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1 ian-associated gammacoronavirus genomes from cloacal and oropharyngeal swabs of clinically healthy fe
2 eabirds and 21.3% [12.9-31.8] in mammals, in cloacal and rectal swabs).
3 ] in seabirds, 2.1% [0.4-6.1] in mammals) in cloacal and rectal swabs.
4 lts with the lyophilized beads was tested on cloacal and tracheal swabs from experimental birds inocu
5  between males and females (iv), and whether cloacal and tracheal swabs might be used to detect herpe
6 ious virus could be detected in lung tissue, cloacal, and oropharyngeal swabs.
7 -like body form, with its deregionalized pre-cloacal axial skeleton, has been explained as either hom
8 the pronephric kidney and stabilizes primary cloacal cilia.
9  and exhibit anterior cysts and destabilized cloacal cilia.
10 d the latency of the male's grab, mount, and cloacal contact responses and also determined the effici
11 opulatory efficiency and the latency to make cloacal contact) were correlated with fertilization rate
12 mum in the fecal precursor (guano; colon and cloacal contents) of both species.
13                             We show that the cloacal defects result from alterations in the morphogen
14 lated gene that has an essential function in cloacal development.
15 ish caused pronephric-outlet obstruction and cloacal dilatation, phenocopying human congenital LUTO.
16 t the cloacal membrane, and suggest that the cloacal ectoderm may be the source of the genital initia
17                                              Cloacal endoderm also gives rise to the epithelial linin
18 ressed at the midline in the fusing urethral/cloacal endoderm and underlying lateral mesoderm of the
19  By restoring Wnt-Fgf8 signaling in Shh(-/-) cloacal endoderm genetically, we revealed that Shh relay
20                       Results of surgery for cloacal exstrophy are not as good, but are encouraging n
21 s and associated malformations in cloaca and cloacal exstrophy are not hopeless problems.
22                                   Cloaca and cloacal exstrophy in most cases are very different anato
23                                              Cloacal exstrophy is a rare, complex defect of the entir
24                                    Of the 41 cloacal exstrophy patients being followed, 7 have not un
25 54 patients with cloaca and 41 patients with cloacal exstrophy to assess anorectal function, urinary
26 Apart from congenital abnormalities, such as cloacal exstrophy, intersex disorders, and an absence of
27                                              Cloacal exstrophy, which is an even more complex spectru
28 ent advances in the treatment of bladder and cloacal exstrophy.
29      We assessed all 16 genetic males in our cloacal-exstrophy clinic at the ages of 5 to 16 years.
30  simultaneously regulating patterning of the cloacal field and supporting an outgrowth signal.
31 distal hox13 genes are essential for correct cloacal formation.
32                      Using a novel assay for cloacal function, we find that larvae with reduced mid-g
33                 Furthermore, the size of the cloacal gland, an accurate indicator of testosterone act
34 d in the resistant line, with intra-nares or cloacal infection resulting in only local shedding and f
35                                    Repair of cloacal malformations has evolved to include the total u
36 rant septation of the hindgut with anomalous cloacal membrane during weeks 6 to 9 of gestation form t
37  an epithelial-epithelial interaction at the cloacal membrane, and suggest that the cloacal ectoderm
38                      Here, we show that peri-cloacal mesenchymal (PCM) progenitors are the major sour
39      Six1 and Eya1 are absent from the intra-cloacal mesenchyme (ICM), a cell mass that divides the c
40  and Eya1 are strongly expressed in the peri-cloacal mesenchyme (PCM) surrounding the cloaca, the ter
41 ordinated morphogenesis of surface ectoderm, cloacal mesoderm and hindgut endoderm.
42                          We examined how the cloacal microbiome of wild Sceloporus virgatus (the stri
43                                          The cloacal microbiome was not affected significantly by hib
44 rated on the Illumina platform revealed that cloacal microbiomes of S. virgatus vary as a function of
45 of projections in the male quail from POM to cloacal motor neurons strongly resembles that in rats, c
46 pinal cord housing motor neurons innervating cloacal muscles involved in reproductive behavior.
47                       Here, we show that the cloacal muscles of the chick originate from somites 30-3
48 otocols, we have determined the aetiology of cloacal muscles.
49  mouse), we show that the development of the cloacal musculature is dependent on proximal leg field f
50            Surprisingly, we found that chick cloacal myoblasts first migrate into the developing leg
51 genesis with hypoplastic genitalia, a single cloacal opening, and persistence of columnar epithelium
52                The development of homologous cloacal/perineal muscles was also examined in the mouse.
53  and only then differentiate into the single cloacal/perineal muscles.
54 mum-likelihood analysis to show that the pre-cloacal primaxial domain of elongate, limb-reduced lizar
55 drogen sensitive targets, the syrinx and the cloacal protuberance.
56 on of a local anesthetic (tetracaine) in the cloacal region prior to courtship and mating.
57             It was previously noted that the cloacal region was preserved(2), but its detailed anatom
58  as a whole in tetrapods from a pre-existing cloacal regulatory machinery.
59                  NDV isolates recovered from cloacal samples of apparently healthy waterfowl and shor
60                                  Shh directs cloacal septation by promoting cell proliferation in adj
61 n of unique perineal structures derived from cloacal septation.
62 gnaling present a fully penetrant failure in cloacal septation.
63 fic function related to structures formed by cloacal septation.
64  ultimately only the presence of a sustained cloacal shedding (and not oropharyngeal shedding) was cr
65 apid transmission and significantly elevated cloacal shedding compared to the parental Anhui/13 H7N9.
66 n chickens, with superior oropharyngeal over cloacal shedding; both viruses transmitted efficiently a
67 hat a change in the relative position of the cloacal signalling centre during evolution has led to an
68 rons: the TPN, RPM, caudifemoralis (CF), and cloacal sphincter (SC).
69 eled the motor neurons innervating the large cloacal sphincter muscle (mSC) that forms part of the fo
70 CR (RT-PCR) was used to screen oropharyngeal/cloacal swab and brain samples from wild Canada geese (B
71  coronavirus was sequenced directly from the cloacal swab of a Canada goose that perished in a die-of
72 his result obtained from the analysis of 153 cloacal swab samples suggests that the presence of the v
73                                    Blood and cloacal swab samples were collected from birds every sev
74 e pan-IAV RT FRET-PCR to oral-pharyngeal and cloacal swab specimens collected from healthy poultry in
75 ppings (25 [25%] of 100), commercial broiler cloacal swabs (17 [17%] of 100), backyard poultry cloaca
76 9/1,839) or 6.3% of their oral-pharyngeal or cloacal swabs (233/3,678) were positive for IAV, and 56.
77 12, 2018, and July 1, 2019: backyard poultry cloacal swabs (n=100), commercial broiler cloacal swabs
78 ry cloacal swabs (n=100), commercial broiler cloacal swabs (n=102), cattle and buffalo rectal swabs (
79 al swabs (17 [17%] of 100), backyard poultry cloacal swabs (one [1%] of 100), chicken meat (13 [13%]
80                  We took paired tracheal and cloacal swabs and fresh feces samples.
81 e IAV hemagglutinin (HA) genome sequences in cloacal swabs from lesser scaups.
82 arison was performed with 1,550 tracheal and cloacal swabs from various avian species and environment
83 ia spp. in domestic birds in China, oral and cloacal swabs of healthy chickens, ducks, geese and pige
84                  Virus was isolated from the cloacal swabs of one contact pheasant for an unprecedent
85 vel species of astrovirus and calicivirus in cloacal swabs of ruddy turnstones (Arenaria interpres) c
86                                              Cloacal swabs were collected from wild-caught lizards ac
87                         Serum, tracheal, and cloacal swabs were randomly collected from 262 birds amo
88 blood, kidney, lungs, spleen, intestine, and cloacal swabs, but not allantoic fluid, serum, or trache
89 rd poultry cloacal swabs, commercial broiler cloacal swabs, cattle and buffalo rectal swabs, human re
90                We collected backyard poultry cloacal swabs, commercial broiler cloacal swabs, cattle
91 tracheal swabs and 81% agreement with VI for cloacal swabs, indicating a high level of accuracy of th
92  higher titers from oropharyngeal swabs than cloacal swabs.
93  33 degrees C, or 36 degrees C, and measured cloacal temperatures and plasma corticosterone concentra
94 d out of the ventral muscle mass towards the cloacal tubercle.
95 on of smoothened in the genital ectoderm and cloacal/urethral endoderm shows that the ectoderm is a d
96 ment, we conditionally removed Fgf8 from the cloacal/urethral epithelium.