCA grant led by QUT)
    Queensland University of Technology
    Open grant
  • 2018 - 2019
    Immunoassay support for the Vaxxas Nanopatch phase 1 clinical trial (SP-1207-022): assessment of CMI
    UniQuest Pty Ltd
    Open grant
  • 2018 - 2019
    CMI assay development for the assessment of influenza-specific T-cell responses
    UniQuest Pty Ltd
    Open grant
  • 2017 - 2018
    Adjuvant therapy for checkpoint inhibitor efficacy in murine oncology models
    UniQuest Pty Ltd
    Open grant
  • 2017 - 2018
    Memory CD8+ T-cell function in squamous cell carcinoma
    Cancer Council Queensland
    Open grant
  • 2016 - 2018
    The influence of local immunosuppression upon the healing of segmental defects in mice
    AO Foundation Research Fund
    Open grant
  • 2016 - 2019
    Aurora A as a novel therapeutic target for HPV-driven cancers (NHMRC Project Grant administered by Griffith University)
    Griffith University
    Open grant
  • 2016
    The Australian human microbiota project-microbe isolation facility
    UQ Major Equipment and Infrastructure
    Open grant
  • 2016 - 2018
    The role of CD4+CD8+ double-positive T-cell regulation of CD8 T-cell responses
    NHMRC Project Grant
    Open grant
  • 2015 - 2017
    Topical application of ORIL007 in two different mouse models
    Oncology Research International Ltd
    Open grant
  • 2015 - 2017
    Deciphering novel control mechanisms in the skin
    ARC Discovery Projects
    Open grant
  • 2014 - 2015
    Chemokine involvement in the differential response of Actinic Keratosis and Squamous Cell Carcinoma to Imiquimod therapy
    Cancer Council Queensland
    Open grant
  • 2012 - 2013
    Characterisation of T-cell immunity in Squamous Cell Carcinoma
    UQ New Staff Research Start-Up Fund
    Open grant
  • 2012
    Manipulating immune tolerance to improve therapeutic vaccine outcome
    UQ Early Career Researcher
    Open grant
  • 2011 - 2023
    Fellowship in Skin Cancer Research in Queensland
    Perpetual Trustees Queensland Limited
    Open grant

Supervision

Availability

Associate Professor James Wells is:
Available for supervision

Looking for a supervisor? Read our advice on how to choose a supervisor.

Supervision history

Current supervision

  • Doctor Philosophy

    Investigating molecular mechanisms of Q-2361 as an enhancer of T cell activation

    Principal Advisor

    Other advisors: Associate Professor Graham Leggatt

  • Doctor Philosophy

    The impact of arginine treatment and arginine depletion on the adoptive transfer of melanoma-specific T cells

    Principal Advisor

  • Doctor Philosophy

    Piecing it Together: Deciphering T cell Receptor-Peptide Recognition

    Principal Advisor

    Other advisors: Professor Brandon Wainwright

  • Doctor Philosophy

    Understanding the role of myeloid lineages in early melanoma establishment

    Principal Advisor

    Other advisors: Associate Professor Arutha Kulasinghe

Completed supervision

Media

Enquiries

For media enquiries about Associate Professor James Wells's areas of expertise, story ideas and help finding experts, contact our Media team:

communications@uq.edu.au