1 We expressed 4 CD23 variants.
2 To separate the roles of LDB1 and mediator in LCR looping,
we expressed a looping-competent but transcription-activation
3 We expressed a tagged form of MAN2A1-FER in NIH3T3 and HEP3B
4 To evaluate the pathological relevance of these peptides,
we expressed Abeta36-40 and Abeta42-43 in Drosophila melanoga
5 Next,
we expressed and purified EGFR and HER3 tail-only constructs.
6 Here,
we expressed and purified full-length porcine INSL3 (pINSL3)
7 We expressed and purified human beta-cardiac myosin subfragme
8 Here,
we expressed and purified the luminal domain of Saccharomyces
9 For a full functional characterization of the L176F mutant
we expressed and purified the mutant protein and measured key
10 We expressed and purified the Rv2633c protein in Escherichia
11 We expressed Arabidopsis IRT1 (AtIRT1) under control of the M
12 We expressed asynchrony as the annual variation in bird pheno
13 To this end,
we expressed Atf1 phosphorylation mutants from a constitutive
14 Using viral vectors taken up at axon terminals,
we expressed chemogenetic actuators selectively in LC neurons
15 number and position of the incorporated chimeric subunits,
we expressed chimeric constructs with subunit dimers.
16 properties of CRY proteins required for circadian function,
we expressed CRY in SCN of Cry-deficient mice using adeno-ass
17 ic interaction of Ad36E4ORF1 in enhancing glycemic control,
we expressed E4ORF1 of Ad36 or Ad5 or fluorescent tag alone b
18 We expressed fluorescent fusions of FtsZ from diverse photosy
19 relationship between MAPT-induced aneuploidy and apoptosis,
we expressed FTLD-causing mutant forms of MAPT in karyotypica
20 in heavy chain (MHC) phosphorylation roles in 3D migration,
we expressed GFP-tagged NMIIA wild-type or mutant constructs
21 We expressed global and regional LV denervation as the percen
22 We expressed human and Caenorhabditis elegans AMPylation enzy
23 To address this,
we expressed human CFH mutants in Pichia pastoris We found th
24 To overcome this deficiency,
we expressed human fucosyltransferase 6 using modified mRNA.
25 anism of the R1441C mutation in the GTPase domain of LRRK2,
we expressed human wild-type or R1441C LRRK2 in dopaminergic
26 We expressed in E. coli VLPs from the bacteriophage AP205 gen
27 We expressed Kv4.2 channels in Xenopus oocytes and measured t
28 Here,
we expressed milligram quantities of functional full-length P
29 In this study,
we expressed MpPR-1 proteins in a yeast model lacking endogen
30 Using a state-of-the-art strategy,
we expressed multiple complementary reporter molecules from t
31 When
we expressed MuPKS heterologously in yeast, yellow pigments a
32 To define the intrinsic motifs that regulate coupling,
we expressed mutant CaV2.1 alpha1 subunits on a CaV2.1 null b
33 We expressed mutant GlyRs in HEK293T cells, and electrophysio
34 To evaluate this,
we expressed native and engineered Galpha proteins from soybe
35 We expressed PbENT1 in purine auxotrophic yeast and used radi
36 To test this hypothesis,
we expressed potassium and sodium mechanosensitive ion channe
37 We expressed RABV large polymerase protein (L) in insect cell
38 We expressed recombinant salivary proteins from Lutzomyia int
39 To determine the function of BciD,
we expressed the bciD gene of Chlorobaculum limnaeum strain D
40 As an alternative strategy,
we expressed the canola IKU2 ortholog in Arabidopsis endosper
41 characterize the elusive mechanics of TRPV4 volume-sensing,
we expressed the channel in Xenopus laevis oocytes together w
42 This was found when
we expressed the dose as the conventional total soil concentr
43 To address this discrepancy,
we expressed the entire ectodomain of mouse P-selectin as a m
44 We expressed the mutation in cell lines and primary cultures,
45 aracterize their functions after penetration, in this study
we expressed the Pseudomonas syringae effector HopAI known to
46 To evaluate the functional effects of the novel variant,
we expressed the wildtype or mutant hEAAT1 in mammalian cells
47 We expressed these SI variants in COS-1 cells and analyzed th
48 We expressed these two TOP1MT variants and the double-variant
49 In addition,
we expressed truncated forms and protein chimeras to gain a d
50 When
we expressed wild-type levels of mcm10-m2,3,4 in budding yeas