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Dr Fernanda Cardoso
Dr

Fernanda Cardoso

Email: 
Phone: 
+61 7 344 33402

Overview

Background

Dr Fernanda Cardoso is a Brazil-born Australian dual-citizen researcher interested in venom peptide-based biodiscovery and therapeutics development. Cardoso was awarded an MSc in Molecular Pharmacology and a PhD with an emphasis in Biochemistry and Immunology and is part of the Institute for Molecular Bioscience, where she develops novel therapies for complex neurological diseases. Cardoso has interdisciplinary training in the fields of neuropharmacology, medicinal chemistry and chemical biology and a strong background in drug discovery, which provides the skills to identify naturally occurring or synthetic bioactive molecules and to study their effects in human physiology with applications in neurologic disorders such as chronic pain, irritable bowel syndrome (IBS), and motor neuron disease (MND). Please see Dr Cardoso’s Grants and Publications list for more details.

Before joining the University of Queensland, Dr Cardoso was part of the Queensland Institute for Medical Research, holding a prestigious CAPES Postdoctoral Fellowship. During this period, Cardoso developed unique high-throughput screen platforms for discovering protein and peptide targets of novel therapies to combat infectious diseases and novel helminth-derived bioactives with anti-inflammatory properties. Please see Dr Cardoso’s Publications list for more details.

Dr Cardoso is currently part of the Centre for Drug Discovery and manages several industry and academic projects studying ion channel modulators derived from natural repertoires, particularly venoms, and developing novel, effective drugs to treat neurological disorders.

Availability

Dr Fernanda Cardoso is:
Available for supervision
Media expert

Qualifications

  • Bachelor, Universidade Federal de Minas Gerais (UFMG)
  • Masters (Research) of Biological Sciences, Universidade Federal de Minas Gerais (UFMG)
  • Doctor of Philosophy, Universidade Federal de Minas Gerais (UFMG)

Research interests

  • Chronic pain - Mechanisms of pain and Therapeutics development, Visceral Pain, Irritable Bowel Syndrome

  • Neurodegeneration - Pathophysiology and Therapeutics development

  • Venomics and Pharmacology of Spiders, Cone snails and Snake venoms

  • Structure-function properties of venom peptides and proteins

  • Voltage-gated Ion Channels

Research impacts

Dr. Fernanda Cardoso's research has provided remarkable insights into the discovery and biology of new agents for therapeutical use in complex disorders such as chronic pain, irritable bowel syndrome and motor neuron disease, and vaccinology against tropical diseases. Her ongoing research in ion channel modulators has provided unique leads for treating neuropathic pain and neurodegenerative disorders, which could improve the lives of millions of individuals around the globe, and her past discoveries in vaccine research have the potential to improve the lives of millions of people in Africa, Asia and South America through a vaccine against schistosomiasis.

Works

Search Professor Fernanda Cardoso’s works on UQ eSpace

127 works between 2003 and 2025

121 - 127 of 127 works

2007

Journal Article

The role of the vacB gene in the pathogenesis of Brucella abortus

Miyoshi, Anderson, Rosinha, Gracia M.S., Camargo, Ilana L.B.C., Trant, Cyntia M.C., Cardoso, Fernanda C., Azevedo, Vasco and Oliveira, Sergio C. (2007). The role of the vacB gene in the pathogenesis of Brucella abortus. Microbes and Infection, 9 (3), 375-391. doi: 10.1016/j.micinf.2006.12.004

The role of the vacB gene in the pathogenesis of Brucella abortus

2007

Conference Publication

Vaccine against schistosomiasis: The role of a new tegument protein Sm29 on human and murine protective immune responses

Cardoso, F. C., Gava, E., Macedo, G. C., Kitten, G. T., Mello, A. L., Caliari, M. V. and Oliveira, S. C. (2007). Vaccine against schistosomiasis: The role of a new tegument protein Sm29 on human and murine protective immune responses. 13th International Congress of Immunology, Rio de Janeiro, Brazil, 21-25 August 2007.

Vaccine against schistosomiasis: The role of a new tegument protein Sm29 on human and murine protective immune responses

2006

Journal Article

Identification of a new Schistosoma mansoni membrane-bound protein through bioinformatic analysis

Cardoso, F. C., Pinho, J. M. R., Azevedo, V. and Oliveira, S. C. (2006). Identification of a new Schistosoma mansoni membrane-bound protein through bioinformatic analysis. Genetics and Molecular Research, 5 (4), 609-618.

Identification of a new Schistosoma mansoni membrane-bound protein through bioinformatic analysis

2006

Journal Article

Human antibody responses of patients living in endemic areas for schistosomiasis to the tegumental protein Sm29 identified through genomic studies

Cardoso, F. C., Pacífico, R. N. A., Mortara, R. A. and Oliveira, S. C. (2006). Human antibody responses of patients living in endemic areas for schistosomiasis to the tegumental protein Sm29 identified through genomic studies. Clinical and Experimental Immunology, 144 (3), 382-391. doi: 10.1111/j.1365-2249.2006.03081.x

Human antibody responses of patients living in endemic areas for schistosomiasis to the tegumental protein Sm29 identified through genomic studies

2006

Other Outputs

Membrane protein Sm29 of schistosoma mansoni and uses thereof for treating and diagnosing schistosomiasis

Cardoso, Fernanda C. and Oliveira, Sergio C. (2006). Membrane protein Sm29 of schistosoma mansoni and uses thereof for treating and diagnosing schistosomiasis. WO2007118292A3.

Membrane protein Sm29 of schistosoma mansoni and uses thereof for treating and diagnosing schistosomiasis

2005

Conference Publication

Human IgG3 recognition of Schistosoma mansoni 29 kDa membrane bound protien identified by a bioinformatic approach

Cardoso, F. C., Pacifico, R. N. A. and Oliveira, S. C. (2005). Human IgG3 recognition of Schistosoma mansoni 29 kDa membrane bound protien identified by a bioinformatic approach. XLI Congress of Brazilian Society of Tropical Medicine, Florianopolis, Brazil, 6-10 March 2005.

Human IgG3 recognition of Schistosoma mansoni 29 kDa membrane bound protien identified by a bioinformatic approach

2003

Journal Article

Molecular cloning and characterization of Phoneutria nigriventer toxins active on calcium channels

Cardoso, F. C., Pacífico, L. G., Carvalho, D. C., Victoria, J. M. N., Neves, A. L. G., Chavez-Olortegui, C., Gomez, M. V. and Kalapothakis, E. (2003). Molecular cloning and characterization of Phoneutria nigriventer toxins active on calcium channels. Toxicon, 41 (7), 755-763. doi: 10.1016/S0041-0101(03)00011-4

Molecular cloning and characterization of Phoneutria nigriventer toxins active on calcium channels

Funding

Current funding

  • 2023 - 2026
    Peptide Inhibitors Targeting Sodium Channels to Treat Amyotrophic Lateral Sclerosis
    United States Congressionally Directed Medical Research Programs - Amyotrophic Lateral Sclerosis Research Program
    Open grant

Past funding

  • 2020 - 2023
    Novel multifunctional analgesic sodium channel inhibitors
    NHMRC IDEAS Grants
    Open grant
  • 2018 - 2019
    Development of dual Nav1.1/1.7 inhibitors for the treatment of IBS-related pain
    UniQuest Pty Ltd
    Open grant

Supervision

Availability

Dr Fernanda Cardoso is:
Available for supervision

Before you email them, read our advice on how to contact a supervisor.

Available projects

  • We are seeking enthusiastic students to join our Lab! Please get in touch with us if you want to learn from our fantastic team at the Institute for Molecular Biosciences!

  • Discovery and characterization of bio-active molecules from animal venoms

    We have open positions for Research Students to develop projects in discovery, characterization and structure-function studies of bio-active compounds in animal venoms and other natural repertoires. Students will develop skills in high throughput cellular assays using fluorescence imaging assays, manual and automated whole-cell patch clamp electrophysiology, high performance liquid chromatography, mass spectometry, recombinant expression, peptide synthesis, amongst other state-of-the-art methods and techiniques. Students will also co-author papers and be involved in writting and figures preparation for research publications from their work.

  • Therapeutics development

    We have open positions for Research Students to develop projects in therapies for treating Chronic Pain, Visceral Pain and Motor Neuron Disease. These novel therapies will be developed from bio-active compounds targeting voltage-gated sodium and/or calcium channels. Students will develop skills in manual and automated whole-cell patch clamp electrophysiology, high performance liquid chromatography, mass spectometry, recombinant expression, peptide synthesis, amongst other state-of-the-art methods and techiniques. Students will also co-author papers and be involved in writting and figures preparation for research publications from their work.

  • Other research projects in HDR

    On-going

    Isolation and characterisation of novel analgesic conotoxins - Tianjiao Zhao Doctor Philosophy — Associate Advisor

    Completed

    The unexplored pharmacopeia of Australian spiders: learning from the experts - Hayden Wirth (2022) Science Honours — Principal Advisor

    Peptides targeting sodium channels to treat Motor Neuron Disease - Charan Kotapati (2022) Biomedical Sciences Honours — Principal Advisor

    Structure-Function and Rational Design of a Newly Discovered Spider Venom Peptide Ssp1a at hNaV1.2, hNaV1.3 and hNaV1.7 Yashad Dongol (2020) Doctor Philosophy — Associate Advisor

    Spider-venom peptides targeting ion channels in chronic pain pathways - Amatulla Shakir Nashikwala (2022) Master Coursework — Principal Advisor

    In vitro assessment of human neuroblastoma cytotoxicity induced by snake venoms - Simon Kramer (2022) Summer Research project — Principal Advisor

    Molecular pharmacology and peripheral analgesia of omega-conotoxins- Mahadhi Hasan (2021) Doctor Philosophy — Associate Advisor

    Discovery and Characterisation of Venom Peptide and Small Molecule Modulators for T-type Calcium Channels - Dan Wang (2020) Doctor Philosophy — Associate Advisor

    Molecular interactions between spider peptides and the sodium channel Nav1.1 - Huyiu Hu (2019) Masters Coursework — Principal Advisor

    Structure-function relatioships of the multifunctional spider peptide Tap1a - Saja E Mawlawi (2019) Masters Coursework — Principal Advisor

    Novel ion channels modulators from Australian tarantula venoms - Phil M Choin (2015) Summer Research Project — Associate Advisor

    N-type calcium channels modulators from Australian tarantula venoms - Wan Nur Amalina (2015) Summer Research Project — Associate Advisor

    Isolation and characterization of novel spider venom peptides antagonizing voltage-gated calcium channels - Ching Koon Lim (2014) Masters Coursework — Associate Advisor

    Optimizing the potency and selectivity of a spider-venom peptide that inhibits the analgesic target Nav1.7 - Andelain Erickson (2014) Honours — Associated Advisor

Supervision history

Current supervision

  • Doctor Philosophy

    Selective modulation voltage gated sodium channels to investigate pathophysiology and treatment for motor neuron disease

    Principal Advisor

    Other advisors: Professor Glenn King

  • Doctor Philosophy

    Venom variation in New World pit vipers

    Associate Advisor

    Other advisors: Dr Andrew Walker, Professor Bryan Fry

  • Doctor Philosophy

    Clinical implications and evolutionary insights of Latin American pit viper venom function

    Associate Advisor

    Other advisors: Dr Andrew Walker, Professor Bryan Fry

  • Doctor Philosophy

    Clinical implications and evolutionary insights of Latin American pit viper venom function

    Associate Advisor

    Other advisors: Dr Andrew Walker, Professor Bryan Fry

Completed supervision

Media

Enquiries

Contact Dr Fernanda Cardoso directly for media enquiries about:

  • Analgesics
  • Bio-active peptides
  • Drug discovery
  • Ion channels
  • Irritable bowel syndrome
  • Motor Neuron Disease
  • Neurodegeneration
  • Neurological disorders
  • Pain
  • Snake
  • Spider
  • Toxins
  • Venoms

Need help?

For help with finding experts, story ideas and media enquiries, contact our Media team:

communications@uq.edu.au