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Liu X 75
Showing records 1 to 25 | Display all abstracts from Liu X96292 A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Yang Y
Cell Death and Disease 2021; 12: 1017
95945 Clinical and Ultrasound Biomicroscopic Characteristics of Congenital Fibrovascular Pupillary Membrane-Induced Secondary Glaucoma
Zhu Y
Frontiers in medicine 2021; 8: 763137
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
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
95888 Novel compound heterozygous mutations in identified in a Chinese family with developmental glaucoma
Cai S
Molecular medicine reports 2021; 24:
96378 Isolation of microglia from retinas of chronic ocular hypertensive rats
Zhong H
Open life sciences 2021; 16: 992-1001
95754 Forkhead domain inhibitory-6 attenuates subconjunctival fibrosis in rabbit model with trabeculectomy
Lan C
Experimental Eye Research 2021; 210: 108725
95945 Clinical and Ultrasound Biomicroscopic Characteristics of Congenital Fibrovascular Pupillary Membrane-Induced Secondary Glaucoma
Fang L
Frontiers in medicine 2021; 8: 763137
96199 Association of serum retinol concentration with normal-tension glaucoma
Feng S
Eye 2022; 36: 1820-1825
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
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; Tang L
Experimental Eye Research 2021; 210: 108725
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
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
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
96378 Isolation of microglia from retinas of chronic ocular hypertensive rats
Sun J
Open life sciences 2021; 16: 992-1001
96292 A missense mutation in Pitx2 leads to early-onset glaucoma via NRF2-YAP1 axis
Wang J
Cell Death and Disease 2021; 12: 1017
95754 Forkhead domain inhibitory-6 attenuates subconjunctival fibrosis in rabbit model with trabeculectomy
Liu G
Experimental Eye Research 2021; 210: 108725
96172 Identification and functional study of FOXC1 variants in Chinese families with glaucoma
Yang B
American Journal of Medical Genetics, Part A 2022; 188: 540-547
