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Nuclear receptors as potential therapeutic targets for age-related macular degeneration.
Malek, Goldis.
Afiliação
  • Malek G; Duke University Eye Center, Albert Eye Research Institute, Department of Ophthalmology, Duke University, 2351 Erwin Road, Room 4006, 27710, Durham, NC, USA, gmalek@duke.edu.
Adv Exp Med Biol ; 801: 317-21, 2014.
Article em En | MEDLINE | ID: mdl-24664713
ABSTRACT
Age-related macular degeneration (AMD) is the most important cause of blindness and visual impairment among the elderly. Nuclear receptors represent one of the largest families of transcription factors, with 48 present in the human genome. They are critical regulators and modulators of developmental and physiological processes and are both targets of drugs and chemicals of environmental significance. Many of the cellular processes regulated by nuclear receptors are disrupted in AMD. With this in mind, we recently created a nuclear receptor atlas of retinal pigment epithelial (RPE) cells, cells affected in AMD, highlighting the expression of all the nuclear receptors. The results of which provided scaffold to study individual receptors in aging and disease. This study led to several candidate receptors that have become the focus of detailed studies regarding their mechanistic role in the eye. One example of a nuclear receptor potentially relevant to AMD pathobiology is presented.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Citoplasmáticos e Nucleares / Receptores de Hidrocarboneto Arílico / Epitélio Pigmentado da Retina / Degeneração Macular Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Adv Exp Med Biol Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores Citoplasmáticos e Nucleares / Receptores de Hidrocarboneto Arílico / Epitélio Pigmentado da Retina / Degeneração Macular Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Adv Exp Med Biol Ano de publicação: 2014 Tipo de documento: Article