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Select item 109969361.

Identification of Novel FZD4 Mutations in Familial Exudative Vitreoretinopathy and Investigating the Pathogenic Mechanisms of FZD4 Mutations

Erkuan Dai, Min Liu, Shujin Li, Xiang Zhang, Shiyuan Wang, Rulian Zhao, Yunqi He, Li Peng, Liting Lv, Haodong Xiao, Mu Yang, Zhenglin Yang, Peiquan Zhao

Invest Ophthalmol Vis Sci. 2024 Apr; 65(4): 1. Published online 2024 Apr 1. doi: 10.1167/iovs.65.4.1

PMCID:: PMC10996936

Abstract Article PDF–12M

Select item 89941672.

FZD4 in a Large Chinese Population With Familial Exudative Vitreoretinopathy: Molecular Characteristics and Clinical Manifestations

Jinglin Lu, Li Huang, Limei Sun, Songshan Li, Zhaotian Zhang, Zhaoxin Jiang, Jiaqing Li, Xiaoyan Ding

Invest Ophthalmol Vis Sci. 2022 Apr; 63(4): 7. Published online 2022 Apr 8. doi: 10.1167/iovs.63.4.7

PMCID:: PMC8994167

Abstract Article PDF–4.9M

Select item 83066493.

Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy

Li Huang, Jinglin Lu, Linyan Zhang, Zhaotian Zhang, Limei Sun, Songshan Li, Ting Zhang, Limei Chen, Liming Cao, Xiaoyan Ding

Genes (Basel) 2021 Jul; 12(7): 980. Published online 2021 Jun 27. doi: 10.3390/genes12070980

PMCID:: PMC8306649

Abstract Article PDF–3.8M

Select item 64088214.

Molecular evolutionary and structural analysis of familial exudative vitreoretinopathy associated FZD4 gene

Suman Seemab, Nashaiman Pervaiz, Rabail Zehra, Saneela Anwar, Yiming Bao, Amir Ali Abbasi

BMC Evol Biol. 2019; 19: 72. Published online 2019 Mar 8. doi: 10.1186/s12862-019-1400-9

PMCID:: PMC6408821

Abstract Article PDF–3.5M

Select item 55335815.

TSPAN12 is a Norrin Co-Receptor that Amplifies Frizzled4 Ligand Selectivity and Signaling

Maria B. Lai, Chi Zhang, Jianli Shi, Verity Johnson, Lavan Khandan, John McVey, Michael W. Klymkowsky, Zhe Chen, Harald J. Junge

Cell Rep. Author manuscript; available in PMC 2017 Jul 28.

Published in final edited form as: Cell Rep. 2017 Jun 27; 19(13): 2809–2822. doi: 10.1016/j.celrep.2017.06.004

PMCID:: PMC5533581

Abstract Article PDF–3.1M

Select item 50346916.

WNT Stimulation Dissociates a Frizzled 4 Inactive-State Complex with Gα_12/13

Elisa Arthofer, Belma Hot, Julian Petersen, Katerina Strakova, Stefan Jäger, Manuel Grundmann, Evi Kostenis, J. Silvio Gutkind, Gunnar Schulte

Mol Pharmacol. 2016 Oct; 90(4): 447–459. Published online 2016 Oct. doi: 10.1124/mol.116.104919

PMCID:: PMC5034691

Abstract Article PDF–3.1M

Select item 49686097.

Novel mutations in FZD4 and phenotype–genotype correlation in Chinese patients with familial exudative vitreoretinopathy

Miao Tang, Xiaoyan Ding, Jiaqing Li, Andina Hu, Miner Yuan, Yu Yang, Zongyi Zhan, Zijing Li, Lin Lu

Mol Vis. 2016; 22: 917–932. Published online 2016 Jul 30.

PMCID:: PMC4968609

Abstract Article PDF–2.9M

Select item 46320818.

Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy

Ping Fei, Xiong Zhu, Zhilin Jiang, Shi Ma, Jing Li, Qi Zhang, Yu Zhou, Yu Xu, Zhengfu Tai, Lin Zhang, Lulin Huang, Zhenglin Yang, Peiquan Zhao, Xianjun Zhu

Sci Rep. 2015; 5: 16120. Published online 2015 Nov 4. doi: 10.1038/srep16120

PMCID:: PMC4632081

Abstract Article PDF–883K

Select item 19207889.

Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity

H Kondo, H Hayashi, K Oshima, T Tahira, K Hayashi

Br J Ophthalmol. 2003 Oct; 87(10): 1291–1295. doi: 10.1136/bjo.87.10.1291

PMCID:: PMC1920788

Abstract Article PDF–1.3M

Select item 1098116410.

Investigating the Impact of Dimer Interface Mutations on Norrin's Secretion and Norrin/β-Catenin Pathway Activation

Min Liu, Erkuan Dai, Mu Yang, Shujin Li, Lin Fan, Yining Liu, Haodong Xiao, Peiquan Zhao, Zhenglin Yang

Invest Ophthalmol Vis Sci. 2024 Mar; 65(3): 31. Published online 2024 Mar 22. doi: 10.1167/iovs.65.3.31

PMCID:: PMC10981164

Abstract Article PDF–6.2M

Select item 1078145911.

A regulatory circuit of lncRNA NLGN1-AS1 and Wnt signalling controls clear cell renal cell carcinoma phenotypes through FZD4-modulated pathways

Haifeng Gao, Wei Chen, Gaojian Pan, Hui Liu, Jinke Qian, Weijun Tang, Wei Wang, Shilei Qian

Aging (Albany NY) 2023 Dec 31; 15(24): 15624–15639. Published online 2022 Sep 27. doi: 10.18632/aging.204263

PMCID:: PMC10781459

Abstract Article PDF–1.5M

Select item 864806412.

Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy

Tianchang Tao, Ningda Xu, Jiarui Li, Hongyan Li, Jinfeng Qu, Hong Yin, Jianhong Liang, Mingwei Zhao, Xiaoxin Li, Lvzhen Huang

Invest Ophthalmol Vis Sci. 2021 Dec; 62(15): 4. Published online 2021 Dec 3. doi: 10.1167/iovs.62.15.4

PMCID:: PMC8648064

Abstract Article PDF–3.2M

Select item 738297813.

Frizzled-4 is required for normal bone acquisition despite compensation by Frizzled-8

Priyanka Kushwaha, Soohyun Kim, Gabrielle E. Foxa, Megan N. Michalski, Bart O. Williams, Ryan E. Tomlinson, Ryan C. Riddle

J Cell Physiol. Author manuscript; available in PMC 2021 Oct 1.

Published in final edited form as: J Cell Physiol. 2020 Oct; 235(10): 6673–6683. Published online 2020 Jan 27. doi: 10.1002/jcp.29563

PMCID:: PMC7382978

Abstract Article PDF–1.0M

Select item 720172114.

Role of NDP- and FZD4-Related Novel Mutations Identified in Patients with FEVR in Norrin/β-Catenin Signaling Pathway

Shuai Han, Junhui Sun, Liwei Yang, Ming Qi

Biomed Res Int. 2020; 2020: 7681926. Published online 2020 Apr 27. doi: 10.1155/2020/7681926

PMCID:: PMC7201721

Abstract Article PDF–2.4M

Select item 637737615.

Variable reduction in Norrin signaling activity caused by novel mutations in FZD4 identified in patients with familial exudative vitreoretinopathy

Tian Tian, Xiang Zhang, Qi Zhang, Peiquan Zhao

Mol Vis. 2019; 25: 60–69. Published online 2019 Feb 7.

PMCID:: PMC6377376

Abstract Article PDF–3.3M

Select item 556722816.

A miR-SNP biomarker linked to an increased lung cancer survival by miRNA-mediated down-regulation of FZD4 expression and Wnt signaling

Jing Lin, Roza Zandi, Ruping Shao, Jian Gu, Yuanqin Ye, Jing Wang, Yang Zhao, Alexander Pertsemlidis, Ignacio I. Wistuba, Xifeng Wu, Jack A. Roth, Lin Ji

Sci Rep. 2017; 7: 9029. Published online 2017 Aug 22. doi: 10.1038/s41598-017-09604-4

PMCID:: PMC5567228

Abstract Article PDF–2.2M

Select item 545875817.

Wnt5a promotes Frizzled-4 signalosome assembly by stabilizing cysteine-rich domain dimerization

Zachary J. DeBruine, Jiyuan Ke, Kaleeckal G. Harikumar, Xin Gu, Peter Borowsky, Bart O. Williams, Wenqing Xu, Laurence J. Miller, H. Eric Xu, Karsten Melcher

Genes Dev. 2017 May 1; 31(9): 916–926. doi: 10.1101/gad.298331.117

PMCID:: PMC5458758

Abstract Article PDF–447K

Select item 449740918.

Structure and functional properties of Norrin mimic Wnt for signalling with Frizzled4, Lrp5/6, and proteoglycan

Tao-Hsin Chang, Fu-Lien Hsieh, Matthias Zebisch, Karl Harlos, Jonathan Elegheert, E Yvonne Jones

eLife. 2015; 4: e06554. Published online 2015 Jul 9. doi: 10.7554/eLife.06554

PMCID:: PMC4497409

Abstract Article PDF–6.5M

Select item 436599019.

Next-Generation Sequencing and Novel Variant Determination in a Cohort of 92 Familial Exudative Vitreoretinopathy Patients

Jason Salvo, Vera Lyubasyuk, Mingchu Xu, Hui Wang, Feng Wang, Duy Nguyen, Keqing Wang, Hongrong Luo, Cindy Wen, Catherine Shi, Danni Lin, Kang Zhang, Rui Chen

Invest Ophthalmol Vis Sci. 2015 Mar; 56(3): 1937–1946. Published online 2015 Mar 19. doi: 10.1167/iovs.14-16065

PMCID:: PMC4365990

Abstract Article PDF–923K

Select item 358099220.

Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity

Hiroyuki Kondo, Shunji Kusaka, Aki Yoshinaga, Eiichi Uchio, Akihiko Tawara, Tomoko Tahira

Mol Vis. 2013; 19: 476–485. Published online 2013 Feb 25.

PMCID:: PMC3580992

Abstract Article PDF–1.4M

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PMC Links for Gene (Select 8322) (45)
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Homo sapiens chromosome X protocadherin 11 (PCDH11) mRNA, complete cds, alternat...
Homo sapiens chromosome X protocadherin 11 (PCDH11) mRNA, complete cds, alternatively spliced
gi|13161065|gb|AF332219.1|
Homo sapiens lysyl oxidase-related protein C (LOXC) mRNA, complete cds
Homo sapiens lysyl oxidase-related protein C (LOXC) mRNA, complete cds
gi|14669470|gb|AF338441.1|

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