Yamaji Y - Search Results

1

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

Yoshida S, Yamaji Y, Yoshida A, Ikeda Y, Yamamoto K, Ishibashi T. Yoshida S, et al. Among authors: yamaji y. Mol Vis. 2006 Dec 6;12:1552-7. Mol Vis. 2006. PMID: 17200654 Free article.

2

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

Yoshida S, Yamaji Y, Yoshida A, Noda Y, Kumano Y, Ishibashi T. Yoshida S, et al. Among authors: yamaji y. Hum Genet. 2005 May;116(6):518-24. doi: 10.1007/s00439-005-1269-0. Epub 2005 Mar 3. Hum Genet. 2005. PMID: 15744520

3

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

Yoshida S, Yamaji Y, Yoshida A, Kuwahara R, Yamamoto K, Kubata T, Ishibashi T. Yoshida S, et al. Among authors: yamaji y. Mol Vis. 2006 Dec 6;12:1558-64. Mol Vis. 2006. PMID: 17200655 Free article.

4

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

Yoshimura K, Yoshida S, Yamaji Y, Komori A, Yoshida A, Hatae K, Kubota T, Ishibashi T. Yoshimura K, et al. Among authors: yamaji y. Am J Ophthalmol. 2005 Apr;139(4):733-5. doi: 10.1016/j.ajo.2004.10.002. Am J Ophthalmol. 2005. PMID: 15808183

5

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

Yoshida S, Yamaji Y, Yoshida A, Kuwahara R, Fujisawa K, Ishibashi T. Yoshida S, et al. Among authors: yamaji y. Can J Ophthalmol. 2006 Oct;41(5):614-6. doi: 10.1016/S0008-4182(06)80034-7. Can J Ophthalmol. 2006. PMID: 17016536

6

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

Yoshida S, Ogura A, Ishikawa K, Yoshida A, Kohno R, Yamaji Y, Ikeo K, Gojobori T, Kono T, Ishibashi T. Yoshida S, et al. Among authors: yamaji y. Br J Ophthalmol. 2010 Jun;94(6):795-801. doi: 10.1136/bjo.2009.167072. Epub 2009 Nov 16. Br J Ophthalmol. 2010. PMID: 19919945

7

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

Yamaji Y, Yoshida S, Ishikawa K, Sengoku A, Sato K, Yoshida A, Kuwahara R, Ohuchida K, Oki E, Enaida H, Fujisawa K, Kono T, Ishibashi T. Yamaji Y, et al. Invest Ophthalmol Vis Sci. 2008 Jul;49(7):3151-7. doi: 10.1167/iovs.07-1249. Epub 2008 Mar 3. Invest Ophthalmol Vis Sci. 2008. PMID: 18316703

8

[Molecular genetic analysis of inherited ocular diseases].

Yoshida S, Yamaji Y, Kuwahara R, Murata T. Yoshida S, et al. Among authors: yamaji y. Nihon Rinsho. 2005 Dec;63 Suppl 12:264-8. Nihon Rinsho. 2005. PMID: 16416805 Review. Japanese. No abstract available.

9

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

Yoshida S, Yamaji Y, Kuwahara R, Yoshida A, Hisatomi T, Ueno A, Ishibashi T. Yoshida S, et al. Among authors: yamaji y. Eye (Lond). 2006 Jun;20(6):743-5. doi: 10.1038/sj.eye.6702001. Epub 2005 Jul 8. Eye (Lond). 2006. PMID: 16021188 No abstract available.

10

NEMO mutational analysis in a Japanese family with incontinentia pigmenti.

Tada H, Yoshida S, Yamaji Y, Fujisawa K, Ishibashi T. Tada H, et al. Among authors: yamaji y. Eye (Lond). 2007 Jun;21(6):888-90. doi: 10.1038/sj.eye.6702770. Epub 2007 Mar 30. Eye (Lond). 2007. PMID: 17401323 No abstract available.

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