Y. Yamaji

发表

Gene expression profile of fibrovascular membranes from patients with proliferative diabetic retinopathy

T. Gojobori, K. Ikeo, S. Yoshida, 2009, British Journal of Ophthalmology.

De novo insG619 mutation in PAX2 gene in a Japanese patient with papillorenal syndrome.

S. Yoshida, A. Yoshida, T. Ishibashi, 2005, American journal of ophthalmology.

Prognostic DNA testing and counselling for dominant optic atrophy due to a novel OPA1 mutation.

S. Yoshida, A. Yoshida, T. Ishibashi, 2006, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Rapid genotyping for most common TGFBI mutations with real-time polymerase chain reaction

S. Yoshida, A. Yoshida, T. Ishibashi, 2005, Human Genetics.

CRMP-5-IgG in patient with paraneoplastic optic neuritis with lung adenocarcinoma

S. Yoshida, Y. Murakami, T. Ishibashi, 2007, Eye.

TEM7 (PLXDC1) in neovascular endothelial cells of fibrovascular membranes from patients with proliferative diabetic retinopathy.

E. Oki, K. Ohuchida, S. Yoshida, 2008, Investigative ophthalmology & visual science.

Rapid detection of SAG 926delA mutation using real-time polymerase chain reaction.

S. Yoshida, A. Yoshida, T. Ishibashi, 2006, Molecular vision.

Novel triple missense mutations of GUCY2D gene in Japanese family with cone-rod dystrophy: possible use of genotyping microarray.

S. Yoshida, A. Yoshida, T. Ishibashi, 2006, Molecular vision.

NEMO mutational analysis in a Japanese family with incontinentia pigmenti

T. Ishibashi, Y. Yamaji, K. Fujisawa, 2007, Eye.

Novel mutation in exon 2 of COL2A1 gene in Japanese family with Stickler Syndrome type I

A. Yoshida, T. Hisatomi, T. Ishibashi, 2006, Eye.

Case of novel PITX2 gene mutation associated with Peters' anomaly and persistent hyperplastic primary vitreous

S. Yoshida, A. Ueno, K. Ishikawa, 2010, Eye.