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1 Lateralized behavior was strongly sex related.
2 ins were developmental stage-specific and/or sex-related.
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.
13 o understand the genetic, environmental, and sex-related determinants of age-related hearing loss and
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
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
26 identified significant behavioral and neural sex-related differences in association with a computer-b
34 aim of this study was to determine possible sex-related differences in brain responses to a visceral
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
47 We wished to test previous hypotheses that sex-related differences in mortality and morbidity may b
49 his article describes recent developments in sex-related differences in opioid (morphine) pharmacodyn
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.
58 regeneration potential may arise from innate sex-related differences in the cells' stress responses.
62 al studies have reinforced the importance of sex-related differences in the pathogenesis of cardiovas
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,
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.
73 e aim of this study was to determine whether sex-related differences occur in counterregulatory respo
75 on estrogen, do not play a major role in the sex-related differences of the mouse meibomian gland.
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
87 neurodevelopmental conditions whose striking sex-related disparity (with an estimated male-to-female
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
92 al processes has much potential to elucidate sex-related factors associated with neurological and psy
95 cally induced in zygotes; furthermore, these sex-related gene sets were enriched for secretory pathwa
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
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
107 ht heart catheterization to measure age- and sex-related normative responses of pulmonary capillary w
109 1997, 216 physicians (39.9%) disciplined for sex-related offenses between 1981 and 1994 were licensed
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
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
120 ine the prevalence of HFE mutations, age and sex-related penetrance of different HFE genotypes, inter
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
128 ve dosing in women, up to one fourth of this sex-related risk difference in bleeding is avoidable.
130 uman systemic lupus erythematosus, including sex-related survival differences; female MRL-lpr/lpr mic
133 However, the epidemiological impacts of sex-related variation in animal contact networks have ra
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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