Research theme for competitive and other funds (2)：
2002 - 2003 Significance of complement regulating factor DAF polymorphism for proteinuria developed in th BUF/Mna rat
1999 - 2000 Analysis of kidney phenotype in the perlecan mutated mouse in which heparan sulfate side chain is removed by the use of ES cell
Papers (31)：
Morita H, Takagi J, Hirase S, Nomura Y, Imai T, Otake K. Coexistence of Two Endocrine Abnormalities: Pituitary Stalk Interrruption Sydrome (PSIS) and Cushing Syndrome. Ann Clin Case Reo. 2019. 4. 1719-1722
Morita H, Sato Y, Wakayama Y, Ayaki M, Hirase S, Takagi J, Otake K, Inui K, Inoue Y, Yoshimura A, et al. Motor-Dominant Peripheral Neuropathy, Polydactyly, Mental Retardation, Kidney Failure, Diabetes Mellitus, and Developmental Delay in the Absence of Retinal Dystrophy: Specturm of Bardet-Biedl Syndrome (BBS). Biome J Sci & Tech Res. 2019. 22. 5
Could Nutrition Serve as a Promising Therapeutic Strategy for Genetic Disease?
(The 2nd Guangzhou International Forum of Disease Oriented Nutrition and Three Disciplinaries Integration to Improve Management of Kidney Nutrition 2019)
A genetic disease “Alport syndrome”, and proposal for new treatment
(1st Gangzhou International Forum on Disease Oriented Nutrition and Dietition 2018)
Heterozygous mutation of alpha 3 chain of collagen type IV (COL4A3) in a large Japanese pedigree with autosomal dominant Alport syndrome showing a typical ultrastructural change in the glomerular basement membrane (GBM) of the kidney
(The13thInternational Congress of HumanGenetics 2018)
Molecular Architecture of the glomerular basement membrane (GBM) and its abnormalities in kidney diseases.
(BIT’s 8thWorld Gene Convention(WGC) 2017)
