Inositol monophosphatase 1 (IMPA1) mutation in intellectual disability patients impairs neurogenesis but not gliogenesis

Author(s):Show less -

Figueiredo, T. ; Mendes, A. ; Kobayashi, G. ; Moreira, D. ; Oliveira, D. ; Goulart, E. ; Stern, S. ; Kok, F. ; Marchetto, M. ; Santos, R. ; Gage, F. ; Zatz, M.

• Document type: Journal article
• Source: European Journal of Human Genetics; v. 28, n. SUPPL 1, p. 1-pg., 2020-12-01.
• FAPESP's process: 13/08028-1 - CEGH-CEL - Human Genome and Stem Cell Research Center
• Grantee: Mayana Zatz
• Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC
• FAPESP's process: 14/50931-3 - Aging and genetic disorders: genomics and metagenomics
• Grantee: Mayana Zatz
• Support Opportunities: Research Projects - Thematic Grants
• FAPESP's process: 16/09618-5 - What is the role of IMPA1 enzyme in Familial Intellectual Disability?
• Grantee: Thalita Cristina Figueiredo Cunha
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• FAPESP's process: 17/19877-0 - Understanding the role of IMPA1 mutation in hippocampal neurons derived from patients with familial intellectual disability
• Grantee: Thalita Cristina Figueiredo Cunha
• Support Opportunities: Scholarships abroad - Research Internship - Post-doctor