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1 ast as water sprayed on the animal's back or belly.
2 IFs) motoneurons establish around the muscle belly.
3 eep in their mind coexistent troubles in the belly.
4 fect during development evidenced by a white belly.
5 surround a substantial portion of the muscle belly.
6 % decrease in total fibers at the muscle mid-belly.
7 ulted from the broad insertion of the muscle belly.
8 ophy of the adjacent superior oblique muscle belly.
9 e ventral coloration distinguishes the light-bellied agouti (AW) from the agouti (A) allele, and is c
10                                      All eom bellies and tendons exhibited substantial compartmental
11 raphy and CT scanning reveal enlarged muscle bellies and thickened tendons, with low internal reflect
12                 High-fat meats, such as pork belly and beef belly, showed significant correlations be
13 tion of coat color and white spotting of the belly and extremities, suggesting a developmental mutati
14 der of the sheath insinuates into the muscle belly and its anterior aspect blends into the sides of t
15       Seven high-fat matrices of pork brain, belly and liver; horse serum, beef, salmon and avocado w
16  a total 40 mm length to the proximal muscle bellies, and trimmed to 16 mm width.
17 nced meat types (pork loin, pork belly, beef belly, and chicken thigh) was investigated under differe
18 d from slightly concave to convex across the belly, and flattened toward the free edge.
19 et recognition, including Sec15, DLAR, Jelly belly, and PTP69D.
20 us, turned from concave to convex across the belly, and was convex along the free edge.
21 d immunoreactivity within the healthy muscle belly, any detectable immunoreactivity for Xin was indic
22 vex near both commissures and concave at the belly at maximal valve opening.
23 cave near both commissures and convex at the belly at midsystole but convex near both commissures and
24  different sites along and across the muscle belly at rest and during maximum voluntary contraction (
25 ent of the embryonic dorsal/ventral (back-to-belly) axis in pre-gastrula embryos and allowed the assi
26 n various minced meat types (pork loin, pork belly, beef belly, and chicken thigh) was investigated u
27 e of the AML along the M(CC) flips, with the belly being convex to the left atrium at midsystole and
28 generally present in the contour feathers of belly, breast, or legs in Pitohui dichrous, Pitohui kirh
29 graphy of a long-distance migrant, the light-bellied Brent goose (Branta bernicla hrota).
30 m formal training in Seokmun Hoheup, a lower belly-centered breathing practice (mean +/- SD age, 58.1
31     In this study we tested nine Florida Red-bellied Cooters (Pseudemys nelsoni) on their retention f
32 Variance (CoV) across muscles were: anterior belly digastric (5.0%), mylohyoid (8.7%), geniohyoid (5.
33 e clamps at the scleral insertion and muscle belly ends within a physiological chamber.
34                   Among the meat types, pork belly exhibited the highest contaminant levels, followed
35                                    Viscera + belly flap was overall the most stable part, and also ha
36                                    Viscera + belly flap was overall the most stable part, and also ha
37 herring fractions (head, backbone, viscera + belly flap, tail, fillet) from spring and fall, and its
38 nted beneath the superior rectus muscle (SR) belly in anesthetized adult rabbits.
39    We show in Drosophila that secreted Jelly belly (Jeb) and its receptor tyrosine kinase Anaplastic
40                   The secreted protein Jelly belly (Jeb) is required for an essential signalling even
41 We demonstrate that Alk and its ligand Jelly belly (Jeb) play a central role as an anterograde signal
42                           We show that Jelly belly (Jeb) produced by R1-R6 axons interacts with its r
43 ase signaling during NR as its ligand, Jelly belly (Jeb), is constitutively expressed from a glial ce
44            We identified a novel gene, jelly belly (jeb), which is required for visceral mesoderm dev
45 acterize the retinal photoreceptors of spine-bellied (Lapemis curtus) and horned (Acalyptophis peroni
46 ving cooperative species of primate, the red-bellied lemur (Eulemur rubriventer).
47                                          Red-bellied lemurs were found to have gut microbiota with sl
48 bladder malformation associated with a prune-belly-like syndrome, defining an isolated gene defect un
49 he rodent compensatory behaviors of lying on belly (LOB) and Pica.
50                                   The yellow-bellied marmot (Marmota flaviventris) is a social, groun
51 ta set from a hibernating mammal (the yellow-bellied marmot) inhabiting a dynamic subalpine habitat.
52 mporal trends in seasonal survival of yellow-bellied marmots (Marmota flaviventer) and explored the e
53 hen apply it to empirical datasets of yellow-bellied marmots (Marmota flaviventer) and Soay sheep (Ov
54      We used long-term data from wild yellow-bellied marmots (Marmota flaviventer) living in two diff
55 s of individual-based demography from yellow-bellied marmots (Marmota flaviventer) to fit and project
56 hesis in a well-studied population of yellow-bellied marmots (Marmota flaviventer), which spend 7-8 m
57  We apply a similar framework in wild yellow-bellied marmots (Marmota flaviventer).
58 ong-term study of individually marked yellow-bellied marmots (Marmota flaviventris) and documented th
59 imate change on hibernation behavior; yellow-bellied marmots are emerging 38 days earlier than 23 yea
60 r we present the transcriptome from the fire bellied newt Cynops orientalis.
61 luation of mass measurements of the anterior bellies of the digastric, mylohyoid, geniohyoid and tong
62 echniques were used to isolate the extrinsic bellies of the styloglossus and hyoglossus muscles from
63 ackbone conformation with Cas8g spanning the belly of the structure.
64  through a PPG sensor strapped either on the belly or chest of an infant, logging information on hear
65 e two species of African pangolin, the white-bellied pangolin (Phataginus tricuspis) and the giant pa
66                                    The white-bellied pangolin (Phataginus tricuspis) is the world's m
67   We detected population growth in the white-bellied pangolin coinciding with a dry period during the
68                                    The white-bellied pangolin is subject to intense trafficking, feed
69  distinct mitochondrial lineage of the white-bellied pangolin, which was most likely shaped by river
70 defects, and they have short tails and white belly patches of variable size.
71 nts of Niviventer confucianus (Chinese white-bellied rat)-the most abundant rodent-on 11 forested isl
72 he AML along the M(SL) is similar across the belly region at midsystole and early diastole, the CC cu
73  expression and was more abundant in the mid-belly region in both the orbital and global layers.
74  2A-MyHC fibres, which are excluded from mid-belly region in wild-type mice, dominated the orbital la
75  populated the outer global layer in the mid-belly region of the Pitx2(Deltaflox/Deltaflox) mice.
76             Estimated displacement at muscle bellies revealed a pattern never highlighted before that
77  study, we first cloned C6AST genes from pot-bellied seahorse (Hippocampus abdominalis) and analyzed
78 ubclades, we studied pactacin enzymes in pot-bellied seahorse and medaka (Oryzias latipes).
79 rd SQUID from OPM sensors mounted on a novel belly-shape patient interface design with movable sensor
80  were then calculated as the ratio of muscle belly shortening velocity to fascicle shortening velocit
81  High-fat meats, such as pork belly and beef belly, showed significant correlations between GEs and 3
82 a number of temperatures, olive oil, and the belly skin of Rana catesbeiana.
83 tested the effect of the small Steel grizzle-belly (Slgb) deletion on TGCT susceptibility to determin
84  that has an unhinged shell such as a yellow-bellied slider (Trachemys scripta) and a turtle that has
85 ch activated a distinct region of the muscle belly, so that each primary nerve branch and the muscle
86                     Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new spontaneous al
87 Heterozygous KitlSl-20J mice display a white belly spot and intercrossing results in an embryonic let
88                                              Belly spot and tail (Bst) is a semidominant mouse mutati
89                                          The Belly spot and tail (Bst) semidominant mutation, mapped
90     The autosomal semidominant mutation Bst (belly spot and tail) is often associated with small and
91 ackground, produces in heterozygotes a white belly spot with 100% penetrance and very few other anoma
92 0 KO mice that survive birth exhibit a white belly spot, all have persistent fetal vasculature in the
93 eterozygous Pax3(Cre/+) mice display a white belly spot, as do Splotch heterozygotes.
94 the cervical region, as well as a very large belly spot.
95 le, and 32.1% are nonpenetrant for the white belly spot.
96 etermines the presence and size of the white belly spot.
97 at reduced proliferation is the cause of the belly spots in Kit mutants.
98                                 Depigmented 'belly spots' in mice with mutations in the receptor tyro
99 ) mice exhibited pigmentation defects (white belly spots) and simple syndactyly with high penetrance
100 tion of diffuse clones, chimeric stripes and belly spots.
101 yperactivity, abnormal gait, deafness, white belly spotting, and hypoplasia of Mullerian duct derivat
102  intensity and shadow striping), and between belly stripe number and tsetse fly distribution, several
103 roles for residues in the tail, backbone and belly subunits of Cascade that are critical for binding
104 lization via stacking interactions with the "belly" subunits, securing the NTS in place.
105                Here, we tested whether white-bellied sunbirds (Cinnyris talatala), foraging from an a
106  (n = 13), bladder exstrophy (n = 14), prune belly syndrome (n = 12), Hinman syndrome (n = 6), urogen
107 uded posterior urethral valves (n=13), prune belly syndrome (n=4), meningomyelocele (n=2), and urogen
108 to determine the long-term sequelae of prune belly syndrome (PBS) and whether the absence of abdomina
109                                        Prune Belly Syndrome (PBS) is a rare entity, usually found in
110                                        Prune belly syndrome (PBS), also known as Eagle-Barret syndrom
111 l wall laxity are classified as Pseudo Prune Belly syndrome (PPBS).
112 g features were consistent with pseudo prune belly syndrome (PPBS).
113               Final diagnoses included prune belly syndrome (seven cases), posterior urethral valves
114 tting in mice, with a lack of pigment on the belly, tail tip, and paws.
115                 Tactile stimuli on the back, belly, tail, whisker, dorsal forepaws, and dorsal hind-p
116 ommon marmosets (Callithrix jacchus) and red-bellied tamarins (Saguinus labiatus), were highly suscep
117 us macaques), two New World NHP species (red-bellied tamarins; common marmosets) and Syrian hamsters-
118                           We used the yellow-bellied toad (Bombina variegata), an amphibian occupying
119 of the habenular nuclei of the oriental fire-bellied toad, Bombina orientalis, and compared them with
120 igations were performed in the Oriental fire-bellied toad, Bombina orientalis.
121 n the defensive skin secretion of the yellow-bellied toad, Bombina variegata.
122                           Stacking on a full belly: Triangular molecular prisms display electron shar
123 e speed was also recorded from the MG muscle belly under passive conditions.
124  you notice that one fish has died, floating belly-up.
125                                        Black-bellied Whistling-Ducks (Dendrocygna autumnalis; BBWD) a
126 gitorum profundus (FDP) consists of a muscle belly with four neuromuscular regions and a complex inse

 
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