Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Cataract and LOXL1[original query] |
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LOXL1 genetic polymorphisms are associated with exfoliation glaucoma in the Japanese population. Molecular vision 2008 14 1037-40. Mori K, Imai K, Matsuda A, Ikeda Y, Naruse S, Hitora-Takeshita H, Nakano M, Taniguchi T, Omi N, Tashiro K, Kinoshita S |
LOXL1 variants in elderly Japanese patients with exfoliation syndrome/glaucoma, primary open-angle glaucoma, normal tension glaucoma, and cataract. Molecular vision 2008 14 1898-905. Tanito Masaki, Minami Masayoshi, Akahori Masakazu, Kaidzu Sachiko, Takai Yasuyuki, Ohira Akihiro, Iwata Takes |
Lack of association of LOXL1 gene variants in Japanese patients with central retinal vein occlusion without clinically detectable pseudoexfoliation material deposits. Acta ophthalmologica 2015 May 93 (3): e214-7. Tanito Masaki, Hara Katsunori, Akahori Masakazu, Harata Ayano, Itabashi Takeshi, Takai Yasuyuki, Kaidzu Sachiko, Ohira Akihiro, Iwata Takes |
[Evaluation of LOXL1 polymorphisms in exfoliation syndrome in the Uygur population]. [Zhonghua yan ke za zhi] Chinese journal of ophthalmology 2014 Feb 50 (2): 126-32. Ma Yinu, Xie Tingyu, Zhu Guowei, Chen Xue |
Correlation of Aqueous Humor Lysyl Oxidase Activity with TGF-ß Levels and LOXL1 Genotype in Pseudoexfoliation. Current eye research 2016 10 41 (10): 1331-1338. Gayathri Ramakrishnan, Coral Karunakaran, Sharmila Ferdinamarie, Sripriya Sarangapani, Sripriya Krishnamoorthy, Manish Panday, Shantha B, Ronnie George, Vijaya Lingam, Narayanasamy Angayarkan |
Lysyl oxidase-like 1 polymorphisms in a southwestern Greek cataract population with pseudoexfoliation syndrome. Clinical ophthalmology (Auckland, N.Z.) 2016 10 161-6. Panoutsopoulos Alexios A, Gartaganis Vassiliki S, Giannakopoulos Marios P, Goumas Panos D, Anastassiou Evangelos D, Gartaganis Sotirios |
Association of LOXL1 Gene Polymorphisms with Exfoliation Glaucoma Patients. Iranian journal of public health 2019 Oct 48 (10): 1827-1837. Taghavi Elham, Daneshvar Ramin, Noormohammadi Zahra, Modarresi Seyed Mohammad-Hossein, Sedaghat Mohammad Re |
Insights into the genetic basis of retinal detachment.
Human molecular genetics 2020 Mar 29 (4): 689-702. Boutin Thibaud S, Charteris David G, Chandra Aman, Campbell Susan, Hayward Caroline, Campbell Archie, , Nandakumar Priyanka, Hinds David, , Mitry Danny, Vitart Veroniq |
Associations of polymorphisms in LOXL1 and copper chaperone genes with pseudoexfoliation-syndrome-related cataract in a Chinese Uygur population. International ophthalmology 2020 Apr . Jing Qinghe, Li Dan, Gao Wei, Zhang Fan, Lu Yi, Jiang Yongxia |
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- Page last updated:Apr 16, 2024
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