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1 in a crop affects plant resistance to generalist pathogens, we infected a collection of wild and domesticated tomato acce
2                                                       Here, we infected a small group of male rhesus (Macaca mulatta) and
3                                               In this study we infected autoimmune-susceptible DRB1*0401.AEo and non-susc
4 I-resistant AIVs is associated with in vivo susceptibility, we infected BALB/c mice with recombinant AIVs with R292K (ma8
5                                                             We infected biglycan knockout (KO) and wild-type (WT) C3H mic
6                                                             We infected boa constrictors and ball pythons by cardiac inje
7                                                             We infected boa constrictors and ball pythons with purified r
8                                                       Thus, we infected C57BL/6 mice with two populations of Chlamydia mu
9                                                             We infected cardiomyocytes using a short hairpin RNA lentivir
10                                                             We infected cells from Eptesicus fuscus with MERS-CoV and mai
11                            To simulate ascending infection, we infected EEC aggregates with commensal and pathogenic bact
12  mortality; whereas to include the role of barrier defences we infected flies by dusting the cuticle with fungal spores.
13                    To drive type 1 immunity in CNS tissues, we infected GL261 tumor-bearing mice with attenuated rabies v
14 of human corneal epithelial (HCE) cells to HSV-1 infection, we infected HCE cells at three different dosages of HSV-1 and
15                                    To test this hypothesis, we infected heterozygous STING N153S mice with murine gammahe
16                                                             We infected Huh7 and Huh7.5.1 cells and primary human hepatoc
17  strain-specific effects of IAV NS1 on human DC activation, we infected human DCs with a panel of recombinant viruses wit
18                                               However, when we infected human macrophages, the mutant triggered a lower l
19 e effects of excess IL-18 on virus-induced immunopathology, we infected Il18-transgenic (Il18tg) mice with lymphocytic ch
20                                                       Here, we infected Irf1 (-/-) mice with two distantly related arthri
21 determine if YopE or YopT triggers pyrin dephosphorylation, we infected lipopolysaccharide (LPS)-primed murine macrophage
22 f abortive infection in driving CD4(+) T cell loss in vivo, we infected macaques with simian-human immunodeficiency virus
23                                                             We infected macrophage and intestinal epithelial cell lines w
24                           To investigate these differences, we infected male and female mice of different age groups with
25 is, necroptosis, and apoptosis during Salmonella infection, we infected mice and macrophages deficient for diverse combin
26                                        To investigate this, we infected mice depleted of platelet GPVI or CLEC2 by antibo
27 idate the role of Notch signaling during fungal infections, we infected mice expressing the pan-Notch inhibitor dominant
28 velop a TB model that more closely resembles human disease, we infected mice with an ultra-low dose (ULD) of between 1-3
29                                                             We infected mice with chronic lymphocytic choriomeningitis vi
30 ess the role of UNC93B and TLR for MHV68 infection in vivo, we infected mice with MHV68.
31                                    To test this hypothesis, we infected mice with viruses coadministered with a single do
32                                                             We infected murine RAW264.7 macrophages with Mycobacterium ma
33                                                       Here, we infected myeloid cell cultures with VEEV to identify the c
34                                                             We infected neonatal C57BL/6 or C3H mice with H. pylori or tr
35                                                             We infected nonhuman primate cell cultures and then crab-eati
36                                                             We infected nontransformed human intestinal enteroid cultures
37                                    To test that hypothesis, we infected Pompe cells and then assessed the VZV infectious
38                    To investigate this phenomenon in vitro, we infected primary CD4+ T cells with an HIV construct expres
39                                                             We infected primary fibroblasts isolated from domestic cats (
40                                                             We infected RdRP mice and wild-type (WT) mice with various do
41 esponses and the role of immune responses in pathogenicity, we infected rhesus macaques with Borrelia turicatae (a new wo
42                                                       Here, we infected rhesus macaques with simian-human immunodeficienc
43       To increase our understanding of the immune response, we infected the retinal pigment epithelial (RPE) cell line, A
44 f virulence determinants or the evaluation of therapeutics, we infected them with a green fluorescent protein-expressing
45                                To study neural development, we infected three-dimensional cortical organoids with HCMV.
46                              To address this knowledge gap, we infected two genetic models of Nod1 deficiency with the H.
47                                                             We infected two induced pluripotent stem cell (iPSC) lines an
48 ted a screen of mice from the Collaborative Cross (CC) that we infected with influenza, severe acute respiratory syndrome
49     To explore approaches to classify susceptibility to TB, we infected with MTB dendritic cells (DCs) from putatively re
50                                    To test this hypothesis, we infected young adult mice with either of two genetically d