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1                                              zoo-1 knockdown results in lethality during elongation,
2 investigate the effects of inbreeding in 119 zoo populations, encompassing 88 species of mammals, bir
3 cropsies of white (n = 3) and black (n = 13) zoo rhinos were sampled in several locations yielding 18
4 t 254 zoo workers for antibodies to SV40; 25 zoo workers with direct contact with nonhuman primates a
5 uslike particles (VLPs) was used to test 254 zoo workers for antibodies to SV40; 25 zoo workers with
6 d approach to a comprehensive dataset on 258 zoo-housed bonobos that includes weight and length growt
7          We use a global dataset of over 450 zoos to develop a model of how zoo composition and socio
8                                            A zoo-blot probed at moderate stringency with labeled cDNA
9 halitic placental and marsupial animals at a zoo in Germany and in wild yellow-necked field mice (Apo
10 ies BC) and of two historical baboons from a zoo via shotgun metagenomics.
11     Another risk factor is being born into a zoo rather than being imported from the wild, with poor
12  but seemingly irregular configurations of a zoo of topological vortices and antivortices.
13 26), which suggests that the popularity of a zoo's collection relative to the types and numbers of sp
14  additives in dietary and fecal samples of a zoo-housed polar bear.
15 ng transmission electron microscopy reveal a zoo of topologies, and polarization displacement mapping
16       Hybridization of a GLP cDNA probe to a zoo blot demonstrated multiple signals in nonhuman prima
17 ing from de-mixing of elastic monopoles to a zoo of unusual colloidal crystals formed by high-order m
18 esented 4- to 8-year-old children visiting a zoo in Scotland (N = 109) with a task in which the perce
19 cancer-related mortality using data on adult zoo mammals (110,148 individuals, 191 species) and map a
20 torquatus, both in Africa and in an American zoo.
21 (Odocoileus virginianus) in a North American zoo.
22 Cercopithecus lhoesti) from a North American zoo.
23 e families housed in multiple North American zoos.
24 sian and African elephants at North American zoos.
25 (ASV, Faith PD and Shannon) was higher among zoo gorillas than among those in the Cameroonian forest,
26  of collaborations between entomologists and zoo personnel as a means of enhancing research and publi
27 xonomic orders incorporating lab, field, and zoo sites.
28 r screening wild populations and private and zoo collections of Mediterranean tortoises.
29  Dietary protein levels selected by wild and zoo polar bears were low and similar to selection observ
30 e retroviruses infect laboratory workers and zoo workers, zoonotic retrovirus transmission has not be
31 emoved tortoises for food, oil, museums, and zoos, they also colonized the archipelago resulting in t
32                    One risk factor for Asian zoo elephants is being moved between institutions, with
33 the 10 were males, and 3 of the 10 worked at zoos.
34 only females, with males being moved between zoos for mating, but perhaps they should be kept togethe
35 oximity to other species and to humans, both zoo workers and visitors, provides the potential for cro
36 n among those in the Cameroonian forest, but zoo and Cameroonian chimpanzees showed no difference.
37 ach, measured protein:fat ratios selected by zoo polar bears offered dietary choice and examined pote
38  in neural crest development is supported by zoo blot hybridizations that reveal extensive conservati
39 geneous environmental conditions provided by zoos.
40  the UK, (2) to develop a way of calculating zoo popularity in terms of the species kept within a col
41                    Altogether, our stem cell zoo uncovered general scaling laws governing species-spe
42 antial 'dwell times' in the Centre by common zoo standards and the addition of new engagement element
43 in parallel to the cadherin-catenin complex, zoo-1 loss of function reduces the dynamic recruitment o
44                    Tested in two conditions, zoo-housed apes (2 gorillas, 5 chimpanzees) were familia
45     This research shows that the current DFT zoo of approximations does not constitute a transparent
46  from eight other NHP species in a different zoo show the same pattern of convergence, and that semic
47 e new RNA world, which may contain a diverse zoo of new architectures and mechanisms.
48 e and general approach to generate an entire zoo of new anisotropic colloids.
49 hoerus africanus) from Africa and a European zoo was determined.
50         Conducted in Cameroon and a European zoo, this integrative study elucidates these processes,
51 atric chimpanzees and gorillas in a European zoo.
52 zees (Pan troglodytes) housed at 32 European zoos were measured for 25-hydroxyvitamin D(2), 25-hydrox
53  and adolescent bonobos housed in 5 European zoos to study the role of personality similarity in dyad
54 dividuals were born in captivity in European zoos and hosted a strikingly low diversity of fecal micr
55 0 elephants to show that animals in European zoos have about half the median life span of conspecific
56  through bonobo networks across six European zoos.
57   Analysis of woolly monkey colonies at five zoos indicated that WMHBV infections occurred in most of
58                                          For zoo-housed polar bears, fed on a lipid-rich diet of fish
59    Personality research has implications for zoo animal welfare, as it can further our understanding
60 elated with generated popularity ratings for zoos based on the species kept within a collection and a
61 lied upon to remove deleterious alleles from zoo populations.
62  and increase the in situ contributions from zoos, helping to reduce global biodiversity loss.
63                       We show that data from zoos and aquariums in the Species360 network can signifi
64 cies across Australia, including government, zoos, and nongovernment organizations.
65 easing the importance of maintaining healthy zoo populations.
66 t of over 450 zoos to develop a model of how zoo composition and socio-economic factors directly and
67                                     However, zoo and sanctuary apes ingested a greater ratio of water
68 epletion measures of water turnover (L/d) in zoo- and rainforest-sanctuary-housed apes (chimpanzees,
69 lated human polyomaviruses) was increased in zoo workers with direct contact with nonhuman primates (
70 h log density, but decreased among pandas in zoo 2 compared to zoo 1, during summer compared to winte
71 n the ground, age and higher among pandas in zoo 3 compared to zoo 2, but decreased with number of ne
72                              Giant pandas in zoo like enclosures had a similar FMR (14,182 kJ/day) to
73 om the wild, with poor adult survivorship in zoo-born Asians apparently being conferred prenatally or
74                            Water turnover in zoo and sanctuary apes was similar to estimated turnover
75 hat may contribute to sex ratio variation in zoo populations.
76 reasingly conducted on direct public view in zoo settings.
77                                           In zoos, we found strong evidence that this variation gener
78 grated management programs for arthropods in zoos are commonplace.
79 of Asian elephants (Elephas maximus) born in zoos and causes disease in the wild.
80 of all captive Asian elephant calves born in zoos in the United States and Europe since 1980.
81                Animals under managed care in zoos and aquariums are ideal surrogate study subjects fo
82 Asian elephants; unlike African elephants in zoos, this species' infant mortality is very high (for e
83 A crossed from African to Asian elephants in zoos.
84                                Thus, even in zoos, where environmental pressures are largely reduced,
85  using data from mammalian species housed in zoos and aquariums worldwide, we show that ongoing hormo
86 arthropods of medicoveterinary importance in zoos.
87 which animals are most beneficial to keep in zoos in terms of financial and conservative value is rea
88 ive study of turtles and tortoises living in zoos and aquariums, we show that ~75% of 52 species exhi
89 hina tiger (P.t. amoyensis) persists only in zoos.
90 and by establishing insurance populations in zoos (COIc).
91 es and whose captive breeding populations in zoos are not self-sustaining.
92 tries and in captive breeding populations in zoos is a highly lethal hemorrhagic herpesvirus disease
93 eterinary importance are well represented in zoos, and an ample literature documents their influence
94  from 129 avian and 324 mammalian species in zoos worldwide between 1980 and 2021.
95 ctancy in 528 mammal and 648 bird species in zoos.
96 timber camps), and its adult survivorship in zoos has not improved significantly in recent years.
97  their behavioural diversity in three Indian zoos.
98             The viral sequence from infected zoo lions belonged to clade V, and a single mutation of
99 f captive brown bears in a relatively large, zoo-type enclosure and compared those values to previous
100 ns and non-human primates (NHP) from a local zoo.
101 red in most of the animals at the Louisville zoo but not at four other zoos in the United States.
102 annotation graphical user interface, a model zoo and a human-in-the-loop pipeline to facilitate the a
103 o highlight the changing practices of modern zoos over a near half-century timescale.
104                                         Most zoos keep only females, with males being moved between z
105                    Here, the effect of a new zoo-based primate research centre on visitor behaviour,
106 arge-scale genetic study of the private (non-zoo) captive tiger population in the United States, also
107 st stress and/or obesity as likely causes of zoo elephants' compromised survivorship.
108 l role in anaerobic bacterial degradation of zoo- and phytosterols and shows only little similarity t
109 igate the physical and biological drivers of zoo- and ichthyoplankton aggregations at the edge of a d
110 the first study to combine the modalities of zoo-FISH and array CGH between different avian species.
111  functional genomics and cancer mortality of zoo mammals' data.
112 servation action including reintroduction of zoo-born tamarins into forest fragments 1984-2000, incre
113 la microbiota more closely resembled that of zoo chimpanzees than of Cameroonian gorillas.
114  To observe the distribution and location of zoos across the UK, (2) to develop a way of calculating
115 gs emphasise the importance and potential of zoos as public engagement centres for the biological sci
116                                  The role of zoos has shifted markedly from their origins in the nine
117 nalysing the impact of the changing roles of zoos on captive animals during the late 20th and 21st ce
118  contact with nonhuman primates and 15 other zoo workers (23% vs. 10%, respectively; P=.01) were sero
119  at the Louisville zoo but not at four other zoos in the United States.
120  mammals), and which are dissimilar to other zoos achieve higher numbers of visitors and contribute t
121 ncing: one group from six cheetahs in a U.S. zoo and two lions in a European circus, and the other gr
122 ified cDNA libraries, direct cDNA selection "zoo" blotting, cDNA screening, and identification of 24
123 plify extinction risks, especially in small, zoo-maintained populations which is of particular concer
124 l infection of TMUV in mammals, specifically zoo dolphins in Thailand, offering insights into its evo
125                                Surprisingly, zoo gorilla microbiota more closely resembled that of zo
126                                 We find that zoos with many animals, large animals, high species rich
127 provides a step towards finding order in the zoo of strongly interacting complex systems.
128 ses detected were of human serotypes, in the zoo population, only 15% of picornaviruses detected in N
129 ameroonian humans and great apes than in the zoo, virome convergence between Cameroonian humans and g
130  mice (Apodemus flavicollis) at and near the zoo.
131 scale assembly, generate the pedigree of the zoo-managed population, reaffirm the close genetic relat
132 n-theoretic language, thereby organizing the zoo of implicated chemical and mechanical signaling proc
133 fying individual reactive species within the zoo.
134 ndividual reactive intermediates within the "zoo" of organometallic species that form on catalytic su
135 normal and pathological neuronal aging, this zoo of aging-animal variants will facilitate analysis bo
136 d biomagnification factor (BMF(F)) for three zoo-housed polar bears who experience seasonal periods o
137  decreased among pandas in zoo 2 compared to zoo 1, during summer compared to winter, and also with a
138 and higher among pandas in zoo 3 compared to zoo 2, but decreased with number of nests, sociality, tr
139                  Higher-protein diets fed to zoo polar bears during normal care were concurrent with
140              Hybridisation of NBR2 probes to zoo blots showed that the NBR2 gene is present in human
141 troviruses at three research centers and two zoos identified no SIV, SRV, or STLV infection in 187 pa
142 and 59 other mammalian species living in two zoos and in the wild.
143 ants, human evolutionary studies, and typing zoo animals of unknown origin (for use in captive breedi
144 ected quarterly from 21 elephants at five UK zoos.
145                               Unfortunately, zoo-managed individuals currently face a high prevalence
146 eces, (p 0.019, R(2) between elephant within zoo - 0.608).

 
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