Overview of Cytochrome P450 1B1 gene mutations in patients with primary congenital glaucoma.
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CYP1B1-mediated Pathobiology of Primary Congenital GlaucomaRare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and ManagementOcular cytochrome P450s and transporters: roles in disease and endobiotic and xenobiotic dispositionGenetic, Biochemical and Clinical Insights into Primary Congenital GlaucomaIn silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma.Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.Carrier frequency of CYP1B1 mutations in the United States (an American Ophthalmological Society thesis).A novel methodology for enhanced and consistent heterologous expression of unmodified human cytochrome P450 1B1 (CYP1B1).Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases.Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity.A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent.Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.Cyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway.Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.Potential role of CYP1B1 in the development and treatment of metabolic diseases.Primary congenital and developmental glaucomas.Aryl hydrocarbon receptor (AHR): "pioneer member" of the basic-helix/loop/helix per-Arnt-sim (bHLH/PAS) family of "sensors" of foreign and endogenous signals.Defective CYP1B1 causes GlaucomaAnalysis of CYP1B1 Gene Mutations in Patients with Primary Congenital Glaucoma.Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study.Mutation spectrum of CYP1B1 in Chinese patients with primary open-angle glaucoma.Research progress on human genes involved in the pathogenesis of glaucoma (Review).
P2860
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P2860
Overview of Cytochrome P450 1B1 gene mutations in patients with primary congenital glaucoma.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
@en
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
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type
label
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
@en
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
@nl
prefLabel
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
@en
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
@nl
P2093
P1476
Overview of Cytochrome P450 1B ...... h primary congenital glaucoma.
@en
P2093
P304
P356
10.1016/J.EXER.2011.07.009
P577
2011-08-16T00:00:00Z