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1 viral attachment to cell surface glycans and junctional adhesion molecule A.
2 aged myofibres through the modulation of the junctional adhesion molecule-A.
4 ing occludin, claudin-5, zonula occludens-1, junctional adhesion molecule-A, and endothelial cell-sel
5 cumulation of vascular endothelial-cadherin, junctional adhesion molecule-A, and platelet/endothelial
6 ent of key TJ proteins: occludin, claudin-1, junctional adhesion molecule-A, and zonula occludens-1.
10 V attachment and entry is mediated by feline junctional adhesion molecule A (fJAM-A), which binds to
11 1b(-/-), and CD18(null) mice with wild-type, junctional adhesion molecule-A(-/-), ICAM-1(null), ICAM-
12 attachment to cell surface carbohydrate and junctional adhesion molecule A (JAM-A) and internalizati
13 (T1L/53) and type 3 Dearing/55 (T3D/55) use junctional adhesion molecule A (JAM-A) as a receptor.
14 Mammalian orthoreoviruses use glycans and junctional adhesion molecule A (JAM-A) as attachment rec
17 trocyte TJs of claudin 1 (CLDN1), CLDN4, and junctional adhesion molecule A (JAM-A) subunits is induc
18 he cytoplasmic tail of the ZO-1 PDZ3 ligand, junctional adhesion molecule A (JAM-A) to determine how
25 ll adhesion molecule (PECAM; CD31), CD99 and junctional adhesion molecule A (JAM-A), but apparently n
31 pression of tight junction proteins, such as junctional adhesion molecule-A (JAM)-A, occludin, and zo
32 mab, two humanized IgG4s which bind to human Junctional Adhesion Molecule-A (JAM-A) and alpha4 integr
33 n reovirus binds to cell surface glycans and junctional adhesion molecule-A (JAM-A) and enters cells
34 protein sigma1 engages glycan receptors and junctional adhesion molecule-A (JAM-A) and is thought to
35 vel of integral membrane proteins: occludin, junctional adhesion molecule-A (JAM-A) and N-cadherin at
37 ted expression of the tight junction protein junctional adhesion molecule-A (JAM-A) in the HepG2 huma
49 s contain the tight junction proteins JAM-A (junctional adhesion molecule A), occludin, and cingulin.
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