1 macokinetics, target occupancy, and immunological analysis,
we chose 10 mg/kg every 2 weeks as the dose for further devel
2 We chose 218 ChR chimeras from two SCHEMA libraries and assay
3 We chose 3 of these antibodies, denoted as 1C1, 3B10, and 2H7
4 stomize the areas of the ONH and visual field to correlate,
we chose a 30 degrees sector centered on the largest defect s
5 For this purpose,
we chose a conditioning regimen composed of treosulfan (14 g/
6 f pharmacokinetic, pharmacodynamic, and safety information,
we chose a dose of 1000 mg every 2 week for the dose-expansio
7 For this purpose
we chose a non-self-complementary DNA duplex containing the b
8 To demonstrate this principle,
we chose a photocleavable linker and found that installation
9 As complex stimuli,
we chose a set of well-controlled moving naturalistic texture
10 We chose a threshold of 2 h in view of its relevance in time-
11 In our response, we explain why
we chose an existing and internationally recognized delineati
12 We chose articles that assessed the association between cereb
13 As reference enzyme,
we chose cytochrome P450 BM3 that is restricted by NADPH depe
14 To evaluate the capabilities of this system,
we chose eight targets, some of which were difficult to overe
15 Here,
we chose enhanced green fluorescent protein as a model system
16 We chose examples ranging from well separated vesicles to den
17 We chose from 200 southern African, clade C envelope-pseudoty
18 After recruiting 48 mostly small media outlets,
we chose groups of these outlets to write and publish article
19 We chose K. pneumoniae for our in vivo model, since K. pneumo
20 As a consensus raft marker,
we chose monomeric GFP linked via a glycosylphosphatidylinosi
21 We chose not to optimize the model's parameters to replicate
22 We chose one human kinase, ZAP-70, to simulate using molecula
23 We chose ricolinostat 160 mg once daily on days 1-21 of a 28
24 We chose several representative examples to highlight the opp
25 For experimental evaluation,
we chose six sequences from each of the eight templates by ob
26 Here,
we chose the contour length of the unfolded polypeptide as a
27 For this purpose,
we chose the pilus protein FimG from Gram-negative bacteria a
28 behind our first paper on the fusiform face area (FFA): how
we chose the question, developed the methods, and followed th
29 We chose the second transmembrane segment, S2, of a voltage-g
30 We chose thiocillin as a model system, a thiopeptide in the r
31 amyloidogenic, single-point mutations in the alpha-domain,
we chose three specific mutations to address the effects that
32 Given the growing interest in xenobiology projects,
we chose to compare the structural features of XNA polymers a
33 We chose to concentrate on the evaluation of the molecular ro
34 Therefore,
we chose to conduct a multicenter non-randomized trial, in wh
35 We chose to design new molecular probes based on the structur
36 Nevertheless,
we chose to develop an accurate and truly predictive theoreti
37 water conditions in cells subjected to freezing protocols,
we chose to directly analyze their subcellular water states b
38 much as ET-1 is one of the key regulators of vascular tone,
we chose to examine in more detail the effect of OA-NO2 on en
39 Here,
we chose to focus exclusively on deoxygenation-dependent rheo
40 Of those,
we chose to focus on an inhibitor of heat shock protein 90 be
41 We chose to focus on western China because poverty, ethnic di
42 We chose to investigate rab17, whose expression is restricted
43 We chose to investigate the detailed role of CXCR7 in a murin
44 taking place during the misshaping of the developing brain,
we chose to study cells that are representative of the very e
45 We chose to study this question in the context of acute myelo
46 red prominently in our interactome map of proliferation and
we chose to take it forward in our analysis on the basis of i
47 We chose to target the inflammasome, a molecular complex capa
48 We chose to use trehalose, a nontoxic naturally occurring dis
49 For this study,
we chose two well-established HSV-1 infection models: mouse f
50 Therefore,
we chose UV radiation followed by analyses of the total bromi