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In cardiac hypertrophy associated with pathological processe
2018-10-24
In cardiac hypertrophy associated with pathological processes, it has been shown that CSCs participate in the reparative processes (Ellison et al., 2013; Leri et al., 2005); however, extensive damage cannot be completely reversed, indicating that the regenerative potential of these stem Tubastatin A
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CD BMSCs formed heterotopic bone
2018-10-24
CD34+ BMSCs formed heterotopic bone in vivo which corroborate their enrichment in osteoprogenitors. While in the present study, we employed CD34 as a marker that defines a specific lineage within BMSCs, it is plausible that CD34 plays a role in osteoblast differentiation. CD34 plays an important rol
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We would like to thank
2018-10-24
We would like to thank the Gene Expression Core Facility in the Department of Pathology at UCLA for array analysis; BSCRC Flow Core staff Jessica Scholes and Felicia Codrea for their help with FACS sorting; Jonathan Carlson for useful discussion; and Jason Ernst for thoughtful comments on the manusc
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In the parenchymal niche found
2018-10-24
In the parenchymal-niche found in the adult anterior lobe, SOX2-positive MLN4924 were more densely connected to each other than in the MCL-niche, and formed dense cell clusters by E-cadherin (Fig. 1). We previously demonstrated that CAR and ephrin-B2 specifically localize at the apical cell membran
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Discussion A genome scale location analysis using published
2018-10-24
Discussion A genome-scale location analysis using published data (Gifford et al., 2013) was performed to identify surface proteins that have promoters occupied by POU5F1(OCT4)/SOX2/NANOG (OSN). In total, 30 (6%) of the 496 proteins identified on the surface of hPSCs have promoters occupied by OSN (
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The NAD dependent protein silent information regulator Sir i
2018-10-24
The NAD-dependent protein silent information regulator 2 (Sir2) is a deacetylase for histones and other proteins and a key regulator of life span in several organisms. Sirtuin (SIRT)1 of the Sirtuin family is the closest homolog of yeast Sir2 in mammals and has critical functions in the regulation o
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br Results br Discussion We undertook this study
2018-10-24
Results Discussion We undertook this study in an attempt to unravel the epigenetic mechanisms involved in the silencing of the FMR1 gene in fragile X syndrome by the use of a fibroblast line carrying an unmethylated full mutation. There have been several attempts to study epigenetic silencing
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The analysis of the transcriptome of
2018-10-24
The analysis of the transcriptome of OXM-treated HSPCs was revealing. First, the data showed very clearly that the mRNA levels of mTERT were not different between treated and untreated animals. In vitro studies by others have shown that OXM can enhance telomerase activity through estrogen receptor-m
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br Experimental Procedures br Author Contributions br Acknow
2018-10-24
Experimental Procedures Author Contributions Acknowledgments Introduction Duchenne muscular dystrophy (DMD) is a severe muscular degenerative disease caused by loss-of-function mutations in the dystrophin gene located on the X chromosome. The dystrophin gene consists of 79 exons, and dis
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Another question to address is the potential influence of th
2018-10-24
Another question to address is the potential influence of the degree of maturity of prepubertal donor tissue on the success of transplantation. Donor age-dependent differential gene expression and subsequent protein expression have been reported in tissue grafts. This could alter the initial ability
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The majority of the characterized NETs bind
2018-10-24
The majority of the characterized NETs bind lamins and/or chromatin binding proteins (Harr et al., 2016; Kind et al., 2013; Wong et al., 2014). Chromatin proteins in pluripotent stem mao inhibitor display hyperdynamic plasticity (Chen and Dent, 2014; Meshorer et al., 2006). During differentiation,
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Collectively we have evaluated the impact
2018-10-24
Collectively, we have evaluated the impact of a MODY5-causing point mutation (S148L) in the HNF1B gene on human pancreas development using a unique human stem cell model. We report molecular phenotypes (up- and down-regulation of pancreatic genes) when HNF1B is increasingly expressed from days 7 to
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The present study indicated that induction of glutamatergic
2018-10-24
The present study indicated that induction of glutamatergic markers by nucleotides involved the P2Y4-Gq signaling axis. Expression of the P2Y4 nucleotide receptor was transiently augmented in the course of neuronal differentiation of ESCs, which is coincident with the window of nucleotide-induced vG
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Previous reports have described ESC based differentiation
2018-10-24
Previous reports have described ESC-based differentiation in collagen gels to study the developmental events of vasculogenesis and angiogenesis (Feraud et al., 2001; Hermant et al., 2007). However, these were not optimized for the assessment of more fundamental aspects of vessel induction, patternin
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Traditionally testing of hPSC lines for gross chromosomal ch
2018-10-24
Traditionally, testing of hPSC lines for gross chromosomal changes employed karyology by chromosome banding of metaphase topotecan Supplier (Amps et al., 2011; Baker et al., 2007). Although karyotyping allows examination of the entire cell genome in a single assay, an often overlooked issue in eval
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