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1 hest expression in the nervous system and in pharyngeal muscle.
2 ction coupling in the Caenorhabditis elegans pharyngeal muscle.
3 o specifically activate ceh-22 expression in pharyngeal muscle.
4 oline receptor subunit that functions in the pharyngeal muscle.
5 alcium-dependent processes in the C. elegans pharyngeal muscle.
6 MC, and it is required for MC stimulation of pharyngeal muscle.
7 dant to those of mlc-2 in both body-wall and pharyngeal muscle.
8 ly rescues a ceh-22 mutant when expressed in pharyngeal muscle.
9 as observed in motor neurons, intestine, and pharyngeal muscle.
10 r the hyperpolarizing effect of glutamate on pharyngeal muscle.
11 genitors of the second heart field (SHF) and pharyngeal muscles.
12 y activates neurotransmission from M4 to the pharyngeal muscles.
13 as L1 larvae lacking most or all ABa-derived pharyngeal muscles.
14 utants, ubc-9(RNAi) animals lack ABa-derived pharyngeal muscles.
15 ex muscles and indirectly by controlling the pharyngeal muscles.
16 kx2-5, which is expressed exclusively in the pharyngeal muscles.
17 is restricted to the somatic, visceral, and pharyngeal muscles.
18 atially restricted to somatic, visceral, and pharyngeal muscles.
19 he green fluorescent protein is expressed in pharyngeal muscles.
20 le precursors that form most of the juvenile pharyngeal muscles.
21 arynx are no longer dye-coupled to posterior pharyngeal muscles.
23 ults indicate that the mechanical effects of pharyngeal muscle activation depend not only on the regi
24 decerebrate cats to determine the effect of pharyngeal muscle activation on airway pressure-area rel
26 acheotomized cats to determine the effect of pharyngeal muscle activation on the pharyngeal airway.
30 is the earliest known gene expressed in the pharyngeal muscles and is likely regulated directly by f
31 response to environmental conditions within pharyngeal muscles and is recognized by the nuclear horm
34 , a ceh-22 target normally expressed only in pharyngeal muscle, and a synthetic reporter construct co
35 gating enzymes are necessary for ABa-derived pharyngeal muscle, and we hypothesize that TBX-2 functio
37 ement, termed DE3, is strongly active in the pharyngeal muscles, and we identified two short oligonuc
38 the posterior pharynx demonstrates that all pharyngeal muscles are dye-coupled in wild-type animals;
39 ated cholinergic transmission from MC to the pharyngeal muscles by activating the Gsalpha signaling p
40 Tropomyosin I gene in somatic body-wall and pharyngeal muscles by binding to DNA sequences within th
41 glutamate-gated chloride channel (AVR-15) on pharyngeal muscle, causing complete pumping inhibition.
44 successfully profiled proteins expressed in pharyngeal muscle cells, and in the process, identified
46 show that ectopic overexpression of slo-1 in pharyngeal muscle confers sensitivity of the muscle to e
48 ults indicate that the mechanical effects of pharyngeal muscle contraction depend on the airway level
49 ne eat-5, which is required for synchronized pharyngeal muscle contractions, and find that it is a ne
52 asic ontogenetic motif underlies cardiac and pharyngeal muscle development and evolution in chordates
53 s paper, we examine the role CEH-22 plays in pharyngeal muscle development and gene activation by (a)
59 tructive sleep apnea (OSA) require increased pharyngeal muscle dilator activation during wakefulness
60 Null and gain-of-function mutations affect pharyngeal muscle excitability in ways that are consiste
61 quiescence during DTQ results from a loss of pharyngeal muscle excitability, whereas feeding quiescen
62 lier/OLF/EBF) orchestrates the transition to pharyngeal muscle fate both by promoting an MRF-associat
63 agonism underlies a fundamental heart versus pharyngeal muscle fate choice that occurs in a conserved
67 d pha-1 have strongly synergistic effects on pharyngeal muscle gene expression; in addition, a pha-1
69 shes pumping, and optogenetic stimulation of pharyngeal muscle in these animals causes abnormal contr
70 esults indicate that selective activation of pharyngeal muscles in cats frequently results in greater
72 Extracellular physiological recordings from pharyngeal muscle of hypomorphic mutants show alteration
73 netically encoded calcium indicators, in the pharyngeal muscle of the nematode worm Caenorhabditis el
75 g UNC-89-A and -B primarily in body-wall and pharyngeal muscle, one internal promoter directing expre
76 s, intestinal epithelial cells, neurons, and pharyngeal muscle) or state-selective (heat-shock) promo
77 Mitoflash activity in Caenorhabditis elegans pharyngeal muscles peaked on adult day 3 during active r
79 gh levels of signaling through GAR-3 inhibit pharyngeal muscle relaxation and impair feeding--but do
81 olecular mechanisms that govern heart versus pharyngeal muscle specification within this lineage rema
82 rm an ancient conserved regulatory state for pharyngeal muscle specification, whereas their regulator
83 essential for development of the ABa-derived pharyngeal muscles, specification of neural cell fate in
84 ription similarly to DE3 specifically in the pharyngeal muscles, suggesting it may be an essential si
85 mal enhancer mediates expression in a single pharyngeal muscle, the donut-shaped m8 cell at the poste
86 k suggested that DAF-5 and DAF-3 function in pharyngeal muscle to regulate gene expression, but our a
87 nitors are primed to activate both heart and pharyngeal muscle transcriptional programs, which progre
88 nhancer activity is primarily limited to the pharyngeal muscles, we hypothesize that de209 also binds
89 our results and previous calcium imaging of pharyngeal muscles, we propose a model that explains how
91 d, starvation induces excessive autophagy in pharyngeal muscles, which in turn, causes damage that ma
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