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1 d within the Caenorhabditis elegans foregut (pharynx).
2 etected in RIP, PQR, and PDA or -B or in the pharynx.
3 xcessively large particles from entering the pharynx.
4 morphogenesis of the Caenorhabditis elegans pharynx.
5 atic H. influenzae colonization of the human pharynx.
6 cells modulate FGF8 signaling in the caudal pharynx.
7 ntext that there may be excess tissue in the pharynx.
8 wall muscle and to the posterior half of the pharynx.
9 oblem is deposition of adipose tissue in the pharynx.
10 olved in the development and function of the pharynx.
11 cartilage patterning in the zebrafish larval pharynx.
12 function of other nicotinic receptors in the pharynx.
13 behavioral responses in the adult and dauer pharynx.
14 nase (MEK) 4 whose promoter is active in the pharynx.
15 dvanced through the rostral trachea into the pharynx.
16 iated molecules are present in the patient's pharynx.
17 ion of FGF-2 and similar FGFs in the ventral pharynx.
18 to a defect in neuromuscular control of the pharynx.
19 strips in the presence or absence of ventral pharynx.
20 f the thymus/parathyroid primordium from the pharynx.
21 pharynx and heart and that of Nkx2.3 in the pharynx.
22 the trunk into repetitive arrays of ventral pharynx.
23 omitant slowing of the pumping action of the pharynx.
24 in mesodermal and endodermal tissues of the pharynx.
25 ression of the X-linked mlc-1(+) gene in the pharynx.
26 t-shaped m8 cell at the posterior end of the pharynx.
27 at both mlc-1 and mlc-2 are expressed in the pharynx.
28 lc-2 performs a nearly essential role in the pharynx.
29 rgan identity for the Caenorhabditis elegans pharynx.
30 he A bands of body-wall muscles, but not the pharynx.
31 sential excitable cells such as those of the pharynx.
32 squamous epithelium that is adjacent to the pharynx.
33 leased at several different locations of the pharynx.
34 h thymus fate specification extends into the pharynx.
35 to homeostasis abnormalities in the head and pharynx.
36 muscles of face, mouth, tongue, larynx, and pharynx.
37 destroyed the integrity of the intestine and pharynx.
38 trains and H. haemolyticus isolated from the pharynx.
39 ells, specifically inhibited regrowth of the pharynx.
40 is a bacterium that resides within the human pharynx.
41 t-2 is localized mainly to the intestine and pharynx.
42 an primordia to completely separate from the pharynx.
43 to an FGF8-soaked bead placed dorsal to the pharynx.
44 specification of some of the neurons in the pharynx.
45 ng a predetermined threshold volume into the pharynx 2 cm above the upper esophageal sphincter, direc
46 hibits pumping of the Caenorhabditis elegans pharynx, a myogenic muscular pump for feeding, and found
49 -the counting of extra cells of the anterior pharynx--a quantitative technique that can be used to de
52 rs of the oral and nasal cavity, larynx, and pharynx and accounts for approximately 350,000 deaths pe
53 echanically couples the buccal cavity to the pharynx and anterior epidermis ("Epithelialization"), an
54 t take a stereotype path rostrally along the pharynx and are thought to reach their target sites via
55 l crest cells (CNCC) migrate into the caudal pharynx and arterial pole of the heart to form the outfl
56 ermal precursor, giving rise to cells of the pharynx and body muscle among others, while its sister E
57 35-null mutation fail to generate MS-derived pharynx and body muscle, and instead generate ectopic PA
59 am-negative bacteria that colonize the human pharynx and can cause respiratory tract infections, such
62 Anterior definitive endoderm, the future pharynx and foregut lining, emerges from the anterior pr
64 Electromyographic responses recorded from pharynx and hand were used as a measure of cortico-motor
65 ion of Nkx2.6 overlaps that of Nkx2.5 in the pharynx and heart and that of Nkx2.3 in the pharynx.
69 ows younger ages at diagnosis of oral cavity/pharynx and kidney cancers, possibly reflecting accelera
71 ng down chs-2 by RNAi caused a defect in the pharynx and led to L1 larval arrest, indicating that chi
72 a ceh-51 null mutation arrest as larvae with pharynx and muscle defects, although these tissues appea
74 g (50-70 ms) latency reflex responses in the pharynx and oesophagus, were used to condition the corti
77 ected stream projects along the floor of the pharynx and reaches as far rostrally as the floor of the
78 FGF-8 and BMP-2 are present in the ventral pharynx and secondary heart field/outflow myocardium, re
80 iac crescent and in the heart outflow tract, pharynx and spleen when linked directly to lacZ or when
81 es as a receptor for GAS colonization of the pharynx and support the potential efficacy of disrupting
82 x muscles, and was also deposited around the pharynx and the gonad, in the spermatheca and at the dis
83 y may alter the mechanical properties of the pharynx and the role of obesity in the pathogenesis of s
84 The ability to cause infection at both the pharynx and the skin ("generalist" strains) is correlate
86 of the compact formation (which supplies the pharynx) and to the loose formation (larynx), whereas th
87 the prenasal sinus, nasopharyngeal duct, and pharynx, and at lower densities in the oral and velar ch
91 rough the midline of the developing face and pharynx, and its participation in formation of a single
92 sms-1 isoform is expressed in the C. elegans pharynx, and its transgene rescues the sms-1 mutant phen
93 euronal cell groups innervating soft palate, pharynx, and larynx as well as diaphragm, intercostal, a
94 ting the dilator muscles of the soft palate, pharynx, and larynx, but abnormal respiratory mechanics
98 e hindbrain, enter the gut mesenchyme at the pharynx, and migrate as strands of cells to the terminal
100 ia can result from dysfunction at the mouth, pharynx, and oesophagus and may predispose individuals t
102 f its organs are incorporated into the adult pharynx, and several drivers of this clade are expressed
104 assembly was placed spanning from stomach to pharynx, and subjects were studied for 2 hours after a h
105 evelopment of a second epithelial organ, the pharynx, and suggest how these differences lead to organ
107 g1 gland cells located adjacent to M4 in the pharynx, and these defects can be partially rescued by M
108 ion"), and (3) a concomitant movement of the pharynx anteriorly and the epidermis of the mouth poster
112 ells, which migrate into the caudal, ventral pharynx at stage 14, block a signal from the ventral pha
114 ed, resulting in the maintenance of a thymus-pharynx attachment and a subsequent inability of the thy
116 dermis of the mouth posteriorly to bring the pharynx, buccal cavity, and mouth into close apposition
117 ng odds ratios for cancer of the oral cavity/pharynx but not larynx cancer suggests additional factor
121 stomeres in C. elegans develop into foregut (pharynx) cells in response to the selector gene PHA-4/Fo
122 tivity downregulating Fgf8 expression in the pharynx, decreasing cell survival during mandibular outg
123 ess) pathway components, including posterior pharynx defect (POP-1)/TCF, APC related/adenomatosis pol
124 on coordinated gene expression, mediated by pharynx defective (PHA)-4/FoxA in combination with addit
125 homolog (PSNEN, alias, Pen-2), and anterior pharynx defective 1 (APH-1), the four components of the
127 ar (EC) domain, presenilin-1 (PS1), anterior pharynx defective 1, and presenilin enhancer 2 in the tr
128 esenilins (PS1 and PS2), nicastrin, anterior pharynx defective phenotype 1 (APH-1), and PS enhancer 2
130 other membrane proteins [nicastrin, anterior pharynx defective-1 (APH-1), and presenilin enhancer-2 (
131 n enhanced clearance of Abeta in an anterior pharynx-defective (APH)-1alpha/-1beta-dependent manner.
132 sed of presenilin, nicastrin (NCT), anterior pharynx-defective 1 (APH-1), and presenilin enhancer 2 (
133 plex consisting of presenilin (PS), anterior pharynx-defective 1 (APH-1), nicastrin (NCT), and presen
134 plex components: PS1, nicastrin and anterior pharynx-defective 1 (APH1) but not presenilin enhancer 2
135 castrin, presenilin enhancer 2, and anterior pharynx-defective 1 that mediates the intramembrane prot
136 n and the accessory proteins APH-1 (anterior pharynx-defective 1) and nicastrin, triggers the endopro
137 se complex, composed of presenilin, anterior-pharynx-defective 1, nicastrin, and presenilin enhancer
138 nilin (PS); nicastrin (Nct); APH-1 (anterior pharynx-defective-1); and presenilin enhancer-2 (PEN-2).
139 pment of the Caenorhabditis elegans foregut (pharynx) depends on coordinated gene expression, mediate
141 pha-1 has long been considered essential for pharynx development on the basis of its mutant phenotype
144 4 years), anal (difference = 4), oral cavity/pharynx (difference = 2), and kidney cancers (difference
147 tract, the point where the outflow joins the pharynx does not move caudally as it normally should, th
149 ances, during normal eating, food enters the pharynx during the preparatory phase before a swallow is
151 ialization of the second pair of jaws in the pharynx, enhances the ability of fishes to process hard
152 ers: lip and oral cavity; nasopharynx; other pharynx; esophageal; stomach; colon and rectum; liver; g
153 nesis, conserved molecular programs regulate pharynx, esophagus, liver, and pancreas development in t
154 ding cancers of the larynx, oral cavity, and pharynx, esophagus, pancreas, kidney, bladder, and lung;
155 ses bulbar, muscle weaknesses (face, tongue, pharynx, etc) and reduced response to conventional immun
159 cancer cell lines (bladder RT4, breast MCF7, pharynx FaDu, ovarian SKOV3, and prostate PC3 and DU145)
160 ty (SCC1), larynx (SCC5), tongue (OSC19) and pharynx (FaDu), with grape seed proanthocyanidins (GSPs)
161 pidly growing squamous cell carcinoma of the pharynx, FaDu, to approximately 7.5 days for the slower
163 zothiazepine S107, establishing the nematode pharynx for studying specific CPVT mutations and for dru
164 ae because VAV-1 function is required in the pharynx for synchronous contraction of the musculature.
165 ed a pulling force exerted by the elongating pharynx (foregut) on the anterior epidermis during C. el
166 e found that the M3 neurons of the C.elegans pharynx form fast inhibitory glutamatergic neuromuscular
170 tamate by photolysis of caged glutamate to a pharynx from which the two M3 neurons were removed produ
173 mutants display morphogenetic defects in the pharynx, gut, and muscle quadrants, in addition to the d
174 n neural crest-derived cells had reached the pharynx had no effect on myocardial calcium transients.
177 ly, ulcerative lesions also developed at the pharynx, histo-pathologic findings of which were not dif
178 eous SCC, including those of the oral cavity/pharynx (HR, 5.60; 95% CI, 4.18-7.50) and lung (HR, 1.66
179 ransmitted from outside the pharynx into the pharynx in a manner analogous to how the mammalian auton
182 xpressed in epithelial cells of the skin and pharynx in the p63+/+ mouse, it is undetectable in these
184 s with microspheres show that the C. elegans pharynx, in combination with the buccal cavity, is tuned
185 itability and area of representation for the pharynx increased, while esophagus representation decrea
187 We show that SMA-3 Smad is expressed in pharynx, intestine and hypodermis, as has been previousl
188 nd that fibulin-1C has specific roles during pharynx, intestine, gonad and muscle morphogenesis, bein
189 ghly specialized non-endodermal cells of the pharynx into fully differentiated intestinal cells in in
190 ignal is likely transmitted from outside the pharynx into the pharynx in a manner analogous to how th
191 ith the separation of the primordia from the pharynx is disrupted, resulting in the maintenance of a
192 abditis elegans as a novel tool, because its pharynx is evolutionarily related to the vertebrate hear
194 ene expression in the Caenorhabditis elegans pharynx is regulated in part by organ-specific signals,
195 ion assay in which ejection of the planarian pharynx is selectively induced by brief exposure of anim
198 e defect in C. elegans feeding behavior: the pharynx is unable to pump rapidly in the presence of foo
199 ic contraction of the Caenorhabditis elegans pharynx is unique in that the network of 12 neurons, inc
200 nt regions (e.g., the tip of the head vs the pharynx) is processed in different regions of the suboes
201 , the risks of cancer in the oral cavity and pharynx, kidney, thyroid, colon, leukemia, lung, melanom
202 alcoholism; cancers of the mouth, esophagus, pharynx, larynx, and liver combined; breast cancer in wo
204 ., rostral-central nucleus); 2) soft palate, pharynx, larynx, and tracheobronchial tree (e.g., dorsal
206 Alcohol causes cancers of the oral cavity, pharynx, larynx, oesophagus, and liver, and causes a sma
207 l (Mo12) motor nuclei innervate jaw, facial, pharynx/larynx/esophagus, and tongue muscles, respective
208 Injection of minute amounts of water in the pharynx leads to a long-duration lower esophageal sphinc
209 ke was associated with reduced risk of oral, pharynx, liver, colon, prostate, endometrial cancer and
210 olytic streptococcal infection affecting the pharynx, lower lip, and gingiva of a healthy 19-year-old
214 of the AVR-15 ivermectin-binding channel on pharynx muscle, is to target AVR-14 and AVR-15, which ar
215 te cats, the pharyngeal (0.5-1.0 ml water in pharynx (N=6)) or esophageal (1-3 ml air in esophagus (N
217 uld predict that during nasal breathing, the pharynx of a tracheostomized patient would be exposed to
218 and adult stages and along the length of the pharynx of adult worms, as well as the cyclic expression
222 umin (BSA) labelled a pair of neurons in the pharynx of both sexes and five cells in the ventral cord
223 introduced CPVT inducing mutations into the pharynx of Caenorhabditis elegans, which we previously e
224 lococcus aureus, isolated from the rectum or pharynx of patients with KD, secretes toxic shock syndro
227 versed the deleterious effect of the ventral pharynx on myocardial calcium transients and proliferati
229 e conclude that introduction of GAS into the pharynx or into deep tissues results in rapid induction
230 Single electrical stimuli applied to the pharynx or oesophagus had no effect on the response to c
231 rectal gonorrhea underwent swabbing from the pharynx or rectum 7 and 14 days following treatment.
232 oedema (defined as swelling of lips, tongue, pharynx, or face during ACE inhibitor use and no swellin
233 esult of breast cancer; cancers of the lung, pharynx, or intrathoracic organs; other cancer; respirat
236 jor risk factor for cancers of the mouth and pharynx (oral cancer), but the differential risks by bev
239 n the nascent digestive tract, including all pharynx precursors at the time they are restricted to a
240 ies provide the first description of how the pharynx primordium develops into an epithelial tube, and
241 3 was observed at gap junctions in the adult pharynx, providing supporting evidence that innexins are
246 hem in muscle tissue, motor neurons, and the pharynx, reveal that these peptides have potent bioactiv
247 n microscopic reconstruction of the anterior pharynx revealed evidence for synapses from I2 onto musc
248 : melanoma (RR, 3.36 in men, 3.52 in women); pharynx (RR, 2.77 in men, 2.81 in women); lung (RR, 1.37
249 outinely treated with radiotherapy (oral and pharynx, salivary gland, rectum, anus, larynx, lung, sof
250 Nrf and Skn-1 proteins, and suggest that the pharynx selector function of CncB is highly conserved on
251 = 11.5), liver (SIR = 3.6), oral cavity and pharynx (SIR = 2.6), respiratory (SIR = 2.6), leukemia (
252 4.68; 95% CI, 3.81 to 5.70), oral cavity and pharynx (SMR = 3.66; 95% CI, 3.16 to 4.22), and larynx (
254 ormalized for grams of protein for nasal and pharynx specimens and for mL-gram of protein for sputum.
256 a, SW1736 thyroid, DU-145 prostate, and FADU pharynx-squamous sarcoma) as well as the P-388 murine ly
257 s of markers for the original differentiated pharynx state; hence, there is no apparent requirement f
258 pression extended to the lateral side of the pharynx, suggesting a compensatory function of Nkx2.5 in
259 (e.g., formation of the dorsal ridge and the pharynx) take place almost normally in rpr-deficient emb
261 just prior to or just after hatching with a pharynx that appears fully formed but is not properly at
262 ctional neuron in the Caenorhabditis elegans pharynx that can both stimulate peristaltic contractions
263 lts in elevated FGF8 signaling in the caudal pharynx that disrupts secondary heart field development.
264 found that myocardium cultured with ventral pharynx that had not yet contacted neural crest cells ha
265 including the development of a supernumerary pharynx (the feeding organ of the animal) and the produc
268 ted, vaccinated cattle was restricted to the pharynx throughout both the early and the persistent pha
271 ults show that the entropy of the C. elegans pharynx tissues increases as the animal ages, but a shar
274 anterior heart field (AHF) migrate from the pharynx to contribute to the early myocardium of the out
275 necting sugar-sensitive taste neurons in the pharynx to neural circuits that control the drive to ing
276 itoring the entire pressure profile from the pharynx to the stomach along with pressure topography pl
277 ormation of a common lumen that connects the pharynx to the stomach, serving both as trachea and as e
278 icities of the rhythms range from subsecond (pharynx) to seconds (gonadal sheath) to minutes (defecat
280 ts to relate these properties to GAS skin or pharynx tropism and invasiveness are of great interest.
281 Among neurons expressing drivers in the pharynx, two projection patterns can be distinguished in
290 at stage 14, block a signal from the ventral pharynx, we cultured stage 12 chick heart tube or myocar
291 of Nkx2.5 and Nkx2.6 in the formation of the pharynx, we generated and analyzed Nkx2.5 and Nkx2.6 dou
292 inspiration of the rostral, mid-, and caudal pharynx were analyzed for airway size and pharyngeal wal
294 asses of corpse: early deaths with a swollen pharynx (which we call 'P deaths'), and later deaths wit
297 ized by local growth of the bacterium in the pharynx with pseudomembrane formation or, less commonly,
298 data suggest that PHA-4 and DAF-12 endow the pharynx with transcriptional plasticity to respond to di
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