ライフサイエンスコーパス: cheek

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

2 outdoor air and number of lentigines on the cheek.

3 solitary, slowly growing tumor of the right cheek.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

20 300, or 1000 impulses of shock wave on both cheeks at energy levels 0.1 mJ/mm(2).

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

22 Cheek cell DHA and arachidonic acid in phospholipids wer

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 Solid hamster cheek pouch carcinoma xenografts were then established i

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

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

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

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

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

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

62 12-dimethylbenz(a)anthracene-treated hamster cheek pouch model of carcinogenesis using multiphoton la

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

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

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

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

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

68 12-dimethylbenz[a]anthracene-treated hamster cheek pouch mucosa tissues.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

85 thelial cells of arterioles from the hamster cheek pouch.

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

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

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

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

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

91 The cheek pouches were harvested for histologic and histoche

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

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

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

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

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

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

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

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

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

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

102 4: subject relax their cheeks without any cheek support.

103 he subjects stiffen their cheeks without any cheek support.

104 Cheek swab samples were obtained for DNA analysis from 1

105 DNA was isolated from cheek swab samples.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 2: the tester support the subject's cheeks with their hands.

122 1: the subjects support their cheeks with their hands.

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

124 4: subject relax their cheeks without any cheek support.

125 3: the subjects stiffen their cheeks without any cheek support.