ライフサイエンスコーパス: feral

1 ragers in coastal California from 1999, when feral A. mellifera populations were low due to Varroa de

2 Feral adult female cynomolgus macaques were ovariectomiz

3 Our analyses indicate that adaptations to feral and domestic environments involve different genomi

4 ses a contagious and often lethal disease of feral and domestic swine.

5 ly reported seroprevalence in SIVsm-infected feral and household pet sooty mangabeys.

6 infections in rural Sierra Leone, where both feral and pet sooty mangabeys harbor divergent members o

7 Sequencing and heteroduplex analysis of one feral animal-derived SIV showed a mosaic genome containi

8 Feral animals represent an important problem in many eco

9 rom exposure to Brucella-infected livestock, feral animals, or wildlife or frequently via consumption

10 ting for two-thirds of the MHC haplotypes in feral animals.

11 Captive monkeys and feral apes have been reported to only rarely "spontaneou

12 ent blood cultures from a woman and from two feral barn cats.

13 t litter, keeping cats indoors, reducing the feral cat population, and protecting the play areas of c

14 tion by introduced species, particularly the feral cat, Felis catus, and European red fox, Vulpes vul

15 example of dwarfing of a large mammal - the feral cattle of Amsterdam Island, southern Indian Ocean,

16 The origins and uniqueness of feral cattle on Chirikof Island, Alaska, are uncertain.

17 We have previously shown that Kauai Island's feral chickens are a highly variable and admixed populat

18 nments involve different genomic regions and feral chickens show some evidence of adaptation at genes

19 intestinal tract of free-range, broiler and feral chickens.

20 ed to reconstruct in vitro the microbiota of feral chickens.

21 ecological changes in weedy environments if feral crop plants or hybrids formed with compatible weed

22 of bovine origin, but isolates from badgers, feral deer, sheep, humans, and a pig were included.

23 3.7%; P=.0005), suggesting that they are not feral descendants of hospital isolates.

24 an infectious cell line circulating in many feral dog populations.

25 Homologous DRB exon 2 sequences from 36 feral domestic cats throughout the world plus from three

26 ed from 35 genera of animals that were wild, feral, domesticated, or otherwise held captive in the Un

27 Feral fish outnumber wild populations, leading to a poss

28 enic activity measured in water extracts and feral fish that have been shown to be in population decl

29 Here we show that in female feral fowl most copulations are coerced, and that female

30 investigated male reproductive senescence in feral fowl, Gallus gallus domesticus, where socially dom

31 ction and spatial memory affect space use of feral hogs (Sus scrofa).

32 Therefore, the resulting feral honeybee population of south Texas was best viewed

33 We followed feral horses (Equus caballus) in three populations for a

34 s, fruit flies, pipefish, wild mallards, and feral house mice.

35 SA SSTI at SUH were more likely to represent feral isolates of nosocomial origin.

36 Here we map selective sweeps in feral Kauai chickens using whole-genome sequencing.

37 Feral livestock may harbor genetic variation of commerci

38 Analysis of gag region sequences showed that feral mangabeys in one small troop harbored four distinc

39 e present in free-living barn populations of feral mice and pet store mice with diverse microbial exp

40 MMMol, a Japanese feral mouse cell line, is an exception in that these cel

41 color variants of their principal prey, the feral pigeon Columba livia, presumably because targeting

42 reeds have made substantial contributions to feral pigeon populations.

43 Several plumage types are found in feral pigeons (Columba livia), but one type imparts a cl

44 ect of plumage coloration on the survival of feral pigeons.

45 NA was amplified from one farmed pig and two feral pigs and characterized by nucleotide sequencing to

46 mporal changes in the genetic structure of a feral population from the southern United States undergo

47 estes size) is associated with T levels in a feral population of Soay sheep, resident on St. Kilda, S

48 Eighteen feral populations of B. napus also showed a strong tende

49 istory strategies (often reported in wild or feral populations) relating to parental investment were

50 rge groups of monkeys randomly selected from feral populations, suggesting that the capacity for depr

51 l genome sequences representing domestic and feral populations.

52 utions from a racing breed to North American feral populations.

53 c, hybrid, and transgenic plants in wild and feral populations.

54 New data from feral rats point to the regulatory influences on mesocor

55 rs that limit extensive gene transfer in the feral setting.

56 g an env gene that was homologous with other feral SIVsm env genes in the troop but having a gag gene

57 Polymorphisms among inbred mouse strains and feral species suggest that mutations responsible for the

58 Since feral strains of S. cerevisiae are dimorphic and have a

59 8, 0.6%), farmed swine (267/648, 41.2%), and feral swine (9/306, 2.9%).

60 Feral swine are globally known as one of the most destru

61 When pre-emergence culling of feral swine caused population declines, it was effective

62 history of Marfan syndrome and recreational feral swine hunting.

63 Feral swine rooting commonly exceeds 20 cm in depth, esp

64 early response to the FMDV-like pathogen in feral swine was unwarranted while response to the CSFV-l

65 ife-histories in hypothetical populations of feral swine with different contact structures (homogenou

66 phylogenetic relationship between VACV-IOC, feral VACV established in nature, and the ancestor-like

67 hypothesis that CTGV-like viruses represent feral VACV that evolved in parallel with VACV-IOC after

68 (3) rice (Oryza sativa), often infested with feral weedy rice, which interbreeds with the crop; and (