Detrimental effects of Notch1 signaling activated by cadmium in renal proximal tubular epithelial cells

بواسطة Fujiki, K, Inamura, H, Matsuoka, M
الحاوية / القاعدة Cell Death Dis (2014)

Corneal amyloidosis caused by Leu518Pro mutation of βig-h3 gene

بواسطة Hirano, K., Hotta, Y., Fujiki, K., Kanai, A.
منشور في 2000

An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

بواسطة Hotta, Y, Hayakawa, M, Fujiki, K, Shinohara, K, Sado, K, Kanai, A, Yanashima, K
منشور في 1993

Mutations in the Norrie disease gene: a new mutation in a Japanese family.

بواسطة Isashiki, Y, Ohba, N, Yanagita, T, Hokita, N, Hotta, Y, Hayakawa, M, Fujiki, K, Tanabe, U
منشور في 1995

H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people

بواسطة Chau, H M, Ha, N T, Cung, L X, Thanh, T K, Fujiki, K, Murakami, A, Kanai, A
منشور في 2003

Genetic evidence for CFTR dysfunction in Japanese: background for chronic pancreatitis

بواسطة Fujiki, K, Ishiguro, H, Ko, S, Mizuno, N, Suzuki, Y, Takemura, T, Yamamoto, A, Yoshikawa, T, Kitagawa, M, Hayakawa, T, Sakai, Y, Takayama, T, Saito, M, Kondo, T, Naruse, S
منشور في 2004