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1 lls and transduction of cells expressing the coxsackievirus and adenovirus receptor.
2 and reveal a direct interaction between the coxsackievirus and adenovirus receptor and the immune sy
3 tudy demonstrates that hiPSC-CMs express the coxsackievirus and adenovirus receptor, are susceptible
4 s 259 and 260 in the cytoplasmic tail of the coxsackievirus and adenovirus receptor (CAR) are known t
5 While group B coxsackieviruses (CVB) use the coxsackievirus and adenovirus receptor (CAR) as the rece
6 ruses into target cells is expression of the coxsackievirus and adenovirus receptor (CAR) at the cell
10 associated with the widespread expression of coxsackievirus and adenovirus receptor (CAR) in normal h
17 we demonstrate that in the adult brain, the coxsackievirus and adenovirus receptor (CAR) is located
22 rity of adenovirus serotypes can bind to the coxsackievirus and adenovirus receptor (CAR) on human ce
23 protein serves this purpose, binding to the coxsackievirus and adenovirus receptor (CAR) present on
25 In this study, a zebrafish homologue of the coxsackievirus and adenovirus receptor (CAR) protein was
28 novirus serotype 5 fiber protein engages the coxsackievirus and adenovirus receptor (CAR) to bind cel
29 oding the murine homolog (mCAR) of the human coxsackievirus and adenovirus receptor (CAR) were isolat
31 s many adenoviruses infect cells through the coxsackievirus and adenovirus receptor (CAR), group B ad
42 binds with high affinity to the cell surface coxsackievirus-and-adenovirus receptor (CAR), and penton
45 es), cardiac fibrosis, apoptosis, lower CAR (Coxsackievirus and adenovirus receptor) expression and C
48 FP(A20) exhibited up to 50-fold increases in coxsackievirus- and-adenovirus-receptor-independent tran
49 beta, tumor-derived growth factor beta; CAR, coxsackievirus and adenovirus receptor; MLV, murine leuk
51 presence of varied concentrations of soluble coxsackievirus and adenovirus receptor showed that the o
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