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1 tures as a shallow, irregular RPE elevation (SIRE).
2 tured by self-identified race and ethnicity (SIRE).
3 oup size and the number of offspring weaned (sired).
4 ome monitoring is recommended for those with SIRE.
5 r the markers that were polymorphic in their sire.
6 eek to maximise the number of offspring they sire.
7  continued offspring production from a given sire.
8 this system depends upon the genotype of the sire.
9 nd < 100 mum in height were subclassified as SIRE.
10 eneous racial categories and who had missing SIRE.
11  DLS-like and 51 also fulfilled criteria for SIRE.
12 sition compared to those from ewe and stable sire.
13 nty-four eyes (10.3%) were identified with a SIRE.
14 prenatally stressed (F2-S) or control (F2-C) sires.
15 sires but more daughters than sons via small sires.
16 ended from N-ethyl-N-nitrosourea-mutagenized sires.
17 ce born to N-ethyl-N-nitrosourea-mutagenized sires.
18 ed with WWII and the repeated use of popular sires.
19 ed ovaries and Y-sorted semen from two Angus sires.
20  absent in male offspring of cocaine-exposed sires.
21  embryos derived from high and low fertility sires.
22 bility of gametes from genetically desirable sires.
23 ating of Col1a2(oim/+) dams to Col1a2(oim/+) sires.
24 ly the male offspring of cocaine-experienced sires.
25 alysis of two SIRE-1 subclones revealed that SIRE-1 contains a long, uninterrupted, ORF between the 3
26                                              SIRE-1 is a family of several hundred dispersed copies o
27                 DNA sequence analysis of two SIRE-1 subclones revealed that SIRE-1 contains a long, u
28                            The assignment of SIRE-1 to the copia/Ty1 family was confirmed by comparis
29                                     A 2.4 kb SIRE-1-specific fragment was recovered from a soybean cD
30 arge, copia/Ty1-like retroelement designated SIRE-1.
31 ; DLS: 23% vs. no DLS 9.9%; SIRE: 22% vs. no SIRE 11%).
32 6 sexually active males; 1,227 reported they sired 2,323 pregnancies (69% live births, 1% stillbirths
33 ed twenty-seven male survivors reported they sired 2,323 pregnancies, and 1,915 female survivors repo
34 7% vs. no IE 6.3%; DLS: 23% vs. no DLS 9.9%; SIRE: 22% vs. no SIRE 11%).
35 8,140 genotyped Angus cattle including 7,486 sires, 72,688 dams and 205,966 offspring.
36    Our GIA calls were highly concordant with SIRE (95%) and aligned well with reference populations o
37 e not surgically sterile were less likely to sire a pregnancy than siblings (hazard ratio [HR], 0.56;
38  sired infants, and the most successful male sired a much lower percentage of infants (18%) than repo
39 ly associated with a decreased likelihood of siring a pregnancy (per 5000 mg/m(2) increments: HR 0.82
40      Compared with siblings, the HR for ever siring a pregnancy for survivors who had an AAD score =
41 re associated with a decreased likelihood of siring a pregnancy in male survivors of childhood cancer
42                   Among survivors, the HR of siring a pregnancy was decreased by radiation therapy of
43                             Risk factors for siring a pregnancy were evaluated using Cox proportional
44 -15), 2445 (62%) siblings reported having or siring a pregnancy, of whom 2201 (90%) individuals repor
45 ter, 4149 (38%) survivors reported having or siring a pregnancy, of whom 3453 (83%) individuals repor
46 n P. incarnata and explored the fruiting and siring ability of both flower types.
47 S (adjusted HR, 3.41; 95% CI, 2.26-5.14), or SIRE (adjusted HR, 2.83; 95% CI, 1.68-4.75).
48                            The same stallion sired all F(2)s such that the two full-sibling families
49 ized to test for statistical associations of sire alleles with progeny response to S. enterica serova
50 n of SD(+) spermatids so that SD/SD(+) males sire almost exclusively SD-bearing progeny rather than t
51 h aberrantly low TRDs that were all multiply sired, although the role this might play in natural popu
52 dicate that the probability that a male will sire an EPO in an available brood is the primary source
53  male to sire EPO, the male's probability of siring an EPO in an available brood and the number of of
54 ch effects: these are a t-test of the paired sire and dam pseudovalues from the jackknife procedure a
55 (mostly targeting Class I/Copia-Ivana- Copia-SIRE and LINEs elements).
56 o estimate hazard ratios for associations of SIRE and nSES with prostate cancer outcomes in the VA an
57                               The results of SIRE and PZA were 100% reproducible between the two inst
58 nificant at the genomewide level in both the sire and the dam-based analyses.
59 ecording schemes) were simulated to validate SIRE and to assess their impact on the precision, accura
60 bserved providing care for eggs they did not sire and which are not kin.
61 males with higher composite cognitive scores sired and raised more offspring.
62        The analysis included 1794 sons of 14 sires and 206 genetic markers distributed across all 29
63 that were increased in the sperm of stressed sires and associated with reduced hypothalamic-pituitary
64 the F1 offspring of alcohol-exposed C57Bl/6J sires and CD-1 dams do not exhibit fetal growth restrict
65 type were over-represented in offspring from sires and dams heterozygous for both LCAD and VLCAD muta
66 ted breeding values of 804 Holstein-Friesian sires and pertained to three bTB indicator traits: i) po
67 osomes 1, 2, 3, 5, 14, 18, 20 and 21) in the sires and progeny were genotyped for the markers that we
68 codes two cytochrome c synthetases (CcmF and SirE) and two apocytochrome c chaperones (CcmI and SirG)
69 and males on the number of offspring weaned (sired) and on the number of offspring weaned (sired) sur
70 setting, self-identified race and ethnicity (SIRE), and nSES.
71 IF), ethambutol (EMB) (collectively known as SIRE), and pyrazinamide (PZA) drug susceptibility testin
72  designs consisting of 2000 sons, 20 related sires, and their ancestors.
73 ing chromosome-wide significance in both the sire- and dam-based analyses in POP 1, and genome-wide s
74 ionately likely to share paternity when they sired any chicks.
75       Y chromosome diversity caused males to sire approximately 63% to approximately 98% female proge
76 gaster, the last male to inseminate a female sires approximately 80% of subsequent progeny.
77  and other biologic differences according to SIRE are frequently reported.
78                            Infected dams and sires are both able to transmit ZIKV to the offspring, m
79 rkoman lineage and that English Thoroughbred sires are largely responsible for the predominance of th
80 We introduce an experimental design in which sires are mated to multiple dams, some of which are unre
81 based on self-identified race and ethnicity (SIRE) are well documented, yet these variables have hist
82 ealizing the enormous potential of surrogate sires as a tool for dissemination and regeneration of ge
83 eriod, their 21 mothers, and all 24 possible sires) at 17 microsatellite marker loci and assigned pat
84                                       In the sire-based analysis, 1695 offspring with trait records a
85 as applied whereby QTL were detected using a sire-based linkage analysis, a sparse SNP marker map and
86                                 Initially, a sire-based QTL analysis was used to detect linkage group
87            These findings support the use of SIRES bicistronic vectors for a better assessment of the
88 ple dams, some of which are unrelated to the sire but others are genetically related owing to an arbi
89 s produce more sons than daughters via large sires but more daughters than sons via small sires.
90              Male AB6F1 (A/JCr dam x C57BL/6 sire) but not B6AF1 (B6 dam x A/J sire) mice developed s
91        Further, our workflow could expand on SIRE by (i) detecting the ancestry of patients that usua
92 and SB records from 90,393 primiparous cows, sired by 1122 bulls, distributed over 935 herd-calving y
93                                Using embryos sired by a heterozygous male, we demonstrate germline tr
94 a preferred male, and one when offspring are sired by a less preferred male.
95 s by the same female: one when offspring are sired by a preferred male, and one when offspring are si
96 nclude that female birds invest more in eggs sired by a preferred male, and raise the possibility tha
97  of female and castrated male pigs that were sired by boars represented by 4 breeds.
98                                The offspring sired by extrapair mates were no more fit in terms of re
99 in fertility, and almost 100% of female pups sired by G-AR(-/y) males younger than 15 weeks carried t
100 ins only from further investment in children sired by her son, and thus has less incentive to assist
101                                         Eggs sired by larger males are less vulnerable to predation (
102 IMA-specific Tregs expand during pregnancies sired by males expressing alloantigens with overlapping
103 ecause there is reduced viability of progeny sired by males with a checkpoint-activating defect in th
104 ng the performance of maternal half-siblings sired by males with different call durations.
105  highly polyandrous: 47% of 682 litters were sired by more than one male.
106               Moreover, heterozygous embryos sired by pi6(-/-) fathers show reduced viability in uter
107  in terms of recruitment than were half-sibs sired by social mates.
108  correlated with the proportion of offspring sired by that male.
109 oods, with fewer than 25% of offspring being sired by the caring male, although caring males sired pr
110 ly correlated with the proportion of progeny sired by the first male to mate relative to tester males
111 wn that fish nests often contain embryos not sired by the nest-tending male (because of cuckoldry eve
112 ng that outcrossed sibs within families were sired by the same father.
113 -generation full-sibling reference families, sired by the same stallion, in which there are 61 indivi
114 been inferred from the proportion of progeny sired by the second male in double-mating experiments [6
115  was found between the proportion of progeny sired by the second-mating male relative to tester males
116  male donors, they do not reject the fetuses sired by those same donors.
117        Paternity analysis within clutches co-sired by two males revealed that female preferences for
118                                              SIRE can be used as a screening tool on routine structur
119 ics of the embryo production system, and (3) sire can have a large effect on embryonic development be
120 ely explanation for observations of multiply sired clutches in marine turtles is that these are succe
121 s to cocaine and stress, we examined whether sire cocaine taking would influence fear-associated beha
122 legs from twenty lamb of different sexes and sires (colour stable and labile) were aged using in-bag
123 included 1102 Italian Brown Swiss bulls with sire conception rate records genotyped with 454k single
124                      Pasture trees had fewer sires contributing to mating events, but pollen dispersa
125 MP-responsive element-binding protein to the SIRE; (d) cotransfection of a human C/EBPbeta expression
126 GFP and RFP-labelled donor gonadal cells and Sire Dam Surrogate mating, we demonstrate that chicks de
127 lable from the half-sib pedigree design: the sire, dam and genotypic estimates.
128 cing data of a minimum of three individuals (sire, dam and offspring), RatesTools provides a list of
129                     Genotype analysis of the sire, dam, ten clinically unaffected siblings, and an af
130 wadays, the availability of genotyped trios (sire-dam-offspring) in the livestock industry enables th
131 lotype panel (128 haplotypes sampled from 32 sire/dam/offspring trios phased in a previous study) led
132           Approximately 29% of diploid males sired daughters, showing their ability to produce viable
133 ns found in the literature, when the between-sire degrees of freedom were small.
134  of study eyes (P < 0.001) with IE, DLS, and SIRE developed eMNV compared with those without these fe
135 pic strategy was to choose a single mouse to sire each generation using criteria designed to select a
136                                      Puddler-sired eggs contain 2 to 4 times more sodium than those c
137                           Longer-lived sperm sired embryos with increased survival and a reduced numb
138 umber of broods available to a focal male to sire EPO, the male's probability of siring an EPO in an
139 6J crosses, the offspring of alcohol-exposed sires exhibited fetal growth restriction, enlarged place
140  inherited the callipyge mutation from their sire express the phenotype.
141                            In summary, males siring extra-pair offspring in neighboring nests assist
142  dawn chorus, egg-laying and male success in siring extra-pair young, providing new evidence that art
143  subtle steric and electronic effects in the SiRe facial approach transition structure, which favor t
144 ce of selection and genetic background (n=33 sire families for GHR; n=14 sire families for NPY; n=36
145 es for GHR; n=14 sire families for NPY; n=36 sire families for GNRHR).
146 background (n=33 sire families for GHR; n=14 sire families for NPY; n=36 sire families for GNRHR).
147    Trait data from a total of 772 hens in 67 sire families from one generation of the pedigree dam li
148  < 0.05) negative substitution effects on US sire fertility (SCR).
149 R = 0.95) and of the substitution effects on sire fertility (SCR, R = 0.6) between the US and IL samp
150 vel genomic strategies for improving service sire fertility in Brown Swiss cattle.
151  unravel the genomic architecture underlying sire fertility in Holstein dairy cattle.
152 significant (p = 0.03) negative effect on IL sire fertility.
153 variants and biological processes underlying sire fertility.
154                     Furthermore, p53-/- mice sired fewer offspring than p53+/+ mice did when both gro
155 maintained on the same diet as their dam and sire for 6 months.
156 ved territories but still chose high-quality sires for their progeny.
157                     Remarkably, offspring of sires from both paternal stress groups displayed signifi
158                                         When sires from T. castaneum are mated to conspecific and het
159 espect to disease etiology or outcome across SIRE groups may not be meaningful; in fact, these differ
160                             Lamb from labile sire had significantly higher fat melting point than the
161                  Samples from ram and labile sire had significantly higher pH and saturated FAs and r
162 ating of Mstn(tm1Sjl/+) dams to Col1a2(oim/+)sires had a 15% increase in torsional ultimate strength,
163 drug-naive male offspring of cocaine-exposed sires have memory formation deficits and associated redu
164 hat are successful in sperm competition also sire healthy offspring.
165                                              SIRE implements a flexible Bayesian algorithm which acco
166 tomy, and YY males were significantly poorer sires in competition with their XY counterparts.
167 o for dams in female-pregnant species versus sires in male-pregnant species.
168  requires specific adjustment and the use of sires in the pedigree is only possible when mating of qu
169 x (homeodomain protein) IRES (abbreviated as SIRES) in place of the encephalomyocarditis (EMCV) IRES
170 aternal relatives of females with which they sired infants, and the most successful male sired a much
171 es lacking Heterochromatin Protein 1E (HP1E) sire inviable embryos that undergo catastrophic mitosis.
172 ntercrosses indicates that the effect of the sire is determined by the sperm genotype at Om or a locu
173 populations, the variation segregating among sires is greater than that found in an earlier study for
174 m and analyzed using both BD BACTEC MGIT 960 SIRE Kit and standard diffusion disk assays to identify
175      Matings between carrier dam and carrier sire led to a reduction of up to -203.46% in pregnancy s
176 l of our approach to address the ancestry of sire lines.
177                                              SirE located in the sir gene cluster is required for the
178 -living nematode species Rhabditis sp. SB347 sire &lt;5% male progeny.
179 will be F1s and first-generation backcrosses sired mainly by the outcrossing lineage, together with s
180  selectively increased in the NAc of cocaine-sired male (but not female) offspring.
181 oxidase (Dao1) in the hippocampus of cocaine-sired male progeny.
182 cial purebred lines, including three broiler sire (male) lines and two broiler dam (female) lines, we
183 erved in wild orangutans, infanticide by non-sire males has been predicted to occur due to their extr
184 rtality when compared to non-carrier dam and sire matings.
185  and determinants of disease on the basis of SIRE may be identified in these studies.
186  x C57BL/6 sire) but not B6AF1 (B6 dam x A/J sire) mice developed spontaneous insulin resistance, NAF
187 as males carrying Slx and Slxl1 duplications sire more female offspring, which directly correlates wi
188 l condition outcompete older males [2-8] and sire more infants [9-12].
189               Males carrying Slxl1 deletions sire more male offspring, whereas males carrying Slx and
190                                Sneaker males sire more offspring posthumously, indicating that sperm
191 male remates, and that the second males that sire more progeny either induce females to store and use
192 s is advantageous to both sexes: large males sire more young than small males, and large females have
193           Rare males acquired more mates and sired more offspring compared to common males and, as pr
194                    East-facing capitula also sired more offspring than west-facing capitula and under
195 d with perfumes mated with more females, and sired more offspring, than untreated, equal-aged, contro
196 tions revealed that conspecific pollen tubes sired more than 98% of seedlings.
197 converge on a small proportion of males that sire most young.
198 ond male to copulate with a female typically sires most of her offspring.
199                                  Because the SIRE motif is composed of a c/EBP binding site and a cAM
200 the genetic literature on polygamy rates and sire numbers per clutch in invertebrate animals that bro
201 iterature on rates of multiple paternity and sire numbers per clutch in viviparous fishes vs. mammals
202 tion via the stallion Nearctic (b.1954), the sire of the most influential stallion of modern time, No
203 ry associates are often, but not always, the sires of their current infants [16, 20-22].
204   The sterol-independent regulatory element (SIRE) of the LDL receptor (LDLR) promoter mediates oncos
205 isrupted Prm1 or Prm2 alleles, but failed to sire offspring carrying the 129 genome.
206       Finally, yellow-throated sneaker males sire offspring via secretive copulations and often share
207  hybrid males with motile sperm still cannot sire offspring.
208 some genes produced haploid male gametes and sired offspring after assisted reproduction.
209       TB-RBP-null male mice were fertile and sired offspring but had abnormal seminiferous tubules an
210                    Both hPRSS55 rescue lines sired offspring; RES GPI males exhibited partially resto
211 uality territories, pairing with females and siring offspring, than yearlings with intermediate pluma
212 ent attacks increase a male's probability of siring offspring.
213 d with an unrelated male, the unrelated male sired on average twice as many offspring as either broth
214                                 Inbred males sired only one-fifth as many surviving offspring as outb
215 erty; all 5 males and 4 females subsequently sired or delivered litters following transplantation.
216 ith sires potentiated USV after contact with sires or strange males.
217 sis, survivors had a decreased likelihood of siring or having a pregnancy versus siblings (male survi
218 lus a virgin female (aunt), their biological sire, or a castrated male.
219 e monoecious individuals was ~ 1/3 poorer at siring outcrossed offspring than pollen from monoecious
220 termine the number of offspring each subject sired over his lifetime and during the study period.
221  skew is high, with the most successful male siring over three times as many young as the next most s
222 rage %ViableSperm (54.7%) measured in an 860-sire population.
223 clearance events and open-pollinated progeny sired post-clearance.
224                             Pups reared with sires potentiated USV after contact with sires or strang
225                                              Siring probability also showed inbreeding depression and
226 ated additive genetic variance in extra-pair siring probability was larger, although the 95% credible
227            Failure of mab-23 mutant males to sire progeny is due primarily to defective sex muscle-me
228                    In contrast, male cocaine-sired progeny exhibited enhanced expression of cue-condi
229  proteins in the hippocampus of male cocaine-sired progeny, some of which were enhanced near the Dao1
230 as enhanced in female, but not male, cocaine-sired progeny.
231 ed by the caring male, although caring males sired proportionally more offspring in a given clutch th
232  analysis revealed that with few exceptions, SIRE provides unbiased, accurate parameter estimates ass
233 dkn1a expression in the accumbens of cocaine-sired rats.
234  cocaine self-administration in male cocaine-sired rats.
235                                              SIRE represents a new tool for analysing a wide range of
236 in a four-path selection model that included sire(s) of bulls (SB), sire(s) of cows (SC), dam(s) of b
237 n model that included sire(s) of bulls (SB), sire(s) of cows (SC), dam(s) of bulls (DB), and dam(s) o
238  among paternal parents if different parents sire seeds within an ovary.
239 , male morph flowers were more successful in siring seeds.
240 uciferase [rl]) placed between EMCV IRES and SIRES segments.
241             Introducing a 90 d delay between sire self-administration and breeding reversed both coca
242 nite NE-MNV, and all 6 graded positively for SIRE (sensitivity, 100%).
243 ng that OM induction is mediated through the SIRE sequence in conjunction with a strong activator bou
244 nc finger transcription factor Egr1 with the SIRE sequence in OM-stimulated HepG2 cells.
245         In vitro, the binding of Egr1 to the SIRE sequence is weak, but is strikingly enhanced in the
246                                          The SIRE sequence overlaps the previously described TATA-lik
247              Eyes whose OCT images display a SIRE sign are at higher risk of having subclinical NE-MN
248 fspring production from daughters to sons as sire size increases.
249 er we introduce a novel software tool called SIRE (standing for "Susceptibility, Infectivity and Reco
250 most consistent predictor of male extra-pair siring success across bird species, yet the mechanisms u
251 to ovule fertilisation, governing subsequent siring success and seed production.
252 class (yearling or older) on male extra-pair siring success is relative or absolute.
253   We tested this prediction by assessing the siring success of monoecious individuals of the plant Me
254                                              Siring success of non-CMS hermaphrodites was higher than
255  in a substantial increase in the extra-pair siring success of yearling males compared to the "contro
256                               Low extra-pair siring success of yearling males may be a consequence of
257 sults provide clear evidence that extra-pair siring success of yearlings can increase and that it dep
258                Alternatively, low extra-pair siring success of yearlings may be independent of the pr
259                                       Biased siring success was not the result of differential embryo
260            Differences in patterns of annual siring success were best explained by age-dependent patt
261 n because increased male allocation enhances siring success when eggs are abundant.
262 ired) and on the number of offspring weaned (sired) surviving to breeding age (two proxies of direct
263                       Aggressive culling and sire testing were used to minimize its prevalence; howev
264 received pollen from a far greater number of sires than trees within remnant forest.
265 icated that male, but not female, progeny of sires that self-administered cocaine displayed reduced c
266 ment in male, but not female, progeny of rat sires that self-administered cocaine.
267 ration in male, but not female, offspring of sires that self-administered cocaine.
268 Bdnf promoters was increased in the sperm of sires that self-administered cocaine.
269  as a sterol-independent regulatory element (SIRE) that is critically involved in OM-, transcription
270 te groups where the chance for the killer to sire the next infant is high.
271  in the other group animals were fertile and sired the normal number of pups/litter.
272 turally kill another male's pups so they can sire their own offspring.
273  2 to 4 times more sodium than those control-sired; this difference is already apparent in eggs laid
274 line transfer of nongenetic information from sire to offspring must include certain components, such
275 rafts showed the gene expression mediated by SIRES to be 4- and 8-fold higher, respectively, than EMC
276 was created by crossing four outbred broiler sires to dams of two highly inbred lines.
277 e sires to produce sons and sperm from small sires to produce daughters.
278                Females used sperm from large sires to produce sons and sperm from small sires to prod
279 ysis used only the offspring of heterozygous sires to reduce the influence of selection and genetic b
280               On average, male morph flowers sired twice as many seeds as hermaphroditic flowers.
281 splants, the recipient mice were fertile and sired up to 80 per cent of progeny from donor cells.
282                                The cKO males sired up to two litters but became infertile due to coll
283 ally as a self-identified race or ethnicity (SIRE) variable.
284 ere found to be significantly higher for the SIRES vectors than for the EMCV IRES vectors.
285  within a single ejaculate are equivalent at siring viable offspring.
286            The positive predictive value for SIRE was 25% and the negative predictive value was 100%.
287                               The absence of SIRE was identified in 209 of 227 eyes without NE-MNV (s
288 (Prlr) Prlr-IRES-Cre-tdtomato reporter mouse sires, we show that the circuitry activated during pater
289            Singleton pregnancies to a single sire were established by embryo transfer and thereafter
290                                              Sires were exposed during breeding and lactation.
291 evaluated, the Gal3 and Gal7 SNPs in broiler sires were found to be associated with antibody producti
292 m of cocaine- relative to saline-experienced sires were identified.
293 95 offspring with trait records and their 20 sires were successfully genotyped for the SNPs on the sp
294 ed males, including new alphas and rare beta sires, were disproportionately likely to share paternity
295 ating, as well as the total offspring number sired when males were second to mate were maximized at a
296  downstream tk gene is 12-fold greater using SIRES when compared with EMCV IRES.
297 anced in the male progeny of cocaine exposed sires, which also have BLA synaptic plasticity deficits.
298  the mutation inactivating both ACE isozymes sire wild-type and heterozygous offspring at an indistin
299 benefit from high-quality territories and/or sires with high-quality genes.
300 al behavior and the age at which males first sire young is unexpected.

 
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