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3 n family age at onset, r=0.22 individual and parental age at death, and r=0.32 individual and mean fa
4 n family age at onset, r=0.38 individual and parental age at death, and r=0.40 individual and mean fa
5 age at onset, r=0.58 between individual and parental age at death, and r=0.69 between individual and
6 death was significantly correlated with both parental age at onset and at death and with mean family
7 ath) or the GRN group (r=0.22 individual and parental age at onset, r=0.18 individual and mean family
8 her the C9orf72 group (r=0.32 individual and parental age at onset, r=0.36 individual and mean family
9 he MAPT group (r=0.45 between individual and parental age at onset, r=0.63 between individual and mea
10 per base pair per generation (at an average parental age of 7.5 yr), much lower than found in direct
11 s that the male mutation bias is stable with parental ages and cast further doubt on the assumption t
12 : (1) cancer and mutation spectra along with parental ages were similarly distributed; (2) ascertainm
14 , Dot1l maternal deletion did not affect the parental allele-specific expression of imprinted genes,
17 ed by differences in DNA methylation between parental alleles at specific regulatory elements known a
21 uplexes are packaged with an equal amount of parental and newly synthesized histones in the wake of t
22 Targeted cloning, mapping, and sequencing of parental and novel telomeric restriction fragments (TRFs
23 ns, disrupting previous correlations between parental and offspring environments, and interfering wit
24 monstrate the broad utility of using matched parental and transformed cells for small molecule inhibi
25 ng a series of genetic crosses that separate parental and zygotic contributions, we show that the H2A
29 ent, does not compromise the affinity of the parental antibody, and utilizes chemically stabilized si
31 or more reactions in the past 12 months and parental anxiety significantly predicted higher levels o
34 s a co-evolved system for credibly signaling parental attention to secondarily altricial infants.
35 or clpP2(-) knockdown strains but not in the parental bacteria, despite significant induction of hsp2
36 lly derived mimics of gliadin epitopes and a parental bacterial protein that is naturally processed b
39 hat parent-offspring conflict and associated parental benefits explain variation in fledging age amon
43 rmore, segregation analysis of F2 progeny of parental C57Bl/6N and Balb/C mice revealed that polymorp
45 portant role on the emergence of coordinated parental care and that considering environmental variabl
47 dy identified a number of nuclei involved in parental care in birds and suggests similar regulatory m
49 ic adaptive contexts such as mate selection, parental care, coalition signaling, and group cohesion.
51 ce-like preference evolved in the context of parental care, solitary species should not exhibit it.
52 ornamentation typically occurs in taxa with parental care, suggesting that selection arising from so
54 rying beetles under two different regimes of parental care: Some populations were allowed to supply p
56 on that circulating tumor cells resemble the parental cell line, but not lung-metastatic cells, sugge
61 internalized through integrins expressed in parental cells, in a tissue specific manner, as a key st
62 SR1 mutant cells were injected along with WT parental cells, tumor growth was enhanced with mutant ce
63 lls showed stronger E2F2 expression than the parental cells, while E2F2 inhibition sensitized the res
70 that ornamented plumage is favored by strong parental choice for chicks with more extreme ornamentati
71 ism further emphasizes the important role of parental chromatin in development and could provide the
73 ocal exchange of genetic information between parental chromosomes and is essential for fertility.
75 ajority of known epigenetic marks present in parental chromosomes during primordial germ cell develop
76 The exchange of genetic information between parental chromosomes in meiosis is an integral process f
77 e subtle morphological differences among the parental, circulating tumor cells, and lung metastatic c
78 ntative viruses of all three genotypes and a parental clade 2.3.2.1a strain (H5N1-R0) infected and re
79 gainst cancer cells and that activity of the parental clone, or functional avidity of selected gamma9
80 8% of the haploids in hybrids maintain their parental compartment status at B6/Cast divergent compart
84 hange, the weight of evidence indicates that parental conditioning over generations is not a panacea
87 in M. decorus, conform to the predictions of parental conflict: first, reciprocal F1s exhibit size di
91 gies to expand adolescent inclusion: waiving parental consent requirements, allowing adolescents to i
92 utions exhibiting higher expression than its parental construct (by a factor of 10) as well as the ab
94 parents; parental separation; bullying; and parental criminal conviction, with data collected on mul
97 pression or if the adoptive home experienced parental death or divorce during childhood/adolescence.
98 , and this effect is likely mediated both by parental depression and the continuity or disruption of
101 n forked DNA at 3.9 angstrom, revealing that parental DNA enters the ZF sub-ring and strand separatio
102 results complete the DNA path from entry of parental DNA into CMG to exit of daughter DNA from PCNA.
104 s (28%), reduction in open defecation (13%), parental education (10%), maternal nutrition (5%), econo
105 , economic improvement (19.5%), increases in parental education (14.9%), and better piped water acces
106 ed change in HAZ, with key factors including parental education (24.7%), maternal nutrition (19.3%),
111 ation on height at ages 1 to 69 years and on parental education were pooled allowing the analyses at
112 sts that the SES inequalities, in particular parental education, are related to global aspects of cor
113 with persistent differences across levels of parental education, household income, and household food
114 maternal and newborn health care, increased parental education, migration to urban areas, and reduce
116 , we evaluate the potential for sex-specific parental effects in a freshwater population of three-spi
118 associated with suicidal ideation, and that parental emotional support may be protective; (c) Adhere
119 rational plasticity or parental effects-when parental environments alter the phenotype of future gene
120 nisms cope with environmental stressors when parental environments are highly predictive of offspring
123 the nematode Caenorhabditis elegans and that parental exposure of animals to P. vranovensis promotes
125 dity involves transmission of the effects of parental exposure to the offspring through epigenetic ch
130 ses and controls, the two other studies used parental family history of Alzheimer's disease to define
132 adaptively and cause hybrids to fall between parental fitness peaks, with potential consequences for
134 ediates antitumor efficacy comparable to the parental FOLR1-TCB whereas a noncleavable control Prot-F
137 onse and avoided H/L ratio alteration in the parental generation exposed to high environmental temper
140 Here we map genomic interactions for each parental genome (including the X chromosome), using an o
142 isms, when the two pronuclei first meet, the parental genomes are separated by four pronuclear membra
143 na disassembly and subsequent merging of the parental genomes into a single nucleus after mitosis.
145 lterations are being examined in relation to parental gonadal dose, reconstructed using questionnaire
146 ncies, but the potential impact of assessing parental gonadal mosaicism has not been considered.
153 We sought to determine the association of parental history of atopic disease with AD in offspring.
154 t differ between subjects with and without a parental history of dementia, but were significantly cor
157 however, the effects are small compared with parental history, particularly for bipolar disorder.
158 s (DEGs) were identified in association with parental Holocaust exposure (FDR-adjusted p < 0.05); mos
161 and immune-related genes in association with parental Holocaust exposure with differential effects ba
163 brids were inferred in silico based on their parental inbred lines using single nucleotide polymorphi
165 n of pregnancy, the most specialized form of parental investment among vertebrates, is the rejection
166 indicative of an adaptive seasonal shift in parental investment in response to a deteriorating offsp
168 otypes differed from 2n = 28 chromosomes for parental Ixodes spp. ticks, and both increase and decrea
171 ants are 6, 10, and 14 mo of age can enhance parental language input and whether this, in turn, chang
173 ng a role for the chick ornamentation in the parental life-history strategy, perhaps as a reliable si
175 xation rates and photosynthetic induction in parental lines of a soybean nested association mapping (
180 ol achievement and resilience, and an intact parental marriage can substantially buffer these adverse
181 genotypes from this study can be targeted as parental materials to improve existing common bean germp
182 nvasive, and adhesive in vitro compared with parental MCF7 cells, and this phenotype was mediated by
183 gs, liver, and bone marrow, all derived from parental MDA-MB-231 triple-negative breast cancer cells.
184 monomineralic anorthosites appear to require parental melts saturated in plagioclase only but where a
185 emotional neglect; parental substance abuse; parental mental illness or suicide attempt; violence bet
186 ed by offspring sex and presence of reported parental mental illness, with adjustment for covariates.
188 ndividual mediators of this association were parental monitoring and involvement (indirect effect = 1
190 gned protective factors (positive parenting, parental monitoring and supervision, food security at ho
191 representing the pairwise combination of 11 parental monoclonal antibodies against CD73 was generate
192 Experimental down-regulation of Bsnd in the parental mouse strain phenocopied the severe cystic kidn
193 e first time, we show that CIMVs-MSCs retain parental MSCs phenotype (Sca-1(+), CD49e(+), CD44(+), CD
194 economic background, usage of eyeglasses and parental myopia was assessed by a questionnaire before v
196 divergent stress-induced mortality based on parental origin in mice with equivalent dystrophin expre
198 ant to embryonic reprogramming, resulting in parental origin-specific monoallelic gene expression.
200 persistence of POE varies between different parental pairs, perduring for at least 10 generations in
201 inantly cis controlled and largely reflected parental patterns, providing a genetic basis for inherit
203 s the quality of life (QOL) of children from parental perspective but little is known about the child
207 h after further mapping and validation in bi-parental populations will be useful for development of s
209 variables (i.e., sex of the exposed parent, parental posttraumatic stress disorder, age at Holocaust
210 tween families, to understand the context of parental preference and to determine whose fitness inter
213 The mechanisms that control how the two parental pronuclei fuse in the first mitosis of the embr
219 cohort based was undertaken using an online parental questionnaire, clinical visits including struct
226 2-month) visits were evaluated together with parental report of AD diagnosis by a health care provide
227 nea index and any aggregation parameter, but parental report of snoring was positively associated wit
229 ld employment configuration was derived from parental reports: both parents full-time, male-breadwinn
230 sex (typically males) commonly require more parental resources, these sex differences are not curren
232 posure in childhood/adolescence consisted of parental self-reports of smoking and participants' serum
233 r suicide attempt; violence between parents; parental separation; bullying; and parental criminal con
234 used Cre driver lines, in most cases with a parental sex bias related to Cre expression in sperm or
238 ts, cotinine <1.0 ng/mL); and 3) nonhygienic parental smoking (1-2 smoking parents, cotinine >=1.0 ng
239 g parents, cotinine <1.0 ng/mL); 2) hygienic parental smoking (1-2 smoking parents, cotinine <1.0 ng/
240 e persistent negative influences of prenatal parental smoking and youth substance use as they are mod
242 ons of this study include the self-report of parental smoking information and the possibility of resi
244 exposed, participants exposed to nonhygienic parental smoking were at higher risk of poor (lowest qua
245 re observed at both time points for prenatal parental smoking, life events, and negative affect and s
246 ors, such as early testosterone exposure and parental socialization, work together in the development
247 age at conception, maternal education level, parental socio-economic status, gestational age, breast-
250 RNA-Seq analyses were conducted on hexaploid parental species (S. alterniflora and S. maritima), thei
251 urally occurring hybrids as well as in their parental species and explore links between migratory tra
253 aches to analyze the differences between the parental species and the hybrids, and determined the ori
254 uch species hybridize, migratory traits from parental species can combine maladaptively and cause hyb
257 reduce genetic variation in daughter versus parental species, a common pattern is the recurrence of
261 development (score on the Wolke scale), and parental stimulation (Home Observation for Measurement o
265 eric proteins in which VacA m1 segments of a parental strain were replaced by corresponding m2 sequen
268 ical, or emotional abuse; emotional neglect; parental substance abuse; parental mental illness or sui
270 activation of EMT-related gene networks than parental Suit2 cells, and forced overexpression of ST6Ga
273 exual RNA replication mechanisms involve one parental template, whereas sexual RNA replication mechan
277 udied participants, examined associations of parental trauma-related variables (i.e., sex of the expo
278 ell lines was concordant with the respective parental tumor and characteristic for the respective tum
279 cancer cell able to propagate/phenocopy the parental tumor and recapitulate tumor heterogeneity.
281 and genomic profiles of their corresponding parental tumors is crucial when analyzing their biologic
282 The chromosomal aberration patterns of the parental tumors were largely maintained in the cell line
285 ng a steeper transcription gradient than the parental virus and generation of defective interfering R
286 timized, SHIV-AE16W proved comparable to the parental virus, and SHIV-325cH demonstrated markedly enh
299 f SHM that was reduced by half compared with parental WT Ramos B cells, demonstrating that the CTNNBL