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期刊名:Molecular vision

缩写:MOL VIS

ISSN:1090-0535

e-ISSN:N/A

IF/分区:1.4/Q3

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共收录本刊相关文章索引3930
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Kevin Gregory-Evans,Cheryl Y Gregory-Evans Kevin Gregory-Evans
The fovea is an anatomic specialization of the human retina critical for high visual acuity, color vision, and contrast sensitivity. The molecular and cellular pathways directing this focal topography are still to be determined. Abnormaliti...
Dorota Wicher,Danuta Sielska-Rotblum,Urszula Zawadzka-Wiech et al. Dorota Wicher et al.
Purpose: Retinoblastoma, the most common eye tumor in children, can occur in hereditary or nonhereditary forms. In the hereditary form, various germline alterations, single nucleotide (SNVs) or copy number variations (CNV...
Moncef Ould Hamou,Maureen Masset,Célia Weber et al. Moncef Ould Hamou et al.
Purpose: Diabetes is a chronic inflammatory disease that may damage the blood-retinal barrier, leading to diabetic retinopathy (DR). Blood-retinal barrier rupture may subject the retinal pigmented epithelial cells to a hy...
Hirohiko Kakizaki,Heebae Ahn,Muhammad Abumanhal et al. Hirohiko Kakizaki et al.
Purpose: To characterize the distribution of reticular fibers in the human sclera and explore their potential role in the pathogenesis of pathologic myopia and posterior staphyloma. ...
Tomoaki Araki,Masamitsu Shimazawa,Shinsuke Nakamura et al. Tomoaki Araki et al.
Purpose: We screened 28 female cynomolgus monkeys (CMs) and 25 female rhesus monkeys (RMs) for white dots (WDs) in the macula and detected several animals with WDs in colonies at the Shin Nippon Biomedical Laboratories, L...
Guangrong Zhao,Dayou Ding Guangrong Zhao
Bietti crystalline dystrophy (BCD), an autosomal recessive inherited retinal disorder caused by mutations in the CYP4V2 gene, has long remained therapeutically challenging. Recent advances in adeno-associated virus-based gene therapy have e...
Mangesh Bawankar,Bhaswati Sengupta,Sujata Malik et al. Mangesh Bawankar et al.
Purpose: To characterize the aggregation behavior of the γD-crystallin protein in an acidic environment with a focus on the formation of intermediate species. The research employs fluorescence correlation spectroscopy to...
Zainab Akhtar,Kiran Afshan,Yumei Li et al. Zainab Akhtar et al.
Purpose: Cyclic nucleotide-gated (CNG) channels are ligand-gated ion channels that transduce light signals into electrical signals in the retinal photoreceptors. Pathogenic variants in CNG channel genes are reported to ca...
Andreas Koller,Susanne Maria Brunner,Julia Preishuber-Pflügl et al. Andreas Koller et al.
Purpose: Cysteinyl leukotriene receptor 1 (CysLTR1), originally described as a proinflammatory G protein-coupled receptor, has been shown to possess diverse nonimmunological properties. One of these functions is to modula...
Qiwei Wang,Xiaoshan Lin,Dongni Wang et al. Qiwei Wang et al.
Purpose: Hair anomalies represent a common associated symptom of congenital cataracts. Early diagnosis is crucial for treatment and predicting prognosis. However, the insidious and nonspecific nature of the symptoms in yo...