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
- 2024-12
- 2025-01
-
br Materials and methods br Results br Discussion
2018-10-20
Materials and methods Results Discussion The present study showed that CBL treatment enhanced the survival of grafted NSCs in APP tg mice. In contrast, in the vehicle-treated group there was decreased survival of transplanted neuroblasts that was worse in the APP tg mice. This is consistent
-
To derive hiPSC from patient fibroblasts we adopted
2018-10-20
To derive hiPSC from patient fibroblasts, we adopted previous protocols (Okita et al., 2011; Rasmussen et al., 2014) and electroporated the patient\'s skin fibroblasts with episomal plasmids expressing human OCT4, SOX2, L-MYC, KLF4, NANOG, LIN28, and short hairpin RNA against TP53. To demonstrate th
-
br Experimental Procedures br Author Contributions
2018-10-20
Experimental Procedures Author Contributions Acknowledgments We would like to thank Karthik Arumugam, Lucia Marucci, and Elisa Pedone for critically reading the manuscript; Bruno Di Stefano for suggestions to iPSC generation experiments; and Vanessa Chigancas and Neus Romo for technical sup
-
br Experimental Procedures br Acknowledgments br Introductio
2018-10-20
Experimental Procedures Acknowledgments Introduction Induced pluripotent stem apigenin (iPSCs) can be generated by introducing OCT4, SOX2, KLF4, and c-MYC (Takahashi et al., 2007; Takahashi and Yamanaka, 2006) or other combinations of reprogramming factors (Stadtfeld and Hochedlinger, 2010
-
We exploited the fact that the eHBs
2018-10-20
We exploited the fact that the eHBs were trapped as progenitors to analyze the effect of specific growth factors upon them and uncovered a central role for FGF (Figure 6). These data are consistent with studies in which FGF promoted the expansion of BL-CFCs derived from human or murine ESCs (Faloon
-
Consistent with our in vitro
2018-10-20
Consistent with our in vitro data, two recent genetic studies in the mouse provide strong in vivo evidence that Pdx1 is a bona fide transcriptional repressor. By E11.5, the pancreatic buds in Pdx1 null mutant embryos arrest and begin to regress (Ahlgren et al., 1996; Offield et al., 1996). Recently,
-
Small molecules have demonstrated great potential
2018-10-20
Small molecules have demonstrated great potential in modulating cellular fate and functions. A milestone work showed that mouse iPSCs were successfully induced from mouse embryonic fibroblasts (MEF) via six chemical molecules, in the absence of Yamanaka reprogramming factors (Hou et al., 2013). Rece
-
Barasertib br Results br Discussion Many key pluripotency
2018-10-20
Results Discussion Many key pluripotency TFs bind within close proximity to specific genomic locations and therefore cooperatively control the expression of key genes (Chen et al., 2008). Overlapping functional TF Barasertib (Whyte et al., 2013) ensure the stability of the overall transcripti
-
A growing amount of evidence indicates that
2018-10-20
A growing amount of evidence indicates that PSCs initiate their differentiation program from the G1 phase of the EPZ 005687 where they are most susceptible to specification cues (Chetty et al., 2013; Jonk et al., 1992; Mummery et al., 1987; Pauklin and Vallier, 2013; Sela et al., 2012; Singh et al.
-
In mouse embryos both the developing retina and
2018-10-20
In mouse embryos, both the developing retina and the ventral hypothalamus show strong Rax expression (Ikeda et al., 2005; Wataya et al., 2008; Wilson and Houart, 2004). Consistent with previous studies (Ikeda et al., 2005; Wataya et al., 2008), we confirmed that SHH agonists upregulated Rax in mESCs
-
The mechanisms involved in reprogramming somatic cells to
2018-10-20
The mechanisms involved in reprogramming somatic D-Luciferin Supplier to iPSCs by the Yamanaka factors remain poorly understood. Because of the low efficiency and slow kinetics of most reprogramming systems, molecular events that direct somatic cells to pluripotency have been difficult to define. R
-
Nepicastat HCl An increase in the PGC number
2018-10-20
An increase in the PGC number caused by dnd RNA injection does not exceed 3-fold, even if a high level of Dnd expression occurs in many cells. It is likely that an additional factor essential for PGC specification exists in medaka, which shows expression and PGC-specifying activity similar to dnd bu
-
br Experimental Procedures br Author Contributions br Acknow
2018-10-20
Experimental Procedures Author Contributions Acknowledgments Introduction The onset of puberty is regulated by a small population of hypothalamic gonadotropin-releasing hormone (GnRH) neurons, which secrete GnRH decapeptide to the hypophyseal portal system. Unlike other neuroendocrine ce
-
In in vivo animal models we observed no
2018-10-20
In in vivo animal models, we observed no rejection signs in the iPS-RPE allografts of MHC-matched monkeys (DrpZ1 and DrpZ17); for example, fundus photographs revealed no exudation, FA showed no vascular leakage of fluorescein, and OCT indicated there was no retinal edema around the transplanted RPE
-
Hello world!
2018-07-29
16170 records 1078/1078 page Previous First page 上5页 107610771078