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1  images of the distribution of lipids within nerve tissue.
2 lution mass analysis of lipids desorbed from nerve tissue.
3 members are in coelomocytes and adult radial nerve tissue.
4 ge, as assessed by light microscopy of optic nerve tissue.
5 hese tumors relative to non-neoplastic optic nerve tissue.
6 d with SEC31B expression in heart and tibial nerve tissue.
7 ffness of healthy versus tumor-bearing optic nerve tissue.
8 rmacokinetics and distribution in peripheral nerve tissue.
9 nd mitochondrial membrane potential in these nerve tissues.
10 unt and activity of the ETC enzymes from the nerve tissues and, thus, can be applied to evaluate the
11 ts from brain, liver, astrocytes, as well as nerve tissue, and performance is evaluated by using pure
12 CA (R115P) present in the patient's affected nerve tissue but not in blood DNA.
13                  NCSCs freshly isolated from nerve tissue can be directly transplanted in vivo, where
14 inding chemotherapeutic agents in peripheral nerve tissues cannot by itself account for their associa
15                                              Nerve tissue contains a high density of chemical synapse
16 n the absence of immune cells in an in vitro nerve tissue culture model and in Rag1-knockout (Rag1-/-
17 n is regulated by the developmental stage of nerve tissue, decreasing markedly in adult rat cortical
18 ed in tumor samples as compared with control nerve tissue, defining a schwannoma-typical signature.
19               Thus, even for small blocks of nerve tissue, dense connectomic mapping requires the ide
20 nes, replacing the less efficient and unsafe nerve-tissue-derived rabies vaccines, the burden of this
21 expression and their localization in sciatic nerve tissue during EAN, using a semiquantitative compet
22                                        Optic nerve tissue from an individual with NMO did not differ
23 ity of lipid ions in spinal cord and sciatic nerve tissues from rats exposed to DCA.
24  muscle, vasculature, and promote peripheral nerve tissue growth when using autologous populations of
25 on of the extracellular matrix in peripheral nerve tissue in MS.
26 rength at the lesion site and is nontoxic to nerve tissues in earthworms and mammals, we have also de
27 roducts (AGEs), which accumulate in diabetic nerve tissue, increased M1 and decreased M2 gene express
28             We demonstrate that degenerating nerve tissue is targeted by preexisting endogenous antib
29 onjunctiva, sebaceous glands, and muscle and nerve tissues labeled moderately to intensely for both m
30 ve potential of the autograft, all facets of nerve tissue must be incorporated in a combinatorial the
31 ell lines as compared with normal peripheral nerve tissues, normal astrocytes and immortalized melano
32                                In peripheral nerve tissue, the alpha4(V)-NTD is localized to the regi
33 and multiple sclerosis spinal cord and optic nerve tissues to describe in detail the distribution of
34  obtained sufficient macaque brain and optic nerve tissues to detect PrP.
35 s vaccines have evolved from the first crude nerve tissue vaccines developed by Louis Pasteur and his
36                               The peripheral nerve tissue was infiltrated with dendritic cells, CD4(+
37 an immediate enzymatic dissociation of fresh nerve tissue while maintaining high cell viability, impr

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