ライフサイエンスコーパス: sea lion

1 ated on free-ranging otariids (fur seals and sea lions).

2 ity to assess the prevalence of ZcAV in live sea lions.

3 losely related to those adapted to seals and sea lions.

4 pi were obtained from control and chronic DA sea lions.

5 his mixing zone region have been optimal for sea lions.

6 since the last common ancestor of seals and sea lions.

7 ith thick myelin sheaths (elephant seal: 9%, sea lion: 7%) and thin myelin sheaths (elephant seal: 91

8 and thin myelin sheaths (elephant seal: 91%, sea lion: 93%).

9 is the first description of coxiellosis in a sea lion and suggests that exposure to sea lions may be

10 and a naturally occurring condition in wild sea lions and simultaneously advance general knowledge o

11 Populations of seals, sea lions, and sea otters have sequentially collapsed ov

12 rvational and experimental studies of seals, sea lions, and walruses reveal elements of vocal develop

13 Because sea lions are dynamic foragers that rely on flexible nav

14 California sea lions are one of the major marine mammal species alo

15 Sea lions are susceptible to a wide variety of viruses,

16 sites in 48 healthy dolphins and 18 healthy sea lions, as well as those of adjacent seawater and oth

17 Distributions of Steller sea lions at sea displayed self-similar fractal patterns

18 rmine if the spatial distribution of Steller sea lions at sea displayed similar scaling properties to

19 dent patterns in the distribution of Steller sea lions at sea or linkages with SST may have been appa

20 s indicate that the distributions of Steller sea lions at sea were more influenced by bathymetry than

21 northern anchovy (Engraulis mordax), and in sea lion body fluids.

22 rom 2000-2010 to estimate probabilities of a sea lion born in one DPS being seen within the range of

23 no prior data on structural connectivity in sea lion brains, with or without neuropathology.

24 We analyzed >22,000 sightings of 4,172 sea lions branded as pups in each DPS from 2000-2010 to

25 olphin, which evolved independently from the sea lion but displays similar feeding behavior, also has

26 d serum albumin concentration, but only in a sea lion colony exposed to anthropogenic environmental i

27 ntibody concentration during early Galapagos sea lion development were higher in a colony exposed to

28 a lions previously exposed to DA (chronic DA sea lions) display hippocampal neuropathology similar to

29 Chronic DA sea lions displayed hippocampal neuron loss in patterns

30 for comparison with samples from California sea lions during unexplained disease outbreaks.

31 n an effort to find linkages between Steller sea lions (Eumetopias jubatus) and their environment, th

32 ion trends support the separation of Steller sea lions (Eumetopias jubatus) into a western distinct p

33 ghest prevalence and abundance in California sea lion feces.

34 This ELISA provides a tool for testing live sea lions for ZcAV exposure and is valuable for subseque

35 reported in the lungs of captive California sea lions involved in a mortality event.

36 us, hippocampal neuropathology of chronic DA sea lions is similar to that of human patients with temp

37 Significantly, California sea lion isolates formed a unique group, providing evide

38 in a sea lion and suggests that exposure to sea lions may be a risk factor for contracting Q fever.

39 re deployed on 10 groups of juvenile Steller sea lions (n=52) at eight different locations within the

40 , we surveyed the fecal virome in California sea lions of different ages and health statuses.

41 e decline of the endangered New Zealand (NZ) sea lion (Phocarctos hookeri) is linked to latent levels

42 Additionally, distributions of Steller sea lion point patterns were examined with respect to me

43 ble persistence of L. interrogans within the sea lion population.

44 ZcAV is prevalent in stranded wild sea lion populations and results suggest that PCR assays

45 We tested whether sea lions previously exposed to DA (chronic DA sea lions

46 n the brainstem, thalamus, and cortex in one sea lion pup and the external anatomy of the brain in a

47 However, 35% of the variability in NZ sea lion pup production is explained by latent by-catch,

48 x, we processed brain sections from seal and sea lion pups for Nissl substance, cytochrome oxidase, a

49 ity of bacteriophages was higher in unweaned sea lion pups than in juveniles and animals in rehabilit

50 viral species were shed by pups and juvenile sea lions, respectively.

51 We find that the sea lion's impressive array of whiskers is matched by a

52 nality of the KIR and most likely led to the sea lion's loss of D0.

53 Pinnipeds (sea lions, seals, and walruses) are notable for many rea

54 ssay (ELISA) to detect antibodies to ZcAV in sea lion serum.

55 th the northern elephant seal and California sea lion spend most of their lives at sea, but each also

56 A pregnant sea lion stranded in the State of Washington was found t

57 to the inactivation of Tas1r2, we found that sea lion Tas1r1 and Tas1r3 are also pseudogenized, consi

58 ed serum and lung samples (n = 96) from wild sea lions that stranded along the California coast were

59 We showed, in a large sample of wild sea lions, that spatial memory deficits are predicted by

60 r receptor function is not restricted to the sea lion: the bottlenose dolphin, which evolved independ

61 dimension were calculated for each group of sea lions using a unit square box-counting method, where

62 nt capsid of Parkville virus, and San Miguel sea lion virus serotype 4 (SMSV4), which are representat

63 The sea lion visual cortex is located at the posterior side

64 to human patients, hippocampal sclerosis in sea lions was unilateral in 79% of cases, mossy fiber sp

65 f wild marine carnivore, three seals and one sea lion, we find that Ly49 and KIR are each represented

66 ained opportunistically postmortem from wild sea lions with and without chronic clinical signs of tox

67 eal (Mirounga angustirostris) and California sea lion (Zalophus californianus) are members of a diver

68 reas of the nervous system of the California sea lion (Zalophus californianus).

69 The endangered Galapagos sea lion (Zalophus wollebaeki) is threatened simultaneou

70 California sea lions (Zalophus californianus) are abundant human-si

71 ira interrogans serovar Pomona in California sea lions (Zalophus californianus) as a case study to il

72 Over 400 California sea lions (Zalophus californianus) died and many others

73 Hundreds of wild California sea lions (Zalophus californianus) exposed to the algal