Projects
Ascertainment of ROR2 mutations in recessive Robinow syndrome and elucidation of the development profile of ROR1 and ROR2 in humans, from early embryo to adult
Institution
St George's University
Project ID
10063
Project Files
Assessing the relevance of organoids to model inter-individual variation within the Human Cell Atlas initiative
Institution
Max Planck Institute for Evolutionary Anthropology
Project ID
200375
Project Files
Assessment of cell cycle state in cephalic epithelium during human midface morphogenesis
Institution
University of California
Project ID
200570
Project Files
Assessment of cell cycle state in cephalic epithelium during human midface morphogenesis [IHGES]
Institution
University of California, San Francisco
Project ID
200673
Project Files
Assessment of cis-acting effects on the expression of neuropsychiatric genes
Institution
King's College London
Project ID
10178
B and T cell developmental origin
Institution
Wellcome Sanger Institute
Project ID
200681
Project Files
Biodiversity Gallery
Institution
Hong Kong Science Museum
Project ID
200255
Biological function and clinical implications of the novel FRMD7 gene; the first gene to be associated with infantile nystagmus
Institution
Leicester University
Project ID
200081
Breakdown of the endoderm during middle ear cavitation
Institution
King's College London
Project ID
200243
Cardiac inflow in human embryos
Institution
Newcastle University
Project ID
200101