University College London Featured PhD Programmes
University College London Featured PhD Programmes
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Biochemistry (cognitive neuroscience) PhD Projects, Programs & Scholarships

We have 6 Biochemistry (cognitive neuroscience) PhD Projects, Programs & Scholarships

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  MVLS Doctoral Training Programme Studentships 2020

Funding Type

PhD Type

 . APPLICATION DEADLINE. 20 JANUARY 2020. Stipend. £15,009 (2019/20 rate). Start Date. 1 October 2020. Fully funded. 3.5 years.
  The influence of Apolipoprotein E genotypes on pathways of neurotransmission measured in vivo. Implications for dementia research
  Dr M De Marco, Prof A Venneri
Applications accepted all year round

Funding Type

PhD Type

Monoaminergic midbrain nuclei are currently emerging as major players in the definition of the pathological changes of early Alzheimer’s disease (AD) stages.
  Discovery and modelling of common molecular mechanisms disrupting hearing in genetic mutations associated with hearing loss
  Prof I D Forsythe, Dr A Lecchini-Visintini
Application Deadline: 12 January 2020

Funding Type

PhD Type

Objectives. Determine the cellular and molecular changes in the auditory brainstem of mice carrying genetic mutations associated with hearing loss and language development and use modelling to evaluate common mechanisms.
  Characterisation of the neuronal receptor for soluble amyloid precursor protein: a route to new therapeutic targets for Alzheimer’s disease
  Prof N Hooper, Prof M J Humphries
Applications accepted all year round

Funding Type

PhD Type

Alzheimer’s disease (AD) is the commonest form of dementia for which currently there is no means of stopping or even slowing the disease.
  MRC DiMeN Doctoral Training Partnership: The in situ 3D molecular structure of Alzheimer’s disease-associated pathology by cryo-electron microscopy
  Dr R Frank, Prof S E Radford, Dr E W Hewitt
Application Deadline: 6 January 2020

Funding Type

PhD Type

Synapses are the microprocessors of the mind that encode and store memories. In Alzheimer’s disease (AD), synapses are damaged by the constituents of abnormal beta-amyloid plaques that accumulate in the brain.
  Oral vitamin D spray as a novel treatment for 22q11 deletion syndrome
  Dr A McNeill, Dr C Mazzà
Applications accepted all year round

Funding Type

PhD Type

22q11 deletion syndrome is the most common genetic disorder, affecting about 1/2500 people (as common as cystic fibrosis). It is due to a small missing piece of chromosome 22 on the long arm (q) at position 11.
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