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Several previous studies support the possibility that RPC
2018-10-20
Several previous studies support the possibility that RPC differentiation into podocytes may be involved in remission of different types of diseases, including proliferative glomerulonephritis (Rizzo et al., 2013), gestational pre-eclampsia (Penning et al., 2014), and diabetic nephropathy (Pichaiwon
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In this study we describe an efficient dCas activator
2018-10-20
In this study, we describe an efficient dCas9 activator with multimeric VP16 activation domain and a simplified method for guide RNA assembly and cloning. We demonstrate that the dCas9 activator can be fused to a dihydrofolate reductase (DHFR)-derived destabilization domain (DD) (Iwamoto et al., 201
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During development extrinsic signals in a progenitor s
2018-10-20
During development, extrinsic signals in a progenitor’s microenvironment provide cues for self-renewal and lineage commitment. Although several growth factors, including fibroblast growth factors (FGFs) 2 (Perantoni et al., 1995), 8 (Perantoni et al., 2005), 9, and 20 (Barak et al., 2012) and epider
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All PGCs differentiated from ESCs
2018-10-20
All PGCs differentiated from ESCs in our study, regardless of differentiation approach or sorting strategy, were capable of implementing ICC erasure at the Snprn ICC. However, unlike E9.5 PGCs from the embryo, the hypomethylated state at this ICC was unstable, and in every case re-methylation was in
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Collectively we have evaluated the impact of
2018-10-20
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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Numerous morphogenetic events are explained by the cell surf
2018-10-20
Numerous morphogenetic events are explained by the cell surface tension model. In equilibrium, surface tension is minimized via coordinated forces generated by cell surface tension and actomyosin-mediated cortical tension, resulting in cell sorting and self-organization (Beysens et al., 2000; Heisen
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inhibitor of apoptosis TPCA reversibly binds to IKK and prev
2018-10-20
TPCA-1 reversibly binds to IKKβ and prevents it from phosphorylating IκBα for degradation and thereby blocks nuclear translocation of NF-κB (Kondo et al., 2008). Our results demonstrate that TPCA-1 may inhibit the stimulatory action of TNF-α on NF-κB. TPCA-1 partially inhibits secretion of constitut
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The detailed molecular mechanisms regarding how
2018-10-20
The detailed molecular mechanisms regarding how H1foo enhances the reprogramming efficiency in iPSC generation and why OSKH-iPSCs exhibit improved quality remain elusive. The higher-order chromatin structure is crucially dependent on architectural chromatin proteins, including the family of linker h
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br Introduction The neocortex also called the dorsal cortex
2018-10-20
Introduction The neocortex, also called the dorsal cortex, is an immensely complex mammalian BIRB796 manufacturer structure that controls higher cognitive functions, such as problem solving and reasoning, sensory perception, emotional processing, and attention. The developing neocortex is popula
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br Results br Discussion The dataset allows a well defined
2018-10-20
Results Discussion The dataset allows a well-defined comparison of protein abundance and phosphorylation in pluripotent Gefitinib and the earliest definitive hNSCs. This contrasts with previous studies that used hESCs and heterogeneous mixtures of differentiated progeny (Brill et al., 2009; R
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To determine whether the inhibition of RSK and
2018-10-20
To determine whether the inhibition of RSK and TTK inhibits neovascularization in vivo, we gave mice LL/2 tumor grafts. Both BI-D1870 and AZ3146, used at doses determined to be non-toxic to animals, significantly improved survival, inhibited tumor growth, and decreased vascular density. In contrast,
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NHS-SS-Biotin manufacturer Here we attempted to reprogram hi
2018-10-20
Here, we attempted to reprogram highly fluorescence-activated cell sorting (FACS)-purified (100% purity) leukemia blasts from three subtypes of B-ALL, t(4;11)/MLL-AF4+, t(1;11)+MLL-EPS15+, and t(12;21)/ETV6-RUNX1 B-ALL, to establish novel iPSC-based disease models to address the developmental impact
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Hello world!
2018-07-29
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