戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 howed bifurcation of the xiphoid process and sternum.
2 tes, also have an eighth rib attached to the sternum.
3  second pairs of ribs normally attach to the sternum.
4 his closure results in severe defects of the sternum.
5 (Synapsida), only limited data exist for the sternum.
6  osteomyelitis of the xiphoid process of the sternum.
7 ive difference was found in artifacts of the sternum.
8 r electrode coil depth >3 mm anterior to the sternum.
9 e shape and relative dimensions of the mouse sternum.
10  narrowing, thickening and elongation of the sternum.
11 tal shelves, shoulder girdle, vertebrae, and sternum.
12 andible and asymmetric fusion of ribs to the sternum.
13 rtebral discs, as well as adjoining ribs and sternum.
14 from lateral plate mesoderm, which forms the sternum.
15 evelopmental patterning of the forelimbs and sternum.
16 ved from the right shoulder (control) to the sternum.
17 development of periosteal innervation of the sternum.
18 ic ganglia along rib periosteum to reach the sternum.
19 F4 are not expressed in the rib cartilage or sternum.
20 e force of the heart is directed towards the sternum.
21  failure of the rib cartilage to contact the sternum.
22 of 226 insertion attempts were made into the sternum; 54 were unsuccessful, with an overall success r
23 clude abnormal attachment of the ribs to the sternum, a reduction in the number of intercostal segmen
24                         Abnormalities of the sternum accompany the rib fusions.
25 ents <1 yr of age who were left with an open sternum after cardiac surgery with cardiopulmonary bypas
26 so displayed a dorsal-ward deflection of the sternum akin to human PE.
27 ardiograms, and photoplethysmograms from the sternum, allowing clinicians to investigate the cardiova
28                                          The sternum also showed low variability (2.96 SD), suggestin
29 lude disruption of the sternebrae within the sternum and abnormal formation of the fibrocartilaginous
30 ive intestinal peptide when they reached the sternum and acquired them after arrival.
31 ded by distance between posterior surface of sternum and anterior surface of spine) was 4.65 (normal
32             The RSS is the region behind the sternum and anterior to the ascending aorta.
33            In addition, fusions were seen in sternum and carpal bones.
34                                Fusion of the sternum and endocardial cushions is impaired in the muta
35  the T-box transcription factor gene Tbx5 in sternum and forelimb formation and show that both struct
36 nd can also explain the linked adaptation of sternum and forelimb morphology correlated with mode of
37 t chip was resected medially adjacent to the sternum and laterally at the level where the chest had a
38 s have midline fusion defects manifesting as sternum and palate abnormalities.
39               Carrier females exhibit milder sternum and palate defects and misshapen pupils.
40 ertial measurement unit, IMU) affixed to the sternum and performed a 10-m walking test.
41 on, the development of mineralization in the sternum and some skull elements was significantly disrup
42  an essential role in the development of the sternum and some skull elements.
43  within megakaryocytes and platelets in both sternum and spleen and platelets in circulation.
44 he craniofacial area, the formation of split sternum and the development of polydactyly.
45   Sound knowledge of neoplasms affecting the sternum and their imaging appearance is essential to arr
46 quivalent dose rate at 1 m (EDR-1m) from the sternum and urinary bladder were obtained.
47 f Tbx5 expression underlies the reduction in sternum and wing size in a flightless bird, the emu.
48                          The anterior nares, sternum, and (future) driveline exit site were cultured
49 .5, and 8.8 muSv/h, respectively, facing the sternum, and 5.1, 10.1, and 9.5 muSv/h, respectively, fa
50 .9 muSv/h, respectively, at the level of the sternum, and 9.3 and 4.7 muSv/h, respectively, at the le
51 altered formation of bones and joints in the sternum, and a reduction in the number of bones in the d
52 ted yellowness indicators from the forehead, sternum, and abdomen.
53 in the number of intercostal segments of the sternum, and abnormal growth of the intercostal segments
54 r viability, ability to form normal ribs and sternum, and extent of skeletal muscle differentiation.
55 , transverse wedge osteotomy of the anterior sternum, and internal support with a steel strut for 6 m
56 ements in repeating series in both limbs and sternum, and is required for normal generation of the fu
57 earm, skull or facial bones, pelvis, ribs or sternum, and lower leg fractures) compared with matched
58 e to simulated implants in the femoral head, sternum, and spine (P = 0.01, 0.01, and 0.03, respective
59  reduction of artifacts in the femoral head, sternum, and spine.
60 characteristics, along with robust scapulae, sternum, and unfused cervical vertebrae, support the int
61 axial somites, the appendicular skeleton and sternum arise from the somatic lateral plate mesoderm, a
62  fusion of the ribs at the midline and bifid sternum as well as delayed sternal ossification.
63 al guidelines: at the anatomical left of the sternum between the 2nd and 5th intercostal space.
64 tures include a large, anteriorly projecting sternum; bizarre, paddle-shaped sternal ribs; and a full
65                                          The sternum bone lies at the ventral midline of the thorax w
66      In the stylopod (humerus and femur) and sternum, bone marrow MSCs express other regionally restr
67 olaminergic properties when they reached the sternum, but these properties subsequently disappeared.
68            Modern mammals have a distinctive sternum characterized by multiple ossified segments, the
69 r the detection of thoracic fractures (ribs, sternum, clavicle, and scapula), 93% for the detection o
70 nt with this shared origin and role of Tbx5, sternum defects are a characteristic feature of Holt-Ora
71                           In particular, the sternum defects are greatly exacerbated.
72  respiratory insufficiency caused by rib and sternum defects in addition to the heart defects.
73 genin-null allele, the resulting embryos had sternum defects resembling homozygous myogenin-null embr
74 e has been removed did not have body wall or sternum defects.
75  bearing homozygous hypomorphic alleles, the sternum developed normally and extensive skeletal muscle
76 the genetic pathways regulating forelimb and sternum development, enabling specific adaptations of th
77                                 We find that sternum evolution was episodic: basal members of Pennara
78 ereby development of the cranial sutures and sternum follows a morphogen mode, whereas development of
79 ctors of SBT, whereas the sacroiliac joints, sternum, foot, anterior ribs 1st-5th, and clavicle were
80 issue level, a blood sample was taped to the sternum for ex vivo radiation with or without shielding.
81 confidence interval [CI], .04-.25), rib, and sternum; for pediatric patients (</=18 years) the patter
82 skeletal muscle and, secondarily, in rib and sternum formation during mouse development.
83 absolute levels of myogenin and that correct sternum formation, skeletal muscle differentiation, and
84 urification of type II collagen from chicken sternums, immunization of mice, clinical assessment of a
85 tients; the strut was placed anterior to the sternum in 9 patients under age 12 and over age 40 years
86  Hox genes pattern the lateral plate-derived sternum in a non-colinear manner, independent from the p
87 side the chest through a defect in the lower sternum in association with anterior diaphragmatic and v
88 , proximal and distal muscles as well as the sternum in mammals and the cleithrum of fish.
89 reviously the earliest report of a segmental sternum in non-mammalian synapsids was in the Middle Tri
90 nterior convex ribs in 10 patients; "tilted" sternum in six; prominent asymmetric costal cartilage in
91              Despite the crucial role of the sternum in tetrapod locomotion, little attention has bee
92  a breach in the normal outline of the lower sternum indicating a sternal deficiency.
93 failure and preserved ejection fraction with sternum intact (n=4).
94                                          The sternum is a stabilizing element in the axial skeleton o
95                                          The sternum is an uncommon site for neoplastic involvement a
96                Neoplastic involvement of the sternum is extremely unusual and should be considered ma
97                                          The sternum is fused with the ribs attaching on either side;
98 )) have malformations in digits, wrists, and sternum joints, regions where Tbx5 is expressed.
99 report a case of tubercular infection of the sternum located in the xiphoid process resulting in its
100                     Lesions arising from the sternum, lungs as well as the pleura can also involve th
101 and perichondrial sheath detachment from the sternum may not be necessary for optimal repair.
102 es of positive cultures were blood (n = 12), sternum/mediastinum (n = 8), and the VAD driveline exit
103 and thoracic vertebral column and defects in sternum morphogenesis.
104                             Among tetrapods, sternum morphology is correlated with the mode of locomo
105 regressions to analyse relationships between sternum morphology, body mass and flight capabilities.
106 ility to breathe, some had relatively normal sternum morphology, suggesting that one or more addition
107 ariations in the anterior chest wall: titled sternum (n = 29), prominent convexity of anterior rib or
108 eding (odds ratio = 0.68; 0.52-0.9) and open sternum (odds ratio = 0.76; 0.61-0.96) were associated w
109         Here, we describe the well-preserved sternum of a gorgonopsian, a group of sabre-toothed syna
110        In contrast to wild-type embryos, the sternum of E17.5 Runx1(Re/Re) embryos showed high levels
111 d enabled metastasis to the lung, liver, and sternum of mice inoculated with 4T07 cells in vivo.
112 sequent disassembly of the radically reduced sternum of mysticete cetaceans was element specific, ref
113 ontrast to the vertebrae and long bones, the sternum of wild-type embryos expresses high levels of Ru
114                       The detector faced the sternum or bladder and was 1 m away from and directly in
115  Hoxd-12 in other lateral plate derivatives (sternum, pelvis) likewise phenocopies several luxoid/lux
116  situations, such as assessment of the ribs, sternum, pelvis, hips, and joints, should be guided by t
117 stomach or pancreas, whereas diseases of the sternum presenting as an epigastric swelling is extremel
118                 Of the skeletal tissues, the sternum received the highest dose with a maximum ROD to
119 iable across the skeleton: the tibia and the sternum respond in opposite ways to G-CSF, and the skull
120                We demonstrate a link between sternum size and forelimb use across avians and provide
121                                              Sternum size increased again in crownward Ornithuromorph
122       Third, double mutant mice show a split sternum that is not detected in mice with any other geno
123 er deposit in the region of the clavicle and sternum; thus, unenhanced thoracic computed tomography (
124  score (chest width divided by distance from sternum to spine) was 4.8.
125 ck the origin of the distinctive "mammalian" sternum to the base of Theriodontia, significantly exten
126 illed-nursing facility ranged from 28% (ribs/sternum) to 47% (pelvis/hip).
127 extending to the midbrain, tongue, incisors, sternum, vertebrae and limbs.
128 logical data to demonstrate that the therian sternum was assembled from pre-existing elements.
129 , bone marrow damage as well as apoptosis in sternum was observed in mice pre-treated with CDX-301.
130                                          The sternum was then reapproximated, and data were collected
131 r, alterations in mutant vertebrae, ribs and sternum were also observed, which appear to stem from a
132 de and greater distance between the lead and sternum were associated with a higher impedance.
133 well as mechanical pain sensitivity over the sternum were determined and the PD-Q scores were calcula
134                      The breast, axilla, and sternum were illuminated with NIR light and the fluoresc
135 e of a skeletal structure can be seen in the sternum, which varies considerably across species.
136                                  An enlarged sternum with a prominent keel is a central feature of th
137 cence of all layers of the wound down to the sternum with no signs of healing after receiving broad s
138 lagiostriata taxa, such as the presence of a sternum with parallel striae, and the presence of a high

 
Page Top