نتائج البحث

CX3CR1–Fractalkine Dysregulation Affects Retinal GFAP Expression, Inflammatory Gene Induction, and LPS Response in a Mouse Model of Hypoxic Retinopathy.

• Authors : Rorex, Colin^1,2 (AUTHOR); Cardona, Sandra M.^1,2 (AUTHOR); Church, Kaira A.^1,2 (AUTHOR)

• Source: International Journal of Molecular Sciences. Feb2025, Vol. 26 Issue 3, p1131. 21p.

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The Role of Fractalkine in Diabetic Retinopathy: Pathophysiology and Clinical Implications.

• Authors : Lee, Cheng-Yung^1,2,3 (AUTHOR); Yang, Chang-Hao^2,3,4 (AUTHOR)

Subjects: *DIABETIC retinopathy; *DIABETES complications; *MICROCIRCULATION disorders

• Source: International Journal of Molecular Sciences. Jan2025, Vol. 26 Issue 1, p378. 18p.

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An Evidence-Based Narrative Review of Scleral Hypoxia Theory in Myopia: From Mechanisms to Treatments.

• Authors : Xiao, Qin^1,2 (AUTHOR) ; Zhang, Xiang¹ (AUTHOR) ; Chen, Zhang-Lin¹ (AUTHOR)

Subjects: *EYE diseases; *VISION disorders; *MYOPIA

• Source: International Journal of Molecular Sciences. Jan2025, Vol. 26 Issue 1, p332. 19p.

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JAG1/Notch Pathway Inhibition Induces Ferroptosis and Promotes Cataractogenesis.

• Authors : Ni, Yan^1,2 (AUTHOR) ; Liu, Liangping^1,2 (AUTHOR) ; Jiang, Fanying^1,2 (AUTHOR)

Subjects: *NUCLEAR factor E2 related factor; *NOTCH signaling pathway; *NOTCH genes

• Source: International Journal of Molecular Sciences. Jan2025, Vol. 26 Issue 1, p307. 15p.

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Stem Cell-Based Therapies for Glaucoma Treatment: A Review Bridging the Gap in Veterinary Patients.

• Authors : de Sousa Moreira, Alícia^1,2,3 (AUTHOR) ; Lopes, Bruna^1,2,3 (AUTHOR) ; Sousa, Ana Catarina^1,2,3 (AUTHOR)

Subjects: *MESENCHYMAL stem cells; *VETERINARY medicine; *VETERINARY ophthalmology

• Source: International Journal of Molecular Sciences. Jan2025, Vol. 26 Issue 1, p232. 22p.

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A Comparative Evaluation of the Genetic Variant Spectrum in the USH2A Gene in Russian Patients with Isolated and Syndromic Forms of Retinitis Pigmentosa.

• Authors : Ogorodova, Natalya¹ (AUTHOR) ; Stepanova, Anna¹ (AUTHOR); Kadyshev, Vitaly¹ (AUTHOR)

Subjects: *VISION disorders; *SENSORINEURAL hearing loss; *RETINITIS pigmentosa

• Source: International Journal of Molecular Sciences. Nov2024, Vol. 25 Issue 22, p12169. 15p.

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Recent Insights into Roles of Hypoxia-Inducible Factors in Retinal Diseases.

• Authors : Lee, Deokho^1,2,3 (AUTHOR); Tomita, Yohei^1,2,3 (AUTHOR); Miwa, Yukihiro^1,3,4 (AUTHOR)

Subjects: *MACULAR degeneration; *HYPOXIA-inducible factors; *RETINAL diseases

• Source: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 18, p10140. 13p.

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Gene Therapy for Achromatopsia.

• Authors : Baxter, Megan F.^1,2 (AUTHOR) ; Borchert, Grace A.^2,3,4 (AUTHOR)

Subjects: *COLOR vision; *COLOR blindness; *GENE therapy

• Source: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9739. 13p.

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Slc4a7 Regulates Retina Development in Zebrafish.

• Authors : Zhuang, Youyuan^1,2,3 (AUTHOR) ; Li, Dandan^1,2,3 (AUTHOR) ; Tang, Cheng^1,2,3 (AUTHOR)

Subjects: *RETINAL degeneration; *VISION disorders; *GENETIC disorders

• Source: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9613. 18p.

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Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9.

• Authors : Stellacci, Emilia¹ (AUTHOR) ; Niceta, Marcello² (AUTHOR) ; Bruselles, Alessandro¹ (AUTHOR)

Subjects: *WHOLE genome sequencing; *MISSENSE mutation; *RETINITIS pigmentosa

• Source: International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 15, p8313. 13p.

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