المؤلفون: Ho, Henry

مصطلحات موضوعية: Norrie disease, Norrin, Tspan12, Wnt/β-catenin pathway, molecular biophysics, none, signaling, structural biology, Eye Proteins, Humans, Wnt Signaling Pathway, Nerve Tissue Proteins, Retina, Animals, Protein Binding

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0rv7k9qh
https://escholarship.org/content/qt0rv7k9qh/qt0rv7k9qh.pdf

المؤلفون: Hsin-Yi Henry Ho

المصدر: eLife, Vol 13 (2024)

مصطلحات موضوعية: signaling, Norrie disease, Wnt/β-catenin pathway, Norrin, Tspan12, Medicine, Science, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://elifesciences.org/articles/98933; https://doaj.org/toc/2050-084X

URL الوصول: https://doaj.org/article/9aea7e51599f42429d675dafdca51d77

المؤلفون: Hsu, S. Tammy^Aff4, Justin, Grant^Aff4, Vajzovic, Lejla^Aff5

المساهمون: Özdek, Şengül, editor^Aff1, Berrocal, Audina, editor^Aff2, Spandau, Ulrich, editor^Aff3

المصدر: Pediatric Vitreoretinal Surgery. :399-407

المؤلفون: Şengül Özdek, Ece Özdemir Zeydanlı, Caroline Baumal, Sandra Hoyek, Nimesh Patel, Audina Berrocal, Ashley Lopez-Cañizares, Hasenin Al-Khersan, Shunji Kusaka, Fukutaro Mano, Subhadra Jalali, Domenico Lepore, Solmaz Akar

المصدر: Türk Oftalmoloji Dergisi, Vol 53, Iss 1, Pp 44-57 (2023)

مصطلحات موضوعية: avascular retina, retinopathy of prematurity, familial exudative vitreoretinopathy, coats disease, incontinentia pigmenti, persistent fetal vasculature, norrie disease, Medicine, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.oftalmoloji.org/archives/archive-detail/article-preview/avascular-peripheral-retina-in-nfants/58684; https://doaj.org/toc/1300-0659; https://doaj.org/toc/2147-2661

URL الوصول: https://doaj.org/article/e34fe9325ef44aa3aafbd00b9fd0c6c0

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المؤلفون: Vincent Le, Gabrielle Abdelmessih, Wendy A. Dailey, Cecille Pinnock, Victoria Jobczyk, Revati Rashingkar, Kimberly A. Drenser, Kenneth P. Mitton

المصدر: Cells, Vol 12, Iss 21, p 2579 (2023)

مصطلحات موضوعية: FEVR, Norrie disease, persistent fetal vascular syndrome, norrin, NDP, FZD4, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/12/21/2579; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/44991ceb75bd4bf8b93a721d0f849f71

المؤلفون: Mahsaw Mansoor, Razek Georges Coussa, Margaret R. Strampe, Scott A. Larson, Jonathan F. Russell

المصدر: American Journal of Ophthalmology Case Reports, Vol 29, Iss , Pp 101798- (2023)

مصطلحات موضوعية: Norrie disease, NDP, Norrin, KDM6A, Kabuki syndrome, Leukocoria, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2451993623000063; https://doaj.org/toc/2451-9936

URL الوصول: https://doaj.org/article/fb780eeb5914483893888a5892956e48

المؤلفون: V. A. Aysina, О. V. Kozhevnikova, О. V. Osipova, A. V. Lashkova

المصدر: Эпилепсия и пароксизмальные состояния, Vol 14, Iss 1, Pp 48-53 (2022)

مصطلحات موضوعية: norrie disease, electroencephalography, epileptic seizures, retinal dysplasia, quality of life, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.epilepsia.su/jour/article/view/774; https://doaj.org/toc/2077-8333; https://doaj.org/toc/2311-4088

URL الوصول: https://doaj.org/article/b207cae3b30c48cc89bc958e94e74298

المؤلفون: Haijun Li, Zhiming Li, Degang Wang, Chuanming Chen, Zhiqiang Chen, Jinhua Wang, Chenxia Xu, Xingsheng Dong

المصدر: Frontiers in Genetics, Vol 13 (2022)

مصطلحات موضوعية: Norrie disease, next-generation sequencing, variant, genetic, NDP, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.870232/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/337160cb36a6469187d5f03ab7c1f58c

المؤلفون: James Wawrzynski, Aara Patel, Abdul Badran, Isaac Dowell, Robert Henderson, Jane C. Sowden

المصدر: Frontiers in Genetics, Vol 13 (2022)

مصطلحات موضوعية: norrie disease, FEVR, retinopathy of prematurity, coats disease, NDP, retinal detachment (RD), Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.884722/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/65a17856df3049389cf8ec0086d7a0b7