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1 the presence of rnhB genes in a yeast and a roundworm.
2 logues also regulate sleep in fruitflies and roundworms.
3 utside arthropods, including human parasitic roundworms.
4 udy feeding in living Caenorhabditis elegans roundworms.
5 ificantly reduced hookworm (93.4% to 85.2%), roundworm (22.8% to 1.4%), and whipworm (86.8% to 59.5%)
6 duced prevalence of hookworm (8.1% to 1.3%), roundworm (28.4% to 0.9%), and whipworm (51.9% to 31.9%)
7 asis (12.6% to 4.6%), hookworm (7.8% to 0%), roundworm (33.5% to 6.1%), and whipworm (42.7% to 8.9%).
8 s (16.7% to 5.3%), hookworm (10.3% to 1.9%), roundworm (34.5% to 2.3%), and whipworm (55.5% to 40.3%)
9 ced prevalence of hookworm (94.0% to 71.8%), roundworm (62.0% to 1.4%), and whipworm (93.1% to 74.5%)
10 aks of eosinophilic meningitis caused by the roundworm Angiostrongylus cantonensis are rarely reporte
12 be defined whether infection with the common roundworm Ascaris or its bystander immunological effects
13 and animals: the whipworm Trichuris sp., the roundworm Ascaris sp., the flatworm Dicrocoelium sp. and
14 hondrial NAD-malic enzyme from the parasitic roundworm Ascaris suum has been studied using a steady-s
17 olved in production of branched acids in the roundworm, Ascaris suum, that demonstrates selectivity f
18 e whipworm Trichuristrichiura, and the large roundworm Ascarislumbricoides, infect upwards of two bil
20 re, we investigate collective feeding in the roundworm C. elegans at this intermediate scale, using q
25 lude: an obscure subfamily of globins in the roundworm Caenorhabditis elegans ; two new superfamilies
26 ned and expressed the PPS-1 protein from the roundworm Caenorhabditis elegans and also subjected this
27 femtosecond laser surgery for axotomy in the roundworm Caenorhabditis elegans and show that these axo
30 ce engineered to carry a fat-1 gene from the roundworm Caenorhabditis elegans can add a double bond i
36 lt depends on the host strain.IMPORTANCE The roundworm Caenorhabditis elegans is a laboratory model o
38 example of condensates is P granules in the roundworm Caenorhabditis elegans that play an important
39 s associated with feeding and fasting in the roundworm Caenorhabditis elegans We identified neural ci
40 a simple serotonin-dependent behavior of the roundworm Caenorhabditis elegans, egg laying, to perform
41 mouse line carrying the fat-1 gene from the roundworm Caenorhabditis elegans, encoding an n-3 PUFA d
43 ive assays with wild-type and mutants of the roundworm Caenorhabditis elegans, we establish a paradig
51 d further that C. elegans and probably other roundworms can be common hosts for B. cereus-group bacte
57 visualization and analysis of 3D images for roundworm, fruitfly, dragonfly, mouse, rat and human.
58 on aging in model systems such as yeast and roundworms have revealed conserved regulation of the pro
59 on following infection with the gut-dwelling roundworm Heligmosomoides polygyrus is critical for prot
60 uding pathogenic nematodes, schistosomes and roundworms, herald a new era in phytochelatin research,
61 identical young adult Caenorhabditis elegans roundworms in a shared environment and performed single-
64 chorism from ancestral hermaphroditism), and roundworms (Nematoda) which have undergone independent t
65 provide services and resources for parasitic roundworms (nematodes) and flatworms (trematodes), colle
68 polygyrus bakeri (Hpb), a murine intestinal roundworm, on the efficacy of an mRNA vaccine targeting
71 terodera glycines Ichinohe) is a microscopic roundworm that feeds on the roots of soybean and is a ma
72 odes (hookworms, whipworms, and Ascaris) are roundworms that infect more than 1 billion of the poores
73 ence that exposure of Caenorhabditis elegans roundworms to 2 simple nutrients, glucose and the polyun
75 ude malaria, leishmaniasis, Chagas' disease, roundworm, whipworm, pinworm, Chinese liver fluke, fleas
76 borne helminths, predominantly flatworms and roundworms, whose life cycles are characterized by a div