1 Braun et al contend that
we did not account for survival, but we did.
2 We did not account for within-country variation in vaccine co
3 We did not detect any morphological or functional changes in
4 We did not detect PI16 expression in neurons or glia in spina
5 However,
we did not detect significant changes in ER stress levels, bu
6 However,
we did not detect significant steady-state currents during UB
7 Although
we did not detect trait coordination with yield stability in
8 Previously we developed a mouse model of GDM, however
we did not evaluate alterations to energy and fat metabolism.
9 htly more affected than men, whereas in children < 15 years
we did not find a sex-specific difference in the prevalence.
10 We did not find a similar class of NW bursting neurons in L2-
11 Among the untreated RM,
we did not find any difference in plasma/CSF or in cell-assoc
12 We did not find any effect of rumination, neither on the inte
13 While searches were biased towards the beacons,
we did not find any evidence that participants successfully e
14 We did not find any studies conducted in midwives nor any stu
15 Furthermore,
we did not find consistent associations between these global
16 We did not find differences among the groups in overall relie
17 We did not find effect modification by HFrEF or HFpEF status.
18 Therefore,
we did not find evidence for a benefit of XTC in the context
19 th stable coronary disease and moderate or severe ischemia,
we did not find evidence that an initial invasive strategy, a
20 effective for escaping pursuing predators in the wild, but
we did not find evidence that cryptic species are less likely
21 We did not find significant differences in fecal microbiota c
22 We did not find significant relationships between baseline SM
23 We did not find that SI variability changed over time, sugges
24 By contrast,
we did not found any biallelic CUBN variants in proteinuric p
25 In this study,
we did not identify a protective association of early childho
26 We did not identify an increased prevalence of ADHD in associ
27 In a case-only analysis,
we did not identify genes with variants shared among more tha
28 We did not identify genetic support for the repurposing of st
29 We did not identify significant associations between retinal
30 While
we did not observe a measurable influence of ozone (0 vs 40 p
31 We did not observe a significant correlation between clinical
32 We did not observe a statistically significant difference in
33 We did not observe any consistent association between residen
34 Nevertheless,
we did not observe any effect of standard treatment in acute
35 In our study,
we did not observe any emergence of antibiotic resistance in
36 We did not observe any lymphatic vessels in spinal dura mater
37 We did not observe changes in modular organization, nodal car
38 We did not observe evident sex differences in the frequency o
39 We did not observe higher concordance for CH within MZ twin p
40 We did not observe impaired motor impulsivity on the stop-sig
41 We did not observe much difference in replicative fitness of
42 Although
we did not observe other developmental or phototransduction d
43 We did not observe reduced tissue eosinophil numbers in assoc
44 ntly between constipated respondents of various ages, while
we did not observe sex-based differences.
45 We did not observe the mediation effect in men.
46 Although
we did not observe the previously described spine loss during
47 Limitations of this study include that
we did not review grey literature and that we were unable to
48 We did not see any consistent associations of second trimeste
49 Significantly, if
we did not use a pan-genomic approach, we would grossly overe
50 gating (DDG) (we use the term DDG-retro to distinguish that
we did not use the real-time R-threshold-based application of