ライフサイエンスコーパス: Vogt

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1 Vogt et al. demonstrate that, in mice, maternal high-fat

2 Vogt-Koyanagi-Harada (VKH) disease affects primarily per

3 worse for uveitis related to Behcet disease, Vogt-Koyanagi-Harada disease, or sympathetic ophthalmia,

4 ced expression in bacteria grown in Dulbecco-Vogt modified Eagle's medium compared to bacteria grown

5 To identify new genetic risk factors for Vogt-Koyanagi-Harada (VKH) syndrome, we conducted a geno

6 ific syndromes, the incidence was greater in Vogt-Koyanagi-Harada syndrome (aHR, 3.37; 95% CI, 1.52 t

7 In this issue of the JCI, Vogt et al. show that the B7 family-related protein V-se

8 ow recognised as separate: B. lantschouensis Vogt n. stat. and B. minshanensis Bischoff n. stat..

9 ncontact method for imaging the palisades of Vogt by correlating OCT and confocal microscopy images.

10 Pigmented palisades of Vogt revealed large superficial squamous cells and small

11 g of the limbus revealed normal palisades of Vogt structure and epithelial transition in the healthy

12 cessfully identified the limbal palisades of Vogt that constitute the corneal epithelial stem cell ni

13 he distinctive structure of the palisades of Vogt was found only in 2 of 6 harvested sites.

14 Palisades of Vogt were absent in all (100.0%) patients, and the corne

15 the thinnest stroma without any palisades of Vogt-like niche structure.

16 s reside, such as rete pegs and palisades of Vogt.

17 ation and anatomy of the limbal palisades of Vogt.

18 found to be involved in the pathogenesis of Vogt-Koyanagi-Harada (VKH) disease.

19 ort the proposed immunologic pathogenesis of Vogt-Koyanagi-Harada disease are discussed.

20 he aspect of Bowman's layer, the presence of Vogt's striae, and stromal opacities.

21 Two reports of Vogt-Koyanagi-Harada syndrome in 4-year-old children are

22 CGA) findings in patients with long-standing Vogt-Koyanagi-Harada (VKH) disease and their correlation

23 ms (SNP) of IL-1 and IL-1R family genes with Vogt-Koyanagi-Harada (VKH) and Behcet's disease (BD) in

24 virus DNA in the vitreous of a patient with Vogt-Koyanagi-Harada syndrome is reviewed.

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