ライフサイエンスコーパス: labial

1 ow (30%) sequence similarity with Drosophila Labial.

2 ssion of Deformed and another homeotic gene, labial.

3 n parallel to, and independently of, that of labial.

4 Sex combs reduced, and Antennapedia but not labial.

5 in a slightly broader endodermal region than labial.

6 attern of spatially restricted expression of labial, a selector gene with a role in cell type specifi

7 regulatory activity does not require direct labial activation by the TGF-beta effector Mad.

8 ion resemble those reported for mutations in labial, an endodermal homeotic gene required for copper

9 conspicuous defect in cuprophilic cells from labial and alpha spectrin mutants was in morphogenesis o

10 eurohemal release sites located on the upper labial and anterior tentacular nerves.

11 sophila embryos is dependent upon endogenous labial and exd, suggesting that the ability of this Hox/

12 The data suggest a model in which labial and extradenticle, separated by only 4 bp, bind t

13 d (Scr) gene specifies the identities of the labial and first thoracic segments in Drosophila melanog

14 Expression of labial and homothorax are required for dpp expression in

15 ss-species functional analysis of Drosophila Labial and its mouse HOX1 orthologs (HOXA1, HOXB1, and H

16 at typically affects exocrine glands--mainly labial and lacrimal--leading to complaints of dry mouth

17 ern snakes (for example, recurved teeth with labial and lingual carinae, long toothed suborbital ramu

18 ed distinct asymmetries in morphology of the labial and lingual sides of the cervical loop during ear

19 ignificantly asymmetrical development of the labial and lingual sides of the cervical loop, which lat

20 generation of odontoblasts and dentin on the labial and lingual sides of unerupted and erupted inciso

21 abnormal ameloblast differentiation on both labial and lingual surfaces.

22 is a single segment-like entity composed of labial and maxillary segment derivatives which produce t

23 l recession were measured at two points (mid-labial and mid-palatal).

24 upernumerary segment that occurs between the labial and T1 segments of RNAiScr first nymphs and is at

25 response element that is a direct target of labial and the homeotic cofactors homothorax and extrade

26 tle Scr and Antennapedia orthologs cause the labial and thoracic appendages, respectively, to be tran

27 I and CeOsm-3 are expressed in amphid, inner labial, and phasmid chemosensory neurons.

28 on which thus becomes predisposed to express labial, and that D-Fos cooperates with signal-activated

29 those cells in homologous discs such as the labial, antennal and leg, but not in cells of dorsally l

30 We show here that the Tribolium labial appendages also develop as antennae in double mut

31 the Tribolium ortholog of Scr, transform the labial appendages to antennae, a result seen in the othe

32 ts results in homeotic transformation of the labial appendages to legs.

33 tes, the inner branches of the maxillary and labial appendages, are formed at metamorphosis.

34 the most prominent development involving the labial aspects of the anterior sextants.

35 They occur more in the mandible on the labial attached gingiva of the anterior teeth.

36 g the lip motor area has opposite effects on labial (ba/pa)- and coronal (da/ta) sounds.

37 Accordingly, labial biopsies from primary Sjogren's syndrome patients

38 uid and may cause pressure resorption of the labial bone, yielding a radiolucency sometimes confused

39 h a failing tooth in the esthetic zone and a labial bony defect of >/=5 mm after removal of a tooth w

40 placement with delayed provisionalization in labial bony defects of >/=5 mm regarding change in MBL.

41 o required for transcriptional repression of labial by high wingless levels.

42 cause DFD protein does not accumulate in the labial cells of Scr mutants, although DFD is required fo

43 ly, Pitx2 regulates formation of the Sox2(+) labial cervical loop (LaCL) stem cell niche in concert w

44 pecific region of Tbx1-positive cells in the labial cervical loop (LaCL, stem cell niche).

45 ic stages led to abnormal development of the labial cervical loop and of the inner enamel epithelial

46 creases DESC proliferation and creates a new labial cervical loop stem cell compartment, which produc

47 labic preference for initiating words with a labial consonant-vowel-coronal consonant sequence (LC).

48 For example, the HOX protein labial cooperatively binds with extradenticle protein to

49 to the bone crest; 2) tooth torque (TT); 3) labial cortical bone thickness (BT) for alveolar and bas

50 esponses involve a series of steps including labial dabbing and probing using their piercing mouthpar

51 ng: the presence of a second, internal outer labial dendrite (OL1); a second cephalic dendrite in the

52 EP2/CEM); an accessory process loop of inner labial dendrite 1; and terminus morphology and epidermal

53 reduced (Scr) regulate the limb genes in the labial disc to give rise to a unique type of appendage,

54 In the labial disc, Pb positively regulates transcription of Sc

55 r results suggests a revised fate map of the labial disc.

56 the expression patterns of both ct and pb in labial discs.

57 expression and also downregulates Dll in the labial discs; discs mutant for both pb and Scr give rise

58 The silk emerges from labial ducts as a nanofibrous fluid gel, flowing over th

59 dorsolateral extension of the maxillary and labial Engrailed stripes (posterior compartments) during

60 midgut, and that endoderm expression from a labial enhancer depends on multiple CREs.

61 p pathway, as dpp signalling is required for labial expression but represses homothorax.

62 ediated reporter gene expression and reduces labial expression in the endoderm.

63 on factors FoxK and Dfos/AP-1 that regulates labial expression in the midgut endoderm.

64 nse factors to confer the precise pattern of labial expression in this region.

65 in the embryo as well as for maintenance of labial expression through larval stages; and that D-Fos

66 Efficient labial expression thus only occurs within a window of in

67 ding sites, whereas FoxK, in turn, regulates labial expression.

68 eractions that are important for forming the labial-extradenticle-DNA complex.

69 ivo this enhancer preferentially responds to labial family members.

70 cation was also blocked by a mutation in the labial gene, which is required for differentiation of cu

71 as not associated with the thickness of both labial gingiva and bone.

72 esentation of the clinical thickness of both labial gingiva and bone.

73 In addition, the thickness of the labial gingiva had a moderate association with the under

74 The labial gingival thickness was moderately associated with

75 Insect larvae, manipulated to reduce labial gland salivary secretions, were used to examine t

76 sorptive columnar cells of the midgut and in labial glands.

77 In eight beagle dogs, a critical-size labial GR defect was surgically induced on bilateral max

78 ds of signs and symptoms of genital and oral-labial herpes.

79 c acid (RA) in this process and by using the labial Hox gene, HoxD1, as a posterior marker.

80 Hox gene essential for embryogenesis is the labial/Hox1 homolog ceh-13, required for more anterior p

81 ed similar DNA-binding patterns of HOXA1 and Labial in mouse cells, while HOXB1 binds to distinct tar

82 orax and decapentaplegic in the mesoderm and labial in the endoderm.

83 il to generate midgut constrictions and lack Labial in the endoderm.

84 s Ultrabithorax in the visceral mesoderm and labial in the subjacent endoderm.

85 elium, while the Hox gene Deformed represses labial in this location, thus limiting its expression an

86 c expression of Hoxb1, Hoxa1, and Drosophila labial in transgenic mice.

87 Pitx2 and beta-catenin are expressed in the labial incisor cervical loop or epithelial stem cell nic

88 present evidence that D-Fos is required for labial induction in the embryo as well as for maintenanc

89 SV-1) not only causes painful recurrent oral-labial infections, it can also cause permanent brain dam

90 ifies maxillary and mandibular identity, and labial is necessary for intercalary segment identity.

91 gnathal segments (mandibular, maxillary, and labial) is best understood in the fly Drosophila melanog

92 have studied this issue with the Drosophila labial (lab) gene and its chicken ortholog gHoxb-1.

93 e mouse Hoxb-1 gene, a homolog of Drosophila labial (lab), is sufficient to direct an expression patt

94 logues of the Drosophila head homeotic genes labial (lab), proboscipedia (pb), and Deformed (Dfd) hav

95 The airway was assessed for oral, labial, laryngeal, and tracheal damage.

96 igonucleotide that is sufficient to direct a labial-like expression pattern in Drosophila embryos.

97 syllabic consonant-vowel (CV) co-occurrence: labial (lip) consonants with central vowels, coronal (to

98 Gingival perfusion was evaluated at labial LLLI attached gingiva.

99 th row development in E. bathystoma in which labial migration of functional teeth was extensive enoug

100 of alveolar bone indicate varying degrees of labial migration of teeth through ontogeny, often alteri

101 a, stimulated parotid saliva, and stimulated labial minor gland saliva were collected from 25 patient

102 Examination revealed telangiectasias on the labial mucosa and nail folds.

103 normal human oral mucosa tissues, including labial mucosa tissue, gingival tissue, and tongue dorsum

104 Imaging of capillary ECG in human labial mucosa was achieved by the use of a 1-mm-diameter

105 ILC1s populated and patrolled the uninfected labial mucosa.

106 (5 x 10 mm) on the maxillary right and left labial mucosa.

107 ged conservatively, but 2 eyes required free labial-mucous membrane grafting for persistent corneal e

108 Free labial-mucous membrane grafting was performed in all cas

109 chanosensory terminal axons entering via the labial nerve define the ventromedial sensory center (VMS

110 f the C beta peptide release site, the upper labial nerve, and its synthesis location, the F- and C-c

111 median (VUM) neurons with cell bodies in the labial neuromere of the subesophageal ganglion.

112 , mandibular neuromere, maxillary neuromere, labial neuromere) of the SEZ at all stages of developmen

113 These studies have uncovered a set of labial olfactory responses to a small spectrum of human-

114 aracterized the AgOR profile within a single labial olfactory sensillum.

115 etent subjects with no prior history of oral/labial or genital herpes possessed HSV-specific T cell i

116 cell-derived ameloblasts exclusively on the labial, or outer, surface of the tooth.

117 possess three sound sources, two oscine-like labial pairs and the unique tracheal membranes, which co

118 pressed in 22 or fewer taste neurons in each labial palp.

119 larged mandibles and greatly enlarged apical labial palpomeres with dense specialized sensory organs,

120 we tested the prediction that maxillary and labial palps are patterned using conserved components of

121 ristles located in the male forelegs and the labial palps are thought to recognize nonvolatile pherom

122 tants lacking taste function in the legs and labial palps have intact pharyngeal sweet taste, which i

123 (226)Ra ranged from 8.9 h for the gills and labial palps to 15.4 h for the muscle.

124 ting strong transformations of maxillary and labial palps to legs.

125 terminal segments of antennae, maxillary and labial palps, and unmodified femora of hind legs, provid

126 tail the expression of eight Gr genes in the labial palps, the fly's main taste organ.

127 pressed in gustatory receptor neurons of the labial palpus, tarsus, and wing anterior margin, but not

128 expression in transgenic mouse embryos and a labial pattern in Drosophila embryos.

129 nubbin (nub) affects antenna morphogenesis, labial patterning, the length of the femoral segment in

130 specificity, as it is capable of switching a Labial-PBC binding site/response element to a Deformed r

131 Normally, multimerized Labial-PBC binding sites are sufficient to trigger a Lab

132 ion (0.5 ppm) in CO(2) concentration through labial pit organs whose receptor neurons project afferen

133 Due to severe labial positioning of the implant fixtures, acceptable p

134 ing single orthologs of the Drosophila genes labial, proboscipedia, Deformed, Sex combs reduced, fush

135 genes are orthologs of the Drosophila genes labial, proboscipedia, zen, Deformed, and Sex combs redu

136 h that initiates the replacement cycle via a labial proliferation bias.

137 eceptive-specific (COLD) cells with nasal or labial receptive fields, whereas nociceptive neurons wer

138 tation (crystallographic texture) within the labial regions of each tooth slice and then correlated w

139 ws that individual members of the vertebrate labial-related genes have multiple roles in different st

140 nding experiments showed that the vertebrate labial-related protein Hoxb1 will cooperatively bind to

141 bility of this Hox/Pbx site to interact with labial-related proteins has been evolutionarily conserve

142 pressed by B cells isolated from sections of labial salivary gland biopsies from two Sjogren's syndro

143 For a third of these subjects, matched labial salivary gland biopsy specimens were also analyze

144 We found that having a labial salivary gland biopsy with focus score >=1 foci/m

145 in SS, we laser capture microdissected (LCM) labial salivary gland epithelia from 8 SS and 8 non-SS c

146 that mirror the immunological activation of labial salivary glands (LSG) infiltrating T cells in pri

147 T cell subsets and of CD8(+) T cells in the labial salivary glands from untreated patients with prim

148 ur teeth with extraoral tissues (gingiva and labial scales) is both plausible and consistent with pat

149 atures for genetic relatedness were found in labial secretions of adult sisters.

150 is differentially expressed in the embryonic labial segment of Manduca as two circular monolayers of

151 identity of the posterior head segments; the labial segment requires Sex combs reduced (Scr) for prop

152 tants, where a partial transformation of the labial segment to a more anterior, maxillary identity ha

153 Thus, in the wild-type labial segment, Cx function is required (directly or ind

154 rt of the posterior maxillary and all of the labial segment, is found to be in common among all four

155 pressed in each abdominal segment and in the labial segment.

156 is a canonical gap gene in the maxillary and labial segments and also plays a gap-like role in the fi

157 bryos, mxp is expressed in the maxillary and labial segments, whereas ectopic expression is observed

158 re composed of portions of the maxillary and labial segments.

159 play a severe loss of Amel expression on the labial side of the lower incisors, as well as enamel hyp

160 nd adhesion properties of ameloblasts on the labial side of these teeth were severely disrupted.

161 sis, where the tooth is held in place on the labial side only.

162 in oscines from neuromuscular control of two labial sources [15-17].

163 BC binding sites are sufficient to trigger a Labial-specific activation response in either Drosophila

164 imaged in the superficial tissues lining the labial sulcus.

165 er degree of crystal organization across the labial surface in comparison with the hypoplastic enamel

166 ssion defects were surgically created on the labial surfaces of the maxillary cuspids of 8 mongrel do

167 o the decayed-filled index; fluorosis on the labial surfaces of the upper permanent central and later

168 tion of the homeotic genes Ultrabithorax and labial, they are also required for transcriptional repre

169 scattering coefficients of the gingival and labial tissues are significantly different from those of

170 t expression pattern generated in vivo, from labial to Deformed.

171 age analysis software for vertical KT height labial to each mandibular incisor.

172 ent evidence that casts doubt on whether the labial to maxillary transformation actually exists in em

173 the keratinized gingival tissue (KT) height labial to the mandibular incisors after active orthodont

174 e in HOX preference in the heterodimer, from labial to Ultrabithorax.

175 r multimeric sites that bind heterodimers of Labial-type Hox and PBC proteins.

176 e patient developed acutely painful oral and labial ulcers accompanied by target skin lesions.

177 1 (HSV-1) most commonly causes recrudescent labial ulcers; however, it is also the leading cause of

178 d right upper premolars and molars (UL, UR), labial upper central incisors (UC), and lingual lower ce

179 e imaging system, the frequency and phase of labial vibrations could not be assessed in relation to t

180 Swabs of labial, vulvar, perineal, perianal, endocervical, and ec

181 Oblique labial wear facets present on numerous small conical man

182 ved signaling cascades activate the Hox gene labial, which is important for the differentiation of co

183 as retained essential ancestral functions of Labial, while HOXB1 and HOXD1 have diverged.

184 However, substituting endogenous Labial with the mouse proteins revealed that HOXA1 has r