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Molecular Basis for Involvement of CYP1B1 in MYOC Upregulation and Its Potential Implication in Glaucoma Pathogenesis

CYP1B1 has been implicated in primary congenital glaucoma with autosomal recessive mode of inheritance. Mutations in CYP1B1 have also been reported in primary open angle glaucoma (POAG) cases and suggested to act as a modifier of the disease along with Myocilin (MYOC). Earlier reports suggest that o...

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Detalles Bibliográficos
Autores principales: Mookherjee, Suddhasil, Acharya, Moulinath, Banerjee, Deblina, Bhattacharjee, Ashima, Ray, Kunal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3448602/
https://www.ncbi.nlm.nih.gov/pubmed/23028769
http://dx.doi.org/10.1371/journal.pone.0045077

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