ライフサイエンスコーパス: bull

1 nvolved was recorded (29 were injured by pit bulls).

2 m observed in mouse as compared to human and bull.

3 ordant with the QTL genotypes of these eight bulls.

4 valuation and comparison of theta among five bulls.

5 uence variants and genotypes of key ancestor bulls.

6 ravest injuries would be those caused by pit bulls.

7 el in veal calves (1718 ng mL(-1)) vs. young bulls (2.8 ng mL(-1)).

8 lls (>/=4 years old), particularly prime-age bulls (6-10 years old), play important roles in predator

9 Insemination from bull A resulted in an average sperm aster diameter of 10

10 Sperm asters organized by bull A-derived sperm had an average quality score of 1.8

11 Three bulls (A-C) were chosen based on varying fertility (A, l

12 e found that on the Seward Peninsula, mature bull:adult cow ratios declined 4-12%/year and short-year

13 , regular Pepsi, Pepsi max, Sprite, 7up, Red Bull and Hype).The limit of detection (LOD) and limit of

14 abundant kokanee were extirpated, and native bull and westslope cutthroat trout are imperiled.

15 Protamines from eutherian mammals, including bulls and humans, also contain multiple cysteine residue

16 adults but affiliated instead with sisters, bulls, and age mates.

17 divergent breeds such as Greyhounds and Pit Bulls, and even some of the skeletal transformations tha

18 Attacks by pit bulls are associated with higher morbidity rates, higher

19 ion identified one highly-influential Jersey bull as the putative source ancestor.

20 score of 1.8, which was higher than that of bull B (1.4; P < or = 0.0005) or bull C (1.2; P < or = 0

21 diameters produced after inseminations from bull B (78.2 microm; 60.8%) or bull C (77.9 microm; 57.8

22 Results with bulls B and C were also significantly different (P < or

23 han that of bull B (1.4; P < or = 0.0005) or bull C (1.2; P < or = 0.0001).

24 inations from bull B (78.2 microm; 60.8%) or bull C (77.9 microm; 57.8%), which themselves displayed

25 .: Fries) (Sl) and Coprinopsis atramentaria (Bull.) (Ca), were studied for their synergistic antioxid

26 Holstein bull calves (n = 15) were experimentally exposed to E. c

27 Lastly, comparison of multiple bull collections showed some to have aberrant x-ray scat

28 ablishing the distribution of nds within the Bull Creek drainage of the Beaver River basin in the Okl

29 The lack of hexagonal nds suggests Bull Creek I is not near any impact site.

30 r report of an abundance spike of nds in the Bull Creek I Younger Dryas boundary soil is confirmed, a

31 Potential hexagonal nds at Bull Creek were found to be more consistent with graphen

32 bulls (SB), sire(s) of cows (SC), dam(s) of bulls (DB), and dam(s) of cows (DC).

33 results indicate a statistically significant bull-dependent difference in diameter of the sperm aster

34 ial organization of the sperm aster was also bull-dependent.

35 from 90,393 primiparous cows, sired by 1122 bulls, distributed over 935 herd-calving year classes.

36 nail densities revealed that herbivorous and bull-dozing snails (Littorina littorea) alone can contro

37 protocols applied for veal calves and young bulls enrolled in this study.

38 Here, Bull et al. show that VRS3 encodes a putative Jumonji C-

39 etermined by a simulated fit of the model of Bull et al. to the pulse radiolysis data.

40 A late-stage immune synapse is commonly a bulls-eye pattern of immune cell receptor-ligand pairs s

41 ompounds and sensory attributes of beef from bulls fed concentrates to slaughter (C), grass silage fo

42 Validated genetic variants associated with bull fertility could prove useful for improving reproduc

43 tudies have investigated cow fertility while bull fertility has received much less consideration.

44 ings can provide opportunities for improving bull fertility via marker-assisted selection.

45 ght genomic regions strongly associated with bull fertility.

46 nscription factor FOXJ3 in the regulation of bull fertility.

47 rogressed a bovine POLLED allele into horned bull fibroblasts.

48 dentify 160 reliable and divergently fertile bulls for a dual strategy of targeted sequencing (TS) of

49 have discovered transposase sequences in the bull frog (Rana catesbeiana) and in the clawed frog (Xen

50 of extracellular K+ on membrane currents of bull frog (Rana catesbeiana) taste receptor cells (TRCs)

51 The 1000 bull genomes project supports the goal of accelerating t

52 In the first phase of the 1000 bull genomes project, we sequenced the whole genomes of

53 Ovibos moschatus) are very social and mature bulls (>/=4 years old), particularly prime-age bulls (6-

54 me of mammalian sperm (human, rhesus monkey, bull, hamster, mouse).

55 ortionately after increases in the number of bulls harvested, and calf:cow ratios declined in the Nor

56 bited the greatest degree of variation among bulls having high and low theta within the DYA-DRB3 inte

57 ng the newly sequenced emerald ash borer and bull-headed dung beetle.

58 reconstructed for two of the most important bulls in the history of the dairy cattle industry, Pawne

59 othesis that the selective harvest of mature bulls may be related to documented changes in population

60 Strict regulation of pit bulls may substantially reduce the US mortality rates re

61 ngle x-ray scattering, we show that isolated bull nuclei achieve slightly lower DNA packing densities

62 Semen from 550 Holstein bulls of high (>/= 1.7; n = 288) or low (</= -2; n = 262

63 WES of all exons in the genome in 24 bulls of high and low fertility identified 484 additiona

64 ients; three patients in this group who had "bull" or "thick" necks did not have full neck extension

65 f three anchoring domains, which together in bull P1 contain 19 Arg residues.

66 es corresponding to specific segments of the bull P1 DNA binding domain.

67 unctional analysis confirmed that sperm from bulls possessing the haplotype showed significantly enha

68 disulfide bonds hold the terminal domains of bull protamine folded back onto the central DNA binding

69 icroscopy and light scattering, we show that bull protamine forms particles with DNA that are morphol

70 ntermolecular disulfide bonds formed between bull protamine molecules within in vitro DNA condensates

71 of the intermolecular sulfur-sulfur bonds of bull protamine results in tighter DNA packing.

72 The importance of the bull protamine terminal domains in controlling the bull

73 or the positions of the cysteine residues in bull protamine that form intermolecular disulfide bonds.

74 analog of the central DNA binding domain of bull protamine was synthesized with phenylalanine replac

75 Folded bull protamine was used to condense DNA in vitro under v

76 ins, do not produce as uniform structures as bull protamine.

77 A model is also presented for the bull protamine.DNA complex in native sperm cell chromati

78 nt backcrossing of female hybrids to savanna bulls replaced the forest nuclear genome.

79 short-term users or severe retinal toxicity (bull's eye maculopathy).

80 20/200 or worse, color vision disturbances, bull's eye maculopathy, and peripheral pigmentary retino

81 ngs included markedly reduced visual acuity, bull's eye maculopathy, foveal hyperpigmentation, peripa

82 r disease or evidence for any other cause of bull's eye maculopathy.

83 ng the p.Arg420Ser mutation presented with a bull's eye maculopathy.

84 er diagnosis, 35% of CD and 51% of CRD had a bull's eye maculopathy; 70% of CRD showed absolute perip

85 Using EMM software, we created a bull's eye precisely matched to that generated by DE-MRI

86 th the Wallowa Mountains in the centre of a 'bull's eye' pattern of valleys and low-elevation mountai

87 thy does not always develop in a parafoveal (bull's eye) pattern, and a pericentral pattern of damage

88 ltage value for that same segment in the EMM bull's eye.

89 four Charolaise heifers and four Charolaise bull's muscles were sampled at slaughter after early and

90 nding beyond the arcades; and 1 (2.5%) had a bull's-eye appearance.

91 migration and consolidation that produce the bull's-eye colonies typically associated with P. mirabil

92 This cycle produces the bull's-eye colony often associated with cultures of P. m

93 o change except in severe cases in which the bull's-eye damage expanded progressively.

94 nal pigment epithelium), and severe (visible bull's-eye damage).

95 in structure, with Th2 cells failing to form bull's-eye IS.

96 The fundi showed bull's-eye macular atrophy and widespread RPE thinning.

97 phy (SD OCT) were performed in patients with bull's-eye maculopathy (BEM) to identify phenotypic mark

98 assess the effect of the processing schemes: bull's-eye map (BEM) uniformity, contrast between the le

99 PCs) form an "immunological synapse" (IS), a bull's-eye pattern composed of a central supramolecular

100 ar, a P. mirabilis colony grows outward in a bull's-eye pattern formed by consecutive waves of rapid

101 actions help to shape and maintain the final bull's-eye pattern of the IS.

102 y anomalies over lunar impact basins display bull's-eye patterns consisting of a central positive (ma

103 Bull's-eye plots indicated that the (111)In signal from

104 y of linear sine-wave gratings over proposed bull's-eye radial gratings is discussed.

105 Th1 cells formed typical "bull's-eye" IS with a ring of adhesion molecules surroun

106 ath selection model that included sire(s) of bulls (SB), sire(s) of cows (SC), dam(s) of bulls (DB),

107 Western blot analysis of llama and bull seminal plasma confirmed immunorecognition of OIF u

108 The dimer of bull seminal ribonuclease (BS-RNase) is also known to be

109 Bull shark abundance was high year-round, but peaked in

110 ion by sharks when they are in areas of high bull shark abundance?

111 ent (ROM) differ in areas of low versus high bull shark abundance?

112 edicted dynamics of stable isotope values in bull shark blood and plasma under different assumptions

113 ich could have negative consequences for the bull shark population and/or induce shifts in behaviour.

114 t to determine to what extent predators like bull sharks (Carcharhinus leucas) in the coastal Evergla

115 (2) How do the movement patterns of bull sharks and tarpon compare, and what proportion of t

116 1) How do the seasonal abundance patterns of bull sharks and tarpon compare?

117 /SIGNIFICANCE: Despite similarities in diet, bull sharks and tarpon showed little overlap in habitat

118 Bull sharks increased their use of upstream channels dur

119 ically concentrated up rivers, where tracked bull sharks were absent.

120 DINGS: We satellite-tagged an apex predator (bull sharks, Carcharhinus leucas) and a sympatric mesopr

121 d osmoregulation to reduce predation risk by bull sharks.

122 his is the case in both beating and arrested bull sperm and in beating sea urchin sperm.

123 Because bull sperm bend to a higher curvature after ADP treatmen

124 rotamine terminal domains in controlling the bull sperm chromatin morphology is indicated by our obse

125 In native bull sperm chromatin, intramolecular disulfide bonds hol

126 is comparable with that observed for native bull sperm chromatin.

127 ologically similar to the subunits of native bull sperm chromatin.

128 Permeabilized and reactivated bull sperm exhibit a marked reduction in beating frequen

129 g change in the stalling force produced by a bull sperm flagella in response to ADP.

130 nerated by a detergent-extracted reactivated bull sperm flagellum during an isometric stall was measu

131 orts a role for beta-defensins in regulating bull sperm function.

132 stiffness of 50 muM sodium vanadate treated bull sperm in the presence of 4 mM ADP, but found no cha

133 In vivo, intact bull sperm microinjected into mature oocytes do not unde

134 stigate systematically swimming of human and bull sperm over a range of physiologically relevant shea

135 Space Agency (ESA) studies demonstrated that bull sperm swim with higher velocity in microgravity (mi

136 o, as evidenced by the treatment of isolated bull sperm with the disulfide bond-reducing agent dithio

137 tion in the absence of BSA in both mouse and bull sperm, and the patterns of phosphorylation were sim

138 erimental evidence from sea urchin sperm and bull sperm.

139 were tested by using detergent-demembranated bull sperm.

140 We documented breeding bulls that traveled >6,500 km round trip from their nata

141 e concordant with the QTL genotypes of eight bulls that were established by segregation analysis.

142 oocytes with sperm from a Bos taurus indicus bull to facilitate parent-specific transcriptome analysi

143 ern Rocky Mountains for two native salmonids-bull trout (BT) and cutthroat trout (CT).

144 e method by forecasting suitable habitat for bull trout (Salvelinus confluentus) in the Interior Colu

145 imatic variation and habitat features in 130 bull trout (Salvelinus confluentus) populations from 24

146 observations with laboratory experiments of bull trout (Salvelinus confluentus), a large freshwater

147 have important conservation implications for bull trout and other imperiled species.

148 Consumption by bull trout at other settings were lower and more variabl

149 We also simulated bull trout consumption and growth during salmon smolt ou

150 One-day consumption by laboratory-held bull trout during the first day of feeding experiments a

151 We then determined whether bull trout genetic diversity was related to climate vuln

152 The degree of binge-feeding by bull trout in the field was slightly reduced but largely

153 ainty, regardless of the climate data set or bull trout model employed.

154 nd a strong gradient in genetic diversity in bull trout populations across the Columbia River Basin,

155 ith linear mixed models, allelic richness in bull trout populations was positively related to habitat

156 Phenotypic records collected on >7,000 bulls used in artificial insemination (AI) were used to

157 valuated in three additional randomly chosen bulls using sperm typing.

158 Seminal plasma from llamas and bulls was used as representative of induced and spontane

159 lite markers in a pedigree of 3,147 Holstein bulls, we fine mapped regions of BTA6 that had previousl

160 acks by other breeds of dogs, attacks by pit bulls were associated with a higher median Injury Severi

161 This first application of WES in AI bulls with divergent fertility phenotypes has identified