165 related articles for article (PubMed ID: 37554197)
1. Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy.
Li S; Yang M; Zhao R; Peng L; Liu W; Jiang X; He Y; Dai E; Zhang L; Yang Y; Shi Y; Zhao P; Yang Z; Zhu X
Genes Dis; 2023 Nov; 10(6):2572-2585. PubMed ID: 37554197
[TBL] [Abstract][Full Text] [Related]
2. Novel truncating variants in
He Y; Yang M; Zhao R; Peng L; Dai E; Huang L; Zhao P; Li S; Yang Z
J Med Genet; 2023 Feb; 60(2):174-182. PubMed ID: 35361685
[TBL] [Abstract][Full Text] [Related]
3. The ER membrane protein complex subunit Emc3 controls angiogenesis via the FZD4/WNT signaling axis.
Yang M; Li S; Liu W; Li X; He Y; Yang Y; Sun K; Zhang L; Tian W; Duan L; Chen H; Yao D; Yang Z; Zhu X
Sci China Life Sci; 2021 Nov; 64(11):1868-1883. PubMed ID: 34128175
[TBL] [Abstract][Full Text] [Related]
4. CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis.
Yang M; Li S; Huang L; Zhao R; Dai E; Jiang X; He Y; Lu J; Peng L; Liu W; Zhang Z; Jiang D; Zhang Y; Jiang Z; Yang Y; Zhao P; Zhu X; Ding X; Yang Z
JCI Insight; 2022 Jul; 7(14):. PubMed ID: 35700046
[TBL] [Abstract][Full Text] [Related]
5. Catenin α 1 mutations cause familial exudative vitreoretinopathy by overactivating Norrin/β-catenin signaling.
Zhu X; Yang M; Zhao P; Li S; Zhang L; Huang L; Huang Y; Fei P; Yang Y; Zhang S; Xu H; Yuan Y; Zhang X; Zhu X; Ma S; Hao F; Sundaresan P; Zhu W; Yang Z
J Clin Invest; 2021 Mar; 131(6):. PubMed ID: 33497368
[TBL] [Abstract][Full Text] [Related]
6. An essential role of the cysteine-rich domain of FZD4 in Norrin/Wnt signaling and familial exudative vitreoretinopathy.
Zhang K; Harada Y; Wei X; Shukla D; Rajendran A; Tawansy K; Bedell M; Lim S; Shaw PX; He X; Yang Z
J Biol Chem; 2011 Mar; 286(12):10210-5. PubMed ID: 21177847
[TBL] [Abstract][Full Text] [Related]
7. Frameshift variants in the C-terminal of CTNNB1 cause familial exudative vitreoretinopathy by AXIN1-mediated ubiquitin-proteasome degradation condensation.
Liu Y; Yang M; Fan L; He Y; Dai E; Liu M; Jiang L; Yang Z; Li S
Int J Biol Macromol; 2024 Feb; 258(Pt 1):128570. PubMed ID: 38096938
[TBL] [Abstract][Full Text] [Related]
8. Mechanisms Underlying Rare Inherited Pediatric Retinal Vascular Diseases: FEVR, Norrie Disease, Persistent Fetal Vascular Syndrome.
Le V; Abdelmessih G; Dailey WA; Pinnock C; Jobczyk V; Rashingkar R; Drenser KA; Mitton KP
Cells; 2023 Nov; 12(21):. PubMed ID: 37947657
[TBL] [Abstract][Full Text] [Related]
9. Identification of novel variants in the FZD4 gene associated with familial exudative vitreoretinopathy in Chinese families.
Xu H; Zhang S; Huang L; Zhao P; Zhang X; Yang Z; Zhang L
Clin Exp Ophthalmol; 2020 Apr; 48(3):356-365. PubMed ID: 31765079
[TBL] [Abstract][Full Text] [Related]
10. Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathy.
Park H; Yamamoto H; Mohn L; Ambühl L; Kanai K; Schmidt I; Kim KP; Fraccaroli A; Feil S; Junge HJ; Montanez E; Berger W; Adams RH
Nat Commun; 2019 Nov; 10(1):5243. PubMed ID: 31748531
[TBL] [Abstract][Full Text] [Related]
11. Disrupted ER membrane protein complex-mediated topogenesis drives congenital neural crest defects.
Marquez J; Criscione J; Charney RM; Prasad MS; Hwang WY; Mis EK; García-Castro MI; Khokha MK
J Clin Invest; 2020 Feb; 130(2):813-826. PubMed ID: 31904590
[TBL] [Abstract][Full Text] [Related]
12. A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy.
Zhao R; Dai E; Wang S; Zhang X; He Y; Peng L; Zhao P; Yang Z; Yang M; Li S
Clin Genet; 2023 Mar; 103(3):320-329. PubMed ID: 36453149
[TBL] [Abstract][Full Text] [Related]
13. Familial exudative vitreoretinopathy (FEVR) in a child with novel microarray-defined deletion of 11q14 previously diagnosed as retinopathy of prematurity (ROP).
López-Cañizares A; Lazzarini TA; Mendoza C; Berrocal AM
Ophthalmic Genet; 2023 Jun; 44(3):313-317. PubMed ID: 36444989
[TBL] [Abstract][Full Text] [Related]
14. A Novel Variant of the FZD4 Gene in a Chinese Family Causes Autosomal Dominant Familial Exudative Vitreoretinopathy.
Yang L; Fu J; Cheng J; Wei C; Zhou Q; Ijaz I; Lv H; Fu J
Cell Physiol Biochem; 2018; 51(5):2445-2455. PubMed ID: 30537745
[TBL] [Abstract][Full Text] [Related]
15. Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.
Mao J; Chen Y; Fang Y; Shao Y; Xiang Z; Li H; Zhao S; Chen Y; Shen L
Ann Med; 2022 Dec; 54(1):3286-3298. PubMed ID: 36411543
[TBL] [Abstract][Full Text] [Related]
16. Heterozygote loss-of-function variants in the LRP5 gene cause familial exudative vitreoretinopathy.
Zhao R; Wang S; Zhao P; Dai E; Zhang X; Peng L; He Y; Yang M; Li S; Yang Z
Clin Exp Ophthalmol; 2022 May; 50(4):441-448. PubMed ID: 35133048
[TBL] [Abstract][Full Text] [Related]
17. Severe Familial Exudative Vitreoretinopathy, Congenital Hearing Loss, and Developmental Delay in a Child With Biallelic Variants in FZD4.
van der Ende SR; Meyers BS; Capasso JE; Sasongko M; Yonekawa Y; Pihlblad M; Huey J; Bedoukian EC; Krantz ID; Ngo MH; McMaster CR; Levin AV; Robitaille JM
JAMA Ophthalmol; 2022 Sep; 140(9):889-893. PubMed ID: 35951321
[TBL] [Abstract][Full Text] [Related]
18. Identification of Two Novel Variants in the
Wang Y; Zhao R; Dai E; Peng L; He Y; Yang M; Li S
Genet Test Mol Biomarkers; 2022 Mar; 26(3):146-151. PubMed ID: 35244470
[No Abstract] [Full Text] [Related]
19. LMBR1L regulates the proliferation and migration of endothelial cells through Norrin/β-catenin signaling.
Liu W; Jiang X; Li X; Sun K; Yang Y; Yang M; Li S; Zhu X
J Cell Sci; 2022 Mar; 135(6):. PubMed ID: 35146515
[TBL] [Abstract][Full Text] [Related]
20. Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy.
Peng Y; Zhao R; Dai E; Peng L; He Y; Li S; Yang M
Eur J Ophthalmol; 2022 Nov; 32(6):3220-3226. PubMed ID: 35037517
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
