1 We further assessed the ability of this EVG nanoformulation t
2 Using this afferent nerve,
we further build a power-free spiking mechanoreceptor system
3 We further caution that behavioural experiments need to consi
4 We further characterize lesion recognition by ATL and directl
5 We further characterized Nck1's proinflammatory role by ident
6 By using in vivo imaging and transfusion experiments,
we further confirmed that senescent erythrocytes that are ret
7 Taken together,
we further delineate DMN function by demonstrating the relati
8 We further demonstrate how fragmentation of THF-doped DOM in
9 We further demonstrate that cross-linking impairs the cholest
10 Here,
we further demonstrate that more than ten fundamental equatio
11 We further demonstrate that the meshes generated by the Geome
12 We further demonstrate that treatment with radiation and poly
13 We further demonstrated its applicability by analyzing glycop
14 We further demonstrated that Msi1 overexpression affects IEC
15 We further demonstrated that SOX9 knockdown increases cellula
16 We further demonstrated that synchrotron-based X-ray imaging
17 Using a benchmark of other LRR protein complexes,
we further demonstrated that the present approach may be broa
18 We further determined associations with change in ADHD sympto
19 We further discuss how these properties contribute to intesti
20 Therefore,
we further discuss practical methods and strategies to mitiga
21 We further discuss the neural mechanisms that support changes
22 We further estimate that, under a 'business-as-usual' climate
23 We further evaluated transmissibility of oral microbiomes fro
24 We further explored its application in the N-glycan profile o
25 We further found that additional important factors are involv
26 We further found that pharmacological inhibition of downstrea
27 n close proximity to subjacent subsarcolemmal mitochondria;
we further found that subjacent subsarcolemmal mitochondria p
28 We further found that the feeding of meat preparations with a
29 We further highlight the strengths of mixed-effects modeling
30 We further identified a marginal increase in mutation rate in
31 We further illustrate the benefits of our methods in applicat
32 We further investigated the molecular network supporting the
33 We further made the annotated data and protein structures rea
34 We further present a theoretical framework to justify our mod
35 We further present advances in animal models that are importa
36 We further replicated 50 genes in an independent GWAS, includ
37 We further report ComGC solution structures from two naturall
38 We further report the cryoEM structure of human CMG bound to
39 We further show that GATIR mice provide an ideal tool for non
40 We further show that Hel2 and Gcn2 are activated by a similar
41 We further show that interruption of Cx43 endocytosis in Abet
42 We further show that loss of both Trp53 and Rb1 disables tran
43 We further show that multiple immune cell populations contain
44 on in wild-type cells also repressed virulence through aphB
We further show that ompR expression was not altered by chang
45 We further show that respiratory burst induces antibiotic tol
46 We further show that RsaD redirects carbon overflow metabolis
47 We further show that the interactions that would maximize eff
48 We further show that those different binding properties direc
49 We further showed that ZmMC1 and ZmMC2, but not ZmMC9, are pr
50 We further validated the functions of 3 new adipose IR genes