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1  of genetic plasticity underlying transverse genetic variability.
2  of congenital infection, exhibits extensive genetic variability.
3  robustness in the face of environmental and genetic variability.
4  different growth conditions and/or inherent genetic variability.
5 s, and managed-breeding strategies to retain genetic variability.
6 ing breeding populations for repositories of genetic variability.
7 y by shared environmental factors and not by genetic variability.
8             This indicates a large degree of genetic variability.
9 f the viral genome and are a major source of genetic variability.
10  contribution of different marked effects to genetic variability.
11 while the American C. dentata had the lowest genetic variability.
12 ross loci, may also lead to heterogeneity of genetic variability.
13 ogy, vascular and metabolic risk factors and genetic variability.
14  are often driven by mechanisms that promote genetic variability.
15 history that continue to influence levels of genetic variability.
16 ructure, extensive glycosylation, and marked genetic variability.
17 es, at least at the scale of intrapopulation genetic variability.
18 rbations of cellular function and individual genetic variability.
19 sulate development against environmental and genetic variability.
20 ctions in both the number of individuals and genetic variability.
21 s6466849, rs10268496) that cover all TAS2R16 genetic variability.
22 s, differential pathological signatures, and genetic variability.
23 de immune detection and/or exhibit extensive genetic variability.
24                          Naturally occurring genetic variability across HIV-1 subtypes causes amino a
25 esponsible for heterogeneity of the level of genetic variability across loci.
26 t differences in copy number are a source of genetic variability among D. v. virgifera.
27                                  To evaluate genetic variability among Entamoeba histolytica strains,
28 en deposition in the heart by exploiting the genetic variability among F2 progeny of 129P2 and FVBN/J
29  (cytb), were analysed in silico to identify genetic variability among the four species and used, sub
30 drial COI regions have been used to estimate genetic variabilities and reconstruct phylogenies.
31 l systems can serve as the interface between genetic variability and alterations in complex behaviora
32 stributions of offspring number on levels of genetic variability and among-population differentiation
33 ntifying its modulation by crop N status and genetic variability and analyzing its ecophysiological d
34                                  The reduced genetic variability and apparent gene deletion in some r
35 by examining the relationship between common genetic variability and brain endophenotype.
36                       Our data highlight the genetic variability and capacity in causing outbreak by
37                                          The genetic variability and covalent modifications associate
38  the ISR was used to determine the worldwide genetic variability and distribution of P. gingivalis, a
39             Despite its high prevalence, the genetic variability and drug resistance characteristics
40 rstanding of such fauna is limited and their genetic variability and evolutionary origins remain poor
41       In this study, we determined levels of genetic variability and gene flow among seven population
42                       A fine balance between genetic variability and genomic stability tunes plastici
43 The Italian and Iberian populations have low genetic variability and high linkage disequilibrium, but
44                  Simplot was used to compare genetic variability and high-speed sequencing was used t
45         The strong associations between IL6R genetic variability and IL-6 concentrations deserve furt
46              Stable naive hPSCs with reduced genetic variability and improved functional pluripotency
47 sts that these differences can contribute to genetic variability and pathologic susceptibility.
48 deficiency virus type 1 (HIV-1), we analyzed genetic variability and PI resistance-associated substit
49 s with maladaptive gene flow or by enhancing genetic variability and reducing inbreeding depression,
50 wever, European populations showed a loss of genetic variability and significant genetic differentiat
51         As diverse agents of selection shape genetic variability and structure within species, we arg
52  constitutes a substantial fraction of total genetic variability and the importance of structural gen
53 d suggest a potential mechanism between MAPT genetic variability and the pathogenesis of neurodegener
54 ld will yield data that can account for both genetic variability and the role of critical development
55 arked effects within chromosomes, background genetic variability, and family heterogeneity.
56                                      Current genetic variability, and inferred past demographic chang
57  multistep nature of viral oncogenesis, host genetic variability, and the fact that viruses contribut
58 oup of scientists expert in the field of HCV genetic variability, and those involved in development o
59            In species whose distribution and genetic variability are shaped by strong selection gradi
60 e the potential to show and emphasise common genetic variability associated with disease.
61               Here, we examine the levels of genetic variability at 13 (seven informative) loci in wi
62 ations (FST > 0.130) and discovered temporal genetic variability at a single site that was on par wit
63 , we examined the association between LP and genetic variability at candidate regulatory regions in 5
64          Notably, by Shannon entropy, higher genetic variability at HBsAg amino acid positions 130, 1
65 ucleotide polymorphisms and found widespread genetic variability at many of these loci.
66 ine the signature of population expansion on genetic variability at microsatellite loci, we consider
67                        Our findings point to genetic variability at the ADIPOR1 locus as a strong det
68                                              Genetic variability at the APOA1/C3/A4/A5 cluster has be
69        Additionally, we show that individual genetic variability at the Apobec1 locus results in diff
70 n polymorphisms comprehensively defining the genetic variability at the IL6 locus with diabetes risk.
71                   Extensive population-level genetic variability at the Salmonella rfb locus, which e
72  of all these diseases are predisposed to by genetic variability at the same loci, strongly suggestin
73                      We investigated whether genetic variability at this locus is a determinant of fr
74                        In the pooled sample, genetic variability at this locus was associated with di
75 ction with other recent studies showing that genetic variability at this same locus are related to ch
76                        There was substantial genetic variability between clinical and laboratory isol
77                                          The genetic variability between phenotypically distinct stra
78                                   Additional genetic variability between the seven B. subtilis 168 is
79 ive hybridization was employed to assess the genetic variability between two distinct clinical isolat
80  group A and group B RS viruses demonstrated genetic variability between years and within individual
81  the two primary threats are slow erosion of genetic variability by drift and short-term lowering of
82 However, female choice can actually increase genetic variability by supporting a higher mutation rate
83                 This study demonstrates that genetic variability can affect the outcome of cardiac su
84       Moreover, they show that intraspecific genetic variability can be as important as strong trophi
85                     With maternal selection, genetic variability can be maintained in the population
86  practice based on these recent discoveries, genetic variability clearly appears to affect pain perce
87 e Yellowstone grizzly bear has low levels of genetic variability compared with other Ursus arctos pop
88            The observed interactions between genetic variability, CVRFs, and MPV and its association
89 ence of a single genome does not reflect how genetic variability drives pathogenesis within a bacteri
90 rstly, it is responsible for the creation of genetic variability during meiosis by directing the form
91 kely to be responsible for the generation of genetic variability, even within inbred lines.
92             We sought to identify any common genetic variability exerting a large effect in risk for
93              We aimed to identify any common genetic variability exerting a moderate to large effect
94              Genotyping studies suggest that genetic variability exists among P. gingivalis strains;
95                             According to the genetic variability for carotenoids and tocochromanols,
96 ried widely and the genotypes presented high genetic variability for carotenoids and tocochromanols.
97 eders have increased the yield of this crop, genetic variability for conductance has allowed inadvert
98 lymorphisms to explore the full dimension of genetic variability for future cattle genomic research.
99 y a role in the expression of phenotypic and genetic variability for subsequent selection and evoluti
100 become ineffective owing to loss of additive genetic variability for the preferred traits.
101 likely than nonmutator phenotypes to acquire genetic variability from a more diverged set of donor ba
102                                    Extensive genetic variability, generally in gp120 and the gp41 ect
103                  These data show that common genetic variability has a role in the disease.
104    Vascular endothelial growth factor (VEGF) genetic variability has been associated with altered ris
105 how genome structure and pathogen population genetic variability has been shaped by transposable elem
106 uman brain, because tools for assessing this genetic variability have not been available.
107 rames encode enzymes which may contribute to genetic variability, i.e., restriction-modification syst
108 dies have provided information on how common genetic variability impacts on the risk for the developm
109 f GRN is regulated by miRNAs and that common genetic variability in a miRNA binding-site can signific
110     These results suggest that the amount of genetic variability in a population may be an important
111 strongest in Parkinson's disease (PD), where genetic variability in alpha-synuclein expression affect
112 s to hypothesize that it might contribute to genetic variability in ASFV.
113                  Our data show that there is genetic variability in beta-carotene metabolism and may
114              In summary, the distribution of genetic variability in C. quercuum fusiforme is consiste
115 ng, the molecular mechanism(s) through which genetic variability in Chrna7 may contribute to alpha7 n
116 eristics of the virus, including the extreme genetic variability in circulating viral isolates worldw
117        We propose a model where ASE requires genetic variability in cis, a difference in the sequence
118 herapy and suggest that detailed analysis of genetic variability in clinical trial cohorts can lead t
119                                        Thus, genetic variability in CTGF expression directly modulate
120 on wound biology has shown the importance of genetic variability in determining the initial inflammat
121                                              Genetic variability in DNM3 modifies age of onset for LR
122 rait loci (QTLs) were detected that underlay genetic variability in En Interestingly, four of them co
123 can be used as surrogate markers and whether genetic variability in germline ERBB2 (formerly HER2 or
124  trend, as well as the likely high degree of genetic variability in heat tolerance, suggests that mor
125  Despite this, there has been little work on genetic variability in human gene expression and almost
126               Recent claims that patterns of genetic variability in human mitochondria show evidence
127                                  Patterns of genetic variability in human populations are profoundly
128  humans and the mechanisms of maintenance of genetic variability in human populations, and for detect
129  background of myelination, the clinical and genetic variability in hypomyelinating leukodystrophies,
130 strate specific and differential patterns of genetic variability in inhibition of sucrose intake by d
131 ) are believed to contribute strongly to the genetic variability in living beings, in particular thei
132                  Statistical analysis of the genetic variability in mammary tumor latency indicated t
133 ence studies generally confirm the extensive genetic variability in modern maize is consistent with a
134 been an abundance of publications describing genetic variability in molecules relevant to transplant
135 he concomitant use of other drugs and common genetic variability in monoamine regulation present addi
136 e gene content, functional significance, and genetic variability in natural microbial communities.
137 polysaccharides) of triticale as well as the genetic variability in nutritional composition have been
138        These data indicate the importance of genetic variability in opioid modulation of sucrose inta
139 orphisms (tSNPs) accounting for > 92% of the genetic variability in PLA2G2A were identified and disti
140 ain the incidence of secondary infection and genetic variability in populations containing or lacking
141  natural selection has resulted in high CD36 genetic variability in populations of African descent.
142 relatively unbiased picture of the extent of genetic variability in protein sequences within populati
143 nts, platelet dysfunction can be a result of genetic variability in proteins that mediate inside-out
144        The molecular mechanisms that mediate genetic variability in response to alcohol are unclear.
145  Although recombination is a major source of genetic variability in retroviruses, no recombinant stra
146  been underway to control this parasite, but genetic variability in S. japonicum populations could re
147 uman EPHX2 mutations may in part explain the genetic variability in sensitivity to ischemic brain inj
148 for previously reported associations between genetic variability in serotonin transporter function an
149 f hypervariable genes can negate the lack of genetic variability in species such as B. anthracis and
150                Our analyses demonstrate that genetic variability in the alpha-synuclein gene is a ris
151                                   Therefore, genetic variability in the alpha2-macroglobulin gene is
152 Escherichia coli pathotypes reveal extensive genetic variability in the argW-dsdCXA island.
153                                              Genetic variability in the behavioral responses of exper
154 d the presence of the hmuR gene and revealed genetic variability in the carboxy terminus of hmuR in P
155           Together, these data indicate that genetic variability in the CRP gene is associated with s
156                             We conclude that genetic variability in the HNF-4gamma gene is unlikely t
157 rs in mice reveal an important potential for genetic variability in the imprinting process, and also
158 s novel insight into the association between genetic variability in the leptin gene and anemia in HIV
159 suggested that in many neurological diseases genetic variability in the loci predisposing subjects to
160                   Examination of the role of genetic variability in the long-term evolution of clades
161 c sequencing to evaluate the contribution of genetic variability in the pathogenesis of amyotrophic l
162 o warfarin was more strongly associated with genetic variability in the pharmacologic target of warfa
163  idea that they may serve as a reservoir for genetic variability in the PKD1 gene.
164                     The observed significant genetic variability in the response of wheat to heat str
165                            While the limited genetic variability in these animals prevents us from ma
166                           Here, we show that genetic variability in these regions can be explained by
167              Investigation of the effects of genetic variability in this gene on brain function could
168 s studies have targeted the contributions of genetic variability in this system to human brain activi
169                However, the contributions of genetic variability in this system to individuals' cogni
170  pulsed characters and the expected level of genetic variability in those control variables.
171 eflect an inducible mechanism that generates genetic variability in times of stress.
172 hese studies emphasize the potential role of genetic variability in transplantation, and provide the
173  exome, and Sanger sequencing to analyze the genetic variability in TREM2 in a series of 1092 patient
174 at genome size is negatively correlated with genetic variability, independent of phylogeny, body size
175                                              Genetic variability influences susceptibility to the pot
176 tions have been made that would suggest that genetic variability influencing allograft survival reach
177 controlled breeding practices has segregated genetic variability into distinct dog breeds that posses
178                                              Genetic variability is a hallmark of RNA virus populatio
179  used to detect biological pathways in which genetic variability is associated to variation in gene e
180 nding-oligomerization domain function due to genetic variability is associated with an increased susc
181   Therefore, knowledge of its DNA genome and genetic variability is central to preventing and treatin
182 ng individual organisms of which significant genetic variability is displayed.
183 a strongly discontinuous model for how human genetic variability is distributed and shows how individ
184                    We hypothesized that this genetic variability is driven by immune selection pressu
185 eletions (<1Kb), a significant proportion of genetic variability is due to copy number variation (CNV
186                                     Although genetic variability is known to greatly impact on the hu
187 bjected to regulation by naturally occurring genetic variability is of relevance for the understandin
188 accelerate bacterial adaptation when desired genetic variability is present within DNA fragments of u
189 or chaperone function in the context of high genetic variability is proposed.
190 lity and disease, and have shown that common genetic variability is unlikely to explain the entire ge
191 ene copy number variation, a major source of genetic variability, is important for several genes that
192 iduals extinguish conditioned fears, such as genetic variability, learning capacity and conditions un
193 is issue of Neuron, Cruchaga et al. identify genetic variability linked to altered levels of tau prot
194                                         Such genetic variability may be important for ACVr disease in
195                                         Host genetic variability may contribute to susceptibility of
196 is reasonable to expect that a wide range of genetic variability may exist given all of the different
197                      Although a high rate of genetic variability may facilitate viral escape and pers
198  activity based on drug-drug interactions or genetic variability may therefore influence glibenclamid
199 olerance to various stresses and loss of the genetic variability needed to correct that.
200 E on the offspring appear to be moderated by genetic variability, neurobehavioral disinhibition, and
201 t a single site that was on par with spatial genetic variability observed over distances of 15,000 km
202 ery little is known about the occurrence and genetic variability of (pro)phages within the Bifidobact
203 ty of a phiKMVvirus to dramatically increase genetic variability of a co-infecting phage), highlighti
204 ed by functional studies and analysis of the genetic variability of AGER in patients with CF.
205 specific drugs a nd vaccines is the study of genetic variability of allpublicly available HCV sequenc
206                  Almost all theories for the genetic variability of characters assume measurements on
207                        Here we report on the genetic variability of comC and comD within Streptococcu
208 e phenotypic and mutational spectrum and the genetic variability of DNAJC3, we analyzed 8,603 exomes,
209 ak similarities in many cases, suggestive of genetic variability of erp genes among these bacteria.
210                     We further estimated the genetic variability of gut microbes, with Bacteroides sp
211 mers or probe mismatches related to the high genetic variability of HDV and, possibly, to the complex
212 tudy this question making use of the natural genetic variability of human populations, which allows u
213                                     The host genetic variability of immune response to HIV and immune
214 viruses was used to assess the impact of the genetic variability of influenza A(H3N2) viruses on infl
215 butes in phenotypically relevant ways to the genetic variability of many organisms.
216 ructures of recently evolved halophytes, the genetic variability of model plants, and endemic halophy
217 s result is mirrored by field surveys of the genetic variability of natural strains of yeast.
218                                          The genetic variability of nine genes in 12 isolates and str
219                                Assessing the genetic variability of plant performance under heat and
220                                              Genetic variability of Plasmodium falciparum underlies i
221   We assessed the impact of the whole common genetic variability of PROX1 (80 SNPs) on type 2 diabete
222 rapies and vaccines that may bypass the wide genetic variability of RNA viruses.
223                   Here, we characterized the genetic variability of RSV during 5 seasons, and evaluat
224 eport, for the first time, we associated the genetic variability of SCN4A with the development of ess
225            Overall, our data reveal that the genetic variability of Seg-10/NS3 differentially modulat
226                                          The genetic variability of SIVsm strains among PCs may influ
227 r account for only a small proportion of the genetic variability of tested diseases.
228                                          The genetic variability of the ADIPOQ gene and circulating a
229              The differential regulation and genetic variability of the ALS genes results in a divers
230                            Here we show that genetic variability of the gene encoding PKCalpha (PRKCA
231                       We also predicted that genetic variability of the genes conferring resistance t
232 nderstanding of the population structure and genetic variability of the genus Mycobacterium, we condu
233                               Because of the genetic variability of the HIV-1 envelope glycoproteins
234                                              Genetic variability of the host may have large impact on
235 erogeneous disease such as HCM with the vast genetic variability of the human genome, and high freque
236                                 For example, genetic variability of the mu-opioid receptor (MOR)-enco
237               The present study examined the genetic variability of the PePHD in patients receiving I
238                                              Genetic variability of the PFam54 gene array suggests th
239 tion of the disease may be influenced by the genetic variability of the plcD region.
240                                   Levels and genetic variability of the PON1 position 192 isoforms (G
241                      Our study revealed high genetic variability of the S. epidermidis genome, new ma
242  this study, we focused our attention on the genetic variability of the TAS2R16 gene, encoding for on
243 (RSV) within communities may result from the genetic variability of the virus and associated evolutio
244 cine will need to overcome the extraordinary genetic variability of the virus, where most variation o
245  accomplishing these goals is the tremendous genetic variability of the virus, with some genes differ
246                                          The genetic variability of these isolates within phylogeneti
247 ium; however, the prevalence, expression and genetic variability of this protein in native marine mic
248        A multilocus genetic score reflecting genetic variability of this signature is associated with
249 on mutations within rdxA, possibly revealing genetic variability of this trait in C. jejuni due to sp
250 nown regarding the generation and effects of genetic variability of virus replication in the natural
251 used on epidemiological investigation of the genetic variability of well-documented strains of Y. pes
252  associated with GRN haploinsufficiency, and genetic variability on the wild-type GRN allele might ha
253 her evidence of the important role that host genetic variability plays in the determination of diseas
254                                              Genetic variability, population structure and gene flow
255                     To better understand the genetic variability present among pediatric strains and
256                               The remarkable genetic variability present within the species is reflec
257         Single-clone algal cultures (lacking genetic variability) produced short cycle periods and ty
258 known to be metabolized by enzymes with this genetic variability (range, P =.006-P<.001).
259               In worldwide populations, SNCA genetic variability remains the most reproducible risk f
260  targets contribute significantly to the non-genetic variability seen within and across individuals,
261 rvival of Egfrtm1Mag homozygous embryos, the genetic variability segregating within the outbred popul
262                  Our findings establish that genetic variability, smoking, and COPD all influence CST
263                                      The low genetic variability suggests that evolutionary pressure
264 which species are able to retain more useful genetic variability than they 'should', for example by e
265 d may serve as a mechanism for meningococcal genetic variability that avoids the fitness costs encoun
266 is circuitry may arise, in part, from common genetic variability that contributes to risk for MDD.
267 ed to use a genome-wide approach to identify genetic variability that directly affects LRRK2 Gly2019S
268        Recent work has emphasised the marked genetic variability that exists in the Fc receptor locus
269      In view of the pronounced antigenic and genetic variability that has been noted in the Osps of o
270  valuable in providing new insights into the genetic variability that is present in a particular spec
271                         Potential sources of genetic variability that may contribute to the disorder'
272 is driven by the advantages conferred by the genetic variability that results from transposition, in
273 nted by other researchers to identify common genetic variability that results in minor and moderate r
274  characterized by significant phenotypic and genetic variability the genetic matrix has a strong infl
275 sis; the classical vs balance hypothesis for genetic variability; the neutral theory of molecular evo
276 t transformation, but limitations imposed by genetic variability, tumor heterogeneity, availability o
277 ears offered a unique opportunity to examine genetic variability under natural conditions.
278                                 Knowledge of genetic variability underlying drug resistance and other
279  selection, which is predicted to reduce the genetic variability underlying such traits.
280                                              Genetic variability was also assessed, for sister pairs
281                                Although some genetic variability was detected among the five isolates
282                                         High genetic variability was found for En under both scenario
283                                              Genetic variability was measured in terms of polymorphis
284                                  The role of genetic variability was tested by comparing triploids ge
285 0 sequences from various BTV strains display genetic variability, we assessed the impact of different
286                                      Despite genetic variability, we found no difference in the sever
287 SNPs genotypes, explaining >92% of the locus genetic variability, were determined in 519 patients wit
288 he weight given to within- and between-breed genetic variability, were used in order to estimate the
289 xpansive growth to water deficit has a large genetic variability, which is higher than that of photos
290 inese chestnut C. mollissima had the highest genetic variability, while the American C. dentata had t
291  into the mechanistic and network effects of genetic variability, with improved statistical power to
292 opulations in T-705-treated mice had greater genetic variability, with more frequent transversion eve
293 y is reflected in substantial ecological and genetic variability within and among Trichinella taxa, a
294  mapping within the linkage region suggested genetic variability within DNM3 as an age-of-onset modif
295    The selected plants were cloned to reduce genetic variability within each genotype.
296 d comparative genomics provides a measure of genetic variability within natural populations and ident
297                                 The study of genetic variability within natural populations of pathog
298                                              Genetic variability within populations was high relative
299           TFV is a substrate for ABCC10, and genetic variability within the ABCC10 gene may influence
300                                              Genetic variability within the groups was assessed by re

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