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1            Lateralized behavior was strongly sex related.
2 ins were developmental stage-specific and/or sex-related.
3 cuit led to dis-inhibition or elimination of sex-related aggression, respectively.
4       Additionally, significant decreases in sex-related alcohol consumption were observed in both gr
5 etermining loci affect the evolution of both sex-related and non-sex-related genes.
6  responsible for the initial average bias in sex-related beliefs and for a bias in updating expectati
7 e that prenatal stress can induce long-term, sex-related changes in the sensitivity of the cardiovasc
8 ribute to human gender development, and most sex-related characteristics are influenced by socializat
9 ic gene expression pattern data reveal clear sex-related characteristics, indicative of an unambiguou
10 al antagonism, calls for a unified theory of sex-related chromosome evolution, incorporating, for exa
11 e gender identity, and some, though not all, sex-related cognitive and personality characteristics.
12        The authors conclude that a specific, sex-related cytoarchitectural SDApc parameter shows left
13 o understand the genetic, environmental, and sex-related determinants of age-related hearing loss and
14 osis (CF); however, a mechanism to explain a sex-related difference has remained elusive.
15 were reported (21 men and 26 women), with no sex-related difference in age of diagnosis (51.5 vs 56.5
16 ibution showed inconsistent results, and any sex-related difference in disease risk has not been adeq
17                                 However, the sex-related difference in risk of all-cause events was m
18                                         This sex-related difference may reflect differences in health
19                                           No sex-related difference was present.
20 D) RE was -0.52 (2.95) diopters (D), with no sex-related difference.
21 otential confounding with typically observed sex-related differences (e.g., body composition), predic
22 tions than men, but the mechanisms for these sex-related differences and the impact of hormone therap
23 This study was designed to determine whether sex-related differences exist in methionine cycle kineti
24 ults demonstrate that significant (P < 0.05) sex-related differences exist in the expression of numer
25                                              Sex-related differences exist in the structure and funct
26 identified significant behavioral and neural sex-related differences in association with a computer-b
27                     Numerous reports suggest sex-related differences in atherosclerosis.
28                                              Sex-related differences in basal right ventricular endoc
29                                              Sex-related differences in behavior are extensive, but t
30   The contribution of dosing to the observed sex-related differences in bleeding is unknown.
31           In addition, there are significant sex-related differences in body composition and in the c
32                                              Sex-related differences in body composition were narrowe
33 ted differences in medication adherence, and sex-related differences in body size.
34  aim of this study was to determine possible sex-related differences in brain responses to a visceral
35                                      We find sex-related differences in communication patterns in a l
36  anatomic basis and/or mechanism(s) of these sex-related differences in COPD are unknown.
37 pioid receptor distribution and for age- and sex-related differences in delta opioid receptor densiti
38     Our objectives were to evaluate age- and sex-related differences in events among LQTS patients re
39 s a potential disease modifier that underlie sex-related differences in FSHD by protecting against my
40   In addition, the influence of aromatase on sex-related differences in gene expression is predominan
41 mones seem to contribute little to the known sex-related differences in gene expression of the lacrim
42 hese findings provide the first insight into sex-related differences in IBS subjects compared with HC
43 r third ventricles than men, consistent with sex-related differences in intracranial volume.
44                                     Age- and sex-related differences in LAA dimensions exist.
45                     In contrast, significant sex-related differences in leucine flux (P < 0.02) were
46 th-related phenotypes and even contribute to sex-related differences in longevity.
47   We wished to test previous hypotheses that sex-related differences in mortality and morbidity may b
48                                     Age- and sex-related differences in neuron number are negligible.
49 his article describes recent developments in sex-related differences in opioid (morphine) pharmacodyn
50                 This study sought to examine sex-related differences in outcomes related to periphera
51                                        These sex-related differences in PAD risk also differed by age
52 l cross-sectional area could be explained by sex-related differences in paraspinous musculature.
53  of the factors contributing to the observed sex-related differences in platelet biology is warranted
54 ilize a community-based approach to identify sex-related differences in risk factors for sudden cardi
55 tors impact observed age-related changes and sex-related differences in skeletal muscle metabolism.
56                                           If sex-related differences in survival are independent of p
57                            We aimed to study sex-related differences in temporal trends in short- and
58 regeneration potential may arise from innate sex-related differences in the cells' stress responses.
59                                              Sex-related differences in the developmental trajectory
60                                              Sex-related differences in the frequency power distribut
61         Our results may suggest there may be sex-related differences in the myocardial response to is
62 al studies have reinforced the importance of sex-related differences in the pathogenesis of cardiovas
63             This distinct phenotype suggests sex-related differences in the pathophysiology of athero
64                                              Sex-related differences in the perception and modulation
65 iew is to provide a summary of the principal sex-related differences in the presentation, clinical co
66 f the literature and meta-analyses estimates sex-related differences in the prevalence of periodontit
67   These findings support our hypothesis that sex-related differences in the salivary glands are due,
68                                There were no sex-related differences in these response patterns.
69 e of this study was to clarify the impact of sex-related differences in transcatheter aortic valve im
70 ivo to help elucidate the molecular basis of sex-related differences in transcription, which are wide
71 erences in response to treatment, suggesting sex-related differences in underlying pathophysiology.
72                 Distinguishing familial from sex-related differences may facilitate efforts to unders
73 e aim of this study was to determine whether sex-related differences occur in counterregulatory respo
74 ogen biosynthesis, plays a major role in the sex-related differences of the meibomian gland.
75 on estrogen, do not play a major role in the sex-related differences of the mouse meibomian gland.
76               However, little is known about sex-related differences related to PVI procedures.
77                                              Sex-related differences should be taken into account to
78                               No significant sex-related differences were found in fasting homocystei
79 ter or genetic eNOS deficiency abolished the sex-related differences.
80 y controls (HCs) and to identify the role of sex-related differences.
81 ersensitive sites, with 1,284 showing robust sex-related differences.
82 ing exercise capacity and impact on age- and sex-related differences.
83                    There were no significant sex-related differences.
84 t of insulin-like peptide (ILP) signaling in sex-related differentiation processes is attracting incr
85  findings add substance to the view that the sex-related dimension of symmetry/asymmetry is integral
86  CF, although the mechanisms underlying this sex-related disadvantage are unknown.
87 neurodevelopmental conditions whose striking sex-related disparity (with an estimated male-to-female
88                The basis for this intriguing sex-related distinction is unknown.
89 ability estimates as a function of normative sex-related diversity in brain structure, as well as neu
90 es for fat-free mass tended to attenuate the sex-related effect (P = 0.08), adjustment for muscle mas
91                                      Because sex-related effects influence treatment goals, treatment
92 al processes has much potential to elucidate sex-related factors associated with neurological and psy
93           This study therefore suggests that sex-related factors influence the RA penetrance associat
94                                          The sex-related factors involved in the disease are not know
95 cally induced in zygotes; furthermore, these sex-related gene sets were enriched for secretory pathwa
96             It has been widely observed that sex-related genes are copied from sex chromosomes and in
97  regions that control the expression of many sex-related genes, including Sry (sex-determining region
98 ence and expression of apparently functional sex-related genes, the distribution of mating-type genes
99 ct the evolution of both sex-related and non-sex-related genes.
100 sfers, conservation and evolutionary rate of sex-related genes.
101  months, 2.17 [3.88] vs 3.73 [6.86]) but not sex-related HIV risk behaviors and in a lower severity s
102 portion of all disciplinary orders that were sex related increased from 2.1% in 1989 to 4.4% in 1996
103 ediated acute inflammation and an unexpected sex-related involvement in PAF-induced anaphylaxis.
104  Strikingly, microsporidian genomes harbor a sex-related locus with the same genes in the same order.
105 in structure and to identify the patterns of sex-related neuroanatomical variability associated with
106                                        Major sex-related neuroendocrine changes take place during pub
107 ht heart catheterization to measure age- and sex-related normative responses of pulmonary capillary w
108                                     Age- and sex-related occurrence of events was analyzed in 479 pro
109 1997, 216 physicians (39.9%) disciplined for sex-related offenses between 1981 and 1994 were licensed
110    A total of 761 physicians disciplined for sex-related offenses from 1981 through 1996.
111 umber of physicians disciplined per year for sex-related offenses increased from 42 in 1989 to 147 in
112  the discipline of physicians who commit any sex-related offenses is an important public health issue
113            Discipline against physicians for sex-related offenses is increasing over time and is rela
114                               Discipline for sex-related offenses was significantly more severe (P<.0
115 h all physicians, physicians disciplined for sex-related offenses were more likely to practice in the
116 nificantly more severe (P<.001) than for non-sex-related offenses, with 71.9% of sex-related orders i
117  for non-sex-related offenses, with 71.9% of sex-related orders involving revocation, surrender, or s
118 eference curves exhibit established age- and sex-related patterns of development, including dramatic
119 (1.28, 0.98-1.66), without clear allergy- or sex-related patterns.
120 ine the prevalence of HFE mutations, age and sex-related penetrance of different HFE genotypes, inter
121 vation places ILP signaling at the center of sex-related phenomena in early animal development.
122 robability of ASD as a function of normative sex-related phenotypic diversity in brain structure and
123 highlight the need for considering normative sex-related phenotypic diversity when determining an ind
124 ated genes suggests the existence of cryptic sex-related processes.
125 le of the rapid evolution that characterizes sex-related proteins in numerous lineages.
126          Our data suggest a complex age- and sex-related regulation of adiponectin secretion or clear
127 ale urine sniffing test (FUST), a measure of sex-related reward-seeking behavior.
128 ve dosing in women, up to one fourth of this sex-related risk difference in bleeding is avoidable.
129                               We assessed if sex-related survival difference following community-acqu
130 uman systemic lupus erythematosus, including sex-related survival differences; female MRL-lpr/lpr mic
131 er than the majority of genes coding for non-sex-related traits.
132        We support research that investigates sex-related variables in hypothesis-driven studies of an
133      However, the epidemiological impacts of sex-related variation in animal contact networks have ra
134            This highlights the importance of sex-related variation in host behaviour when managing an
135                         However, many of the sex-related variations in biological process, molecular
136  and genotype-specific; however, many of the sex-related variations in gene ontologies and KEGG pathw
137 The following variables were examined: donor sex, related versus nonrelated donation, operative time,

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