ライフサイエンスコーパス: nonprimate

1 many other cortical regions in primates and nonprimates.

2 9 (hCD59), but does not react with CD59 from nonprimates.

3 , and little evidence exists with regards to nonprimates.

4 Therefore, novel nonprimate AAV vectors or compartmentalized delivery may

5 output via an interposed interneuron seen in nonprimates and the fast direct monosynaptic connections

6 ther, these findings suggest a promising new nonprimate animal model and provide a database that will

7 rmine whether these can serve as appropriate nonprimate animal models for metabolic studies.

8 ed in humans and thus may serve as excellent nonprimate animal models for metabolic studies.

9 Nonprimate animal models of HIV-1 infection are prevente

10 tation system (LIPS) assay to screen several nonprimate animal species.

11 Although nonprimates are known to show similar behavior (e.g., co

12 experiments collected from both primates and nonprimates, assessing the types of information that ani

13 auditory system of monkeys resemble those of nonprimates, but the organization at cortical levels is

14 rk, we have modeled the latter strategy in a nonprimate by replacing the X-linked mouse green pigment

15 of human, nonhuman primate (mouse lemur) and nonprimate (cat, tree shrew) lacritin coding sequences r

16 When analyzed by primate versus nonprimate categories, only primates preferred the novel

17 The virus evolves in this novel nonprimate cell adaptive landscape.

18 pted to grow efficiently in primate and some nonprimate cell lines but not in cells of murine origin.

19 A panel of nonprimate cell lines varied widely in susceptibility to

20 s are also infected by the virus and whether nonprimate cells are permissive for RNA replication.

21 E(538) are conserved between all primate and nonprimate CMVs.

22 TUs, but only 13 (3%) of genes, both lacked nonprimate conservation and localized to gaps in the hum

23 nt the first detailed expression profiles of nonprimate-derived adeno-associated viruses, namely, bov

24 n genes (n = 492) and typically did not have nonprimate DNA and protein homologies.

25 iously demonstrated that pseudotyping of the nonprimate equine infectious anemia virus (using the len

26 are distinctly lower than that observed with nonprimate eutherian mammals (45-70%).

27 ence for both predictions and suggest that a nonprimate has knowledge of its own cognitive state.

28 In contrast, several experiments with nonprimates have found that animals can take into accoun

29 Nonprimate hepacivirus (NPHV) is the closest known relat

30 determine the natural host of the only known nonprimate hepacivirus (NPHV), CHV, which is also the cl

31 The closest homolog of HCV is the equine nonprimate hepacivirus (NPHV), which shares similar feat

32 Equine hepacivirus (EHCV; nonprimate hepacivirus) is a hepatotropic member of the

33 ort the identification in domestic dogs of a nonprimate hepacivirus.

34 Among these novel viruses, the nonprimate hepaciviruses (NPHV) that infect horses are t

35 The recent identification of nonprimate hepaciviruses in dogs and then in horses prom

36 galagos, therefore, is more complex than in nonprimates, indicating that it has been altered with th

37 Nonprimates, it has been argued, lack such rule transfer

38 Nonhuman primate and nonprimate lacritin coding sequences were extracted from

39 ems to track spatial dynamics of primate and nonprimate lentiviral genomic RNAs (HIV-1 and feline imm

40 Nonprimate lentiviral vectors may offer safety advantage

41 tended these findings to the integrases of a nonprimate lentivirus and a more distantly related alpha

42 However, the mechanism by which the nonprimate lentivirus BIV Vif inhibits bovine APOBEC3 pr

43 constructed gene transfer systems based on a nonprimate lentivirus, bovine immunodeficiency virus.

44 mic organization is intermediate between the nonprimate lentiviruses and their more derived primate c

45 t distinct mechanisms evolved in primate and nonprimate lentiviruses to reconcile uracil misincorpora

46 All viruses, including primate and nonprimate lentiviruses, a Betaretrovirus, a Gammaretrov

47 amination of the Rev trans activators of two nonprimate lentiviruses, visna virus and equine infectio

48 ry system, whose structural differences from nonprimate macrosmatic species have recently gained mome

49 ined with eyeblink conditioning paradigms in nonprimate mammalian animal models including the rabbit.

50 ddition, such sites also exist frequently in nonprimate mammalian genomes, although AAV integrates si

51 ctions of this hypothesis are confirmed in a nonprimate mammalian order, Rodentia, through an analysi

52 bohydrate-specific IgE antibodies present on nonprimate mammalian proteins were incriminated recently

53 Of the nonprimate mammalian species with developing comparative

54 n synthetase (FS), is widely expressed among nonprimate mammalian species.

55 ductase (XOR) activity in humans relative to nonprimate mammalian species.

56 This epitope is produced in large amounts in nonprimate mammals and New World monkeys due to the intr

57 mitive "blue-yellow" axis of color vision in nonprimate mammals are largely unexplored.

58 c concern for another, it is unclear whether nonprimate mammals experience a similar motivational sta

59 These mice are unique among nonprimate mammals in that, similar to humans, they lack

60 Most nonprimate mammals possess dichromatic ("red-green color

61 vide further evidence that in primates as in nonprimate mammals the cortical input streams include a

62 e a rapid expansion from one or two genes in nonprimate mammals to at least seven members in primates

63 d from four New World primates or nine other nonprimate mammals, as well as to human gingival epithel

64 In contrast to Liat1 genes of nonprimate mammals, Liat1 genes of primates are subtelom

65 teins are highly conserved among primate and nonprimate mammals, suggesting purifying selection throu

66 biosynthesis is catalyzed by this enzyme in nonprimate mammals.

67 homologous to the entopeduncular nucleus of nonprimate mammals.

68 t synthesizes alpha-Gal epitopes in cells of nonprimate mammals.

69 ferences between human prolactin and that of nonprimate mammals.

70 However, results in nonprimates may not be predictive of transduction in the

71 wn about the annotation and transcriptome of nonprimate MSY.

72 s higher than the neuronal density of V1s in nonprimates or many other cortical regions in primates a

73 interest in the use of nonhuman, especially nonprimate, organs.

74 to potently inhibit HIV-1, whereas selected nonprimate orthologs have no such activity.

75 The alpha1,3GT gene is active in marsupials, nonprimate placental mammals, lemurs (prosimians) and Ne

76 nes, but embryonic in prosimian primates and nonprimate placental mammals, the evolution of fetal rec

77 Major nonprimate-primate differences in cortico-genesis includ

78 ori has been suggested, but is not proven in nonprimate reservoirs.

79 , might correspond to the local-edge cell in nonprimate retinas, which serves finer acuity at low tem

80 nique species selectivity for primate versus nonprimate RIP1.

81 in human hippocampus resemble those found in nonprimate slow wave sleep, quantitative studies of thes

82 This makes the quail retina an excellent nonprimate small animal model for studying the metabolic

83 Nonprimate sources of AAVs may be useful to identify add

84 1% had sequence conservation in at least one nonprimate species compared with 67.5% for functional co

85 tes, the capacity for selective attention in nonprimate species has never been quantified.

86 ile chronic treatment with beta3 agonists in nonprimate species leads to uncoupling protein 1 up-regu

87 ng evidence yet of analogical reasoning in a nonprimate species, as apes alone have spontaneously exh

88 feature of a centrally presented stimulus in nonprimate species.

89 can be usefully modeled in nonhuman and even nonprimate species.

90 al inputs in cells from multiple primate and nonprimate species.

91 es may be more common in humans than in some nonprimate species.

92 rallel on bovine retinas for comparison to a nonprimate species.

93 apted to the human host and unable to infect nonprimate species.

94 s on several species, lacritin's presence in nonprimate tears or other tissues has not been explored.

95 Nonprimate (ungulate or feline) lentiviruses might provi

96 s and thus more pinwheels than similar-sized nonprimate V1s, which explains why primates have better

97 imeter) than many other cortical regions and nonprimate V1s; we also show that V2 is 1.7 times as den

98 pted pathogen that does not cause disease in nonprimate vertebrate hosts, while Salmonella enterica s

99 ays in primates and "sluggish/W" pathways in nonprimate visual systems.

100 al rectus muscle of the cat, a highly visual nonprimate with frontally placed eyes.