Поиск по каталогу |
(строгое соответствие)
|
- Профессиональная
- Научно-популярная
- Художественная
- Публицистика
- Детская
- Искусство
- Хобби, семья, дом
- Спорт
- Путеводители
- Блокноты, тетради, открытки
Estrogen Receptors. Differential regulation of downstream signalling
В наличии
Местонахождение: Алматы | Состояние экземпляра: новый |
Бумажная
версия
версия
Автор: Sudipta Maitra and Debabrata Das
ISBN: 9783659327568
Год издания: 2013
Формат книги: 60×90/16 (145×215 мм)
Количество страниц: 76
Издательство: LAP LAMBERT Academic Publishing
Цена: 30358 тг
Положить в корзину
Способы доставки в город Алматы * комплектация (срок до отгрузки) не более 2 рабочих дней |
Самовывоз из города Алматы (пункты самовывоза партнёра CDEK) |
Курьерская доставка CDEK из города Москва |
Доставка Почтой России из города Москва |
Аннотация: Evolution supports multicellular organisms for their better coordination and regulation of body functions. Estrogens regulate a variety of signal transduction pathways involving broad range of gene functions. Estrogen receptors (ERs) can act as transcription factors and are also capable of modulating functions of other transcription factors, thereby regulating gene expression by at least two distinct mechanisms, i.e. protein-protein interactions in the chromosome and activation of signal transduction pathways at the plasma membrane. These mechanisms function in addition to the classical mechanism of ER action. Thus, the possible convergence of genomic and nongenomic actions at multiple response elements provides extremely fine degree of control for the regulation of transcription by ERs. It is evident that genes that are regulated by ERs are of two types: those that contain ERE and those that do not. The latter genes contain binding sites for a variety of heterogeneous transcription factors. Further, discovery of GPER as an estrogen receptor and their ability to start membrane initiated as well as genomic actions is changing the concept of E2 signalling.
Ключевые слова: gene expression, Gpr30, Cancer., Estrogen Receptor, GPER, Estrogen response element, Nongenomic action