Daiji Kiyozumi Selected Research

Fraser Syndrome

1/2020	Genetic mutation of Frem3 does not causeFraser syndrome in mice.
5/2012	Basement membrane assembly of the integrin α8β1 ligand nephronectin requires Fraser syndrome-associated proteins.
7/2011	Fused pulmonary lobes is a rat model of human Fraser syndrome.
4/2010	Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genes.
8/2006	Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!

Daiji Kiyozumi Research Topics

Disease

5	Fraser Syndrome 01/2020 - 08/2006
3	Syndactyly (Polysyndactyly) 05/2012 - 08/2006
1	Male Infertility (Male Sterility) 01/2019
1	Bilateral Frontoparietal Polymicrogyria 01/2013
1	Epidermolysis Bullosa Dystrophica (Dystrophic Epidermolysis Bullosa) 05/2012
1	Blister (Bulla) 04/2010

Drug/Important Bio-Agent (IBA)

5	Proteins (Proteins, Gene)FDA Link 01/2020 - 08/2006
1	Male Contraceptive Agents (Male Contraceptives)IBA 01/2019
1	G-Protein-Coupled Receptors (Receptors, G Protein Coupled)IBA 01/2013
1	LigandsIBA 05/2012
1	IntegrinsIBA 05/2012
1	nephronectinIBA 05/2012
1	FurinIBA 04/2010