ライフサイエンスコーパス: leopard

1 cies (lion, tiger, leopard, jaguar, and snow leopard).

2 s were more complex in the tiger than in the leopards.

3 nant of the lifetime reproductive success in leopards.

4 Female leopards also cared for sons longer than daughters, in l

5 s (additionally recorded in South Africa) in leopard and aggressive contexts.

6 ridization between the ancestors of the snow leopard and lion lineages.

7 e mutations in SHP2 cause clinically similar LEOPARD and Noonan syndromes, two of several autosomal-d

8 rpreting communication behaviours of clouded leopards and other solitary felids.

9 nt antelope (impala) and its main predators (leopards and wild dogs) with a series of manipulative fi

10 the related developmental disorders Noonan, LEOPARD, and cardiofaciocutaneous syndromes.

11 s in Indonesian Borneo are novel for clouded leopards, and contrary to previous descriptions of their

12 viour primarily appears to be a strategy for leopards, and possibly other short-term cachers, to redu

13 jeopardising their own survivorship, female leopards apparently "hedge their bets" with current offs

14 en the domestic cat (F. catus) and the Asian leopard cat (Prionailurus bengalensis).

15 s, (4) puma group, (5) Lynx genus, (6) Asian leopard cat group, (7) caracal group, and (8) bay cat gr

16 igree between the domestic cat and the Asian leopard cat, this map was generated entirely with domest

17 as a species-specific strain of FIV, and the leopard cat, which has a domestic cat FIV strain in one

18 include the large African carnivores (lion, leopard, cheetah, and spotted hyena), where FIV is widel

19 distinctions increase the urgency of clouded leopard conservation efforts, and if affirmed by morphol

20 y presence drives leopard distribution, that leopard density exhibits a negative response to tiger oc

21 We found that clouded leopards displayed 10 distinct communication behaviours,

22 We found that prey presence drives leopard distribution, that leopard density exhibits a ne

23 Alarm calls given in response to leopards, eagles, and snakes could be well distinguished

24 e/absence data of seven species (golden cat, leopard, forest elephant, forest buffalo, western gorill

25 ecture of the dorsal nucleus of the Northern leopard frog (Rana pipiens pipiens), which is a homolog

26 f the forebrain and midbrain in the northern leopard frog (Rana pipiens) and common American toad (Bu

27 11/N20/R103-variant, oocytes of the Northern Leopard frog (Rana pipiens) contain another homologue of

28 y animal model for M. marinum disease in the leopard frog (Rana pipiens), a natural host species.

29 cells within the reticular formation of the leopard frog have an organization similar to that found

30 The leopard frog optic tectum is the principal target of the

31 rasitic flatworms) in the declining northern leopard frog Rana pipiens.

32 (spotted frog), Rana berlandieri (Rio Grande leopard frog) and Rana pipiens (Northern leopard frog).

33 nde leopard frog) and Rana pipiens (Northern leopard frog).

34 ferent synapse of saccular hair cells of the leopard frog, Rana pipiens.

35 l nerve were identified and described in the leopard frog, Rana pipiens.

36 are present in the hypoglossal nerve of the leopard frog, Rana pipiens.

37 velopment of its serotonergic neurons in the leopard frog.

38 frogs, American toads (Anaxyrus americanus), leopard frogs (Lithobates pipiens) and spring peepers (P

39 s crucifer), Pacific treefrogs (P. regilla), leopard frogs (Lithobates pipiens), and Cascades frogs (

40 analysis of EphA and ephrin-A expression in leopard frogs (Rana pipiens and utricularia), species ca

41 l granulomatous infection in immunocompetent leopard frogs (Rana pipiens).

42 is of novel antimicrobial peptide genes from leopard frogs, Rana.

43 nd during chronic granulomatous infection of leopard frogs, suggesting that Erp function is similarly

44 superficial tectal locations in a series of leopard frogs.

45 sing data from 2032 prey items killed by 104 leopards from 2013 to 2015, we built generalized linear

46 As for many lizards, the leopard gecko (Eublepharis macularius) can self-detach i

47 are likely to control such behaviors in the leopard gecko and also are candidate neural substrates f

48 ss this question, we identified areas of the leopard gecko brain that express androgen receptor (AR)

49 The leopard gecko is a lizard lacking sex chromosomes, depen

50 ic development determines gonadal sex in the leopard gecko, Eublepharis macularius.

51 Host species included Gila monster, leopard gecko, fat-tail gecko, blue-tongued skink, Tokay

52 The leopard gecko, like many oviparous reptiles, lacks sex c

53 Leopard geckos (Eublepharis macularius) possess a large

54 In male leopard geckos (Eublepharis macularius), the incubation

55 otype in a 13-generation pedigree of captive leopard geckos, Eublepharis macularius, a TSD reptile.

56 We generated a new high-quality leopard genome assembly, as well as two wild Amur leopar

57 Golden cat and leopard had the lowest occurrence rates in the region, w

58 airoviruses, and are hereafter designated as Leopards Hill virus (LPHV).

59 Leopards hoisted 51% of kills.

60 dae (domestic cat, tiger, lion, cheetah, and leopard), Hominidae, and Bovidae genomes.

61 the factors motivating such behaviour among leopards in the Sabi Sand Game Reserve, South Africa, as

62 sociated with the length of maternal care in leopards in the Sabi Sand Game Reserve, South Africa.

63 he scent marking behaviours of Sunda clouded leopards in the wild.

64 b.com/mz2/imotifs and can be run on Mac OS X Leopard (Intel/PowerPC).

65 ve recognized Panthera species (lion, tiger, leopard, jaguar, and snow leopard).

66 Mutations in leopard (leo), encoding Connexin 41.8 (Cx41.8), a gap ju

67 linically similar but distinctive disorders, LEOPARD (LS) and Noonan (NS) syndromes.

68 We further argue that leopards may select smaller-sized prey than predicted by

69 survival and residual reproductive value of leopard mothers against the benefits derived from matern

70 Leopard mothers appear sensitive to their offspring's de

71 he 37 living species of Felidae, the clouded leopard (Neofelis nebulosa) is generally classified as a

72 tiger (Panthera tigris altaica) and clouded leopard (Neofelis nebulosa).

73 The clouded leopard, Neofelis nebulosa, is an endangered semiarborea

74 be saved and survival prospects for the Amur leopard not only in China, but also through imperative c

75 pulation genetic variation among 109 clouded leopards of known geographic origin (Figure 1A, Tables S

76 riable roaring phrases, when confronted with leopards or crowned eagles.

77 sting vocalizations of their main predators, leopards or eagles.

78 is; snow leopard, P. uncia; jaguar, P. onca; leopard, P. pardus; and lion, P. leo.

79 nthera genus species: tiger, P. tigris; snow leopard, P. uncia; jaguar, P. onca; leopard, P. pardus;

80 Leopards Panthera pardus exhibit a unique form of short-

81 , puma (Puma concolor), lion (Panthera leo), leopard (Panthera pardus), and Pallas' cat (Otocolobus m

82 our ability to document and monitor clouded leopard populations.

83 genera Profelis (serval) and Panthera (snow leopard) provides further evidence for karyotypic conser

84 and MITF), Kallmann (CHD7 and SOX10), Noonan/LEOPARD (PTPN11), CHARGE (CHD7), or Kabuki (KMT2D).

85 de and developed a distribution model of the leopard's historical range in northeastern China over th

86 metric analysis of the pelages of 57 clouded leopards sampled throughout the species' range.

87 exual organisms as examples: ravens, spotted leopards, sea butterflies, and liverworts.

88 Such low survival may be driven by leopard seal Hydrurga leptonyx predation, particularly p

89 Our results suggest that without leopard seal predation, this population would most likel

90 f a kill being kleptoparasitized varied with leopard sex and age, prey size and vulnerability, vegeta

91 of a representative cartilaginous fish, the leopard shark, Triakis semifasciata.

92 These pigment clumps produced a striking leopard-spot pattern on fundus autofluorescence imaging.

93 We have generated iPSCs from patients with LEOPARD syndrome (an acronym formed from its main featur

94 Multiple lentigines/LEOPARD syndrome (LS) is a rare, autosomal dominant diso

95 LEOPARD syndrome (LS) is an autosomal dominant "RASopath

96 aling is exemplified by the observation that LEOPARD syndrome (LS) patients possess inactivating PTPN

97 In LEOPARD syndrome (LS) patients, mutations in the protein

98 LEOPARD syndrome (multiple Lentigines, Electrocardiograp

99 1 mutations causing other diseases including LEOPARD syndrome and leukemias.

100 of cardiomyocytes derived from patients with LEOPARD syndrome and LQTS has shed light on the molecula

101 ome cases, and PTPN11 mutations cause 90% of LEOPARD syndrome cases.

102 juvenile myelomonocytic leukemia (JMML) and LEOPARD syndrome frequently carry a second, somatically

103 ow that in vitro-derived cardiomyocytes from LEOPARD syndrome iPSCs are larger, have a higher degree

104 A major disease phenotype in patients with LEOPARD syndrome is hypertrophic cardiomyopathy.

105 ns increase SHP2 phosphatase activity, while LEOPARD syndrome mutants are catalytically impaired, rai

106 How do catalytically impaired LEOPARD syndrome mutants engender gain-of-function pheno

107 Our study reveals that LEOPARD syndrome mutations weaken the intramolecular int

108 ndicate that previously enigmatic aspects of LEOPARD syndrome pathogenesis can be explained by the co

109 derived from a healthy brother of one of the LEOPARD syndrome patients.

110 bryos with those injected with mRNA encoding LEOPARD syndrome point mutations, we identify a phosphat

111 Consequently, LEOPARD syndrome SHP2 mutants bind upstream activators p

112 2 mutants are constitutively active, whereas LEOPARD syndrome SHP2 mutants exhibit reduced phosphatas

113 individuals) and two of six individuals with LEOPARD syndrome without PTPN11 mutations have missense

114 ) caused by Danon disease, Vici syndrome, or LEOPARD syndrome, but not in HCM caused by mutations in

115 Noonan and LEOPARD syndromes are developmental disorders with overl

116 ermline mutations in PTPN11 cause Noonan and LEOPARD syndromes, which have overlapping clinical featu

117 Female leopards that suffered higher rates of kleptoparasitism

118 st hoisting is a key adaptation that enables leopards to coexist sympatrically with high densities of

119 Leopards typically elicited sequences consisting of a sn

120 Duration of care exhibited by female leopards varied markedly, from 9 to 35 months.

121 rd genome assembly, as well as two wild Amur leopard whole genomes.

122 s between the Siberian tiger and the clouded leopard with 93% accuracy.

123 rence data of the critically endangered Amur leopard worldwide and developed a distribution model of