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 imates and little attention paid thus far to nonprimates.
2 9 (hCD59), but does not react with CD59 from nonprimates.
3  many other cortical regions in primates and nonprimates.
4 , and little evidence exists with regards to nonprimates.
5                             Therefore, novel nonprimate AAV vectors or compartmentalized delivery may
6 a manner not dissimilar to that seen in most nonprimate and noncarnivore mammals, and lacks certain f
7 output via an interposed interneuron seen in nonprimates and the fast direct monosynaptic connections
8 ther, these findings suggest a promising new nonprimate animal model and provide a database that will
9 rmine whether these can serve as appropriate nonprimate animal models for metabolic studies.
10 ed in humans and thus may serve as excellent nonprimate animal models for metabolic studies.
11                                              Nonprimate animal models of HIV-1 infection are prevente
12 tation system (LIPS) assay to screen several nonprimate animal species.
13                                     Although nonprimates are known to show similar behavior (e.g., co
14 experiments collected from both primates and nonprimates, assessing the types of information that ani
15 auditory system of monkeys resemble those of nonprimates, but the organization at cortical levels is
16 rk, we have modeled the latter strategy in a nonprimate by replacing the X-linked mouse green pigment
17 of human, nonhuman primate (mouse lemur) and nonprimate (cat, tree shrew) lacritin coding sequences r
18              When analyzed by primate versus nonprimate categories, only primates preferred the novel
19              The virus evolves in this novel nonprimate cell adaptive landscape.
20 pted to grow efficiently in primate and some nonprimate cell lines but not in cells of murine origin.
21                                   A panel of nonprimate cell lines varied widely in susceptibility to
22 s are also infected by the virus and whether nonprimate cells are permissive for RNA replication.
23 E(538) are conserved between all primate and nonprimate CMVs.
24  TUs, but only 13 (3%) of genes, both lacked nonprimate conservation and localized to gaps in the hum
25 nt the first detailed expression profiles of nonprimate-derived adeno-associated viruses, namely, bov
26 n genes (n = 492) and typically did not have nonprimate DNA and protein homologies.
27 iously demonstrated that pseudotyping of the nonprimate equine infectious anemia virus (using the len
28 are distinctly lower than that observed with nonprimate eutherian mammals (45-70%).
29 ence for both predictions and suggest that a nonprimate has knowledge of its own cognitive state.
30        In contrast, several experiments with nonprimates have found that animals can take into accoun
31                                              Nonprimate hepacivirus (NPHV) is the closest known relat
32 determine the natural host of the only known nonprimate hepacivirus (NPHV), CHV, which is also the cl
33     The closest homolog of HCV is the equine nonprimate hepacivirus (NPHV), which shares similar feat
34                    Equine hepacivirus (EHCV; nonprimate hepacivirus) is a hepatotropic member of the
35 ort the identification in domestic dogs of a nonprimate hepacivirus.
36               Among these novel viruses, the nonprimate hepaciviruses (NPHV) that infect horses are t
37                 The recent identification of nonprimate hepaciviruses in dogs and then in horses prom
38  galagos, therefore, is more complex than in nonprimates, indicating that it has been altered with th
39                                              Nonprimates, it has been argued, lack such rule transfer
40                         Nonhuman primate and nonprimate lacritin coding sequences were extracted from
41 ems to track spatial dynamics of primate and nonprimate lentiviral genomic RNAs (HIV-1 and feline imm
42                                              Nonprimate lentiviral vectors may offer safety advantage
43 cruits CBFbeta as the noncanonical cofactor, nonprimate lentiviral Vif proteins have developed differ
44 tended these findings to the integrases of a nonprimate lentivirus and a more distantly related alpha
45          However, the mechanism by which the nonprimate lentivirus BIV Vif inhibits bovine APOBEC3 pr
46 nvolved in virus budding.IMPORTANCE FIV is a nonprimate lentivirus that infects domestic cats and cau
47 constructed gene transfer systems based on a nonprimate lentivirus, bovine immunodeficiency virus.
48        The surface envelope glycoproteins of nonprimate lentiviruses and betaretroviruses share seque
49        The surface envelope glycoproteins of nonprimate lentiviruses and betaretroviruses share seque
50 mic organization is intermediate between the nonprimate lentiviruses and their more derived primate c
51 ficiency virus, has a modest or no effect on nonprimate lentiviruses equine infectious anemia virus a
52 t distinct mechanisms evolved in primate and nonprimate lentiviruses to reconcile uracil misincorpora
53           All viruses, including primate and nonprimate lentiviruses, a Betaretrovirus, a Gammaretrov
54 amination of the Rev trans activators of two nonprimate lentiviruses, visna virus and equine infectio
55 ry system, whose structural differences from nonprimate macrosmatic species have recently gained mome
56 ined with eyeblink conditioning paradigms in nonprimate mammalian animal models including the rabbit.
57 ddition, such sites also exist frequently in nonprimate mammalian genomes, although AAV integrates si
58 ctions of this hypothesis are confirmed in a nonprimate mammalian order, Rodentia, through an analysi
59 bohydrate-specific IgE antibodies present on nonprimate mammalian proteins were incriminated recently
60                                       Of the nonprimate mammalian species with developing comparative
61 encoding Vgamma9, Vdelta2, and BTN3 in a few nonprimate mammalian species.
62 n synthetase (FS), is widely expressed among nonprimate mammalian species.
63 ductase (XOR) activity in humans relative to nonprimate mammalian species.
64 This epitope is produced in large amounts in nonprimate mammals and New World monkeys due to the intr
65 mitive "blue-yellow" axis of color vision in nonprimate mammals are largely unexplored.
66 c concern for another, it is unclear whether nonprimate mammals experience a similar motivational sta
67 lycosylated proteins, whereas mice and other nonprimate mammals express this epitope.
68                  These mice are unique among nonprimate mammals in that, similar to humans, they lack
69                                         Most nonprimate mammals possess dichromatic ("red-green color
70 vide further evidence that in primates as in nonprimate mammals the cortical input streams include a
71 e a rapid expansion from one or two genes in nonprimate mammals to at least seven members in primates
72 d from four New World primates or nine other nonprimate mammals, as well as to human gingival epithel
73                                 In birds and nonprimate mammals, both the retinotectal and retinogeni
74                In contrast to Liat1 genes of nonprimate mammals, Liat1 genes of primates are subtelom
75 teins are highly conserved among primate and nonprimate mammals, suggesting purifying selection throu
76 ride that is present in cells and tissues of nonprimate mammals.
77  biosynthesis is catalyzed by this enzyme in nonprimate mammals.
78  homologous to the entopeduncular nucleus of nonprimate mammals.
79 t synthesizes alpha-Gal epitopes in cells of nonprimate mammals.
80 ferences between human prolactin and that of nonprimate mammals.
81                          However, results in nonprimates may not be predictive of transduction in the
82 wn about the annotation and transcriptome of nonprimate MSY.
83 s higher than the neuronal density of V1s in nonprimates or many other cortical regions in primates a
84  interest in the use of nonhuman, especially nonprimate, organs.
85  to potently inhibit HIV-1, whereas selected nonprimate orthologs have no such activity.
86 The alpha1,3GT gene is active in marsupials, nonprimate placental mammals, lemurs (prosimians) and Ne
87 nes, but embryonic in prosimian primates and nonprimate placental mammals, the evolution of fetal rec
88                                        Major nonprimate-primate differences in cortico-genesis includ
89 ori has been suggested, but is not proven in nonprimate reservoirs.
90 , might correspond to the local-edge cell in nonprimate retinas, which serves finer acuity at low tem
91 nique species selectivity for primate versus nonprimate RIP1.
92 in human hippocampus resemble those found in nonprimate slow wave sleep, quantitative studies of thes
93     This makes the quail retina an excellent nonprimate small animal model for studying the metabolic
94                                              Nonprimate sources of AAVs may be useful to identify add
95         This exon is homologous to exon 2 in nonprimate species but contains a start codon that would
96 1% had sequence conservation in at least one nonprimate species compared with 67.5% for functional co
97 at would render drug treatments developed in nonprimate species entirely ineffective if applied to pr
98 tes, the capacity for selective attention in nonprimate species has never been quantified.
99 ile chronic treatment with beta3 agonists in nonprimate species leads to uncoupling protein 1 up-regu
100 ypes and scopes of attentional mechanisms in nonprimate species remain underexplored.
101 ng evidence yet of analogical reasoning in a nonprimate species, as apes alone have spontaneously exh
102 feature of a centrally presented stimulus in nonprimate species.
103 apted to the human host and unable to infect nonprimate species.
104 in primates, yet it is largely unexplored in nonprimate species.
105 can be usefully modeled in nonhuman and even nonprimate species.
106 al inputs in cells from multiple primate and nonprimate species.
107 es may be more common in humans than in some nonprimate species.
108 rallel on bovine retinas for comparison to a nonprimate species.
109  are organized similar to those described in nonprimate species; (b) the topographic organization of
110 s on several species, lacritin's presence in nonprimate tears or other tissues has not been explored.
111                                           In nonprimates, there is evidence for CP for sound and colo
112                                              Nonprimate (ungulate or feline) lentiviruses might provi
113 s and thus more pinwheels than similar-sized nonprimate V1s, which explains why primates have better
114 imeter) than many other cortical regions and nonprimate V1s; we also show that V2 is 1.7 times as den
115 pted pathogen that does not cause disease in nonprimate vertebrate hosts, while Salmonella enterica s
116 ays in primates and "sluggish/W" pathways in nonprimate visual systems.
117 al rectus muscle of the cat, a highly visual nonprimate with frontally placed eyes.

 
Page Top