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22-3
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Glaucoma Dialogue
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Author #27172
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Liu X
74
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Liu X
96172
Identification and functional study of FOXC1 variants in Chinese families with glaucoma
Wang X
American Journal of Medical Genetics, Part A
2022; 188: 540-547
95888
Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Cai S
Molecular medicine reports
2021; 24:
95754
Forkhead domain inhibitory-6 attenuates subconjunctival fibrosis in rabbit model with trabeculectomy
Lan C
Experimental Eye Research
2021; 210: 108725
96378
Isolation of microglia from retinas of chronic ocular hypertensive rats
Zhong H
Open life sciences
2021; 16: 992-1001
96292
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Yang Y
Cell Death and Disease
2021; 12: 1017
96199
Association of serum retinol concentration with normal-tension glaucoma
Pang R
Eye
2022; 36: 1820-1825
96249
Aqueous humor proteomic analysis of acute angle-closure glaucoma with visual field loss
Xu J
Annals of translational medicine
2021; 9: 1611
95945
Clinical and Ultrasound Biomicroscopic Characteristics of Congenital Fibrovascular Pupillary Membrane-Induced Secondary Glaucoma
Zhu Y
Frontiers in medicine
2021; 8: 763137
96292
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Li X
Cell Death and Disease
2021; 12: 1017
95888
Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Zhang D
Molecular medicine reports
2021; 24:
96172
Identification and functional study of FOXC1 variants in Chinese families with glaucoma
Liu X
American Journal of Medical Genetics, Part A
2022; 188: 540-547
95754
Forkhead domain inhibitory-6 attenuates subconjunctival fibrosis in rabbit model with trabeculectomy
Tan J
Experimental Eye Research
2021; 210: 108725
96199
Association of serum retinol concentration with normal-tension glaucoma
Feng S
Eye
2022; 36: 1820-1825
95945
Clinical and Ultrasound Biomicroscopic Characteristics of Congenital Fibrovascular Pupillary Membrane-Induced Secondary Glaucoma
Fang L
Frontiers in medicine
2021; 8: 763137
96249
Aqueous humor proteomic analysis of acute angle-closure glaucoma with visual field loss
Zhao L
Annals of translational medicine
2021; 9: 1611
96378
Isolation of microglia from retinas of chronic ocular hypertensive rats
Yu H
Open life sciences
2021; 16: 992-1001
95888
Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Jiao X
Molecular medicine reports
2021; 24:
96249
Aqueous humor proteomic analysis of acute angle-closure glaucoma with visual field loss
Liu X
Annals of translational medicine
2021; 9: 1611
96292
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Wang J
Cell Death and Disease
2021; 12: 1017
96378
Isolation of microglia from retinas of chronic ocular hypertensive rats
Sun J
Open life sciences
2021; 16: 992-1001
96172
Identification and functional study of FOXC1 variants in Chinese families with glaucoma
Li Y
American Journal of Medical Genetics, Part A
2022; 188: 540-547
95754
Forkhead domain inhibitory-6 attenuates subconjunctival fibrosis in rabbit model with trabeculectomy
Tang L
Experimental Eye Research
2021; 210: 108725
95945
Clinical and Ultrasound Biomicroscopic Characteristics of Congenital Fibrovascular Pupillary Membrane-Induced Secondary Glaucoma
Zhong Y
Frontiers in medicine
2021; 8: 763137
96199
Association of serum retinol concentration with normal-tension glaucoma
Cao K
Eye
2022; 36: 1820-1825
96292
A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Tan J
Cell Death and Disease
2021; 12: 1017
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