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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
16                     The inframe deletion and insertion mutations abrogated the transcriptional activa
17                                              Insertion mutations affect the frequency and distributio
18                        A recessive P-element insertion mutation affecting dU2AF38 causes a reduction
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
21                                     Deletion-insertion mutation and colony immunoblotting confirmed t
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
27                    The implications of these insertion mutations are discussed.
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
31                                      A T-DNA insertion mutation at this locus impairs root curling, s
32  MMR and LLR repair pathways, we constructed insertion mutations at HIS4 that form loops of varying s
33                         To determine whether insertion mutations at Lvis1 affect a known proto-oncoge
34                                              Insertion mutations at seven sites in the protease gene
35 tigated by characterizing the effects of two insertion mutations at the AtSS3 gene locus.
36                                         Each insertion mutation bears a unique sequence tag called a
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
39         The phenotypic similarity of the two insertion mutations, both of which were cis-acting, sugg
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
43            One of its monogenic causes is an insertion mutation [c.304ins (GCG)(7)] on the X chromoso
44  These experiments demonstrate that, rarely, insertion mutations can develop in the HIV type 1 protea
45                                 Deletion and insertion mutations confirmed that the FGL sequence was
46    By isolating nearly all the somatic viral insertion mutations contributing to disease in these str
47                                         This insertion mutation cosegregated closely with the osm1 ph
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),
51                          A series of alanine insertion mutations designed to interrupt the hydrophobi
52 erived macrophages (BMDMs), we identified an insertion mutation disrupting the H. capsulatum homolog
53           Results show that the deletion and insertion mutations do not significantly change the seco
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
59                                     The hpuA insertion mutation exerted a polar effect, abolishing ex
60                               Removal of the insertion mutation from this recombinant restored replic
61 he effects of specific EGFR and HER2 exon 20 insertion mutations from NSCLC patients that had clinica
62      Complementation analyses with different insertion mutations further defined and confirmed the se
63 e AI were compound heterozygotes for a novel insertion mutation (g.12946_12947insAGTCAGTACCAGTACTGTGT
64                                              Insertion mutations generated by REMI have facilitated t
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
68  delta mutants, including suppression of the insertion mutation his4-912 delta.
69 . pertussis mutant, SK6, containing a TnphoA insertion mutation in a Bvg-repressed gene (vrg6) was de
70                          First, a transposon insertion mutation in a gene encoding a subunit of hydro
71                                           An insertion mutation in a putative PG acetylase gene (desi
72                                 However, the insertion mutation in accF abolished detectable uptake o
73           Homozygous plants carrying a T-DNA insertion mutation in AtSPP, spp-2, could not be recover
74  parallel to bmp signaling, we identified an insertion mutation in bmp4.
75                                   A nonpolar insertion mutation in C. rodentium espB was constructed
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
80                                           An insertion mutation in gldB was polar on gldC, suggesting
81                  A previously described 4-bp insertion mutation in GRN exon 2 comprised the majority
82  an in-frame deletion of cdh and a kanamycin insertion mutation in lpxH, covered by pKJB5.
83 h temperatures, we constructed a chromosomal insertion mutation in lpxP, the structural gene for the
84       Moreover, the virus that contained the insertion mutation in m09 exhibited a titer similar to t
85    In contrast, the virus that contained the insertion mutation in M83 exhibited a titer of at least
86                                           An insertion mutation in mga (the multigene activator) down
87        NT1 or UIA5 harboring pYDH208 with an insertion mutation in mocC failed to utilize MOP as the
88                                   A deletion-insertion mutation in msbB, a gene that encodes a lipid
89 d by selecting for the correction of a 16-bp insertion mutation in one of the tk sequences.
90                                           An insertion mutation in one of these genes, Mx4885, caused
91                                 A transposon insertion mutation in pgant3 or RNA interference to pgan
92                                           An insertion mutation in ppk causes a decrease in adaptive
93                                           An insertion mutation in the abcA gene resulted in cells di
94 eterozygous, exon 37, six-base pair in-frame insertion mutation in the affected patient and aunt but
95 Pase activity, can fully complement a lethal insertion mutation in the ATTOC159 gene.
96                 A B. subtilis strain with an insertion mutation in the citB gene was devoid of aconit
97 tification of a long-lived mutant bearing an insertion mutation in the cyclin gene clg1(+).
98  mutations, including a newly isolated T-DNA insertion mutation in the gene encoding the ethylene rec
99                      We obtained a recessive insertion mutation in the gene encoding yeast TBP-associ
100                             We identified an insertion mutation in the gene Sfn in repeated epilation
101 ssociated with a hypomorphic retroviral-like insertion mutation in the Gria4 gene, encoding one of th
102                                           An insertion mutation in the hsp16.6 gene resulted in lower
103                         Strains harboring an insertion mutation in the lpxL(htrB) gene, which encodes
104                    Embryos homozygous for an insertion mutation in the LRP6 gene exhibit developmenta
105                                           An insertion mutation in the metL gene of Salmonella typhim
106  direct association with a transgene-induced insertion mutation in the mouse.
107 es the transcriptional effects of a Ty delta insertion mutation in the promoter of the HIS4 gene, a p
108         In a murine skin infection model, an insertion mutation in the response regulator gene, trxR,
109                                           An insertion mutation in the sbo gene also conferred loss o
110          Re-sequencing revealed that a 54-bp insertion mutation in the upstream region of miR-15a-16
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
113                                  A P-element insertion mutation in this interval exhibits a similar d
114 rders of magnitude, whereas a strain with an insertion mutation in tolB showed no reduction in CTXphi
115                                           An insertion mutation in traI abolished the production of A
116 , the implication is that the two-amino-acid insertion mutation in Vif contributes significantly to t
117                    A mutant strain having an insertion mutation in vnfY has 10-fold less vnf dinitrog
118 eltaICP4), and in1814, a virus containing an insertion mutation in VP16.
119                       A nonpolar chromosomal insertion mutation in wzyPaO11 in P. aeruginosa PA103 co
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
122                                        T-DNA insertion mutations in ACA10, but not in the two other A
123                                        T-DNA insertion mutations in ADA2b and GCN5 were found to have
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
126 se genes by salt stress was blocked by T-DNA insertion mutations in AtS1P and AtbZIP17.
127                                      Similar insertion mutations in attR had no significant effect on
128 rimination between wild-type and deletion or insertion mutations in BRCA1 and BRCA2 with CE-based HDA
129 he generation of relatively large (31-codon) insertion mutations in cloned genes.
130                                              Insertion mutations in crr or ptsI of the phosphoenolpyr
131               We identified three pseudoexon insertion mutations in dystrophinopathy patients, two of
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.
135                                              Insertion mutations in EGFR and HER2 both occur at analo
136             Strains carrying combinations of insertion mutations in eight candidate loci were created
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
139               We identified two heterozygous insertion mutations in exon 1 of TNFRSF11A in affected m
140                                              Insertion mutations in frzS caused both vegetative sprea
141                                   Transposon insertion mutations in Gemin3 are larval lethals and als
142                                    Predicted insertion mutations in genes of interest can be identifi
143 nic suppressors of axr2-1 or in a screen for insertion mutations in IAA genes.
144 is study, we used sequence substitutions and insertion mutations in lasBp-lacZ fusion plasmids to exp
145          We systematically made deletion and insertion mutations in loop 1 then monitored splicing ac
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
148                                              Insertion mutations in purG and purI prevent thiamine sy
149                                  Previously, insertion mutations in rimJ, a gene encoding the N-termi
150 xhibited by DeltabipA strains and identified insertion mutations in rluC.
151  selected as suppressors of Ty or solo delta insertion mutations in Saccharomyces cerevisiae have ide
152                                              Insertion mutations in sprA and sprB did not significant
153                          Construction of hel insertion mutations in strain H. influenzae Rd demonstra
154                                         Base insertion mutations in the anticodons of two different E
155         Here, we report the effects of T-DNA insertion mutations in the Arabidopsis GGB gene, which e
156  repair of DSBs in plants, we isolated T-DNA insertion mutations in the Arabidopsis homologs of the K
157                    Our results indicate that insertion mutations in the cytoplasmic tail of the MuLV
158 terogeneity resulting from gene deletion and insertion mutations in the E. chaffeensis genome.
159               We constructed a large pool of insertion mutations in the env gene and analyzed the fit
160 e, we used transposon IS903phikan to isolate insertion mutations in the flp-1 gene (formerly designat
161                                              Insertion mutations in the fsr operon affected biofilm f
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
164                                        T-DNA insertion mutations in the single gene that encodes AtUB
165                       The transposons create insertion mutations in the target gene, allowing phenoty
166                 All possible combinations of insertion mutations in the three genes encoding the acyl
167             R. meliloti derivatives carrying insertion mutations in this locus displayed an N,N,N',N'
168 cterization demonstrated that the transposon insertion mutations in three of the Cds mutants (SR53, S
169                     V. cholerae strains with insertion mutations in tolQ, tolR, or tolA were reduced
170                                              Insertion mutations in two Vibrio cholerae genes, cya an
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
173                   Analysis of a panel of IE1 insertion mutations indicated that disruption of a highl
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
176                          The high density of insertion mutations into Cre allowed us to identify an u
177 d pair of promoters, we introduced point and insertion mutations into the basal elements of the promo
178 he introduction of inactivating deletion and insertion mutations into the E6 or E7 gene.
179 length have been extended by construction of insertion mutations into the uncF(b) gene adding amino a
180                                           An insertion mutation introduced into the gene directly dow
181 cesses that are disrupted by point and small-insertion mutations introduced into potyvirus HC-Pro.
182                                          The insertion mutation is lethal, arresting embryonic develo
183                  Interestingly, this p6(Pol) insertion mutation is often selected in viruses with the
184 selected as suppressors of Ty and solo delta insertion mutations is Saccharomyces cerevisiae have ide
185                                  Deletion or insertion mutations lead to a frameshift that causes mis
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
188 o of them (N771GY and A767-V769dup) are rare insertion mutations located in exon 20.
189          UV melting experiments confirm that insertion mutations lower mt-tRNA(Ser) melting temperatu
190                                              Insertion mutations made with Tn10d(T-POP) can cause tet
191                                   One of the insertion mutations mapped to pseudogene Msed_1517 and e
192 ndings suggest that the analysis of 31-codon insertion mutations may provide a simple approach for ch
193          Mice lacking GlcNAc-TIII due to the insertion mutation Mgat3tmlPst (termed Mgat3neo), exhibi
194                                           An insertion mutation near the upstream promoter for Parp-e
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
198                                   A deletion-insertion mutation of 7169 fur resulted in upregulation
199                   We have identified a T-DNA insertion mutation of Arabidopsis (ecotype C24), named s
200                                           An insertion mutation of fldA was constructed and was letha
201                            In Delta rppA, an insertion mutation of rppA, the PSII gene transcripts we
202 ense, we isolated a mutant with a transposon insertion mutation of sitA, which encodes the periplasmi
203                                           An insertion mutation of the sensor-regulator gene eliminat
204           We have tested wild-type 1a and 18 insertion mutations of 1a and found a perfect correlatio
205             These mutations were found to be insertion mutations of different transposable elements w
206                                       Finger insertion mutations of human immunodeficiency virus type
207                           However, a Tn5 Lac insertion mutation, Omega7536, has been isolated which s
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
210          The effects of the substitution and insertion mutations on termination efficiency at the pyr
211 onformational changes and the effects of the insertion mutations on the kinetics of the transition.
212           We measured the effects of fingers insertion mutations on the misincorporation and excision
213 tes and analyzed the effect of these various insertion mutations on viral phenotypes.
214                                        Of 14 insertion mutations, only IE1(I425) and IE1(I553) failed
215                              We find that an insertion mutation or deletion of HSP104 results in inab
216  by a prion protein (PrP) octapeptide repeat insertion mutation originates from southeast England.
217                                              Insertion mutations outside of the WD domains were wild
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
221                            The G57V and 30:H insertion mutations represent the first CLCN5 mutations
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-
224                                              Insertion mutations show that ARABIDOPSIS CRINKLY4 is re
225                                  Analyses of insertion mutations showed that accA through accE are re
226 ne genes and (2) suppression of Ty and delta-insertion mutations (Spt(-) phenotype).
227                                      Somatic insertion mutations, such as those caused by the inserti
228     Ba1 transduced five distinctly different insertion mutations, suggesting that transduction was ge
229                                    Also, the insertion mutation tended towards fixation in commercial
230                                There was one insertion mutation that added 12 codons and one missense
231                             We also found an insertion mutation that adds another six pairs of CT . A
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
234                                           An insertion mutation that disrupted the fliI open reading
235                                           An insertion mutation that disrupts relA blocks the activat
236                                           An insertion mutation that disrupts the putative comF-flgM
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
241                          We show by deletion-insertion mutations that ftsL and divIC are dispensable
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
244                 Eleven were base deletion or insertion mutations that led to a frameshift and, along
245  led to the identification of 174 transposon insertion mutations that mapped to 13 individual genes.
246                In addition, we have isolated insertion mutations that render this organism defective
247 ntitatively the abilities of 134 independent insertion mutations to (i) make stable viral RNA, (ii) a
248                    The region containing the insertion mutation was cloned, sequenced, and found to c
249                                           An insertion mutation was constructed in pilEL and introduc
250                                           An insertion mutation was constructed in the rpoS gene on t
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
254                  The ratio of deletionrcolon;insertion mutations was 4.1.
255 ction relationships in gB, a panel of linker-insertion mutations was generated throughout the coding
256                        Using a panel of espB insertion mutations, we describe two regions on either s
257                        Twenty-five dipeptide insertion mutations were classified as permissive for in
258                                              Insertion mutations were constructed for four hre genes
259                                              Insertion mutations were constructed in each of the 12 g
260                   Substitution, deletion and insertion mutations were corrected with different freque
261                                              Insertion mutations were found in both genes.
262          In this study, a total of 28 linker insertion mutations were generated throughout the length
263                                              Insertion mutations were identified in genes that are re
264                                              Insertion mutations were introduced into depA, depB, pha
265  in the stress tolerance of S. mutans UA159, insertion mutations were introduced into the genes encod
266                                              Insertion mutations were isolated in cya and crp of Yers
267 cy to T790M and S768N mutations, the exon 20 insertion mutations were sensitive to PF00299804.
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
270                                         This insertion mutation, which segregates in a dominant manne
271                                 EGFR exon 20 insertion mutations, which are typically located after t
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
274                             A double-guanine-insertion mutation within a run of guanines in the herpe
275                We have identified a deletion/insertion mutation within exon D of the human biotinidas
276 ast to iscS or hscA, a strain having a polar insertion mutation within the cysE-like gene was readily
277                              Specific lysine insertion mutations within Acm1 promoted its ubiquitinat
278                  Attempts to place non-polar insertion mutations within either A. vinelandii iscS or

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