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1 As as regulators of TSSG and copy gains of a drug resistance gene.
2 ribozymes that cleave a sequence in the marA drug resistance gene.
3  spleen necrosis virus (SNV) or the neomycin drug resistance gene.
4 l-time adaptive changes in expression of the drug-resistance gene.
5  autograft can be protected by transfer of a drug-resistance gene.
6 th alterations in the level of expression of drug resistance genes.
7 inant DNA products, and the presence of both drug resistance genes.
8 f cytotoxins and expresses a number of known drug resistance genes.
9 d illustrate an in vivo approach for finding drug resistance genes.
10 ating power to prospectively detect emerging drug resistance genes.
11 ontain important antigenic and anti-malarial drug-resistance genes.
12 d for selection in combination with multiple drug resistance gene 1 (MDR1) could have an enhanced eff
13 n of drug resistance proteins, such as multi-drug resistance gene-1 P-glycoprotein (MDR1) and multidr
14 s in two previously unreported P. falciparum drug resistance genes, an acetyl-CoA transporter (pfact)
15 n an attP-containing plasmid together with a drug resistance gene and the integrase on a separate pla
16  recent evolutionary selection both in known drug resistance genes and at new loci, and these varied
17                  The availability of the two drug resistance genes and of several unique restriction
18 ds, R1 and RP4, both of which carry multiple drug resistance genes and were shown to impose an initia
19 tive-negative, but the positive and negative drug-resistance genes are replaced with differently colo
20 tures based on the permanent activation of a drug-resistance gene by the Cre recombinase.
21 ed a point mutation (homologous marker) or a drug-resistance gene cassette (non-homologous marker).
22 ited amplification and overexpression of the drug resistance gene CKS1B, which we recapitulated in hy
23 binant progeny carrying different numbers of drug resistance gene copies at the same locus, silencing
24             3' traps incorporating different drug resistance genes could be readily exchanged, simply
25 tases, can be used to efficiently excise the drug resistance gene during reverse transcription.
26 an undergo the next cycle of P1 transduction/drug resistance gene excision.
27 ey can be used to monitor viral oncogene and drug-resistance gene expression in transplant patients a
28 s is introduced into the cells to excise the drug resistance gene flanked with the lambda attL and la
29 e marrow cells through the introduction of a drug resistance gene, followed by subsequent administrat
30                          However, the use of drug resistance genes for the selection of expression pl
31  strategies for in vivo cell selection using drug resistance genes have had disappointing outcomes an
32                                 It carries a drug resistance gene, hyg, and a 290-bp repeat sequence
33                 Expression of the selectable drug resistance gene in retroviral vectors used for gene
34 ymorphisms (SNPs) in 4 Plasmodium falciparum drug resistance genes in 668 archived parasite-positive
35 y generated a line that excises loxP-flanked drug resistance genes in all tissues, including the germ
36 py number heterogeneity and the emergence of drug resistance genes in cancer.
37 for amplifying oncogenes in human tumors and drug resistance genes in cultured mouse cells.
38 ce by activating its own expression and many drug resistance genes in response to antibiotics.
39                    The expression of several drug-resistance genes, including MRP and p53, increases
40 depends on the chromosomal neighborhood of a drug-resistance gene inserted at different positions of
41         Often, however, the presence of this drug resistance gene interferes with the normal locus an
42                             Incorporation of drug resistance genes into gene vectors has 2 important
43 tumor cell proliferation, and 4) transfer of drug resistance genes into hematopoietic stem cells to i
44  One approach to this goal is to incorporate drug resistance genes into vectors to enable in vivo sel
45 fer a methylguanine methyltransferase (MGMT) drug-resistance gene into normal bone marrow cells.
46 r for cancer gene therapy is the transfer of drug-resistance genes into bone-marrow stem cells for my
47                          In this vector, the drug resistance gene is expressed in avian cells from th
48 umber of random integration sites at which a drug resistance gene is expressed.
49                                 Generally, a drug resistance gene is inserted with the modified gene
50 tarting with the 5" end: LTR, gag, pol, env, drug resistance gene, lac operator, ColE1, LTR.
51 lective conditions showed that the cassette (drug resistance gene-lac operator-ColE1) insert was pres
52 photropic retrovirus containing the multiple drug resistance gene leads to gene transfer not observed
53 cumulation, or amplification of the multiple drug resistance gene (MDR).
54 th factor receptor (EGFR) and human multiple drug resistance gene (MDR-1).
55                The most frequently expressed drug resistance genes, MDR1 and MRP1, occur in human tum
56 odel of gene therapy the P140K mutant of the drug resistance gene methylguanine methyltransferase (MG
57 rge animals - dogs and humans - with a novel drug-resistance gene, MGMT, which is not expressed in no
58                              We inserted the drug resistance genes neo and ble, conferring resistance
59 , sequence types (ST), and presence of known drug resistance genes of E. coli isolates that caused me
60 adily exchanged, simply by selecting for the drug-resistance gene of the replacement vector.
61 The PSTB2 gene is allelic to the pleiotropic drug resistance gene, PDR17, and is homologous to SEC14,
62 ivo is to include in the retroviral vector a drug resistance gene, such as the P140K mutant of the DN
63 lper plasmid and restores the integrity of a drug resistance gene, thereby affording a direct selecti
64 combinase-expressing cassette and remove the drug-resistance gene, thus speeding up the generation of
65 s to breed an animal carrying a loxP-flanked drug resistance gene to an animal that expresses Cre rec
66 f normal host tissue by delivering cytotoxic drug resistance genes to marrow precursor cells and ther
67 s far greater than that observed in previous drug-resistance gene transfer studies.
68 uce transcription of multiple or pleiotropic drug resistance genes via increased expression of a zinc
69 ng a ribozyme targeted to a site in the marA drug resistance gene was constructed to contain an optim
70 trol region (rHS432A(gamma)*), but lacking a drug-resistance gene, we investigated the relationship b
71                                  A number of drug resistance genes, whose products include mutant for
72 ed that transfer of a vector that combines a drug-resistance gene with anti-BCR/ABL antisense (AS) se

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