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br Experimental Procedures A detailed version
2018-10-20
Experimental Procedures A detailed version of our Experimental Procedures can be found in the Supplemental Experimental Procedures. All animal experiments were approved by the Danish Council for Supervision with Experimental Animals (#2011/561-1966). AR was performed at P1 as previously described
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Introduction Reprogramming somatic cells to induced pluripot
2018-10-20
Introduction Reprogramming somatic cholinesterase inhibitor to induced pluripotent stem cells (iPSCs) holds great promise for disease modeling and therapeutic applications. Among the challenges that remain is the extended time frame and variable efficiency of transcription factor-based reprogrammi
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Mesenchymal stem cells MSCs from adult
2018-10-20
Mesenchymal stem RG2833 (MSCs) from adult tissues, with their ability to differentiate into several cell types, chondrocytes included, have been investigated as an alternative cell source (Dennis et al., 1999; Pittenger et al., 1999; Prockop, 1997). Unfortunately, despite their easy isolation and i
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Meanwhile in vitro studies of neural
2018-10-20
Meanwhile, in vitro studies of neural induction from hPSCs have suggested that radial arrangements of columnar neuroepithelial cells, termed neural rosettes, can differentiate toward peripheral nervous system (PNS) lineages (Chambers et al., 2009; Kim et al., 2010) and reported evidence of neural cr
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Based on these principles we
2018-10-20
Based on these principles, we speculated that the use of rBC2LCN as a cargo of cytotoxic agent would provide an efficient strategy to eliminate hPSCs. Here we generated a recombinant lectin-toxin fusion protein by fusing rBC2LCN with 23 kDa of a catalytic domain of Pseudomonas aeruginosa exotoxin A
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Multi electrode array approaches have been
2018-10-20
Multi-electrode array approaches have been proposed as a tool for detecting functional changes in electrically excitable cells, including neurons, exposed to drugs or toxins and allow use in high throughput studies (McConnell et al., 2012). Although there are a number of electrophysiological measure
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We generated immortalized BMSC clones to perform detailed an
2018-10-20
We generated immortalized BMSC clones to perform detailed analysis of functional diversity in BMSC subtypes to levels not previously described. Similar immortalization techniques (e.g., hTERT combined with human papillomavirus E6/E7) have been used for the clonal analysis of BMSCs, which found OAC,
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br Introduction Chronic kidney diseases CKDs
2018-10-20
Introduction Chronic kidney diseases (CKDs) affects ∼10% of the population and represent a major global health burden (Eckardt et al., 2013). Worldwide, the number of patients with end-stage renal disease (ESRD) receiving renal replacement therapy is estimated at more than 1.4 million, with an an
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In previous tumor studies we have used
2018-10-20
In previous tumor studies, we have used a p53-null syngeneic mouse model to mimic p53 loss of function in human breast cancer. This model was developed by transplanting p53-null mammary epithelium into the cleared mammary fat pads of wild-type, syngeneic Balb/c-recipient mice, resulting in spontaneo
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The present study indicated that induction of
2018-10-20
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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Obviously T changes are not
2018-10-20
Obviously, T2 changes are not specific for certain alterations in tazarotene current, as modulators with different modes of action (ATX-II, Bay K-8644, E-4031) all result in similar changes. Moreover, relaxation time was also prolonged by EMD-57033, a relatively pure calcium sensitizer that prolong
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Here we describe the generation of the first L MYC
2018-10-20
Here we describe the generation of the first L-MYC-immortalized human NSC line derived from human fetal brain, for brevity referred to as LM-NSC008. We find that the LM-NSC008 line is chromosomally normal, and overexpresses several stem cell-associated genes. LM-NSC008 cells proliferate faster than
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Hello world!
2018-07-29
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