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1 in a clinical HIV-1 isolate with the MNR 69 insertion mutation.
2 richia coli, each containing a single random insertion mutation.
3 henotype identical to that of a deletion and insertion mutation.
4 S16 homolog through analysis of a transposon insertion mutation.
5 wever, pcfG was unable to complement an ltrB insertion mutation.
6 ts with the C-deletion than those with the C-insertion mutation.
7 del of autism mimicking an autism-associated insertion mutation.
8 tion of a cryptic splice donor site from the insertion mutation.
9 ue predisposition of these two serotypes for insertion mutations.
10 from the phenotypes arising from transposon insertion mutations.
11 issense, nonsense, splice site, and deletion/insertion mutations.
12 a cytoplasmic domain deletion and TM domain insertion mutations.
13 patients with de-novo Thr790Met and exon 20 insertion mutations.
14 n was identified in K14: a heterozygous 1 bp insertion mutation (242insG) upstream of the R125C mutat
15 In merodiploid strains carrying deletion or insertion mutations abolishing the synthesis of AdhE pro
19 Disruption of the rpoS gene by a transposon insertion mutation also prevented acetate-induced acid t
20 entation analysis indicated that a fimI'-kan insertion mutation and a fimI frameshift mutation produc
22 of segregants are those carrying homozygous insertion mutations and allelic triplications, which hav
23 FLT3 receptor is activated by juxtamembrane insertion mutations and by activation loop point mutatio
24 osons are mobile genetic elements that cause insertion mutations and contribute to genome rearrangeme
25 haracterize novel FGFR2 extracellular domain insertion mutations and demonstrate that they are both o
26 s the expression of Ty1 transposable element insertion mutations and genes whose products are require
28 s revealed that gH is relatively tolerant of insertion mutations, as 15 of 22 mutants permitted norma
29 The TREX1 proteins containing R114H and the insertion mutations aspartate at position 201 (D201ins)
30 of exons 2 to 4 of PAX9 revealed a cytosine insertion mutation at nucleotide 793, leading to a prema
32 MMR and LLR repair pathways, we constructed insertion mutations at HIS4 that form loops of varying s
37 at the paired sites, and the introduction of insertion mutations between the sites demonstrated that
38 cytotoxin, but this deletion and several cag insertion mutations blocked induction of synthesis of pr
40 marker and correction of a single base pair insertion mutation by gene targeting, and in all cases o
41 etermined that even small inserts can target insertion mutation by this method and that the insertion
42 ffected family members revealed two separate insertion mutations (c.539-540insT and c.948-949insATGGC
44 These experiments demonstrate that, rarely, insertion mutations can develop in the HIV type 1 protea
46 By isolating nearly all the somatic viral insertion mutations contributing to disease in these str
48 lation, we found only about one-third of the insertion mutations cosegregated with a mutant phenotype
49 wth; and (iv) the deleterious effects of the insertion mutation depend on the presence of the process
50 pleiotropic recessive Arabidopsis transposon insertion mutation, designated hyponastic leaves (hyl1),
52 erived macrophages (BMDMs), we identified an insertion mutation disrupting the H. capsulatum homolog
54 DNA polymerase theta (Poltheta) promotes insertion mutations during alternative end-joining (alt-
55 o new familial cases with novel missense and insertion mutations, each occurring within the T-box dom
56 ruses were constructed by introducing linker insertion mutations either outside the IgG Fc binding do
57 ormed genetic screening for single P-element insertion mutations, enabling us to recover 2500 lethal
58 ne identified by the embryo-defective lethal insertion mutation encodes an RPS16 homolog and has been
61 he effects of specific EGFR and HER2 exon 20 insertion mutations from NSCLC patients that had clinica
63 e AI were compound heterozygotes for a novel insertion mutation (g.12946_12947insAGTCAGTACCAGTACTGTGT
65 s in viral DNA synthesis were induced by the insertion mutation H224, which has been reported to inhi
66 alone, supporting data suggesting that this insertion mutation has polar effects on downstream genes
67 nblocking activity and that all three finger insertion mutations have threefold-decreased sensitivity
69 . pertussis mutant, SK6, containing a TnphoA insertion mutation in a Bvg-repressed gene (vrg6) was de
76 icity defect is partially complemented by an insertion mutation in cbrA that also causes overexpressi
77 551 insertion as well as a separate deletion-insertion mutation in cspA decreased the capacity of S.
78 The capacities of isogenic strains with an insertion mutation in emm49; with a deletion mutation in
79 . burgdorferi, we examined the effects of an insertion mutation in flaB on the amounts of proteins en
83 h temperatures, we constructed a chromosomal insertion mutation in lpxP, the structural gene for the
85 In contrast, the virus that contained the insertion mutation in M83 exhibited a titer of at least
94 eterozygous, exon 37, six-base pair in-frame insertion mutation in the affected patient and aunt but
98 mutations, including a newly isolated T-DNA insertion mutation in the gene encoding the ethylene rec
101 ssociated with a hypomorphic retroviral-like insertion mutation in the Gria4 gene, encoding one of th
107 es the transcriptional effects of a Ty delta insertion mutation in the promoter of the HIS4 gene, a p
111 These sequences contained a two-amino-acid insertion mutation in the Vif gene, which was also obser
112 page was the cause of the original germ-line insertion mutation in this family and that the same mech
114 rders of magnitude, whereas a strain with an insertion mutation in tolB showed no reduction in CTXphi
116 , the implication is that the two-amino-acid insertion mutation in Vif contributes significantly to t
120 nes, Fgf8, Fgf3 and Fgf4, sustain activating insertion mutations in 10%, 42% and 6% of the tumors, re
121 -specific mutagenesis system to create short insertion mutations in a region of the gene known to be
124 e and pathogenesis, we created random TnphoA insertion mutations in an H. ducreyi 35000 library clone
125 ellularly by growth adjacent to strains with insertion mutations in any of the other six xanthomonadi
128 rimination between wild-type and deletion or insertion mutations in BRCA1 and BRCA2 with CE-based HDA
132 This is the first study that documents that insertion mutations in E. chaffeensis that cause attenua
133 we examine the fitness effects of 18 random insertion mutations in E. coli in two resource environme
134 clinical isolate strain V583, we constructed insertion mutations in each of the response regulators.
137 lements in Escherichia coli produces diverse insertion mutations in either a targeted plasmid or a ch
138 stablished mouse lines with loss of function insertion mutations in Ero1l and Ero1lb encoding ERO1alp
144 is study, we used sequence substitutions and insertion mutations in lasBp-lacZ fusion plasmids to exp
146 n contrast to htrB, extracts of strains with insertion mutations in msbB are not defective in transfe
147 , we evaluated the spectrum of protease gene insertion mutations in patient isolates and analyzed the
151 selected as suppressors of Ty or solo delta insertion mutations in Saccharomyces cerevisiae have ide
156 repair of DSBs in plants, we isolated T-DNA insertion mutations in the Arabidopsis homologs of the K
160 e, we used transposon IS903phikan to isolate insertion mutations in the flp-1 gene (formerly designat
162 y a single gene in Arabidopsis thaliana, and insertion mutations in the Hsp90C gene are embryo lethal
163 but attempts to isolate similar mutants with insertion mutations in the region downstream of the gdhA
168 cterization demonstrated that the transposon insertion mutations in three of the Cds mutants (SR53, S
171 lt pathogenesis were interrupted by the IVET insertion; mutations in other ipx genes are necessary to
172 Analyses of a series of site-directed IE1 insertion mutations indicated that a helix-loop-helix (H
174 HIS4 expression of his4-912delta, a promoter insertion mutation induced by the Ty1-912 long terminal
175 wild-type levels, while introduction of the insertion mutation into wild-type Vif sequences resulted
177 d pair of promoters, we introduced point and insertion mutations into the basal elements of the promo
179 length have been extended by construction of insertion mutations into the uncF(b) gene adding amino a
181 cesses that are disrupted by point and small-insertion mutations introduced into potyvirus HC-Pro.
184 selected as suppressors of Ty and solo delta insertion mutations is Saccharomyces cerevisiae have ide
186 te mutations, nonsense mutations, and a 1-bp insertion mutation, leading to a frameshift and prematur
187 V-1) thymidine kinase (tk) gene with a 16-bp insertion mutation linked to either a defective HSV-2 tk
192 ndings suggest that the analysis of 31-codon insertion mutations may provide a simple approach for ch
195 plications containing palindromic frameshift insertion mutations near an HO nuclease recognition site
196 ns on the locus where novel gene deletion or insertion mutations occurred, resulting in the net loss
197 bstitution mutations to complex deletion and insertion mutations occurring in autosomal dominant and
202 ense, we isolated a mutant with a transposon insertion mutation of sitA, which encodes the periplasmi
208 d the effect of the dipeptide fingers domain insertion mutation on strand transfer activity using two
209 dies measuring the influence of a tolC::Tn10 insertion mutation on the expression of an acrA::lacZ re
211 onformational changes and the effects of the insertion mutations on the kinetics of the transition.
216 by a prion protein (PrP) octapeptide repeat insertion mutation originates from southeast England.
218 not bimolecular activation was disrupted by insertion mutations placed immediately downstream of I44
219 n genomic analyses show higher deletion than insertion mutation rates and stronger purifying selectio
220 ficant increase was observed in deletion and insertion mutation rates but no increase in the overall
222 the protein's N-terminal region, the alanine insertion mutations S44[A] and K48[A], and the substitut
223 hifts in protein degrees of freedom with the insertion mutations show mutual compensation for the E2-
228 Ba1 transduced five distinctly different insertion mutations, suggesting that transduction was ge
232 onally, we have identified a pseudoknot loop insertion mutation that appears to point to a genetic in
233 rafish Danio rerio as a site of a retrovirus-insertion mutation that caused severe defects during emb
237 unrelated families, we observed an identical insertion mutation that had occurred in a polycytidine t
238 genesis (STM) to conduct a screen for random insertion mutations that affect colonization in the suck
239 identified a subset of EGFR and HER2 exon 20 insertion mutations that are sensitive to existing coval
240 by isolating bacteriophage MudI1734-induced insertion mutations that blocked the growth-stimulatory
242 his region, there are two, allelic, lethal P-insertion mutations that identify one of these new trith
243 lfon-m-anisidide] were found with transposon insertion mutations that inactivate any of six T4-encode
245 led to the identification of 174 transposon insertion mutations that mapped to 13 individual genes.
247 ntitatively the abilities of 134 independent insertion mutations to (i) make stable viral RNA, (ii) a
251 . aerogenes was cloned and sequenced, and an insertion mutation was generated and shown to be linked
252 tified, cloned, and sequenced and a deletion/insertion mutation was introduced into M. catarrhalis st
253 ene was cloned and sequenced, a deletion and insertion mutation was introduced into N. gonorrhoeae, a
255 ction relationships in gB, a panel of linker-insertion mutations was generated throughout the coding
265 in the stress tolerance of S. mutans UA159, insertion mutations were introduced into the genes encod
268 the mutants bearing the D67N and K70R or 69 insertion mutations, whereas the Q151M mutation seems in
269 utant B. subtilis strain carrying a deletion-insertion mutation which removed the entire splAB operon
272 y genes essential for A motility, transposon insertion mutations with defective A motility were studi
273 son has been constructed and used to isolate insertion mutations with tetracycline-conditional phenot
276 ast to iscS or hscA, a strain having a polar insertion mutation within the cysE-like gene was readily
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