1 We explored a novel mechanism of TLR3 up-regulation that is i
2 Using ITPR3, AHR and NMU as examples,
we explored and validated how the genetic variations contribu
3 In this study,
we explored benzylidine cyclohexanone derivatives with non-po
4 In this study,
we explored FA-gene interactions between the missense APOE po
5 In this study,
we explored for the first time, to our knowledge, the role of
6 We explored genome-wide association studies of chronic lympho
7 In this work
we explored if an atlas-based comparison approach reveals sha
8 To explain these results,
we explored modified Langmuir-Hinshelwood type pathways that
9 ture of the muscarinic M2 receptor in complex with iperoxo,
we explored potential agonists that lacked the highly conserv
10 We explored relationships between ASD and residential locatio
11 We explored risk factors for CSF discordance and escape in pa
12 We explored sex-specific DNA methylation in the cord blood of
13 a 'barometer' of energy demands relative to energy intake,
we explored the causes and consequences of variation in body
14 Here
we explored the climatic and geological drivers of a particul
15 m GVHD prophylaxis, conditioning regimen, and donor source,
we explored the correlation of 10 previously identified bioma
16 In this study,
we explored the detection of ZIKV antigen in a defined leukoc
17 In this study,
we explored the diversity of protease- and IgG subclass-restr
18 We explored the dynamics of sunspot-producing magnetic fields
19 In this study,
we explored the effects of chemical modifications to a natura
20 We explored the factors motivating such behaviour among leopa
21 We explored the functional reorganization of the central and
22 We explored the functionality of two terminal PKS modules tha
23 Here
we explored the genetic mechanism underlying the expression o
24 Here
we explored the growth and functions of Drosophila cortex gli
25 Here,
we explored the impact of conditional deletion of Bmal1 in en
26 Using a zebrafish ncx1 mutant,
we explored the impacts of impaired Ca(2+) homeostasis on myo
27 We explored the landscape of BCAs at nucleotide resolution in
28 Finally,
we explored the limit of our architecture in terms of bytes p
29 We explored the mechanisms involved in the regulation of [Pyr
30 In this study,
we explored the molecular determinants and potential mechanis
31 urally occurring WS-linked gain-of-function Cxcr4 mutation,
we explored the possibility that the lymphopenia in WS arises
32 Accordingly,
we explored the potential of four silica-based materials (MCM
33 We explored the potential role of tissue degeneration and rem
34 mouse endothelial-derived EOMA cell line as a model of HE,
we explored the regulatory effect of platelets.
35 We explored the relationship between the physical nanoenviron
36 We explored the relationship between TMAO and all-cause morta
37 We explored the relationships between the level of protection
38 Therefore,
we explored the role of CCL7 in mast cell activity and motili
39 Herein
we explored the use of microfluidic devices or microchambers
40 Herein
we explored the value of functional magnetic resonance imagin
41 We explored this in this study while accounting for the timin
42 We explored this possibility by demonstrating consistent hist
43 Here
we explored this possibility by means of transcranial magneti
44 We explored,
through mathematical modeling and simulations, t
45 We explored topical vaginal application as an approach to ini
46 We explored two strategies to generate suitable pLAIVs.
47 We explored,
using individual patient data, week 13 circulati
48 Given reports of CD151 expression on T cells,
we explored whether CD151 would mark T cells in a hyperactiva
49 ing pregnancy with child body composition have been unclear.
We explored whether SCB intake during pregnancy was associate
50 Herein
we explored whether urinary proteomic biomarkers specific for