ライフサイエンスコーパス: nemestrina

1 roots from mice and pigtail monkeys (Macaca nemestrina).

2 C interactions in pigtailed macaques (Macaca nemestrina).

3 PET of the pregnant nonhuman primate (Macaca nemestrina).

4 s inoculation of pig-tailed macaques (Macaca nemestrina).

5 T lymphocytes of pig-tailed macaques (Macaca nemestrina).

6 44 C. trachomatis-infected macaques (Macaca nemestrina).

7 travenously into pig-tailed macaques (Macaca nemestrina).

8 gp substrate, in the nonhuman primate Macaca nemestrina.

9 n immunodeficiency virus SHIV89.6P in Macaca nemestrina.

10 tive against SHIV89.6P viral challenge in M. nemestrina.

11 lateral tip of the central sulcus in Macaca nemestrina.

12 e cells of rats, mice, and the monkey Macaca nemestrina.

13 uated DeltaGY in pig-tailed macaques (Macaca nemestrina), a species in which SIVmac239 infection typi

14 and huIgG binding characteristics of the M. nemestrina activating FcgammaRIIa (mnFcgammaRIIa) and in

15 ike A. trivirgatus, genomic sequencing of M. nemestrina and M. fascicularis identifies a CypA retrotr

16 The discovery of TRIMCyp in both M. nemestrina and M. fascicularis indicates that TRIMCyp ex

17 Notably, exon 7 is absent from both M. nemestrina and M. fascicularis TRIMCyp.

18 te, and dorsal prefrontal cortices of Macaca nemestrina and Macaca fascicularis to analyze the organi

19 RT-PCR of total RNA from M. nemestrina and Macaca fascicularis yielded three TRIMCyp

20 om RF tissues of two macaque species, Macaca nemestrina and Macaca mulatta.

21 cial learning in pig-tailed macaques (Macaca nemestrina) and adult humans (Homo sapiens).

22 es obtained from pig-tailed macaques (Macaca nemestrina) and rhesus macaques (Macaca mulatta).

23 Pig-tailed macaques (Macaca nemestrina) and rhesus monkeys (Macaca mulatta), two non

24 V2 of six amblyopic macaque monkeys (Macaca nemestrina) and two visually normal controls.

25 s-infected macaques (16 Macaca mulatta, 1 M. nemestrina, and 1 M. cyclopis) with Enterocytozoon infec

26 acaques, Macaca fascicularis, M. mulatta, M. nemestrina, and M. leonina.

27 Because Macaca nemestrina animals are susceptible to some human immunod

28 ically catheterized pregnant monkeys (Macaca nemestrina) at 118-125 days gestation (term=172 days) re

29 l margin and pars plana from monkeys (Macaca nemestrina) between 1 and 15 years of age were stained w

30 trivulgaris and the Old World monkey Macaca nemestrina by using immunocytochemical labeling for anti

31 s to 28 days) in pig-tailed macaques (Macaca nemestrina), challenged intravenously with a virulent st

32 which over 90% of pigtailed macaques (Macaca nemestrina) coinoculated with SIV/17E-Fr and SIV/DeltaB6

33 egion in macaque monkeys (Macaca mulatta, M. nemestrina) could be used to identify a homologous regio

34 Macaca nemestrina do not express TRIM5alpha; therefore, we aske

35 ces cloned from an SIVMneCL8-infected Macaca nemestrina during clinical latency and just after the on

36 lysis of two male pigtailed macaques (Macaca nemestrina) experimentally infected with XMRV.

37 y virus (SHIV) SF162P3 in 10 pregnant Macaca nemestrina females and their offspring.

38 We studied macaque monkeys (Macaca nemestrina) for which we have detailed psychophysical da

39 We found that pigtail macaque (Macaca nemestrina) hepatic cells derived from induced pluripote

40 -7, which we have provisionally named Macaca nemestrina herpesvirus 7 (MneHV7).

41 human embryonic stem cells (hESC) and Macaca nemestrina-induced PSC (iPSC) line-7 with cytokines in t

42 us salpingeal autotransplant model of Macaca nemestrina infected with Chlamydia trachomatis serovar E

43 ed LN tissue of a pig-tailed macaque (Macaca nemestrina) infected with SIVMne.

44 evaluated in a group of six macaques (Macaca nemestrina) infected with the molecularly cloned, modera

45 nd function of 27 pigtailed macaques (Macaca nemestrina), infected intravenously with a virulent HIV-

46 nt transduction of pigtailed macaque (Macaca nemestrina) long-term repopulating cells using VSV-G-pse

47 ation in vitro in pig-tailed macaque (Macaca nemestrina) lymphocytes.

48 iate cortical area V2 of the macaque (Macaca nemestrina, Macaca fascicularis) for the orientation of

49 l tract-tracing in nonhuman primates (Macaca nemestrina, Macaca fascicularis, Macaca mulatta) to exam

50 We used primate (Macaca nemestrina/Macaca fascicularis) tracing studies and 3D r

51 A total of 11 Macaca nemestrina macaques were inoculated with NC mutant SIV e

52 ency virus SHIV-89.6P infection in 11 Macaca nemestrina macaques.

53 (Macaca fasicularis), and pig-tailed (Macaca nemestrina) macaques.

54 and V2 of six female macaque monkeys (Macaca nemestrina) made amblyopic by artificial strabismus or a

55 used by monkeys (pigtailed macaques: Macaca nemestrina) means submission (immediate behavior) or sub

56 e model, such as the pigtail macaque (Macaca nemestrina; Mn), is crucial.

57 in the female upper genital tract, a Macaca nemestrina model was used.

58 us (SIV)-infected pig-tailed macaque (Macaca nemestrina) model, but this is poorly characterized.

59 Here we show that Macaca nemestrina monkeys can directly control stimulation of m

60 n V1 of two experimentally strabismic Macaca nemestrina monkeys.

61 from an animal society model system (Macaca nemestrina, n=48).

62 Neither M. nemestrina nor M. fascicularis TRIMCyp could restrict HI

63 Sixteen Macaca nemestrina (pigtailed macaques) from 18 to 29 years of a

64 Two macaques (Macaca nemestrina) received infusions of T cells transduced to

65 MCyp alleles described for M. mulatta and M. nemestrina, restricts human immunodeficiency virus type

66 l fibromatosis-associated herpesvirus-Macaca nemestrina (RFHVMn) and -Macaca mulatta (RFHVMm).

67 l fibromatosis-associated herpesvirus Macaca nemestrina (RFHVMn), the pig-tailed macaque homolog of K

68 HV-like herpesvirus, provisionally named "M. nemestrina rhadinovirus type 2 (MneRV-2)," with close si

69 usly reported increased susceptibility of M. nemestrina to HIV-1 infection in vivo.

70 cript at the 5' terminus of exon 7 in all M. nemestrina TRIM5 cDNA clones examined.

71 ere are 18 amino acid differences between M. nemestrina TRIM5eta and Macaca mulatta TRIM5alpha, some

72 nesthetized amblyopic monkeys (female Macaca nemestrina), using 96-channel "Utah" arrays to record fr

73 captive group of pigtailed macaques (Macaca nemestrina), we show that a policing function, performed

74 autografts in subcutaneous pockets in Macaca nemestrina were characterized.

75 ion, the fallopian tubes of 40 female Macaca nemestrina were inoculated with Chlamydia trachomatis an

76 Macaca nemestrina were more likely to develop severe neurologic

77 Pregnant Macaca nemestrina were treated with ethanol (1.8 g/kg b.wt.) 1

78 Pigtailed macaques (Macaca nemestrina) were coinoculated with an immunosuppressive

79 aca mulatta) and pig-tailed macaques (Macaca nemestrina) were inoculated intravenously with rhadinovi

80 s (SIV)-infected pig-tailed macaques (Macaca nemestrina) were treated with four antiretroviral drugs

81 nteraction in the pig-tailed macaque (Macaca nemestrina), which is used in preclinical evaluation of

82 Barr (EBV)-like virus isolated from a Macaca nemestrina with CD8(+) T-cell mycosis fungoides-cutaneou

83 I/II) seronegative pigtailed macaque (Macaca nemestrina) with a cutaneous T-cell lymphoma.

84 tudy by infecting pigtailed macaques (Macaca nemestrina) with a genetically reconstructed strain of h

85 ically catheterized pregnant monkeys (Macaca nemestrina) with either group B streptococcus (GBS) at 1

86 infection of pigtailed (PT) macaques (Macaca nemestrina) with one isolate of SIVagm results in an imm

87 , we infected six pigtailed macaques (Macaca nemestrina) with reconstructed influenza A/Texas/36/91 v

88 of SIV-infected pig-tailed macaques (Macaca nemestrina) with the combination of 9-R-(2-phosphonometh