ライフサイエンスコーパス: tarsal

1 nae) responds to disturbance by activating a tarsal adhesion mechanism by which it secures a hold on

2 skeletal dysplasias characterized by carpal/tarsal and epiphyseal abnormalities, are caused by mutat

3 -2, and MMP-14 have integral roles in carpal/tarsal and epiphyseal bone development.

4 A proximal tarsal attachment suggests that blepharoptosis procedure

5 The eyelid lamellae and tarsal attachments of the levator aponeurosis in particu

6 of diffuse bone marrow edema (median of 6.5 tarsal bones versus 2 adjacent bones, of 14 total bones;

7 first (to our knowledge) nondental remains (tarsal bones) attributed to Purgatorius from the same ea

8 and fusions of the vertebrae and carpal and tarsal bones.

9 Although the distance from the superior tarsal border to Whitnall's ligament increased significa

10 r's muscle attach proximally at the superior tarsal border.

11 gnal implements the patterning activity of a tarsal boundary and regulates the transcription of sever

12 Clinical symptoms of the tarsal coalition frequently follow a sequence of sprains

13 Tarsal coalition is a common abnormality of the hindfoot

14 The diagnosis of the tarsal coalition is made on the oblique radiograph of th

15 rowth, to stiff or painful manifestations of tarsal coalition, collagen abnormalities, neurologic dis

16 andidates that underlie some forms of carpal/tarsal coalition, conductive deafness, scoliosis, and cr

17 atfoot is an uncommon means of identifying a tarsal coalition.

18 Three of 10 had moderate scarring of the tarsal conjunctiva and lid margins and also moderate dry

19 on swab specimens taken from the right upper tarsal conjunctiva of 240 children aged 1 to 5 years liv

20 at are differentially expressed in the upper tarsal conjunctiva of subjects with TT.

21 sion cytology of the lower eyelid margin and tarsal conjunctiva to measure cytokine expression by qua

22 mation of the crypts is likely the result of tarsal conjunctiva trauma with lamellar de-epithelializa

23 coagulum within the fistulous tracts of the tarsal conjunctiva was the site of pathologic features i

24 ociated with evidence of inflammation in the tarsal conjunctiva, although it is not clear whether the

25 mucous membrane grafting to replace scarred tarsal conjunctiva, specialized contact lenses (PROSE),

26 or intense inflammatory infiltration on the tarsal conjunctiva.

27 0001), bulbar conjunctival (P < 0.0021), and tarsal conjunctival (P < 0.0046) epithelia; tarsal conju

28 nd peripheral corneal epithelium, bulbar and tarsal conjunctival epithelia, tarsal conjunctival strom

29 Recurrence was associated with tarsal conjunctival inflammation (OR: 2.4; 95% confidenc

30 njection) provided complete control of giant tarsal conjunctival OSSN (MD, 20 mm) over a 1-month peri

31 bilateral moderate to severe upper and lower tarsal conjunctival papillary reaction, without corneal

32 r evidence of epilation, in association with tarsal conjunctival scarring.

33 r evidence of epilation, in association with tarsal conjunctival scarring.

34 Five of 28 patients had mild tarsal conjunctival scarring.

35 tarsal conjunctival (P < 0.0046) epithelia; tarsal conjunctival stroma (P < 0.0274); and lid margin

36 m, bulbar and tarsal conjunctival epithelia, tarsal conjunctival stroma, and lid margin.

37 , but rarely are nevi found in the fornix or tarsal conjunctival surface.

38 Tarsal conjunctival swab samples were collected for RNA

39 mbia were examined for signs of disease, and tarsal conjunctival swab samples were collected.

40 The antennal transformation and tarsal deletions caused by ss loss-of-function mutations

41 that bowl has a role at an earlier stage in tarsal development.

42 he contact lens may be retained by the upper tarsal edge, presents an anatomical hazard for contact l

43 lved, resulting in missing digit, carpal and tarsal elements.

44 Further, the deep, flat base and tarsal facets imply that its midfoot had no ape-like mid

45 In this manner, lines inhibits proximal tarsal fates and promotes medial and distal tarsal fates

46 tarsal fates and promotes medial and distal tarsal fates.

47 by the limbal form, 33% were affected by the tarsal form, and 19% were affected by the mixed form.

48 while the patient with entropion was given a tarsal fracture and ear cartilage grafting as additional

49 c facial features, brachydactyly with carpal-tarsal fusion and extensive posterior cervical vertebral

50 bnormalities including elbow dislocation and tarsal fusion.

51 terized by progressive vertebral, carpal and tarsal fusions, and mild short stature.

52 terized by progressive symphalangism, carpal/tarsal fusions, deafness, and mild facial dysmorphism.

53 e phalanges, coned epiphyses, and carpal and tarsal fusions.

54 and is required for later expression of the tarsal gene bric a brac (bab).

55 Notably, we discovered that tarsal Gr32a-expressing neurons were essential for court

56 it prevents the beetle from maintaining its tarsal hold.

57 expression caused extra digits, carpals, and tarsals in the hands and feet of regenerating limbs, sug

58 oid drops, but the clinical signs of chronic tarsal inflammation persisted until withdrawal of the fa

59 functionally separate from the tal-mediated tarsal intercalation during mid-third instar that we rep

60 t increased the risk of tumor recurrence was tarsal involvement (AJCC T3 stage lesion; HR, 4.12; P =

61 , ultrasonography revealed synovitis at >/=1 tarsal joint or surrounding tendon.

62 in rats by administration of PG-PS, causing tarsal joint swelling and histopathologic changes charac

63 the hind feet were mobile at the transverse tarsal joint.

64 s controlling N signalling boundaries in the tarsal joints are unknown.

65 ures had a finite ability to respond to 20E; tarsal joints lost competence to respond after 32-34 h A

66 for differentiation was structure specific; tarsal joints required higher concentrations of 20E (gre

67 by repressing the transcription of Dl in the tarsal joints.

68 Here we show that the non-canonical tarsal-less (tal) gene (also known as pri), which encode

69 The polycistronic and non-canonical gene tarsal-less encodes several short peptides 11 to 32 amin

70 Here we show that tarsal-less function triggers a cell signal.

71 development and explain the requirements for tarsal-less in this process.

72 Thus tarsal-less is necessary for the intercalation of the ta

73 tarsal-less is required for embryonic and imaginal devel

74 ila legs and may be provided directly by the Tarsal-less peptides.

75 During leg development, this Tarsal-less signal implements the patterning activity of

76 2 gene and regulates the late expression of tarsal-less.

77 al and metatarsal bones to short carpal- and tarsal-like bones.

78 o primary orbital smooth muscle targets, the tarsal muscle and orbital muscle, contained many synapto

79 collagen IV, and fibronectin were absent in tarsal muscle but were robust in pathway tissue.

80 h endoplasmic reticulum and were larger than tarsal muscle cells.

81 superior salivatory nucleus, which activates tarsal muscle parasympathetic nerves, elicited large con

82 than both surrounding connective tissue and tarsal muscle.

83 Tarsals of Eosimias show derived anatomical traits that

84 the site-specific distribution of the carpal-tarsal osteolysis phenotype.

85 owing the greatest abnormality in the carpal-tarsal osteolysis syndromes are regions of subarticular

86 Multicentric carpal-tarsal osteolysis; multicentric osteolysis, nodulosis, a

87 of the leg gap gene dachshund (dac) and the tarsal PD genes, bric-a-brac 2 (bab), apterous (ap) and

88 sis (n = 10), but 8 eyes required additional tarsal pedicle flaps (n = 6, for peripheral necrosis) or

89 The tarsal plate becomes hyperelastic with a loss of intrins

90 FES tarsal plate fibroblasts (TFs) showed an increased contr

91 of attachment was the superior border of the tarsal plate, adjacent to the insertion of Muller's musc

92 body, the iris, the sebaceous glands of the tarsal plate, and the epithelium of the cornea.

93 nto the eyelid that directly attaches to the tarsal plate.Patients presenting with symptomatic blepha

94 of many locomotion parameters, such as gait, tarsal positioning, and intersegmental and left-right co

95 instructive role in the establishment of the tarsal primordium.

96 l portion of the antennal imaginal disc, the tarsal region of each leg disc, and in bristle precursor

97 stal antennal identity, establishment of the tarsal regions of the legs, and normal bristle growth.

98 m of multicentric osteolysis with carpal and tarsal resorption, crippling arthritic changes, marked o

99 equires Distal-less, only the proximal three tarsal rings are Spineless-dependent.

100 ac expression in the antenna and in all four tarsal rings of the leg requires Distal-less, only the p

101 WHO and are in routine practice: bilamellar tarsal rotation (BLTR) and posterior lamellar tarsal rot

102 ndomized to surgery with standard bilamellar tarsal rotation (BLTR) instrumentation or the TT clamp a

103 mellar tarsal rotation (PLTR) and bilamellar tarsal rotation (BLTR).

104 on TT surgery procedures: posterior lamellar tarsal rotation (PLTR) and bilamellar tarsal rotation (B

105 arsal rotation (BLTR) and posterior lamellar tarsal rotation (PLTR).

106 1 year, and 4 years after posterior lamellar tarsal rotation surgery.

107 of joint formation from the distal tibia to tarsal segment 5, while more proximal clones cause melan

108 segments of the leg, the femur and the first tarsal segment, and even different regions of the femur,

109 to Notch, causing fusion and truncations of tarsal segments (tarsomeres) and, like its close relativ

110 and maintenance of a Dl+/Dl- boundary in the tarsal segments highlighting an ancient mechanism for th

111 ss is necessary for the intercalation of the tarsal segments two to four and for the activation of th

112 Elsewhere in the tarsal segments, signalling by DELTA and NOTCH is necess

113 other cells and those of the distal parts of tarsal segments.

114 form the joint between the fourth and fifth tarsal segments.

115 We find that most tarsal sensilla harbor a sour GRN that is specifically a

116 formed in five specimens suspected of having tarsal sinus lesions on the basis of initial imaging fin

117 Tarsal sinus ligaments were evaluated further on initial

118 were reviewed to verify the integrity of the tarsal sinus ligaments.

119 useful for further evaluation of individual tarsal sinus structures.

120 Magnetic resonance (MR) imaging of the tarsal sinus was performed in 10 cadavers.

121 Both pathway cells and superior tarsal smooth muscle cells expressed alpha-smooth muscle

122 Parasympathetic innervation of rat eyelid tarsal smooth muscle normally inhibits sympathetic neuro

123 tal regions of the leg for the expression of tarsal-specific genes including al and bric-a-brac.

124 stal antenna to leg, deletion of distal leg (tarsal) structures, and reduction in size of most bristl

125 fy sour gustatory receptor neurons (GRNs) in tarsal taste sensilla of Drosophila melanogaster.

126 te neither sweet nor bitter taste neurons in tarsal taste sensilla.

127 predigit joint articulation with the carpals/tarsals that are visible in fossils.

128 01 and P < 0.01, respectively), and inferior tarsal tissues (14.0 +/- 1.3-fold growth; P = 0.01).

129 recurrence after operative excision, such as tarsal tumor location and positive surgical margins.