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1 ssion of Deformed and another homeotic gene, labial.
2 n parallel to, and independently of, that of labial.
3  Sex combs reduced, and Antennapedia but not labial.
4 in a slightly broader endodermal region than labial.
5 attern of spatially restricted expression of labial, a selector gene with a role in cell type specifi
6  regulatory activity does not require direct labial activation by the TGF-beta effector Mad.
7 ion resemble those reported for mutations in labial, an endodermal homeotic gene required for copper
8 conspicuous defect in cuprophilic cells from labial and alpha spectrin mutants was in morphogenesis o
9 eurohemal release sites located on the upper labial and anterior tentacular nerves.
10 sophila embryos is dependent upon endogenous labial and exd, suggesting that the ability of this Hox/
11            The data suggest a model in which labial and extradenticle, separated by only 4 bp, bind t
12 d (Scr) gene specifies the identities of the labial and first thoracic segments in Drosophila melanog
13                                Expression of labial and homothorax are required for dpp expression in
14 at typically affects exocrine glands--mainly labial and lacrimal--leading to complaints of dry mouth
15 ern snakes (for example, recurved teeth with labial and lingual carinae, long toothed suborbital ramu
16 generation of odontoblasts and dentin on the labial and lingual sides of unerupted and erupted inciso
17  abnormal ameloblast differentiation on both labial and lingual surfaces.
18  is a single segment-like entity composed of labial and maxillary segment derivatives which produce t
19 l recession were measured at two points (mid-labial and mid-palatal).
20 upernumerary segment that occurs between the labial and T1 segments of RNAiScr first nymphs and is at
21  response element that is a direct target of labial and the homeotic cofactors homothorax and extrade
22 tle Scr and Antennapedia orthologs cause the labial and thoracic appendages, respectively, to be tran
23 I and CeOsm-3 are expressed in amphid, inner labial, and phasmid chemosensory neurons.
24 on which thus becomes predisposed to express labial, and that D-Fos cooperates with signal-activated
25  those cells in homologous discs such as the labial, antennal and leg, but not in cells of dorsally l
26              We show here that the Tribolium labial appendages also develop as antennae in double mut
27 the Tribolium ortholog of Scr, transform the labial appendages to antennae, a result seen in the othe
28 ts results in homeotic transformation of the labial appendages to legs.
29 tes, the inner branches of the maxillary and labial appendages, are formed at metamorphosis.
30 the most prominent development involving the labial aspects of the anterior sextants.
31       They occur more in the mandible on the labial attached gingiva of the anterior teeth.
32 uid and may cause pressure resorption of the labial bone, yielding a radiolucency sometimes confused
33 h a failing tooth in the esthetic zone and a labial bony defect of >/=5 mm after removal of a tooth w
34 placement with delayed provisionalization in labial bony defects of >/=5 mm regarding change in MBL.
35 o required for transcriptional repression of labial by high wingless levels.
36 cause DFD protein does not accumulate in the labial cells of Scr mutants, although DFD is required fo
37 pecific region of Tbx1-positive cells in the labial cervical loop (LaCL, stem cell niche).
38 ic stages led to abnormal development of the labial cervical loop and of the inner enamel epithelial
39 creases DESC proliferation and creates a new labial cervical loop stem cell compartment, which produc
40 labic preference for initiating words with a labial consonant-vowel-coronal consonant sequence (LC).
41                 For example, the HOX protein labial cooperatively binds with extradenticle protein to
42  to the bone crest; 2) tooth torque (TT); 3) labial cortical bone thickness (BT) for alveolar and bas
43 esponses involve a series of steps including labial dabbing and probing using their piercing mouthpar
44 ng: the presence of a second, internal outer labial dendrite (OL1); a second cephalic dendrite in the
45 EP2/CEM); an accessory process loop of inner labial dendrite 1; and terminus morphology and epidermal
46 reduced (Scr) regulate the limb genes in the labial disc to give rise to a unique type of appendage,
47                                       In the labial disc, Pb positively regulates transcription of Sc
48 r results suggests a revised fate map of the labial disc.
49 the expression patterns of both ct and pb in labial discs.
50 expression and also downregulates Dll in the labial discs; discs mutant for both pb and Scr give rise
51  dorsolateral extension of the maxillary and labial Engrailed stripes (posterior compartments) during
52  midgut, and that endoderm expression from a labial enhancer depends on multiple CREs.
53 p pathway, as dpp signalling is required for labial expression but represses homothorax.
54 ediated reporter gene expression and reduces labial expression in the endoderm.
55 on factors FoxK and Dfos/AP-1 that regulates labial expression in the midgut endoderm.
56 nse factors to confer the precise pattern of labial expression in this region.
57  in the embryo as well as for maintenance of labial expression through larval stages; and that D-Fos
58                                    Efficient labial expression thus only occurs within a window of in
59 ding sites, whereas FoxK, in turn, regulates labial expression.
60 eractions that are important for forming the labial-extradenticle-DNA complex.
61 ivo this enhancer preferentially responds to labial family members.
62 cation was also blocked by a mutation in the labial gene, which is required for differentiation of cu
63 as not associated with the thickness of both labial gingiva and bone.
64 esentation of the clinical thickness of both labial gingiva and bone.
65            In addition, the thickness of the labial gingiva had a moderate association with the under
66                                          The labial gingival thickness was moderately associated with
67         Insect larvae, manipulated to reduce labial gland salivary secretions, were used to examine t
68 sorptive columnar cells of the midgut and in labial glands.
69        In eight beagle dogs, a critical-size labial GR defect was surgically induced on bilateral max
70 ds of signs and symptoms of genital and oral-labial herpes.
71 c acid (RA) in this process and by using the labial Hox gene, HoxD1, as a posterior marker.
72  Hox gene essential for embryogenesis is the labial/Hox1 homolog ceh-13, required for more anterior p
73 orax and decapentaplegic in the mesoderm and labial in the endoderm.
74 il to generate midgut constrictions and lack Labial in the endoderm.
75 s Ultrabithorax in the visceral mesoderm and labial in the subjacent endoderm.
76 elium, while the Hox gene Deformed represses labial in this location, thus limiting its expression an
77 c expression of Hoxb1, Hoxa1, and Drosophila labial in transgenic mice.
78  Pitx2 and beta-catenin are expressed in the labial incisor cervical loop or epithelial stem cell nic
79  present evidence that D-Fos is required for labial induction in the embryo as well as for maintenanc
80 SV-1) not only causes painful recurrent oral-labial infections, it can also cause permanent brain dam
81 ifies maxillary and mandibular identity, and labial is necessary for intercalary segment identity.
82 gnathal segments (mandibular, maxillary, and labial) is best understood in the fly Drosophila melanog
83  have studied this issue with the Drosophila labial (lab) gene and its chicken ortholog gHoxb-1.
84 e mouse Hoxb-1 gene, a homolog of Drosophila labial (lab), is sufficient to direct an expression patt
85 logues of the Drosophila head homeotic genes labial (lab), proboscipedia (pb), and Deformed (Dfd) hav
86            The airway was assessed for oral, labial, laryngeal, and tracheal damage.
87 igonucleotide that is sufficient to direct a labial-like expression pattern in Drosophila embryos.
88 syllabic consonant-vowel (CV) co-occurrence: labial (lip) consonants with central vowels, coronal (to
89          Gingival perfusion was evaluated at labial LLLI attached gingiva.
90 a, stimulated parotid saliva, and stimulated labial minor gland saliva were collected from 25 patient
91  Examination revealed telangiectasias on the labial mucosa and nail folds.
92            Imaging of capillary ECG in human labial mucosa was achieved by the use of a 1-mm-diameter
93  (5 x 10 mm) on the maxillary right and left labial mucosa.
94 ged conservatively, but 2 eyes required free labial-mucous membrane grafting for persistent corneal e
95                                         Free labial-mucous membrane grafting was performed in all cas
96 chanosensory terminal axons entering via the labial nerve define the ventromedial sensory center (VMS
97 f the C beta peptide release site, the upper labial nerve, and its synthesis location, the F- and C-c
98 median (VUM) neurons with cell bodies in the labial neuromere of the subesophageal ganglion.
99 , mandibular neuromere, maxillary neuromere, labial neuromere) of the SEZ at all stages of developmen
100        These studies have uncovered a set of labial olfactory responses to a small spectrum of human-
101 aracterized the AgOR profile within a single labial olfactory sensillum.
102 etent subjects with no prior history of oral/labial or genital herpes possessed HSV-specific T cell i
103  cell-derived ameloblasts exclusively on the labial, or outer, surface of the tooth.
104 possess three sound sources, two oscine-like labial pairs and the unique tracheal membranes, which co
105 pressed in 22 or fewer taste neurons in each labial palp.
106 larged mandibles and greatly enlarged apical labial palpomeres with dense specialized sensory organs,
107  we tested the prediction that maxillary and labial palps are patterned using conserved components of
108 ristles located in the male forelegs and the labial palps are thought to recognize nonvolatile pherom
109 tants lacking taste function in the legs and labial palps have intact pharyngeal sweet taste, which i
110 ting strong transformations of maxillary and labial palps to legs.
111 tail the expression of eight Gr genes in the labial palps, the fly's main taste organ.
112 pressed in gustatory receptor neurons of the labial palpus, tarsus, and wing anterior margin, but not
113 expression in transgenic mouse embryos and a labial pattern in Drosophila embryos.
114  nubbin (nub) affects antenna morphogenesis, labial patterning, the length of the femoral segment in
115 specificity, as it is capable of switching a Labial-PBC binding site/response element to a Deformed r
116                       Normally, multimerized Labial-PBC binding sites are sufficient to trigger a Lab
117 ion (0.5 ppm) in CO(2) concentration through labial pit organs whose receptor neurons project afferen
118                                Due to severe labial positioning of the implant fixtures, acceptable p
119 ing single orthologs of the Drosophila genes labial, proboscipedia, Deformed, Sex combs reduced, fush
120  genes are orthologs of the Drosophila genes labial, proboscipedia, zen, Deformed, and Sex combs redu
121 h that initiates the replacement cycle via a labial proliferation bias.
122 eceptive-specific (COLD) cells with nasal or labial receptive fields, whereas nociceptive neurons wer
123 tation (crystallographic texture) within the labial regions of each tooth slice and then correlated w
124 ws that individual members of the vertebrate labial-related genes have multiple roles in different st
125 nding experiments showed that the vertebrate labial-related protein Hoxb1 will cooperatively bind to
126 bility of this Hox/Pbx site to interact with labial-related proteins has been evolutionarily conserve
127 pressed by B cells isolated from sections of labial salivary gland biopsies from two Sjogren's syndro
128       For a third of these subjects, matched labial salivary gland biopsy specimens were also analyze
129 is differentially expressed in the embryonic labial segment of Manduca as two circular monolayers of
130 identity of the posterior head segments; the labial segment requires Sex combs reduced (Scr) for prop
131 tants, where a partial transformation of the labial segment to a more anterior, maxillary identity ha
132                       Thus, in the wild-type labial segment, Cx function is required (directly or ind
133 rt of the posterior maxillary and all of the labial segment, is found to be in common among all four
134 pressed in each abdominal segment and in the labial segment.
135 is a canonical gap gene in the maxillary and labial segments and also plays a gap-like role in the fi
136 bryos, mxp is expressed in the maxillary and labial segments, whereas ectopic expression is observed
137 re composed of portions of the maxillary and labial segments.
138 play a severe loss of Amel expression on the labial side of the lower incisors, as well as enamel hyp
139 nd adhesion properties of ameloblasts on the labial side of these teeth were severely disrupted.
140 in oscines from neuromuscular control of two labial sources [15-17].
141 BC binding sites are sufficient to trigger a Labial-specific activation response in either Drosophila
142 imaged in the superficial tissues lining the labial sulcus.
143 er degree of crystal organization across the labial surface in comparison with the hypoplastic enamel
144 ssion defects were surgically created on the labial surfaces of the maxillary cuspids of 8 mongrel do
145 o the decayed-filled index; fluorosis on the labial surfaces of the upper permanent central and later
146 tion of the homeotic genes Ultrabithorax and labial, they are also required for transcriptional repre
147 t expression pattern generated in vivo, from labial to Deformed.
148 age analysis software for vertical KT height labial to each mandibular incisor.
149 ent evidence that casts doubt on whether the labial to maxillary transformation actually exists in em
150  the keratinized gingival tissue (KT) height labial to the mandibular incisors after active orthodont
151 e in HOX preference in the heterodimer, from labial to Ultrabithorax.
152 r multimeric sites that bind heterodimers of Labial-type Hox and PBC proteins.
153 e patient developed acutely painful oral and labial ulcers accompanied by target skin lesions.
154  1 (HSV-1) most commonly causes recrudescent labial ulcers; however, it is also the leading cause of
155 d right upper premolars and molars (UL, UR), labial upper central incisors (UC), and lingual lower ce
156 e imaging system, the frequency and phase of labial vibrations could not be assessed in relation to t
157                                     Swabs of labial, vulvar, perineal, perianal, endocervical, and ec
158                                      Oblique labial wear facets present on numerous small conical man
159 ved signaling cascades activate the Hox gene labial, which is important for the differentiation of co

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