Full browser ? ▲ F2S F2S2 F2S2P F2T F2T F2T2 F2T2E F2T2EA F3 F3 F3 Key F3 Key F3000 F360 F37 F37/oesophageal cancer-related gene-coding leucine-zipper motif F380 F3A F3EAD F3H F3I F3P F3T F4 F4 Key F4 Key F451 F4A F4AF F4CG F4CP F4E F4f F4f F4H F4J F4K F4L ...
filetype cpp nnoremap<-O3%filetype cpp nnoremap<F9>:vsplitterm
in cooperating with financial institutions, including banks and guarantee agencies, CPCC is aiming to form the platform in helping cultural innovation companies to get funding and financing support by copyright pledge. The platform is more efficient in time, more convenient in process and more afforda...
Download: Download full-size image Fig. 2. Schematic representation of CPP potential in vaccine development. There are two pathways for presentation of protein-based antigens: exogenous and endogenous. Exogenous antigenic proteins are internalized by APCs via endocytosis, which are usually processed to...
Full size image HEK293 cells also form cilia upon serum starvation induction. The temporal expression ofCCP5in HEK293 cells correlates with ciliogenesis in a pattern resembling that in RPE-1 cells (Additional file1: Fig. S1), suggesting a common phenomenon in ciliated cells. We wondered whether...
A further issue relates to whether we have reached a full understanding of the complement of cell types that underlie the RTT disease phenotype and the extent to which we have yet to explore which cell types, when rendered fully functional, will have the largest influence on amelioration of the...
Ben Van Kerkwyk is an Australian researcher, writer and content creator, now living in the United States. He produces the UnchartedX.com website and UnchartedX youtube channel and podcast, focusing on long-form documentaries on various topics dealing with ancient mysteries and the new scientific...
(at). this mutation of p.138 was inherited from his father full size image clinical features of mecp2 mutation carriers overall, poor social interaction was highlighted symptom, but language using and repetitive behavior differ greatly in these three patients. functional impairment was outstanding ...
Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual disability in females. Typical symptoms are onset at month 6–18 after normal pre- and postnatal development, loss of acquired skills and severe intellectual
Download: Download full-size image Figure 1. Elevated Primary miR-208b (pri-miR-208b) Transcript in Female Left Ventricle (A) Genomic organization of myosin heavy chain coding and non-coding genes on chromosome 14 of mouse. qRT-PCR quantification of (B) pri-miR-208b; (C) Myh6; (D) ...