Projects
To Investigate functions of candidate genes in mitochondrial disease with combined respiratory complex deficiency
Institution
Newcastle University
Project ID
200133
Expression of Protocadherins 11X and 11Y during embryonic and fetal brain development
Institution
University of Oxford
Project ID
200132
Isolation and characterisation of stem cells during development of the human heart
Institution
Newcastle University
Project ID
200131
Investigating the relationship between corneal structure and function
Institution
Cardiff University
Project ID
200130
Identification of a novel gene for primary microcephaly in humans
Institution
University College London
Project ID
200129
Dissecting the expression patterns of two isoforms of the gene PCSK6, a gene assiciated with handedness
Institution
University of Oxford
Project ID
200128
The role of cilla-related genes in human embryonic lungs and kidneys
Institution
Kingston University
Project ID
200127
Transplant of human embryonic stem cell and human induced pluripotent stem cell-derived photoreceptors into Crx, Prph2 and rd1 mice
Institution
Newcastle University
Project ID
200126
CYP21 gene and pseudogene expression in human embryos
Institution
Newcastle University
Project ID
200125
Investigation of the endogenous channel modifier LYPD1 in the developing foetus
Institution
Newcastle University
Project ID
200124