ライフサイエンスコーパス: cheek

1 tablishment within tongue, gums, palate, and cheek.

2 cubital and popliteal fossae, nasal tip, and cheek.

3 roquine, capsaicin, or vehicle into the left cheek.

4 outdoor air and number of lentigines on the cheek.

5 ed by a relapsing facial nodule on the right cheek.

6 solitary, slowly growing tumor of the right cheek.

7 lling, miosis, mydriasis and swelling of the cheek.

8 ts was evoked by an air puff to the monkey's cheek.

9 asal tip, narrowing of the forehead and full cheeks.

10 tral plates of this taxon and trilobite free cheeks.

11 distinct feature to trilobite doublure/free cheeks.

12 , creating a gap between the teeth, lips and cheeks.

13 r incisions (0-3) were made into the hamster cheek 1 week apart, or three incisions were done 1 day a

14 f gauze by gently swabbing the inside of the cheek 3 times.

15 asally: injection under the epidermis of the cheek, a site that has a lymphatic drainage into the CLN

16 slightly bowed eyebrows, deep-set eyes, full cheeks, a short nose, and large, fleshy and forward-faci

17 ral plates are considered homologous to free cheeks, Acanthomeridion is recovered sister to trilobite

18 he space between the gums and the inner lips/cheeks along the front and sides of the mouth (test meth

19 tures, such as the forward projection of the cheek among Northeast Asians and compaction of the Europ

20 Skin swabs were collected from the cheek and antecubital fossa (AF) at baseline, age 8 week

21 es of OMG can capture distinct variations in cheek and brow movements with a high degree of accuracy

22 Lateral sliding joints between the cheek and dermal skull roof, as well as independent mobi

23 Male BMD cells migrate into the cheek and differentiate into epithelial cells, an occurr

24 cupuncture points were the external ear, the cheek and face area, and 4 nonspecific points in the hel

25 lling, miosis, mydriasis and swelling of the cheek and face.

26 ed t test: p < 0.001), while DNA yields from cheek and gutter collections from infants were equivalen

27 sts that the ability to laterally expand the cheek and palate was maintained during the fish-to-tetra

28 p and shooting, and radiating along the left cheek and temple.

29 Dogs lap because they have incomplete cheeks and cannot suck.

30 us cooling trend in the nose, but not in the cheeks and chin was observed.

31 childhood, later disseminating to the feet, cheeks and ears.

32 raph was influenced by methods of supporting cheeks and subject's arm position.

33 Midface (cheeks and temples) volumization was performed using the

34 residues, especially in the areas facing the cheeks and tongue.

35 were assessed for eczema and dry skin on the cheeks and/or extensors; impaired skin barrier function,

36 tological reconstructions of the body shape, cheek, and skull roof.

37 es; periocular in 2 cases; and lip, eyebrow, cheek, and upper eyelid in 1 case each.

38 he body such as the volar forearm, forehead, cheeks, and hands.

39 dy sites (volar forearm, antecubital fossae, cheeks, and lesions) in combination with sequencing of S

40 Soft tissue forces of the tongue, cheeks, and lips are known to cause tooth movement and i

41 transplantation included nose, chin, part of cheeks, and lips.

42 300, or 1000 impulses of shock wave on both cheeks at energy levels 0.1 mJ/mm(2).

43 hotillomania, 28.4%; nail biting, 36.6%; lip-cheek biting, 26.1%; other, 20.1%) did not differ on any

44 oked, or (3) stroked and episodically fed by cheek cannulation.

45 Cheek cell DHA and arachidonic acid in phospholipids wer

46 se and noninvasive nature of this technique, cheek cell fatty acids may serve as a marker of the esse

47 ood diary; 6779 women in the cohort provided cheek cell samples, blood samples, or both, which were g

48 s to screen for lung cancer by assessing the cheek cells based on emerging genetic/epigenetic data wh

49 , in RBCs by 101%, in plasma by 139%, and in cheek cells by 73% (P<0.005 versus baseline for all; res

50 vestigate the degree to which fatty acids of cheek cells reflect the fatty acid content of plasma, re

51 d the phospholipid fatty acid content of the cheek cells was determined.

52 Cheek cells were collected on a small piece of gauze by

53 that is easy to access is the buccal mucosa (cheek cells).

54 hee hee, hah hah hah, cheese cheese cheese, cheek cheek cheek, hah hah hah hah hah hah" 30 times per

55 antly associated with shape variation of the cheek, chin, nose and mouth areas.

56 is associated with widening/fullness of the cheeks, contraction of the chin and deepening of the eye

57 the patient while trying to perform a puffed cheek, creating a closed air column under positive press

58 n of the non-linear viscoelastic behavior of cheek cutis and subcutis to inform anatomically-accurate

59 p number and evolutionary outcomes of rodent cheek dentition.

60 Skull roof and cheek disparity decrease during the end-Devonian mass ex

61 uous nasal breathing while puffing out their cheek during image acquisition, preventing the formation

62 aled that trigeminal neurons innervating the cheek exhibited complete segregation of responses to gen

63 d (torso, ear, neck, frenulum, angle of jaw, cheeks [fleshy], eyelids, and subconjunctivae), bruising

64 When compared with the previous Mellits and Cheek formulas, the new formula fits better for infants

65 he assembly and analysis of a northern white-cheeked gibbon (Nomascus leucogenys) genome.

66 d 24 synteny breakpoint regions in the white-cheeked gibbon (Nomascus leucogenys, NLE) in the form of

67 We identified similar proviruses in white-cheeked gibbons; the gibbon insertions cluster within th

68 h hah hah, cheese cheese cheese, cheek cheek cheek, hah hah hah hah hah hah" 30 times per five minute

69 ncluding the teeth, gingival sulcus, tongue, cheeks, hard and soft palates, and tonsils, which are co

70 The formulas of Mellits and Cheek have been recommended to estimate TBW in children

71 looking at another face being stroked on the cheek in synchrony or asynchrony with affective (slow; C

72 ch involved detecting tactile stimuli on the cheek in the presence or absence of a concomitant light.

73 A few aromatase neurons express Fos after cheek injection of capsaicin, formalin, or chloroquine.

74 ites were studied in each subject: forehead, cheek, inner and outer forearm surfaces, lower back and

75 ived a facial allograft, including mandible, cheeks, lips, and chin, in November 2009.

76 ys (Japanese macaques [Macaca fuscata], gray-cheeked mangabey [Lophocebus albigena], rhesus macaques

77 The murine cheek model and behavioral scoring were employed to eval

78 In a murine cheek model of acute itch, intradermal injection IL-20 a

79 In a mouse cheek model, pre-administration of Pam3CSK4 and FSL-1 en

80 major mouse itch models, including the acute cheek model, the histaminergic model, and a chronic itch

81 hough studied extensively in relation to the cheek mucosa, is not elucidated as far as gingival tissu

82 exhibited an elevated warming effect on the cheeks, nose, and chin.

83 manifested as red violaceous plaques of the cheeks, nose, ears, fingers, and toes that progressed to

84 contents in fillet, and those in the breast, cheek, occiput, and tail tissue of three commercial cora

85 the skin of the calf of the hind paw or the cheek of previously sensitized mice with the hapten, squ

86 yielded significantly stronger signals than cheek or gum swabbing.

87 ne, or both, leading to collapse of the lip, cheek, periorbital soft tissues, and palatal competence

88 ue types [eg, colon, liver, lung, esophagus, cheek pouch (oral epithelium), and cells of hematopoieti

89 an (molecular mass, 70 kDa) from the hamster cheek pouch (p < 0.05).

90 , but not in tissue matched, non-tumorigenic cheek pouch (POT2) or pancreatic (KL5N) cell lines.

91 dothelial) conduction pathways along hamster cheek pouch arterioles in vivo (n=64; diameter, 33+/-1 m

92 mast cell-dependent constriction of hamster cheek pouch arterioles that is attenuated by A3AR blocka

93 f vasoconstriction elicited by NA and KCl in cheek pouch arterioles.

94 herapy of early premalignancy in the hamster cheek pouch carcinogenesis model.

95 e changes in MnSOD expression during hamster cheek pouch carcinogenesis, and the effects of MnSOD ove

96 eans of delivering the MnSOD cDNA to hamster cheek pouch carcinoma (HCPC-1) cells in vitro.

97 nd p15(INK4b) were homozygously deleted in a cheek pouch carcinoma cell line (HCPC) and two pancreati

98 Solid hamster cheek pouch carcinoma xenografts were then established i

99 g growth factor beta, induced EMT of hamster cheek pouch carcinoma-1 cells by promoting the expressio

100 of two Hodgkin lymphomas with golden hamster cheek pouch cells, resulting in serially-transplanted (o

101 on in fluorescence in the carcinogen-treated cheek pouch compared with nonilluminated areas.

102 (N = 21) received a single injection in the cheek pouch containing 4 micrograms of PDGF-BB and 4 mic

103 group (N = 19) received an injection in the cheek pouch containing the saline vehicle only, and the

104 ra and microscope were used to image hamster cheek pouch microvessels during and after 532 nm and 106

105 12-dimethylbenz(a)anthracene-treated hamster cheek pouch model of carcinogenesis using multiphoton la

106 thylbenz[a]anthracene (DMBA)-induced hamster cheek pouch model of oral squamous cell carcinoma (SCC).

107 ay be a tumor suppressor gene in the hamster cheek pouch model system.

108 leukocyte capture in vivo using the hamster cheek pouch model.

109 ive importance of the hamster pancreatic and cheek pouch models of carcinogenesis in subsequent mecha

110 Two-dimensional images of hamster cheek pouch mucosa tissues were obtained by scanning the

111 12-dimethylbenz[a]anthracene-treated hamster cheek pouch mucosa tissues.

112 n epithelial dysplasia induced in the buccal cheek pouch of the Syrian golden hamster.

113 tment of head and neck cancer in the hamster cheek pouch oral cancer model is presented.

114 mics morphometric parameters for the hamster cheek pouch retractor muscle.

115 of human melanoma fragments into the hamster cheek pouch stimulated blood vessel growth.

116 for cancer promotion was the hamster buccal cheek pouch that had been treated with a carcinogen (9,1

117 ucosal microcirculation as an in situ assay, cheek pouch tissue was exteriorized in anesthetized (phe

118 imals were killed at periodic intervals, and cheek pouch tissues were excised and examined for MnSOD

119 or (B2R) inhibited plasma leakage in hamster cheek pouch topically exposed to tissue culture trypomas

120 d papillary SCC, n = 7] sites in the hamster cheek pouch were collected in viable, unsectioned tissue

121 lly-induced epithelial tumors in the hamster cheek pouch were treated.

122 rance of macromolecules from in situ hamster cheek pouch which was attenuated by NPC 17647, a selecti

123 In the light of previous findings in the cheek pouch, the properties of vasoconstriction and vaso

124 neutral endopeptidase 24.11 activity in the cheek pouch, two peptidases widely distributed in the mi

125 In arterioles of the hamster cheek pouch, vasodilatation and vasoconstriction can spr

126 ch are absent from arterioles studied in the cheek pouch.

127 tractor muscle, which is contiguous with the cheek pouch.

128 thelial cells of arterioles from the hamster cheek pouch.

129 ed and dark areas was not seen in the normal cheek pouch.

130 e parameters were chosen for working hamster cheek-pouch retractor muscle.

131 si- and contralateral representations of the cheek pouches in macaques.

132 ES-exposed donors were transplanted into the cheek pouches of control or neonatally DES-exposed adult

133 (pits) and the kangaroo rats have fur-lined cheek pouches that allow for greater foraging efficiency

134 ntrast between normal and carcinogen-treated cheek pouches was found at 4-8 days after injection.

135 The cheek pouches were harvested for histologic and histoche

136 Cheek pouches were imaged in vivo and correlated to hist

137 e and/or nociceptive neurons innervating the cheek project to thalamus or LPb.

138 into genital or nongenital (hind paw, tail, cheek) regions.

139 Techniques such as Mustarde cheek rotation, modified rhomboid, and paramedian forehe

140 on behaviours, with olfaction, scraping, and cheek rubbing the most frequently recorded.

141 n Appalachian endemic species, Southern Gray-Cheeked Salamander, and may extend into other species wi

142 (mean yield = 15.0 micro g/two brushes) than cheek samples (mean yield = 7.6 micro g/two brushes) (pa

143 romosome positive buccal epithelial cells in cheek scrapings obtained from five females who had recei

144 (0)Z (C-86/12).The three sugarcane standard cheeks showed relatively higher values of polarization i

145 Immediately after denervation, a piece of cheek skin (approximately 0.5 cm2) was removed bilateral

146 n mice when applied intradermally to nape or cheek skin, (ii) acidified buffer elevated intracellular

147 nfants: 1) brushing the left and right inner cheeks (standard method) and 2) brushing the upper and l

148 o enhances tactile sensitivity on the nearby cheek, suggesting that the space close to the face is in

149 Cheek support and subject's arm position can influence o

150 4: subject relax their cheeks without any cheek support.

151 he subjects stiffen their cheeks without any cheek support.

152 Cheek swab samples were obtained for DNA analysis from 1

153 DNA was isolated from cheek swab samples.

154 Buccal genetic cheek swab, circulating serum dietary carotenoids and lo

155 ative sources of genetic material, including cheek swabs and dried blood spots, is described briefly.

156 We analyzed cheek swabs from 4626 typically developing children 2-mo

157 We used cheek swabs to obtain the genomic DNA of 200 ADHD male p

158 After data collection, cheek swabs were obtained from all children.

159 Cheek swabs, heterogeneous samples consisting primarily

160 is review provides an overview of the puffed cheek technique and its associated pitfalls.

161 The "puffed cheek" technique is routinely performed during CT neck s

162 The evolution of high-crowned cheek teeth (hypsodonty) in herbivorous mammals during t

163 h following extraction of incisor, canine or cheek teeth from 29 adult horses with dental disease.

164 Understanding that cheek teeth function as guides for chewing and tools for

165 legged herbivorous mammals with high-crowned cheek teeth have been viewed as an example of coevolutio

166 volume loss that affects the contours of the cheeks, temples, and orbits and may negatively affect pa

167 orsi can more reliably support the orbit and cheek than soft-tissue free flaps and non-vascularised g

168 We studied stopover behaviour of Grey-cheeked Thrush (Catharus minimus) at a site in northern

169 northwestern (e.g., American Redstart, Gray-cheeked Thrush) or southern (Yellow-billed Cuckoo) popul

170 ntral plates as homologous to trilobite-free cheeks, to trilobite cephalic doublure, or independently

171 sms found on other oral surfaces such as the cheek, tongue, and teeth are added to this number, the b

172 rsus ash-laden forests) triggered convergent cheek-tooth evolution in Cenozoic herbivores.

173 Vertebrates with incomplete cheeks use their tongue to drink; the most common exampl

174 ment (N = 38) spatial incongruence of touch (cheek vs. forehead) was used as a control condition inst

175 roductive outcomes for the endangered golden-cheeked warbler (Setophaga chrysoparia).

176 0), healthy participants were stroked on the cheek while they were looking at another face being stro

177 ue of The Journal of Physiology is the sheer cheek with which the authors decided to use the microdia

178 2: the tester support the subject's cheeks with their hands.

179 1: the subjects support their cheeks with their hands.

180 ely bigger forehead and eyes, and protruding cheeks), with an adaptive function to induce caretaking

181 ng 80% of the scalp, left forehead, and left cheek, with no evidence of metastasis.

182 4: subject relax their cheeks without any cheek support.

183 3: the subjects stiffen their cheeks without any cheek support.