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1 mode of SECM using an iridium oxide-modified microcell.
3 he presence of cytoplast-like structures and microcells containing mitochondria surrounding the micro
4 that use large-scale arrays of silicon solar microcells created from bulk wafers and integrated in di
5 id cell lines by fusion of canine fibroblast microcell donors with immortalized rodent recipient cell
7 of a novel concept of sealed electrochemical microcell for in situ soft X-ray microspectroscopy in tr
10 t of human chromosome 10 was transferred via microcell fusion into a prostate adenocarcinoma cell lin
11 in A9/YAC hybrids was further transferred by microcell fusion into immortal cell lines derived from h
12 nt nondifferentiating phenotype, we utilized microcell fusion to transfer chromosomes from rhabdomyos
14 erred human chromosome 11 into DT40 cells by microcell fusion, and find that the resulting hybrids ar
15 ransferred into a sporadic RCC cell line via microcell fusion, and microcell hybrid clones were teste
20 ve constructed a collection of canine-rodent microcell hybrid cell lines by fusion of canine fibrobla
22 henotype was observed in 16 of 18 individual microcell hybrid clones as evidenced by the complete abr
23 by detailed microsatellite analyses of novel microcell hybrid clones containing transferred fragments
24 cipient cell line and four randomly selected microcell hybrid clones remained tumorigenic in nude mic
26 adic RCC cell line via microcell fusion, and microcell hybrid clones were tested for tumorigenicity i
28 icity was even more strongly pronounced in a microcell hybrid that received an isochromosome 11q deri
29 egion of human chromosome 8 retained in each microcell hybrid was determined by a PCR analysis with s
30 human X chromosome, present in a DT40-human microcell hybrid, has been manipulated using homologous
31 pt elevated in a nontumorigenic Wilms' tumor microcell hybrid, relative to the tumorigenic parental c
32 aft cultures suggests that the chromosome 11 microcell hybrids are actively progressing through the c
34 ene expression was activated in rat hepatoma microcell hybrids containing human chromosome 14, but ex
39 itro growth suppression of the chromosome 11 microcell hybrids in the organotypic rafts correlates we
40 nscription of the human alpha1AT gene in the microcell hybrids initiated at the macrophage promoter.
42 ed efficiently, but in the human and hamster microcell hybrids its copy number is poorly regulated.
43 on between a mouse thymoma cell line, and to microcell hybrids made with a mouse teratocarcinoma cell
47 cus, we prepared and characterized rat/human microcell hybrids that contained either human chromosome
48 into H11 cells and have isolated a number of microcell hybrids that have rescued hepatic gene express
50 Here we describe the use of noncomplemented microcell hybrids to identify small overlapping deletion
51 omosome 11 has restricted the ability of the microcell hybrids to stratify but has not significantly
54 albumin mRNA levels in several extinguished microcell hybrids were reduced at least 500-fold, simila
55 the entire 130-kb region was reorganized in microcell hybrids, and the distributions of DHSs in acti
56 boxykinase, was also affected in some of the microcell hybrids, but expression of these genes was not
57 ow generated and characterized nine melanoma microcell hybrids, each retaining an introduced fragment
59 NA markers, in revertant clones of senescent microcell hybrids, revealed a consensus deletion, spanni
60 e not retained or are not expressed in these microcell hybrids, which suggests the presence of a nove
64 composed of three-electrode electrochemical microcells, integrated on a fluidic platform constructed
66 17 into the breast cancer cell line MCF7 by microcell mediated chromosome transfer (MMCT) results in
75 t region does not occur when it is moved via microcell-mediated chromosome transfer into a de novo me
76 g approach in chicken DT40 cells followed by microcell-mediated chromosome transfer into human erythr
77 eated by a process that included irradiation microcell-mediated chromosome transfer of Hsa21 into rec
79 nd SKOV-3 ovarian carcinoma cell lines using microcell-mediated chromosome transfer techniques to fur
80 ify such suppressor genes, we have conducted microcell-mediated chromosome transfer to introduce huma
82 required for fragile site induction, we used microcell-mediated chromosome transfer to isolate hybrid
91 type hMSH3 or wild-type hMSH6, introduced by microcell-mediated transfer of chromosome 5 or 2, respec
92 estimate the number of senescence genes, and microcell-mediated transfer of chromosomes into immortal
98 an alternate approach using high-efficiency microcell photovoltaics embedded between a pair of plast
99 ll with the composition and structure of the microcell preparations, which showed the presence of cyt
101 processes for creating and manipulating such microcells, together with theoretical and experimental i
105 l performances of the new laser-machined BDD microcell were assessed by differential pulse anodic str
107 ent with room temperature atoms contained in microcells with spin-protecting coating, placed inside a
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