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1.
Stop codon variant in EFEMP1 is associated with primary open-angle glaucoma due to impaired regulation of aqueous humor outflow.
Exp Eye Res
; 241: 109859, 2024 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-38467175
2.
Cortical thickness differences are associated with cellular component morphogenesis of astrocytes and excitatory neurons in nonsuicidal self-injuring youth.
Cereb Cortex
; 33(3): 811-822, 2023 01 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-35253859
3.
Structural brain characteristics and gene co-expression analysis: A study with outcome label from normal cognition to mild cognitive impairment.
Neurobiol Learn Mem
; 191: 107620, 2022 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-35398514
4.
Genetic polymorphism in catechol-O-methyltransferase associated with the functional connectivity of frontostriatal circuits in first episode schizophrenia patients.
Eur J Neurosci
; 51(10): 2134-2142, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-31876034
5.
Neuroprotective effects of C3 exoenzyme in excitotoxic retinopathy.
Exp Eye Res
; 125: 128-34, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24928315
6.
Evaluation of trabecular meshwork-specific promoters in vitro and in vivo using scAAV2 vectors expressing C3 transferase.
Int J Ophthalmol
; 16(8): 1196-1209, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37602341
7.
A novel MYOC heterozygous mutation identified in a Chinese Uygur pedigree with primary open-angle glaucoma.
Mol Vis
; 18: 1944-51, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22876119
8.
Selective corticocortical connectivity suppression during propofol-induced anesthesia in healthy volunteers.
Cogn Neurodyn
; 16(5): 1029-1043, 2022 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-36237410
9.
Polymorphism rs11200638 enhanced HtrA1 responsiveness and expression are associated with age-related macular degeneration.
Eye (Lond)
; 36(8): 1631-1638, 2022 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34326497
10.
Sequence analysis of MYOC and CYP1B1 in a Chinese pedigree of primary open-angle glaucoma.
Mol Vis
; 17: 1431-5, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21655360
11.
Characterization of intraocular pressure responses of the Tibetan monkey (Macaca thibetana).
Mol Vis
; 17: 1405-13, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-21654897
12.
Molecular genetics of familial nystagmus complicated with cataract and iris anomalies.
Mol Vis
; 17: 2612-7, 2011.
Artículo
en Inglés
| MEDLINE | ID: mdl-22025896
13.
Differences in Brain Structural Covariance Network Characteristics in Children and Adults With Autism Spectrum Disorder.
Autism Res
; 14(2): 265-275, 2021 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-33386783
14.
Cortical Thickness Differences Are Associated With Chemical Synaptic Transmission Upregulated Genes in Degeneration of Mild Cognitive Impairment.
Front Aging Neurosci
; 13: 745381, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34776930
15.
Asymmetrical alterations of grey matter among psychiatric disorders: A systematic analysis by voxel-based activation likelihood estimation.
Prog Neuropsychopharmacol Biol Psychiatry
; 110: 110322, 2021 08 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-33838150
16.
Association between structural brain features and gene expression by weighted gene co-expression network analysis in conversion from MCI to AD.
Behav Brain Res
; 410: 113330, 2021 07 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-33940051
17.
Novel compound heterozygous mutations in CYP1B1 identified in a Chinese family with developmental glaucoma.
Mol Med Rep
; 24(5)2021 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-34528698
18.
A mutated CRYGD associated with congenital coralliform cataracts in two Chinese pedigrees.
Int J Ophthalmol
; 14(6): 800-804, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34150533
19.
Predicting the progression of mild cognitive impairment to Alzheimer's disease by longitudinal magnetic resonance imaging-based dictionary learning.
Clin Neurophysiol
; 131(10): 2429-2439, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32829290
20.
Modulation on Glutamic Pathway of Frontal-Striatum-Thalamus by rs11146020 and rs3813296 Gene Polymorphism in First-Episode Negative Schizophrenia.
Front Neurosci
; 14: 351, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32372910