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1 s showed a complete lack of secretion of the mutated form.
2 th expression constructs for both normal and mutated forms.
3 g its over-expression in either wild-type or mutated forms.
4 nvestigate the molecular properties of these mutated forms and their relationship with the resulting
7 ndard Escherichia coli L-ASP to predict what mutated forms could be engineered to retain activity aga
9 and their N-terminal lobes, in wild-type and mutated forms, has been successfully accomplished by sev
12 alpha-syn degradation, suggesting that this mutated form is a bona fide substrate of this degradatio
14 of decorin proteoglycan or protein core as a mutated form lacking any glycosaminoglycan side chains i
16 tutively activated in AML and thus, like its mutated form, might contribute to the altered signaling
17 es indicated that immunization with a single mutated form of 3D7 AMA1 was sufficient to increase the
19 A(.) We have also solved the structures of a mutated form of ALDH2 where Arg-475 is replaced by Gln (
20 dent assays document that cells expressing a mutated form of Bves are severely impaired in the recycl
21 -ray scattering (SAXS) analysis shows that a mutated form of c-Abl, in which the N-terminal cap and t
23 of the misfolded protein mimics zeolin or a mutated form of carboxypeptidase Y (CPY*) also induced a
27 logy showed that cortical expression of this mutated form of CREB during monocular deprivation preven
29 ased on specificity studies conducted with a mutated form of cSN50, a functional nuclear localization
30 animals treated with anti-CD80 mAb or with a mutated form of CTLA4Ig (which does not bind to CD86) re
32 dGal-1 binding, we examined the binding of a mutated form of dGal-1 that weakly dimerizes (monomeric
33 tedly, overexpression of a dominant negative mutated form of Fas-associated death domain protein (FAD
34 ogenase (D-LDH) activity was identified as a mutated form of glycerol dehydrogenase (GlyDH; D121N and
35 -induced cell proliferation, whereas a point-mutated form of Grb14 incapable of binding to FGFR1 enha
36 roteasomal activity, expression of the R120G mutated form of HspB5 (associated with myofibrillar myop
37 (90-94 hours after egg laying) expressing a mutated form of human alpha-Syn (A53T) in dopaminergic (
40 e groups of mice engineered to overexpress a mutated form of human SOD1 (SOD1(G93A)) resulted in an e
41 w PRG-PRP system that employs, as the PRG, a mutated form of human thymidine kinase 2 (TK2) and 2'-de
42 ial epithelial cells overexpressing a kinase-mutated form of IkappaB kinase beta (IKKbeta-KM), the ac
44 activation by stable expression of a kinase-mutated form of IkappaB kinase caused increased and prol
46 s encoded NKG2D binding protein (OMCP) and a mutated form of IL-2 with poor affinity for IL-2Ralpha.
47 l neuronopathy is caused by infection with a mutated form of JCV, leading to a shift in viral tropism
50 estored U50,488-CPA, whereas expression of a mutated form of KOR that could not initiate p38alpha MAP
51 contrast, lentiviral expression in DRN of a mutated form of KOR that fails to activate p38 MAPK requ
53 anced whole-cell K(+) currents produced by a mutated form of Kv2.1 mimicking apoptosis in a mammalian
56 tion-time of flight/mass spectrometry of the mutated form of lipomannan shows a family of phosphatidy
60 ull-length mVps24p are co-transfected with a mutated form of mVps4p (which is defective in ATP hydrol
61 ation by both MyoD and myogenin, including a mutated form of myogenin in which two potential inhibito
62 otor neuron degeneration 2 mice that carry a mutated form of Omi that affects its proteolytic activit
66 in cells in a p53-dependent manner and by a mutated form of p53 that is competent in inducing apopto
68 the Fv fragment of an antibody is fused to a mutated form of PE, induces apoptosis of the MCF-7 breas
71 are, however, reversed by the presence of a mutated form of pRB which cannot be hyperphosphorylated.
73 t immunotoxin comprised of human IL-13 and a mutated form of Pseudomonas exotoxin (IL-13-PE) might af
74 f a chimeric protein composed of IL-13 and a mutated form of Pseudomonas exotoxin (IL13-PE38QQR) to c
75 imeric fusion protein comprising IL-13 and a mutated form of Pseudomonas exotoxin (termed IL13-PE38QQ
76 prised of a circularly permutated IL-4 and a mutated form of Pseudomonas exotoxin [IL4(38-37)-PE38KDE
77 ric protein composed of interleukin-13 and a mutated form of Pseudomonas exotoxin A, IL13-PE38QQR.
81 red with Ad-GFP or PBS controls, whereas the mutated form of Rad GTPase, which can bind GDP but not G
83 specific alterations were not seen when the mutated form of Six3 cDNA was used in similar experiment
84 ormal levels by wild-type SOS2, but not by a mutated form of SOS2 lacking the T168 residue phosphoryl
88 ly, the only selectable marker is gyrB(r), a mutated form of the chromosomal gyrB gene that encodes t
89 d-type form of Vigna aconitifolia P5CS and a mutated form of the enzyme (P5CSF129A) whose feedback in
90 ransgenic mouse model of AD overexpressing a mutated form of the human amyloid precursor protein (APP
91 olfactory system in mice that overexpress a mutated form of the human amyloid-beta precursor protein
93 ssay system is demonstrated in an assay of a mutated form of the human pancreatic ribonuclease gene i
94 odel of ALS (G93A-SOD1) that overexpresses a mutated form of the human SOD1 gene that is a cause of f
95 described a fusion protein between Cre and a mutated form of the ligand binding domain of the estroge
96 uitination was also observed for an inactive mutated form of the molecule (M1WI), suggesting that MAR
97 inant negative inhibition of the HIV PR by a mutated form of the protease and found relative dimeriza
98 uence by combining the high sensitivity of a mutated form of the protein pore Mycobacterium smegmatis
100 roduction in a receptor chimera expressing a mutated form of the rPAFR3i domain (rPACAPR2/rPAFR3imut)
101 ontrol of the scaffold protein STM, a triply mutated form of the stable intracellular protein inhibit
102 d inhibition of the proteolytic process by a mutated form of the ubiquitin-conjugating enzyme Ubc4.
103 either wild type full-length Six3 cDNA or a mutated form of this gene in which the interaction with
111 ed weak inhibition of HDV RNA replication by mutated forms of ADARs defective for deaminase activity.
118 necessary for an ethylene response, because mutated forms of both LeETR4 and LeETR5 confer dominant
122 hreonine) residue but fails to phosphorylate mutated forms of C(4) PEPc in which this specific site h
123 hybridomas transfected to express native or mutated forms of CD4, it was determined that IL-16/CD4 i
124 hybridomas transfected to express native or mutated forms of CD4, it was determined that IL-16/CD4 i
125 hesion properties of fractalkine, we created mutated forms of CX3CR1 that have little or no ability t
128 and 430 of enolase in A. hydrophila SSU; the mutated forms of enolase were hyperexpressed in Escheric
132 ssion, binding, and G protein coupling of 28 mutated forms of FPR in stably transfected Chinese hamst
133 cells, wild-type and several amino-terminal mutated forms of gamma-catenin had similar transforming
135 mouse to determine whether the expression of mutated forms of GluR2 can rescue WT synaptic responses.
137 uires the presence of active enzyme, because mutated forms of heparanase lacking heparan sulfate-degr
138 begin to address these mechanisms, different mutated forms of HSV-1 TK at residue Gln-125 that have d
140 cells expressing full-length and selectively mutated forms of human, murine, and human/murine chimeri
141 40 and Asp1-Glu3 and Lys16-Glu22 of Abeta42) mutated forms of IDE and NMR structures of the full-leng
142 In this regard, we have shown that various mutated forms of IkappaBalpha are potent inhibitors of o
143 clear proteins and viral antigens we studied mutated forms of influenza virus nucleoprotein (NP) that
144 olite 2-hydroxyglutarate (2HG), generated by mutated forms of isocitrate dehydrogenase (IDH1 and IDH2
147 s that inducibly express either wild-type or mutated forms of MCG10 and MCG10as, we found that MCG10
151 re heteroplasmic, meaning that wild type and mutated forms of mitochondrial DNA (mtDNA) coexist in th
152 binding properties of native, precursor, and mutated forms of mitochondrial ssDNA-binding protein (mt
154 s as a homotrimer, and expression of several mutated forms of NF7 in oocytes demonstrated that both t
156 signal transduction and the activity of the mutated forms of NOTCH1 found commonly in human T cell a
157 ls of breast cancer induced by wild-type and mutated forms of oncogenic ErbB2 or the polyomavirus mid
159 nts in vitro yielded both the native and the mutated forms of P90, indicating that the protease prese
163 to lipid droplets coated with perilipin A or mutated forms of perilipin with an intact C-terminal seq
164 Here, we report studies of the affinities of mutated forms of Pex5p for a series of PTS1 peptides and
167 arly to cells expressing either wild type or mutated forms of PSGL-1 in both flow cytometric and roll
171 s of cell lines expressing wild type (WT) or mutated forms of ras or rac were generated and analysed
172 ed a library of plasmids expressing randomly mutated forms of recombinant VacA and identified 10 muta
175 opathy), or expression of the G985R and G93A mutated forms of superoxide dismutase 1 (linked to famil
178 y 55% amino acid identity with Ras proteins, mutated forms of TC21 exhibit the same potent transformi
179 d in the brain of transgenic mice expressing mutated forms of the amyloid precursor protein (Tg2576 m
180 i1-5 and bri1-9 mutant plants, which harbour mutated forms of the brassinosteroid receptor BRI1.
184 cific activities of native StxA1, as well as mutated forms of the enzyme with substitutions in cataly
189 We demonstrate here, through analysis of mutated forms of the protein, that the non-canonical nin
191 e and characterized yeast strains expressing mutated forms of the RNA using a gene shuffle technique.
192 e expressed constructs coding for native and mutated forms of the two major splice variants of the pe
193 are needed to combat the rapid emergence of mutated forms of the virus that are resistant to existin
194 s and OTRs with GRKs and PKC, wild types and mutated forms of these receptor subtypes were stably exp
195 omote biliary excretion of sterols, and that mutated forms of these transporters predispose to sterol
198 ere are two periods of selection against the mutated form, one early on possibly during satellite cel
199 wild-type yeast profilin gene (PFY1) with a mutated form (pfy1-111) that has codon 72 changed to enc
200 ransferase*amphiphysin-SH3 domain, but not a mutated form that cannot bind to dynamin, inhibited both
202 igand binding truncated form, LBD (T), and a mutated form (Thr-->Ala substitution) identified in the
203 beta-catenin, for which only amino-terminal mutated forms transform RK3E epithelial cells, wild-type
204 mice that expressed either the wild-type or mutated forms, using cDNA clones encompassing only the c
205 nel of monoclonal antibodies showed that the mutated forms were indistinguishable from wild-type gB i
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