Yoshida A - 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: yoshida a. 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: yoshida a. 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: yoshida a. Mol Vis. 2006 Dec 6;12:1558-64. Mol Vis. 2006. PMID: 17200655 Free article.

4

Two brothers with gelatinous drop-like dystrophy at different stages of the disease: role of mutational analysis.

Yoshida S, Kumano Y, Yoshida A, Numa S, Yabe N, Hisatomi T, Nishida T, Ishibashi T, Matsui T. Yoshida S, et al. Among authors: yoshida a. Am J Ophthalmol. 2002 Jun;133(6):830-2. doi: 10.1016/s0002-9394(02)01407-1. Am J Ophthalmol. 2002. PMID: 12036680

5

An analysis of BIGH3 mutations in patients with corneal dystrophies in the Kyushu district of Japan.

Yoshida S, Kumano Y, Yoshida A, Hisatomi T, Matsui H, Nishida T, Ishibashi T, Matsui T. Yoshida S, et al. Among authors: yoshida a. Jpn J Ophthalmol. 2002 Jul-Aug;46(4):469-71. doi: 10.1016/s0021-5155(02)00528-2. Jpn J Ophthalmol. 2002. PMID: 12225829

6

Induction of IL-8, MCP-1, and bFGF by TNF-alpha in retinal glial cells: implications for retinal neovascularization during post-ischemic inflammation.

Yoshida S, Yoshida A, Ishibashi T. Yoshida S, et al. Among authors: yoshida a. Graefes Arch Clin Exp Ophthalmol. 2004 May;242(5):409-13. doi: 10.1007/s00417-004-0874-2. Epub 2004 Mar 17. Graefes Arch Clin Exp Ophthalmol. 2004. PMID: 15029502

7

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: yoshida s, yoshida a. Am J Ophthalmol. 2005 Apr;139(4):733-5. doi: 10.1016/j.ajo.2004.10.002. Am J Ophthalmol. 2005. PMID: 15808183

8

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: yoshida a. Can J Ophthalmol. 2006 Oct;41(5):614-6. doi: 10.1016/S0008-4182(06)80034-7. Can J Ophthalmol. 2006. PMID: 17016536

9

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: yoshida a. 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

10

Involvement of macrophage chemotactic protein-1 and interleukin-1beta during inflammatory but not basic fibroblast growth factor-dependent neovascularization in the mouse cornea.

Yoshida S, Yoshida A, Matsui H, Takada Y, Ishibashi T. Yoshida S, et al. Among authors: yoshida a. Lab Invest. 2003 Jul;83(7):927-38. doi: 10.1097/01.lab.0000075642.11787.83. Lab Invest. 2003. PMID: 12861033 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,367 results

Search Page

Filters