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1       This did not generalize to the control irritant.
2 ally to cutaneously applied phenol, an acute irritant.
3 ween protons and piperine, another vanilloid irritant.
4 n an assay with a cockroach, proved potently irritant.
5 ee-base nicotine is bitter and a respiratory irritant.
6 ied in the vapor, and acrolein is a powerful irritant.
7 6%, is a possible carcinogen and respiratory irritant.
8 ha,beta unsaturated aldehyde and respiratory irritant.
9 ent of TRPA1, a key sensor for environmental irritants.
10 matory responses to cutaneous and peritoneal irritants.
11 y airway exposures to allergens and chemical irritants.
12 ell as environmental and endogenous chemical irritants.
13  pungent natural compounds and environmental irritants.
14 y for behavioral responses to these chemical irritants.
15 nd mediates behavioral responses to chemical irritants.
16 pungent natural compounds, and environmental irritants.
17 ion of nociceptors by endogenous and natural irritants.
18 mach less susceptible to damage from luminal irritants.
19 lvents, welding fumes, and other respiratory irritants.
20 hich respond to numerous odorants as well as irritants.
21 tinel for structurally diverse electrophilic irritants.
22 tinocytes treated with certain allergens and irritants.
23 es to protect the host against pathogens and irritants.
24 airway defense against inhaled pathogens and irritants.
25 ncluding mechanical stimulation and chemical irritants.
26 iggers such as allergens, microorganisms and irritants.
27 and the presence of inhalable pollutants and irritants.
28 f environmental exposures like allergens and irritants.
29  in increased penetrability to allergens and irritants.
30 xposure to allergens, pathogens, or chemical irritants.
31 rs chronically exposed to moderate levels of irritants.
32 after chronic exposure to moderate levels of irritants.
33 ons or exposure to allergic and non-allergic irritants.
34 hagous fluids, environmental xenobiotics and irritants.
35 oxyethylene) ammonium chloride (ITDOP); mild irritants: 5% 3-decyloxypropyl-bis(polyoxyethylene) amin
36               Test materials included slight irritants: 5% sodium lauryl sulfate (SLS), polyoxyethyle
37 alkylbenzene sulfonate (LAS); and a moderate irritant: a proprietary detergent (DTRGT).
38 o enhance permeability and susceptibility to irritants; accordingly, increased attention should be gi
39 rritation response in mice elicited by smoke irritants (acrolein, acetic acid, and cyclohexanone).
40          Treatment was associated with local irritant adverse effects.
41 cing toxicity and inflammation induced by an irritant agent.
42 ral, bacterial, and nonmicrobial (toxins and irritants) agents, resulting in production of many diffe
43 though the intestine is routinely exposed to irritant alimentary compounds and inflammatory mediators
44 s sneezing responses to a multitude of nasal irritants, allergens, and viruses.
45 rosols with increasing doses of the chemical irritants allyl isothiocyanate (AITC; also known as must
46  is opposite of that associated with another irritant, ammonia fumes, which elicited an increase in t
47                                     The lung irritant, ammonia, obtained as vapor over a 30% solution
48                                  Despite the irritant and allergenic properties of fungi, early-life
49 mediated, anti-inflammatory activity in both irritant and allergic contact dermatitis animal models.
50 tivated receptor-alpha agonists in models of irritant and allergic contact dermatitis produced in mou
51 er, distinguishing the clinical phenotype of irritant and allergic contact dermatitis remains challen
52 R, GW3965, were examined utilizing models of irritant and allergic contact dermatitis.
53 onest forms of occupational skin disease are irritant and allergic contact dermatitis.
54 ay potent anti-inflammatory activity in both irritant and allergic contact models of dermatitis, requ
55 n made to identify biomarkers to distinguish irritant and allergic patch test reactions, which could
56 IV hypersensitivity, in part due to the dual irritant and antigenic properties of sensitizing chemica
57 he importance of the interaction between the irritant and antigenic properties of sensitizing chemica
58 er show that PAP-1 is not a sensitizer or an irritant and exhibits no toxicity in a 28-day toxicity s
59 zox and etoxazole) elicited a dose-dependent irritant and repellent effect on T. urticae.
60 jury measured at day 1, regardless of ocular irritant and the stromal response measured by the area u
61 nded chemical data set, comprising five skin irritants and 11 contact allergens.
62 s can affect airway inflammatory response to irritants and allergens, but the importance of stress in
63 r challenges, including allergens, exercise, irritants and aspirin.
64 uction machinery through which environmental irritants and endogenous proalgesic agents depolarize no
65 ormal breathing by a myriad of environmental irritants and infectious insults.
66 cautions should be taken against respiratory irritants and molds and to prevent children from becomin
67  one of the primary sensors of environmental irritants and noxious substances.
68 acts as a sensory receptor for environmental irritants and oxidants.
69 echanism that aids in the removal of harmful irritants and parasites(1).
70 tion following long-term exposure to harmful irritants and pollutants, particularly in the airways.
71 el is the molecular target for environmental irritants and pungent chemicals, such as cinnamaldehyde
72 is the first body surface to contact inhaled irritants and report danger.
73 hat they can be activated by various inhaled irritants and/or cold air.
74 pecific allergen sodium lauryl sulfate as an irritant, and appropriate controls.
75   Expression is also activated by a chemical irritant, and is suppressed by topical administration of
76 condary ozonides (SOZ), which are known skin irritants, and a modest change in particle size.
77 rs in the newborn's intestine, pathogens and irritants, and allergens in food.
78 t recognize pathogens, chemical and physical irritants, and damaged cells subsequently initiating a w
79 er that allows the penetration of allergens, irritants, and microbes into a cutaneous milieu that fac
80 on, and extrinsic stimuli such as allergens, irritants, and microbes.
81 PCR analyses of multiple chemical allergens, irritants, and non-sensitizers have identified 10 genes
82 entions to reduce exposures to allergens and irritants, and research on the underlying mechanisms tha
83 multiple symptomatic high-level exposures to irritants; and (iii) possible IIA, that is asthma occurr
84                     Receptors for trigeminal irritants are generally assumed to be located exclusivel
85 ctivated by noxious heat, acid, and alkaloid irritants as well as several endogenous ligands and is s
86 nses in an oxidative stress-induced model of irritant asthma.
87 ons to aeroallergens, contact allergens, and irritants at days 2, 3, and 4.
88 side' world from potentially harmful toxins, irritants, bacteria and other pathogens that also exist
89 gions in the mouth are uniquely sensitive to irritants because they can penetrate through the tissue
90  range of drug substances, non-toxic and non-irritant behavior.
91 s sensory detection of pathogens, toxins and irritants; breakdown of the epithelial barrier is associ
92 ubstances, toxins, venoms, and environmental irritants but that also trigger exuberant allergic react
93 diverse array of environmental and microbial irritants by forming the barrier of epithelial cells int
94                            Detection of such irritants by the trigeminal nerve evokes protective refl
95 ow a strong potentiation of responses to the irritant capsaicin in an acidic environment.
96 s thermal stimuli, protons, and the alkaloid irritant capsaicin open the channel.
97  by noxious heat, acidic pH and the alkaloid irritant capsaicin.
98                                       Airway irritants cause a variety of lung pathologies.
99 rs after treatment, mild and moderate ocular irritants caused a significant increase in corneal thick
100 he epithelium, whereas the mild and moderate irritants caused complete epithelial cell loss with incr
101         On day 1, mild, moderate, and severe irritants caused complete loss of epithelium and disappe
102 nvestigate the kinetics of both allergic and irritant CD (ACD and ICD) in vivo.
103 tact dermatitis (CD), including allergic and irritant CD, are common dermatological diseases and are
104  and includes allergic CD, photoallergic CD, irritant CD, photoirritant CD (also called phototoxic CD
105 nsitive to mechanical stimuli and a range of irritant chemicals (bradykinin, capsaicin, low pH, plate
106           Here we show that noxious heat and irritant chemicals elicit robust escape behaviors in the
107  the tested compounds, i.e., strong and weak irritant chemicals selected from the literature, induced
108 s of the reactive hapten urushiol and by the irritant chemicals sodium lauryl sulfate and PMA.
109                                              Irritant chemicals triggered rapid ATP and ADP release f
110 ated by a range of noxious stimuli including irritant chemicals, acids and heat.
111 rnatants treated with either urushiol or the irritant chemicals.
112 narily conserved detector of temperature and irritant chemicals.
113 nflammation via hapten-specific T cells) and irritants (chemicals that are toxic to epidermal cells).
114                            The environmental irritant chloroform, a naturally occurring small volatil
115 tinocytes treated with certain allergens and irritants, compared with untreated keratinocytes.
116 apsaicin is unique among naturally occurring irritant compounds because the initial neuronal excitati
117 opic dermatitis (AD) as well as allergic and irritant contact dermatitis (ACD, ICD) are characterized
118           Atopic dermatitis (AD), as well as irritant contact dermatitis (ICD) and allergic contact d
119                                              Irritant contact dermatitis (ICD) is caused by direct da
120  In AD patients, there is often a coexisting irritant contact dermatitis (ICD) or allergic contact de
121 rs responsible for the signs and symptoms of irritant contact dermatitis (ICD).
122 flammation and condition immune responses in irritant contact dermatitis and atopic dermatitis.
123  phorbol 12-myristate-13-acetate, a model of irritant contact dermatitis and oxazolone, a model of al
124      No DEGs were found between allergic and irritant contact dermatitis CHE.
125                 We report 7 cases of erosive irritant contact dermatitis due to chlorhexidine glucona
126 ntial biomarkers to distinguish allergic and irritant contact dermatitis in human skin.
127                    Furthermore, allergic and irritant contact dermatitis reactions were exaggerated i
128 cterized by either inflammation alone (acute irritant contact dermatitis, acute allergic contact derm
129 eratinocytes, especially during allergic and irritant contact dermatitis, however, is less well under
130 morphine had no effect on croton oil-induced irritant contact dermatitis, indicating that morphine's
131 he amelioration of the phorbol ester-induced irritant contact dermatitis.
132 m dodecyl sulfate is a well-known inducer of irritant contact dermatitis.
133 iolet-B-induced skin cancers or allergic and irritant contact dermatitis.
134  in allergic contact dermatitis (ACD) and/or irritant contact dermatitis.
135 C motif ligand 1 (CXCL1) in a mouse model of irritant contact dermatitis.
136 sponses in BALB/c mice to oxazolone, but not irritant contact hypersensitivity responses to croton oi
137 elements in the pathogenesis of allergic and irritant contact hypersensitivity.
138  acute stress has no effect on the course of irritant contact sensitivity, an immune reaction that do
139  continuum of irritation that can be termed "irritant contact stomatitis." This may be due to the fac
140 d having a significantly greater effect than irritant control (p < 0.001); however, neither applicati
141 d with age over 50 years and with a negative irritant control containing sodium lauryl sulphate.
142 ans retinoic acid, 5% sodium lauryl sulfate (irritant control), or vehicle were applied under occlusi
143 and bulb may provide an avenue whereby nasal irritants could affect processing of coincident olfactor
144 nstrated that both spontaneous and augmented irritant dermatitis in FVB.delta(-/-) mice were down-reg
145                                       During irritant dermatitis induced by topical application of cr
146                                              Irritant dermatitis is the most common cause of diaper d
147                                              Irritant dermatitis represents innate inflammatory respo
148                                              Irritant dermatitis was induced by applying phorbol 12-m
149            Neither spontaneous nor augmented irritant dermatitis was observed in FVB.beta(-/-) delta(
150 ses (e.g., psoriasis, atopic dermatitis, and irritant dermatitis) triggered by abnormal barrier funct
151 hogenic role for keratinocyte-derived ATP in irritant dermatitis, they also form the basis for a form
152 ocytes may serve as a causative mediator for irritant dermatitis.
153  mouse models of atopic dermatitis and acute irritant dermatitis.
154 emoresponsive capabilities of the trigeminal irritant-detection system.
155  Here we examined the effect of the chemical irritant dextran sodium sulfate (DSS) on intestinal dama
156 ymethane and subsequently exposed to colonic irritant dextran sodium sulfate (DSS).
157 clinician be aware of cutaneous mimickers of irritant diaper dermatitis as well as their treatments.
158  nasal epithelium, requiring that trigeminal irritants diffuse through the junctional barrier at the
159 s are activated by noxious stimuli including irritants (e.g. TRPV1 agonist capsaicin) and inflammator
160 ave been identified, including environmental irritants (e.g., acrolein) and ingredients of pungent na
161  (e.g., allyl isothiocyanate), environmental irritants (e.g., acrolein), and endogenous ligands (4-hy
162  nerve endings can detect certain lipophilic irritants (e.g., mints, ammonia), the epithelium also ho
163 om soy can inhibit inflammation in a contact irritant ear edema mouse model.
164 gic contact dermatitis, and suggest that the irritant effect of chemicals may be mediated through the
165 h PBS or OVA-peptide, indicating a potential irritant effect of drop application.
166 ght into the underlying mechanism of harmful irritant effects in the respiratory tract caused by acci
167 tionally attributed to immunosuppressive and irritant effects of CS on human cells.
168             The nAChR subtype transduces the irritant effects of nicotine in tobacco smoke and, in ce
169 patients, who may be more susceptible to the irritant effects of these dressings.
170 tissue reactions, and diminished burning and irritant effects.
171 e (CYP) which is metabolized to acrolein, an irritant eliminated in the urine.
172  various clinical forms of asthma related to irritant exposure at work.
173              The causal relationship between irritant exposure(s) and the development of asthma can b
174 matory conditions provoked or exacerbated by irritant exposure.
175 d by subcutaneous injections of the chemical irritant formalin substantially increased the release of
176              Distinguishing the allergic and irritant forms of CD often proves challenging in the cli
177 n excitatory ion channel targeted by pungent irritants from mustard and garlic.
178 imilarly evokes a scratch response to remove irritants from the skin.
179 , called wet dog shakes, to remove water and irritants from their back hairy skin.
180  with accidental exposures to high levels of irritant gases depended on cumulative levels of pulp mil
181 s, microbial products and sterile endogenous irritants governs whether the outcome will be with suppr
182 emonstrate that, following stimulation by an irritant, grooming progresses gradually from an early ph
183                                Plant-derived irritants have predominated in this regard, but animal v
184 oreign organisms, damaged cells and physical irritants; however, inappropriately triggered or sustain
185 vironmental and occupational sensitizers and irritants in its pathogenesis and the interaction with b
186         Here, we studied reflex responses to irritants in normotensive Wistar-Kyoto (WKY) rats and sp
187  exposed to a range of physical and chemical irritants in the environment that are known to trigger a
188 eurons and are activated by several chemical irritants in vitro.
189 igeminally mediated reflex reactions to some irritants including acyl-homoserine lactone bacterial qu
190 rrier to allergens as well as other external irritants including infectious agents, and atmospheric p
191                            Environmental air irritants including nanosized carbon black (nCB) can dri
192  where it acts as a sensor for environmental irritants, including acrolein, and some pungent plant in
193  well as for detecting electrophilic sensory irritants, including allyl isothiocyanate.
194 nd to contain significantly more respiratory irritants, including NO(x), CO, and CO(2), and a larger
195 ensor for structurally diverse electrophilic irritants, including small volatile environmental toxica
196 mediators and to a diverse array of volatile irritants, including those found in tear gas and garlic.
197                                     The term irritant-induced (occupational) asthma (IIA) has been us
198 gregation was observed between allergen- and irritant-induced gene profiles.
199                      Acrolein, a respiratory irritant, induces systemic neuroendocrine stress.
200 ier against water loss and pathogen/allergen/irritant invasion.
201       Control of environmental allergens and irritants is essential.
202  injury, information on possible etiology of irritants is very important.
203 a known human carcinogen and mucous membrane irritant, is emitted from a variety of building material
204 ature of bronchial asthma, and inhalation of irritants may facilitate development of nonallergic AHR.
205        These data suggest that allergens and irritants may, in part, break peripheral tolerance by th
206 , but not prevented, by elimination of local irritants, meticulous oral hygiene, and regular periodon
207 ave examined in vivo and in vitro effects of irritants, most focused on events developing hours to da
208   Intramuscular injection of an inflammatory irritant, mustard oil (MO), induces significant edema fo
209 by the same injury [application of a C-fiber irritant, mustard oil (MO), to the hindpaw].
210 e-activity relationships in analogues of the irritant natural product capsaicin have previously been
211                         Do ancient microbial irritants offer early life protection against diabetes?
212 th exposures to fungal taxa considered to be irritant or allergenic in sensitive subjects, yeasts in
213 osures are assumed to provoke wheeze through irritant or allergenic mechanisms, little is known about
214 ve types of cutaneous inflammation caused by irritant or allergic chemicals.
215                                              Irritant or allergic contact dermatitis usually presents
216 n and mycalamide, psymberin does not display irritant or blistering activity.
217 oduction of mineralization in response to an irritant or parasite threat to the mantle organ.
218  cancer, PICCs were rated as appropriate for irritant or vesicant infusion, regardless of duration.
219 itial management includes avoiding causative irritants or allergens (e.g., by wearing impermeable glo
220                          Itching, induced by irritants or allergens that stimulate pruriceptive neuro
221 s) may increase the risk of LRI by acting as irritants or through increasing susceptibility to infect
222 unds attenuate pain behavior in a trigeminal irritant pain model that is known to rely on TRPV4 and T
223 ion-specifically dead cells and a variety of irritant particles, including crystals, minerals, and pr
224 ls but not to microbial molecules or sterile irritant particles.
225  and clears the airways and lungs of inhaled irritants, particulates, pathogens, and accumulated secr
226 ionarily as an adaptive defense against skin irritants, pathogens, or parasites.
227                        Inhalation of noxious irritants/pollutants activates airway nociceptive affere
228 anate (AITC; aka, mustard oil) is a powerful irritant produced by Brassica plants as a defensive trai
229 e trees' because their anesthetic or counter-irritant properties render them useful in the treatment
230      For the skin, Doxil is classified as an irritant rather than a vesicant.
231                                              Irritant reactions can closely resemble allergic ones, a
232  care products have been documented to cause irritant reactions in susceptible individuals, particula
233 sorders varying from straightforward topical irritant reactions, such as those to synthetic pyrethroi
234 tial channel vanilloid subtype 1 (TRPV1), an irritant receptor for capsaicin, the pungent ingredient
235 ework for understanding how a broad-spectrum irritant receptor is controlled by endogenous and exogen
236 te that HQ is an activator of the peripheral irritant receptor transient receptor potential (TRP) cat
237  acidosis activates and sensitizes the human irritant receptor TRPA1 (hTRPA1).
238     Both these modes can be initiated by the irritant receptor TRPA1, which is confined to crypt EC c
239  repellency is the widely conserved chemical irritant receptor TRPA1.
240 be distinguished within the wide spectrum of irritant-related asthma: (i) definite IIA, that is acute
241      Effects of acetaminophen on oxidant and irritant respiratory tract responses to environmental to
242                                           An irritant response induced by chronic exposure of mouse s
243 , acetaminophen greatly increased the reflex irritant response to ETS.
244 own to be integral to a CHS but not an acute irritant response, whereas CD44 does not significantly c
245  and/or potentiates the oxidative stress and irritant responses to an inhaled oxidant: environmental
246 eloped an in vitro assay for potential human irritant responses via the skin, employing human passage
247 oscopy showed that application of the slight irritant resulted in decreased epithelial thickness at 3
248 eated skin contact with contact allergens or irritants, resulting in allergic contact dermatitis (ACD
249  endogenous danger signals and environmental irritants, resulting in the formation and activation of
250 at are presumably involved in signaling oral irritant sensations.
251 ent receptor potential ankyrin 1 (TRPA1), an irritant-sensing channel.
252                                  TRPA1 is an irritant-sensing ion channel expressed in airway chemose
253 al ankyrin 1 (TRPA1) channel functions as an irritant sensor and is a therapeutic target for treating
254 sophila melanogaster orthologue of the human irritant sensor, acts in gustatory chemosensors to inhib
255                  On day 1, mild and moderate irritants showed increasing stromal cell death from 9.8+
256 o function as chemical sensor of noxious and irritant signaling.
257                     Pretreatment with a mild irritant significantly decreased intracellular calcium i
258 lls with low concentrations of ethanol (mild irritant) significantly attenuated injury induced by hig
259 in compared to sodium lauryl sulfate-induced irritant skin reactions.
260 y examined whether repetitive exposure to an irritant stimulant leads to desensitization and whether
261 or the local environment for the presence of irritant stimuli and, when activated, provide input to t
262 ter a single exposure to very high levels of irritant substances; (ii) probable IIA, that is asthma t
263 ess C5aRs and that exposure to environmental irritants such as cigarette smoke modulates the expressi
264                                      Various irritants such as foods, chemicals, friction, thermal/me
265                      Oxidative stresses from irritants such as hydrogen peroxide and ozone (O(3)) can
266 de range of allergens, infectious agents and irritants (such as pollutants) occurring indoors and out
267 s and responds to a wide variety of chemical irritants, such as acrolein in smoke or isothiocyanates
268      TRPA1 is also targeted by environmental irritants, such as acrolein, that account for toxic and
269   This contrasts with most other common oral irritants, such as cinnamaldehyde, capsaicin, and alcoho
270 rodentium but not to that caused by chemical irritants, such as dextran sodium sulfate.
271                                Inhalation of irritants, such as toluene diisocyanate (TDI), stimulate
272 ildren are exposed to multiple environmental irritants, such as viruses and allergens, that are commo
273 emically disparate animal- and plant-derived irritants target the same key allosteric regulatory site
274  activity as measured by the mouse abdominal irritant test (MAIT) when dosed at 100 mg/kg, sc, but di
275 inociceptive activity in the mouse abdominal irritant test (MAIT).
276 nd 21e were very active in the rat abdominal irritant test (RAIT) with ED(50) doses of 0.38 and 0.31
277                          TNBS, an intestinal irritant that induces the development of inflammatory bo
278  stimulation on the muscle and to a chemical irritant that is known to produce pain in humans provide
279 cle beginning on page 2574), have identified irritants that activate transient receptor potential cat
280          Aldehydes are known carcinogens and irritants that can negatively impact health.
281                In response to infections and irritants, the respiratory epithelium releases the alarm
282                       With the slight ocular irritants there was little or no change in corneal thick
283  can be activated by exogenous electrophilic irritants through direct covalent modification, we reaso
284 ized epithelial chemosensors that respond to irritants through the canonical taste transduction casca
285  vivo CM revealed corneal injury with slight irritants to be restricted to the epithelium, whereas th
286  Thus, in CF, the reduced ability of mucosal irritants to stimulate airway gland secretion via SubP m
287                             Multiple inhaled irritants trigger the release of complement components,
288 y dependent on both the concentration of the irritant used and the duration of exposure and was abrog
289 ociceptors and is sensitive to noxious heat, irritant vanilloids, and protons.
290        In summary, repetitive exposure to an irritant vapor results in a specific desensitization to
291 show opposing outcomes of CD39 deficiency in irritant versus allergic contact dermatitis, reflecting
292 , that is activated by a variety of reactive irritants via the covalent modification of cysteine resi
293 ndin inhibitor (indomethacin) or if the mild irritant was administered in calcium-free media.
294         The protection conferred by the mild irritant was directly dependent on both the concentratio
295 psies against four contact allergens and two irritants were analyzed via microarray.
296 ed with sodium lauryl sulfate (SLS), a model irritant, were used to examine early molecular events of
297 hannels are activated by chemically reactive irritants, whereas snake and Drosophila TRPA1 orthologs
298 single or multiple high-level exposure(s) to irritants, whereas this relationship can only be inferre
299 n were induced by both contact allergens and irritants; whereas only contact allergens prompted stron
300 ntration of a damaging agent, termed a "mild irritant," which by itself is not injurious, can attenua

 
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