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1 cin (Van), Linezolid (Lin), and Clindamycin (Clin).
2 inducible and constitutive CliNS, 14.6% were CliNS.
3 g sections dominate the New versus Old World clines.
4 nal, or linkage effects in the remaining two clines.
5 ffects occurred in most, but not all, of the clines.
6 tions positioned at either end of the native clines.
7 s and pigmentation rarely showed elevational clines.
8 warm and cold sites, potentially maintaining clines.
9 435 individuals, demonstrating three genetic clines.
10 nce of contrasting locally adaptive regional clines.
11 ussing instances where patterns differ among clines.
12 size (T-S) responses and latitude-size (L-S) clines.
13 s and targets of selection among the sampled clines.
14 raphy and selection, could contribute to the clines.
15 ecting key diapause traits, forming adaptive clines.
16 ne region can explain many of the amino acid clines.
17                                       3V2640-CLIN-005 (FASCINATE-1) was a randomized, placebo-control
18 reased with one of the two clinical strains (Clin 1, P=0.0006) and decreased by AD-169 (P=0.0016).
19 s tested for both inducible and constitutive CliNS, 14.6% were CliNS.
20                                              Clin 2 and Towne had no effect on MHC class I expression
21 d by one of the two clinical strains of CMV (Clin 2) (P=0.0091 and P=0.0018, respectively).
22 esistance was highest in 2017 (EryNS: 22.8%; CliNS: 22.0%).
23 in Europe, and displays parallel latitudinal clines across continents, providing strong indirect supp
24 suggest that plasticity can cause phenotypic clines across human-modified landscapes.
25            The high frequency of latitudinal clines across the genome indicates that secondary contac
26 ens, Bombus pensylvanicus) exhibit body size clines across the urban gradient, despite a lack of popu
27 ive isolation by comparing site-wise genomic clines against global patterns and identified a breakdow
28                                              CLIn also enables birth-order analysis and genetic manip
29 rge movement of prestin, linear capacitance (Clin) also displays voltage dependence as motors move be
30  differences and evolution across geographic clines among continents of the intertidal grass Spartina
31         We analyzed proportions of EryNS and CliNS among isolates by site, year, risk factors, and em
32 arriers to gene flow along parallel salinity clines and coincides with a physiologically stressful sa
33 ClineHelpR R-package for visualizing genomic clines and detecting outlier loci using output generated
34 dence from natural populations of geographic clines and seasonal cycling, and stable heterotic polymo
35 ore variable and exhibit steeper latitudinal clines and stronger relationships with local environment
36  They are characterized by rapid temperature clines and varied flow disturbance regimes, both of whic
37 t differences parallel latitudinal body size clines, and will influence predicted impacts of climate
38 ears), diapause variation in the latitudinal clines appears to have aided North American flies in ada
39 range, but it is unclear whether elevational clines are consistent among different mountain ranges.
40 evious investigation suggests that many such clines are due to spatially varying selection rather tha
41 tasets documenting changes to gene frequency clines are extremely rare but provide a powerful means o
42  the conditions under which allele frequency clines are more or less likely to evolve as multiple qua
43               In D. melanogaster latitudinal clines are seen for amino acid polymorphisms at the Hex-
44 nterpret and consequently visualize 'genomic clines' are limited, and users must often write custom,
45 rimental approaches, such as sampling across clines, artificial evolution experiments, and resurrecti
46 eutral evolution under this history produces clines as steep as those expected under selection.
47 oci displaying host differences, latitudinal clines, associations with adult eclosion time, and withi
48 lycogen synthesis, parallel the low activity clines at G6PD for reduced pentose shunt flux in norther
49 genotypes, accounting for the observed steep clines at hybrid zones.
50  explicit population genetic model for these clines based on the known genetics of flower color.
51 exon deleted variant appeared mainly in cell clines, but not in most normal tissues.
52 ication resulted in even steeper latitudinal clines by selecting aliens distantly related to natives
53 tory and physiology vary along environmental clines can reveal functional insight into adaptations to
54                              In fact, these 'clines' can explain most of the variation in human popul
55  clinical nanopore Cas9-targeted sequencing (Clin-CATS) for parallel in-depth repeat analysis, we eva
56 onment associations, and spatial and genomic clines demonstrate that two unrecognized species are pre
57 lts provide evidence that recurrent adaptive clines do not necessarily reflect shared adaptive proces
58                                   Phenotypic clines evolved with nonmonotonic (i.e., nonclinal) patte
59 ugal-Tutkin and Urgancioglu in (Graefes Arch Clin Exp Ophthalmol 244:742-6, 2006).
60  (Tugal-Tutkun and Urgancioglu, Graefes Arch Clin Exp Ophthalmol 244:742-6, 2006; Tugal-Tutkun et al.
61 dy in Drosophila melanogaster of latitudinal clines for 23 SNPs embedded in 13 genes (Pgi, Gapdh1, UG
62 The existence of temporally stable frequency clines for In(2L)t in natural populations of Drosophila
63 which may explain the absence of latitudinal clines for PGM allozyme alleles, the lack of association
64                              The latitudinal clines for several Pgm amino acid polymorphisms show tha
65 clades, we find oxygen-dependent altitudinal clines for steady-state levels of protochlorophyllide, e
66  Remarkably, in both species, the geographic clines for the major wing-pattern loci are displaced by
67 to calculate null expectations for body size clines from a thermal perspective, aiding mechanistic in
68 s showed broadly coinciding, steep frequency clines from north to south across this zone beside the f
69 ity was generally concordant with phenotypic clines from the natural populations.
70 sive parallelism, but that steep altitudinal clines generate islands of divergence.
71                    We show that the shape of clines generated by exogenous selection is indistinguish
72 tically with latitude, but evidence for such clines has been lacking.
73 changed, we see five genes where latitudinal clines have been lost or gained and two where the slope
74                 To test whether cyanogenesis clines have evolved in response to the same selective pr
75                    We find that phenological clines have evolved repeatedly throughout the range, dur
76 damage), and climate-associated cyanogenesis clines have evolved throughout the native and introduced
77           Increasing prevalence of EryNS and CliNS iGAS infections in the US is predominantly due to
78 s published in 2012 (Senti et al., J Allergy Clin Immunol, vol 129(5):1290-1296), the current study i
79                 We demonstrated the power of CLIn in the context of the eight central brain type II l
80 te a modified approach of studying genotypic clines in 'mosaic' hybrid zones.
81                                  Elevational clines in [CO(2)] are not as evident, making it challeng
82      The inverted duplication exhibits steep clines in allele frequency in a natural hybrid zone, sho
83                          There were no clear clines in allele frequency or genetic diversity as would
84 highlight the role of host hybridization and clines in altering host-pathogen interactions, dynamics
85                    We identified latitudinal clines in both rates of cooperative nesting and color pa
86 dies utilizing whole-genome data to identify clines in D. melanogaster and several other systems.
87 dients were associated with the evolution of clines in defense in 47% of cities throughout the world.
88        Physiological and genomic elevational clines in different regions can be unique, underlining t
89                                    Body size clines in Drosophila melanogaster have been documented i
90 gation of selection acting along latitudinal clines in Drosophila melanogaster.
91                            We quantify sharp clines in flower color where this species comes into con
92 phical areas and have discovered latitudinal clines in gene frequencies.
93 ostglacial range expansions have resulted in clines in genetic diversity across present-day distribut
94 plotype endemism in southern populations and clines in genetic diversity northward.
95                    We quantified latitudinal clines in genetically determined diapause timing of an i
96                                  Urban-rural clines in melanism were strongest in the largest cities
97 3 North American cities to test for parallel clines in melanism, a genetically based trait associated
98 d, Hex-C), presents a picture of latitudinal clines in metabolic genes prevalent around the branch po
99                              The latitudinal clines in microbiome composition are predicted by metric
100                      We found non-coincident clines in mtDNA and nuclear DNA, mirroring directionalit
101 in Drosophila melanogaster from well-studied clines in North America and Australia.
102 olymorphisms showing significant latitudinal clines in North America, the derived allele is the one i
103                                Environmental clines in organismal defensive traits are usually attrib
104                                   Evaluating clines in phenological traits and the extent and variati
105 ophila melanogaster from the extreme ends of clines in South America and Australia.
106 etween geographic locations and across depth clines in the Caribbean coral, Montastraea cavernosa.
107  extended functionality can evaluate genomic clines in the context of spatial and environmental featu
108  inversions on the third chromosome, and the clines in the inversion frequencies across the southwest
109  S. alterniflora has evolved different trait clines in the native and introduced ranges, showing the
110  phenotype, and allele frequency-environment clines in the native range predict those in the invaded
111 Marked differences were apparent between the clines in the occurrence and magnitude of the significan
112         Sex-biased dispersal created spatial clines in the sex ratio, which influenced offspring prod
113 logical processes associated with these wide clines include cell signaling, olfaction, and pheromone
114 gical processes associated with these narrow clines include physiological and immune responses to the
115             The emm types with >30% EryNS or CliNS included types 77, 58, 11, 83, and 92.
116                                              Clin Infect Dis 2020;73:3183-93.To read the full NIHR Al
117                                Lund, et al., Clin Infect Dis 65:1183-1190, 2017, M.-L.
118                                    EryNS and CliNS infections were most frequent among persons aged 1
119   Notably, these wasps exhibited chromosomal clines, involving chromosome number and decreasing of GC
120 sm collections across north-south geographic clines is useful in the detection of marker associations
121                                 Most (99.8%) CliNS isolates were EryNS.
122 t loci (QTL) showed elevational and climatic clines likely maintained by selection.
123 ough analytical predictions for the width of clines maintained by heterozygote disadvantage fit well
124 eviously reported Est-6 allozyme latitudinal clines may be accounted for by the interaction between s
125                                              Clines may be maintained by diversifying selection acros
126                              Zhao, et al. (J Clin Microbiol 49:3766-3770, 2011) for molecular serotyp
127                         Dien Bard, et al., J Clin Microbiol 59:e00654-21, 2021, ).
128                                        Kahn, Clin Microbiol Rev 19:546-557, 2006, N.
129 structure can be a consequence of geographic clines, not group barriers.
130 also correspond to genetic and morphological clines observed across a range of marine organisms.
131 differences in the spatial scales over which clines occur (40-1600 km).
132 s the world, we reveal ubiquitous and strong clines of decreasing colour lightness towards colder reg
133 rranean Sea with characteristic east to west clines of gene flow.
134 ross 3.4 million individuals from four major clines of global ancestry (approximately 21% non-Europea
135 s and exogenous viability selection generate clines of similar shape, but the comparison has not been
136 smission that plausibly explains latitudinal clines of wMel frequencies on multiple continents.
137  with analyses of changes in neutral genetic clines offers a powerful way to obtain ecologically rele
138 f multi-locus differentiation (i.e., genomic clines) often extend broadly across hybrid zones and the
139  and Slow, are distributed along latitudinal clines on several continents.
140 that is reflected by the presence of allelic clines or local adaptation.
141 sults suggest that recapitulation of genetic clines over latitude and altitude involves extensive par
142 imate and that temperature and precipitation clines predict the invasive performance of particular pr
143                                    Using the Clin Pro tool, the obtained results from MALDI-MS data w
144 uman skin pigmentation is the product of two clines produced by natural selection to adjust levels of
145                                   Geographic clines revealed candidate genes deviating from genome-wi
146          Uncorrected, these allele frequency clines severely confounded inferences of selection.
147 ible (EryNS) and clindamycin-nonsusceptible (CliNS) strains to those with susceptible infections.
148 are structured into three distinct admixture clines stretching between various western and eastern Eu
149 ding mechanistic interpretation of empirical clines such as Bergmann's Rule.
150 In addition, results from basin-wide genomic clines suggested that hybrids and parental forms are ada
151  with BEAST analysis identified two separate clines, suggesting that TBEV spread both east and west f
152 The diversity in genetic architecture of the clines suggests that natural selection has produced simi
153  transgenic cell class-lineage intersection (CLIn) system to assign cells of a particular class to sp
154 oderate with FST=0.084 and fewer latitudinal clines than R. pomonella.
155 ermore, some sublineages demonstrate genomic clines that recapitulate cladogenetic events, suggesting
156 ertain deterministic models - such as linear clines - the regression is constant.
157      For both females and males of all three clines, the generation means were adequately described b
158 y size are often associated with latitudinal clines, thought to be driven by climate gradients.
159 locus basis and examined the distribution of clines to detect those that exhibited signifcantly steep
160  northern and southern ends of each of these clines to produce F(1), F(2), and first backcross genera
161 tosomal markers exhibit asymmetrically broad clines, usually with high frequencies of M. domesticus a
162 a normal (gnomAD) and other databases (LOVD, Clin Var and 100,000 Genomes Project) to determine their
163 s revealed that the evolution of urban-rural clines was best explained by adaptive evolution, but the
164                 Variation in the strength of clines was explained by environmental changes in drought
165           Google Scholar, PubMed, and LARVOL CLIN websites were also searched for reports.
166                         Overall, latitudinal clines were detected in nearly half of all loci genotype
167 t with regional heterogeneity, trait and QTL clines were evident at regional scales (c.
168 enase), the positions and slopes of Fundulus clines were statistically indistinguishable.
169 ce of both isolation by distance and ancient clines, whereas there was no evidence of structure in SE
170  effects as a byproduct of its assessment of Clin, which increases during salicylate treatment as mot
171 nce) traits exhibited geographic or climatic clines, which often remained significant after accountin
172 rary patterns of adaptation to environmental clines will mediate future plant responses to projected
173                                    Three new clines with latitude were detected.
174 lection will form monotonic allele frequency clines with their selective environment, which has led t
175 e width of the chromosomal and mitochondrial clines, with cline centres displaced at least 2.5 km.
176          The recurrent evolution of adaptive clines within a species can be used to elucidate the sel

 
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