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1 nce of molecular motors - a process we term 'skating'.
2  in ratfish, compared to catshark and little skate.
3 rovement was even more pronounced for thorny skate.
4 the homologue in a primitive vertebrate, the skate.
5 r (CD44) at the articular surfaces in little skates.
6 elios, and Eos in Raja eglanteria (clearnose skate), a cartilaginous fish that is representative of a
7                                        Three skate AE isoforms (skAEs) are expressed, and at least sk
8 e ability of the basic domain of dynactin to skate along microtubules is used by dynein to maintain l
9            Prominent expression of Ikaros in skate also is found in the lymphoid Leydig organ and epi
10                                   The Thorny Skate (Amblyraja radiata) is a vulnerable species displa
11  (Anopheles funestus; 200 Mb) and the Thorny Skate (Amblyraja radiata; 2650 Mb).
12 rall most closely resembles mu chains of the skate and human and a new putative antigen binding molec
13                           How have North Sea skate and shark assemblages changed since the early 20th
14 alysis of the cranial neural crest in little skate and zebrafish embryos demonstrated that the transc
15 ygii (bony fish) and Elasmobranchii (sharks, skates and rays).
16                             Pectoral fins of skates and rays, such as the little skate (Batoid, Leuco
17  a dorsoventrally flattened body, similar to skates and rays.
18 as been shown to mediate electroreception in skates and sharks [6].
19 me water repellence, which facilitates rapid skating and plastron respiration under water.
20 hal versus 1.1 to 20 for ringed seal, arctic skate, and beluga whale, respectively).
21               Chondrichthyes - sharks, rays, skates, and chimeras, are among the most threatened and
22 ichthyans (elasmobranchs, such as sharks and skates, and holocephalans, such as chimaeras) to underst
23                  Cartilaginous fish (sharks, skates, and rays) are in the oldest taxon of extant jawe
24 r organization in elasmobranch fish (sharks, skates, and rays) differs from that in other vertebrates
25                Elasmobranchii (i.e., sharks, skates, and rays) forms one of the most diverse groups o
26 hali (chimaeras) and Elasmobranchii (sharks, skates, and rays).
27         Elasmobranch fishes, such as sharks, skates, and rays, use a network of electroreceptors dist
28 h them from their distant relatives, sharks, skates, and rays.
29 lved at all swimming speeds in the clearnose skate; and (iii) critical swimming protocols might misre
30                                              Skates are cartilaginous fish whose body plan features e
31                                   Sharks and skates are representatives of the earliest vertebrates w
32              Elasmobranchs (sharks, rays and skates) are among the most threatened marine vertebrates
33             Elasmobranchs (sharks, rays, and skates) are caught throughout fisheries globally, leadin
34 ewer recreational activities such as in-line skating, are rapidly gaining the recognition they deserv
35 t regional transitions in the differentiated skate axial skeleton.
36  fins of skates and rays, such as the little skate (Batoid, Leucoraja erinacea), show a strikingly un
37 nic anions and steroids, including the major skate bile salt, scymnol sulfate.
38                          In addition, in the skate but not the rat retina, retinal pigment epithelial
39 ontributes to gill arch skeletal polarity in skate by restricting Shh signal transduction and chondro
40 gous sequences from tetrapods, zebrafish and skate can drive reporter gene expression in mouse limbs
41 nel and rectifying Kv channel predicted from skate (cartilaginous fish) ampullary organ electrophysio
42  long-term declines, and the largest (common skate complex) became locally extirpated (as did angelsh
43  that persistence of chondrogenesis in adult skates correlates with ability to spontaneously repair c
44  family revealed that perch Cx35 and Cx34.7, skate Cx35, and mouse Cx36 constitute a novel gamma subg
45 critically endangered species such as common skate (Dipturus batis) and angelshark (Squatina squatina
46 016-17 for the Critically Endangered flapper skate (Dipturus intermedius) in Scotland.
47                                 We find that skate embryos exhibit tetrapod-like anteroposterior nest
48                   Muscle paralysis in little skate embryos leads to joint fusion, suggesting that mus
49      Analysis of joint development in little skate embryos shows the expression of growth differentia
50 keleton has features of the embryonic little skate endoskeleton.
51             Upon hypotonic volume expansion, skate erythrocytes lose solutes via a pathway that requi
52                                              Skate erythrocytes possess numerous tyrosine kinases inc
53                Hypotonic volume expansion of skate erythrocytes rapidly stimulates the tyrosine phosp
54 CT data provided us with the outlines of the skate eye and the location of the retina and this enable
55 o obtain geometrical dimensions of the whole skate eye.
56  in the ectoderm immediately adjacent to the skate GAER, and that these Wnt signals are transduced la
57 OSTalpha-OSTbeta pairs from human, mouse, or skate) generated robust estrone 3-sulfate transport acti
58 ion of Shh signal transduction in developing skate gill arches, and in the formation of ectopic anter
59                                              Skate hepatocyte cDNA was amplified with degenerate olig
60  protein in the KI-IOV was identified as the skate homolog of the mammalian red cell anion exchanger
61 an unusual Sec tail, which is orthologous to skate IgX(short) cDNA.
62 ncrease in exploratory/foraging behaviour in skates in response to EMF and a more subtle exploratory
63 22.5 million people participating in in-line skating in the United States in 1995, about 100,000 were
64 rentiation; it is found, in both the rat and skate, in the ventricular space that ultimately becomes
65 w pads, knee pads, and helmets in preventing skating injuries.
66 clasper development from pelvic fins of male skates is controlled by hormonal regulation of the Sonic
67     Further analyses showed that microtubule skating is a form of one-dimensional diffusion along the
68 s of the shark Scyliorhinus canicula and the skate Leucoraja erinacea and the absence of all HoxC gen
69 enotypic innovation by developing the little skate Leucoraja erinacea as a genomically enabled model.
70 nts of the jaw, hyoid and gill arches of the skate Leucoraja erinacea derive from molecularly equival
71 photoreceptor densities in the retina of the skate Leucoraja erinacea.
72 keleton of elasmobranchs, such as the little skate (Leucoraja erinacea) and bamboo shark (Chiloscylli
73  expressed by electrosensory cells in little skate (Leucoraja erinacea) and functionally couple to me
74 at embryonic development of cartilage in the skate (Leucoraja erinacea) mirrors that of mammals, with
75            We previously demonstrated in the skate (Leucoraja erinacea) that branchial rays derive fr
76                  Here, we demonstrate in the skate (Leucoraja erinacea) that the pseudobranch does, i
77 he gills of a cartilaginous fish, the little skate (Leucoraja erinacea), are in fact endodermally der
78 s and vertebrae in a cartilaginous fish, the skate (Leucoraja erinacea).
79 skeleton of a cartilaginous fish, the little skate (Leucoraja erinacea).
80 he pharyngeal and paired fin skeleton in the skate (Leucoraja erinacea).
81  embryos of a cartilaginous fish, the little skate (Leucoraja erinacea).
82 fate mapping in a cartilaginous fish (little skate, Leucoraja erinacea) shows that the spiracular org
83 rafish) and a cartilaginous fish (the little skate, Leucoraja erinacea).
84  DiI tracing for up to 70 days in the little skate, Leucoraja erinacea, we show that lateral line pla
85 ction product was found and used to screen a skate liver cDNA library.
86                                    Thus, the skate liver P2Y receptor functions as a primitive P2Y AT
87                        We also show that the skate mandibular arch pseudobranch is supported by a spi
88 y analysis of nucleotide alignments show the skate opsin to be homologous to other rod opsins.
89 the similarity of the cytoplasmic domains of skate opsin to those of blue-sensitive visual pigments.
90 n action resembling that of flatfish such as skates or rays.
91                                              Skate orthologs of mammalian GATA-3, GATA-1, EBF-1, Pax-
92                          Srds represents the skate orthologue of mammalian peripherin/rds genes.
93                            Human, mouse, and skate OSTalpha proteins are predicted to contain seven t
94  human P2Y(2), rat P2Y(6), human P2Y(11), or skate P2Y receptors in oocytes resulted in modulation of
95 ply ancestral patterns of gene expression in skate pectoral fins, shedding light on the molecular mec
96    The 5' and 3' untranslated regions of the skate peripherin/rds (srds) cDNA were isolated by the ra
97    To determine the cellular function of the skating phenomenon, dynein and the dynactin microtubule-
98       Cartilaginous fishes (e.g., sharks and skates) possess a postcranial dermal skeleton consisting
99 to functionally complement the corresponding skate proteins by measuring transport of [3H]estrone 3-s
100                        The all-rod retina of skate provides a comparatively simple system in which to
101   The tissue-specific expression patterns of skate PU.1 and Spi-C suggest that these genes share regu
102 s are highly conserved between mammalian and skate PU.1, in marked contrast to lamprey Spi, in which
103 sed a negatively buoyant fish, the clearnose skate Raja eglanteria, and took two approaches: a classi
104 heteroclitus), two elasmobranch species (the skate Raja erinacea and the dogfish Mustelus canis), and
105 ce suggests that hepatocytes from the little skate Raja erinacea express a primitive P2Y ATP receptor
106 rily primitive marine vertebrate, the little skate Raja erinacea, was screened for taurocholate trans
107 t diverging jawed vertebrates, the clearnose skate (Raja eglanteria).
108                   Volume expansion of little skate (Raja erinacea) erythrocytes increases the affinit
109                                              Skates (Raja erinacea and R. ocellata) are among the few
110 a proteins recently identified in the little skate, Raja erinacea, even though the latter exhibit onl
111                                In the little skate, Raja erinacea, the electrosensory primary afferen
112                     Chondrichthyans (sharks, skates, rays and holocephalans) possess paired appendage
113 n the contribution of elasmobranchs (sharks, skates, rays) and actinopterygians (ray-finned fishes) t
114 ll skeleton of cartilaginous fishes (sharks, skates, rays, and holocephalans) exhibits a striking ant
115 ep in the volume-activated taurine efflux in skate red cells.
116                                   Sharks and skates represent the earliest vertebrates with an adapti
117 ast two of the four Ikaros family members in skate resemble the patterns observed in mammals, i.e., i
118 d 9% for Chardonnay, mosquito and the thorny skate, respectively, relative to unreduced primary assem
119       Both immunohistochemistry in the adult skate retina and in situ hybridizations in the adult rat
120 ve cloned and analyzed the opsin cDNA from a skate retina library.
121  molecular basis of visual adaptation in the skate retina, we have cloned and analyzed the opsin cDNA
122 uxes from horizontal cells isolated from the skate retina.
123                                            A skate retinal cDNA library was screened using a mouse pe
124 bridization to clone a novel connexin from a skate retinal cDNA library.
125 ue of peripherin/rds was identified from the skate retinal cDNA library.
126  indicate alterations in the interactions of skate rhodopsin with other proteins in the phototransduc
127                                     However, skate rods are unusual in that they are capable of adapt
128 in the posterior half of the pectoral fin of skate, shark, and zebrafish but in the anterior side of
129 omosome-scale genome sequence for the little skate shows that it preserves many ancestral jawed verte
130 y and three-dimensional conformation-we find skate-specific genomic rearrangements that alter the thr
131 enerate primers and R. eglanteria (clearnose skate) spleen cDNA as template.
132                                              Skates therefore offer a unique model for adult chondrog
133         The receptor was expressed widely in skate tissue and was expressed to a similar extent in ot
134 on and fate-mapping approaches in the little skate to demonstrate that Shh secretion from a signallin
135 can lobster and the electro-sensitive Little skate to electromagnetic field (EMF) emissions of a subs
136                                  However, in skate, transcriptional features of developing cartilage
137     Using cell lineage tracing, we show that skate trunk vertebrae arise through tetrapod-like resegm
138 egg cases indicate that Ambylraja hyperborea skates use the site as an egg case nursery ground.
139 mobranch fishes, including sharks, rays, and skates, use specialized electrosensory organs called amp
140 ization in the ratfish, catshark, and little skate varied both quantitively in tissue mineral density
141  had and whether or not they performed trick skating, was 9.5 (95 percent confidence interval, 2.6 to
142 rovided by batoid fish such as stingrays and skates, we created a biohybrid system that enables an ar
143 earned a motor skill, such as cycling or ice-skating, we can rapidly generalize to novel tasks, such
144 ically isolated external horizontal cells of skate were examined using whole-cell voltage-clamp techn
145 mobranchs (small-spotted catshark and little skate) were characterized using synchrotron radiation an
146 ous fish species (9 sharks, 1 sawfish, and 2 skates), which represents a sister clade to all bony fis

 
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