ARDC Research Link Australia Research Link Australia   BETA Research
Link
Australia
  • ARDC Newsletter Subscribe
  • Contact Us
  • Home
  • About
  • Feedback
  • Explore Collaborations
  • Researcher
  • Funded Activity
  • Organisation
  • Researcher
  • Funded Activity
  • Organisation
  • Researcher
  • Funded Activity
  • Organisation

Need help searching? View our Search Guide.

Advanced Search

Current Selection
Research Topic : SYNAPSE FORMATION
Scheme : NHMRC Project Grants
Clear All
Filter by Field of Research
Orthopaedics (8)
Medical and Health Sciences (7)
Nutritional science (6)
Endocrinology (5)
Haematology (5)
Cell Development (Incl. Cell Division And Apoptosis) (3)
Food properties (incl. characteristics and health benefits) (3)
Applied immunology (incl. antibody engineering xenotransplantation and t-cell therapies) (2)
Cellular Interactions (incl. Adhesion, Matrix, Cell Wall) (2)
Reproduction (2)
Biochemistry And Cell Biology Not Elsewhere Classified (1)
Cellular Interactions (Incl. Adhesion, Matrix, Cell Wall) (1)
Cellular Nervous System (1)
Central Nervous System (1)
Developmental Genetics (incl. Sex Determination) (1)
Enzymes (1)
Foetal Development and Medicine (1)
Gene Expression (1)
Medical infection agents (incl. prions) (1)
Medical microbiology not elsewhere classified (1)
Medical parasitology (1)
Medical physiology not elsewhere classified (1)
Neurogenetics (1)
Nutrigenomics and personalised nutrition (1)
Oral and maxillofacial surgery (1)
Rheumatology and Arthritis (1)
Filter by Socio-Economic Objective
Search did not return any results.
Filter by Funding Provider
National Health and Medical Research Council (77)
Filter by Status
Closed (77)
Filter by Scheme
NHMRC Project Grants (77)
Filter by Country
Australia (1)
Filter by Australian State/Territory
NSW (1)
  • Researchers (0)
  • Funded Activities (77)
  • Organisations (0)
  • Funded Activity

    Synaptic Development In The Abscence Of B2-laminin, Agrin And Rapsyn

    Funder
    National Health and Medical Research Council
    Funding Amount
    $147,117.00
    More information
    Funded Activity

    Molecular Mechanisms Involved In The Formation, Maintenance And Viability Of Synapses.

    Funder
    National Health and Medical Research Council
    Funding Amount
    $213,613.00
    More information
    Funded Activity

    Organisation Of Nerve To Muscle Signalling Molecules

    Funder
    National Health and Medical Research Council
    Funding Amount
    $145,414.00
    More information
    Funded Activity

    Mutations Affecting Nerve - Muscle Connection

    Funder
    National Health and Medical Research Council
    Funding Amount
    $148,460.00
    More information
    Funded Activity

    SEZ6 AND NEURONAL CALCIUM SIGNALLING IN SYNAPSE DEVELOPMENT

    Funder
    National Health and Medical Research Council
    Funding Amount
    $617,685.00
    Summary
    Inappropriate development and function of neuronal circuits is a universal feature of neurological disorders of cognition such as Down syndrome, autism spectrum disorders and Fragile X mental retardation, epilepsy, schizophrenia and Alzheimer�s disease. In these diseases, neurons exhibit abnormal neuronal branches (dendrites) and abnormal connections on dendritic spines. This research is aimed at understanding the mechanisms controlling dendrite development that underpin proper neuronal wiring.
    More information
    Funded Activity

    Protein Partners Of Rapsyn That Regulate Acetylcholine Receptor Clustering

    Funder
    National Health and Medical Research Council
    Funding Amount
    $411,000.00
    Summary
    Spinal nerves control our limb muscles by releasing chemical signals directly onto the surface of muscle fibres that they contact. These chemical signalling contacts are called synapses. They are like the synapses between nerve cells in our brains but easier to study, meaning that we can make more rapid progress in understanding how synapses work. The sensor receptors for chemical signals at the nerve-to-muscle synapse are held in place on the muscle fibre surface by a protein called rapsyn. In .... Spinal nerves control our limb muscles by releasing chemical signals directly onto the surface of muscle fibres that they contact. These chemical signalling contacts are called synapses. They are like the synapses between nerve cells in our brains but easier to study, meaning that we can make more rapid progress in understanding how synapses work. The sensor receptors for chemical signals at the nerve-to-muscle synapse are held in place on the muscle fibre surface by a protein called rapsyn. In turn, rapsyn must be organized by other chemical signals from the nerve, but we don't know exactly how this happens. When the receptors become disorganized at the synapse, in diseases such as Myasthenia Gravis, we lose control of our muscles. This project will employ newly developing techniques of proteomics and genomics to identify new proteins that bind to rapsyn and to test how they work to organize receptors at the synapse. By identifying the proteins that control rapsyn we may be able to develop new treatments for Myasthenia Gravis that restore the function of the synapse with less side effects than current therapies.
    Read more Read less
    More information
    Funded Activity

    MECHANISMS OF TRANSMITTER SECRETION AT PREGANGLIONIC NERVE TERMINALS

    Funder
    National Health and Medical Research Council
    Funding Amount
    $341,169.00
    More information
    Funded Activity

    Protein Phosphorylation Events In Long Term Potentiation

    Funder
    National Health and Medical Research Council
    Funding Amount
    $347,423.00
    More information
    Funded Activity

    Mechanisms Underlying Inhibitory Glycinergic Transmission In The Central Nervous System

    Funder
    National Health and Medical Research Council
    Funding Amount
    $113,307.00
    More information
    Funded Activity

    Neurodevelopmental Role Of Susceptibility Genes For Autism Spectrum Disorders: From Genes To Behaviour

    Funder
    National Health and Medical Research Council
    Funding Amount
    $482,968.00
    Summary
    Autism is a developmental neuropsychiatric syndrome characterised by impairments in three principal domains: social interaction, language and behavioural inflexibility. Autism spectrum disorder (ASD) refers to a group of neurodevelopmental syndromes with the common feature of dysfunctional reciprocal social interaction. In this project we will investigate the role of genes that increase the risk of ASD in the development of behaviours using an animal model. This work will lead to a better unders .... Autism is a developmental neuropsychiatric syndrome characterised by impairments in three principal domains: social interaction, language and behavioural inflexibility. Autism spectrum disorder (ASD) refers to a group of neurodevelopmental syndromes with the common feature of dysfunctional reciprocal social interaction. In this project we will investigate the role of genes that increase the risk of ASD in the development of behaviours using an animal model. This work will lead to a better understanding of the genetic basis of ASD.
    Read more Read less
    More information

    Showing 1-10 of 77 Funded Activites

    • 1
    • 2
    • 3
    • 4
    • 5
    Advanced Search

    Advanced search on the Researcher index.

    Advanced search on the Funded Activity index.

    Advanced search on the Organisation index.

    National Collaborative Research Infrastructure Strategy

    The Australian Research Data Commons is enabled by NCRIS.

    ARDC CONNECT NEWSLETTER

    Subscribe to the ARDC Connect Newsletter to keep up-to-date with the latest digital research news, events, resources, career opportunities and more.

    Subscribe

    Quick Links

    • Home
    • About Research Link Australia
    • Product Roadmap
    • Documentation
    • Disclaimer
    • Contact ARDC

    We acknowledge and celebrate the First Australians on whose traditional lands we live and work, and we pay our respects to Elders past, present and emerging.

    Copyright © ARDC. ACN 633 798 857 Terms and Conditions Privacy Policy Accessibility Statement
    Top
    Quick Feedback