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1 mode of SECM using an iridium oxide-modified microcell.
2 sustainable and efficient performance of the microcells.
3 d (c) DC/AC preamplifier integrated into the microcell and interfaced to a bandpass AC amplifier.
4  catalytic activity, as demonstrated in both microcell and polymer electrolyte membrane cell experime
5                Herein, we develop an on-chip microcell-based total-internal-reflection-fluorescence-m
6 he presence of cytoplast-like structures and microcells containing mitochondria surrounding the micro
7 that use large-scale arrays of silicon solar microcells created from bulk wafers and integrated in di
8 id cell lines by fusion of canine fibroblast microcell donors with immortalized rodent recipient cell
9 tegration of three-electrode electrochemical microcells (ElecCell) and organic photodetectors (OPD) i
10                                          The microcell, fabricated using ultraviolet lithography, at
11 of a novel concept of sealed electrochemical microcell for in situ soft X-ray microspectroscopy in tr
12                                    By fusing microcells from a colon carcinoma cell line with a mitoc
13           Transfer of human chromosome 14 by microcell fusion from non-expressing fibroblasts to rat
14 t of human chromosome 10 was transferred via microcell fusion into a prostate adenocarcinoma cell lin
15 in A9/YAC hybrids was further transferred by microcell fusion into immortal cell lines derived from h
16 nt nondifferentiating phenotype, we utilized microcell fusion to transfer chromosomes from rhabdomyos
17                              We describe the microcell fusion transfer of 100-200 kb self-replicating
18 erred human chromosome 11 into DT40 cells by microcell fusion, and find that the resulting hybrids ar
19 ransferred into a sporadic RCC cell line via microcell fusion, and microcell hybrid clones were teste
20                                 We have used microcell fusion-mediated chromosomal transfer to introd
21 mortal human and rat ovarian tumor cells via microcell fusion.
22                          By a combination of microcell-fusion and deletion-mapping studies, we previo
23            In the present work, we show that microcells have a significant number of mitochondria whi
24 ve constructed a collection of canine-rodent microcell hybrid cell lines by fusion of canine fibrobla
25 the deletions in four of the noncomplemented microcell hybrid cell lines.
26 henotype was observed in 16 of 18 individual microcell hybrid clones as evidenced by the complete abr
27 by detailed microsatellite analyses of novel microcell hybrid clones containing transferred fragments
28 cipient cell line and four randomly selected microcell hybrid clones remained tumorigenic in nude mic
29      The metastatic ability of the resultant microcell hybrid clones was then tested in a standard sp
30 adic RCC cell line via microcell fusion, and microcell hybrid clones were tested for tumorigenicity i
31                    A PCR analysis of various microcell hybrid clones with sequence-tagged site marker
32 icity was even more strongly pronounced in a microcell hybrid that received an isochromosome 11q deri
33 egion of human chromosome 8 retained in each microcell hybrid was determined by a PCR analysis with s
34  human X chromosome, present in a DT40-human microcell hybrid, has been manipulated using homologous
35 pt elevated in a nontumorigenic Wilms' tumor microcell hybrid, relative to the tumorigenic parental c
36 aft cultures suggests that the chromosome 11 microcell hybrids are actively progressing through the c
37                              Two independent microcell hybrids contained a normal chromosome 17 and n
38 ene expression was activated in rat hepatoma microcell hybrids containing human chromosome 14, but ex
39                                              Microcell hybrids containing only the region 10pter-q11
40                         DHS mapping in these microcell hybrids demonstrated that the chromatin struct
41              Grouped together, the four neo6 microcell hybrids had no statistically significant reduc
42             During continuous maintenance of microcell hybrids in MX medium, rare immortal revertant
43 itro growth suppression of the chromosome 11 microcell hybrids in the organotypic rafts correlates we
44 nscription of the human alpha1AT gene in the microcell hybrids initiated at the macrophage promoter.
45 ed for tumorigenicity following injection of microcell hybrids into nude mice.
46 ed efficiently, but in the human and hamster microcell hybrids its copy number is poorly regulated.
47 on between a mouse thymoma cell line, and to microcell hybrids made with a mouse teratocarcinoma cell
48                                              Microcell hybrids of A9 cells with chromosome 16 from th
49                                        Thus, microcell hybrids provide a system in which reproducible
50                                 Rat hepatoma microcell hybrids retaining a derivative human chromosom
51 cus, we prepared and characterized rat/human microcell hybrids that contained either human chromosome
52 into H11 cells and have isolated a number of microcell hybrids that have rescued hepatic gene express
53 albumin gene is extinguished in rat hepatoma microcell hybrids that retain mouse chromosome 1.
54  Here we describe the use of noncomplemented microcell hybrids to identify small overlapping deletion
55 omosome 11 has restricted the ability of the microcell hybrids to stratify but has not significantly
56             One of the metastasis-suppressed microcell hybrids was used for construction of represent
57                                        While microcell hybrids were maintained in selection medium to
58  albumin mRNA levels in several extinguished microcell hybrids were reduced at least 500-fold, simila
59  the entire 130-kb region was reorganized in microcell hybrids, and the distributions of DHSs in acti
60 boxykinase, was also affected in some of the microcell hybrids, but expression of these genes was not
61 ow generated and characterized nine melanoma microcell hybrids, each retaining an introduced fragment
62               In contrast, the chromosome 11 microcell hybrids, HMC 100p4B and HMC 100p5A, form an ep
63 NA markers, in revertant clones of senescent microcell hybrids, revealed a consensus deletion, spanni
64 e not retained or are not expressed in these microcell hybrids, which suggests the presence of a nove
65 ese chromosomes was further established with microcell hybrids.
66 ifferent human chromosomes in whole cell and microcell hybrids.
67 correlate with metastasis suppression in the microcell hybrids.
68  composed of three-electrode electrochemical microcells, integrated on a fluidic platform constructed
69                                 This type of microcell is particularly useful for making electrochemi
70  17 into the breast cancer cell line MCF7 by microcell mediated chromosome transfer (MMCT) results in
71                                              Microcell mediated transfer of a normal human chromosome
72 tatic Dunning AT6.1 prostate cancer cells by microcell-mediated chromosomal transfer.
73 ted copy of the chromosome into SCC lines by microcell-mediated chromosome transfer (MMCT).
74  embryonic stem (ES) cells using irradiation microcell-mediated chromosome transfer (XMMCT).
75                     The combined approach of microcell-mediated chromosome transfer and expression di
76                                      We used microcell-mediated chromosome transfer approach and expr
77                                              Microcell-mediated chromosome transfer has been used to
78                                     When the microcell-mediated chromosome transfer hybrid cells cont
79 t region does not occur when it is moved via microcell-mediated chromosome transfer into a de novo me
80 g approach in chicken DT40 cells followed by microcell-mediated chromosome transfer into human erythr
81 eated by a process that included irradiation microcell-mediated chromosome transfer of Hsa21 into rec
82 n cells with extra chromosome engineered via microcell-mediated chromosome transfer often gain massiv
83 DA-MB-435 breast carcinoma cell line via the microcell-mediated chromosome transfer technique.
84 nd SKOV-3 ovarian carcinoma cell lines using microcell-mediated chromosome transfer techniques to fur
85 ify such suppressor genes, we have conducted microcell-mediated chromosome transfer to introduce huma
86          We tested this possibility by using microcell-mediated chromosome transfer to introduce norm
87 required for fragile site induction, we used microcell-mediated chromosome transfer to isolate hybrid
88                                    PPC-1, by microcell-mediated chromosome transfer.
89 p, a result subsequently confirmed by stable microcell-mediated chromosome transfer.
90 y normal human breast epithelial cells using microcell-mediated chromosome transfer.
91 etastatic AT6.3 rat prostate cancer cells by microcell-mediated chromosome transfer.
92 thelial ovarian cancer cell line, SKOv-3, by microcell-mediated chromosome transfer.
93 n localized to chromosome 3p22-26, by use of microcell-mediated chromosome transfer.
94 the introduction of a normal chromosome 6 by microcell-mediated chromosome transfer.
95                                              Microcell-mediated mtDNA and chromosome transfer can be
96 type hMSH3 or wild-type hMSH6, introduced by microcell-mediated transfer of chromosome 5 or 2, respec
97 estimate the number of senescence genes, and microcell-mediated transfer of chromosomes into immortal
98                                              Microcell-mediated transfer of normal chromosome 11 (chr
99                                Additionally, microcell-mediated transfer of this chromosome in cancer
100  human prostate carcinoma cell line (PC3) by microcell-mediated transfer.
101 lysis with an automated version of the array microcell method (AMCM).
102                                          The microcell Mikrocytos mackini causes Denman Island diseas
103                                              Microcell parasites have independently evolved in severa
104  an alternate approach using high-efficiency microcell photovoltaics embedded between a pair of plast
105 ll with the composition and structure of the microcell preparations, which showed the presence of cyt
106                           Using fluorescence microcells, the assay could detect 15fmol of avian sulfh
107 processes for creating and manipulating such microcells, together with theoretical and experimental i
108 ells suppressed for tumorigenicity following microcell transfer of chromosome 10.
109                                              Microcell transfer of human chromosome 14 from fibroblas
110                                 In contrast, microcell transfer of human chromosome 2 into rat hepato
111 l performances of the new laser-machined BDD microcell were assessed by differential pulse anodic str
112                       Planar electrochemical microcells were micromachined in a microcrystalline boro
113 ent with room temperature atoms contained in microcells with spin-protecting coating, placed inside a

 
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