Archives
- 2018-07
- 2018-10
- 2018-11
- 2019-04
- 2019-05
- 2019-06
- 2019-07
- 2019-08
- 2019-09
- 2019-10
- 2019-11
- 2019-12
- 2020-01
- 2020-02
- 2020-03
- 2020-04
- 2020-05
- 2020-06
- 2020-07
- 2020-08
- 2020-09
- 2020-10
- 2020-11
- 2020-12
- 2021-01
- 2021-02
- 2021-03
- 2021-04
- 2021-05
- 2021-06
- 2021-07
- 2021-08
- 2021-09
- 2021-10
- 2021-11
- 2021-12
- 2022-01
- 2022-02
- 2022-03
- 2022-04
- 2022-05
- 2022-06
- 2022-07
- 2022-08
- 2022-09
- 2022-10
- 2022-11
- 2022-12
- 2023-01
- 2023-02
- 2023-03
- 2023-04
- 2023-05
- 2023-06
- 2023-07
- 2023-08
- 2023-09
- 2023-10
- 2023-11
- 2023-12
- 2024-01
- 2024-02
- 2024-03
- 2024-04
- 2024-05
- 2024-06
- 2024-07
- 2024-08
- 2024-09
- 2024-10
- 2024-11
-
In this study we further show that expression
2018-10-20
In this study, we further show that irak inhibitor of SUV39H1 in HSC is controlled by the highly conserved miR-125 miRNA family. While previously shown to be important regulators of HSC self-renewal and differentiation potential (O\'Connell et al., 2010; Ooi et al., 2010), the contribution of miR-1
-
These data suggest that niches are
2018-10-20
These data suggest that niches are not limited to the governance of stem cells (Wu et al., 2009; Yu et al., 2015a), and the definition of “progenitor niches” may offer new ways to understand the regulation of tissue composition and function. We recently demonstrated that selective deletion of cells
-
Among the repertoire of integrins
2018-10-20
Among the repertoire of integrins, the β1-integrin subunit mediates the attachment of hESCs to fibronectin via the α5β1 heterodimer (Baxter et al., 2009), as well as other commonly used ECM (Braam et al., 2008). Although hESCs cultured on ECM have been shown to express active FAK and AKT (Miyazaki e
-
Hello world!
2018-07-29
15799 records 1054/1054 page Previous First page 上5页 1051105210531054