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71.
Forty-three women who had worked outside of the home prior to becoming pregnant and had returned to the same place of employment after the birth of their children participated in the study. To do so, they responded to a two-part questionnaire asking about their work lives (e.g., level of job satisfaction before, during, and after their pregnancies) and demographic characteristics (e.g., occupation). The results indicated that their job satisfaction was significantly greater before their pregnancies than either during or after their pregnancies. Job satisfaction during pregnancy had a significant, positive correlation with satisfaction with organizational maternity leave policies. Perceived reactions from women's coworkers and supervisors were also examined. Implications for these findings for organizations are discussed. Limitations of the study, and how they might be rectified in future research, are also addressed.  相似文献   
72.
Philosophical Studies - A number of recent theories of quantum gravity lack a one-dimensional structure of ordered temporal instants. Instead, according to many of these views, our world is either...  相似文献   
73.
Current debate in the metaphysics of time ordinarily assumes that we should be realists about time. Recently, however, a number of physicists and philosophers of physics have proposed that time will play no role in a completed theory of quantum gravity. This paper defends fictionalism about temporal thought, on the supposition that our world is timeless. We argue that, in the face of timeless physical theories, realism about temporal thought is unsustainable: some kind of anti-realism must be adopted. We go on to provide an argument against eliminativism about temporal thought. While it doesn't follow from this argument that fictionalism about temporal thought is true, we suggest that this nonetheless shows that fictionalism should be regarded as the preferred view.  相似文献   
74.
Philosophical Studies - Empirical work has lately confirmed what many philosophers have taken to be true: people are ‘biased toward the future’. All else being equal, we usually prefer...  相似文献   
75.
Sleep disturbances are very prevalent in children with developmental delay. Parental-assisted behavioral strategies have been used effectively in school-aged children; however, multimodal treatment for preschool-aged children is lacking. The current study is a preliminary investigation of the effectiveness of a parent group program called Sleepwise designed for young children with developmental delay and incorporating behavioral, communicative, and sensory strategies. Six parents attended three workshop sessions and implemented individualized treatment plans. Initial results revealed significant posttreatment reductions in child sleep disturbances and behavioral problems, with high treatment acceptability ratings by parents. Outcomes were generally maintained at 1-month follow-up.  相似文献   
76.
Previous theory and research suggest that childhood experiences are more likely to generate depressive self-schemas when they focus attention on negative information about oneself, generate strong negative affect, and are repetitive or chronic. Persistent peer victimization meets these criteria. In the current study, 214 youths (112 females) with empirically-validated histories of high or low peer victimization completed self-report measures of negative and positive self-cognitions as well as incidental recall and recognition tests following a self-referent encoding task. Results supported the hypothesis that depressive self-schemas are associated with peer victimization. Specifically, peer victimization was associated with stronger negative self-cognitions, weaker positive self-cognitions, and an elimination of the normative memorial bias for recall of positive self-referential words. Effects were stronger for relational and verbal victimization compared to physical victimization. Support accrues to a model about the social-developmental origins of cognitive diatheses for depression.  相似文献   
77.
Abstract

Background: Transgender stigma is rampant within healthcare systems in the United States. Transgender adults assigned female at birth – including those identifying as transmasculine or non-binary – face unique barriers, such as stigma when accessing sexual and reproductive healthcare labeled as being for “women.” However, transgender and non-binary people are not passive victims to this stigma, and the medical community would benefit from understanding the actions this population takes to resist and reduce transgender stigma in healthcare. Yet, little research has attempted to understand such actions.

Aims: This qualitative study aims to explore how transmasculine and non-binary adults are actively resisting and reducing the impact of transgender stigma in healthcare.

Methods: In-depth semi-structured interviews were conducted with 25 transmasculine and non-binary adults assigned female at birth who were living in a metropolitan area in the mid-Atlantic United States. The research team analyzed qualitative interview data using content analysis.

Results: The 25 participants ranged in age from 21 to 57, with an average age of 33?years old. Six themes were identified related to resisting and reducing transgender stigma in healthcare: (a) using social support; (b) persistence to meet one’s own needs; (c) avoiding mainstream healthcare; (d) advocacy; (e) doing one’s own research; and (f) strategic disclosure of transgender/non-binary identity. We detail how privilege and intersectionality connect to the use of these strategies.

Discussion: Findings indicate there is value in using peer advocates and peer health literacy; in developing and nurturing support groups related to transgender/non-binary health; in developing “allies” employed within the healthcare system; in creating and maintaining lists of culturally responsive health providers and resources about navigating the healthcare system; and in offering trainings related to self-advocacy and health-related activism. These findings can be used to inform future health prevention and intervention efforts with transmasculine and non-binary adults.  相似文献   
78.
Dysfunctions in memory recall lead to pathological fear; a hallmark of trauma-related disorders, like posttraumatic stress disorder (PTSD). Both, heightened recall of an association between a cue and trauma, as well as impoverished recall that a previously trauma-related cue is no longer a threat, result in a debilitating fear toward the cue. Glucocorticoid-mediated action via the glucocorticoid receptor (GR) influences memory recall. This literature has primarily focused on GRs expressed in neurons or ignored cell-type specific contributions. To ask how GR action in nonneuronal cells influences memory recall, we combined auditory fear conditioning in mice and the knockout of GRs in astrocytes in the prefrontal cortex (PFC), a brain region implicated in memory recall. We found that knocking out GRs in astrocytes of the PFC disrupted memory recall. Specifically, we found that knocking out GRs in astrocytes in the PFC (AstroGRKO) after fear conditioning resulted in higher levels of freezing to the CS+ tone when compared with controls (AstroGRintact). While we did not find any differences in extinction of fear toward the CS+ between these groups, AstroGRKO female but not male mice showed impaired recall of extinction training. These results suggest that GRs in cortical astrocytes contribute to memory recall. These data demonstrate the need to examine GR action in cortical astrocytes to elucidate the basic neurobiology underlying memory recall and potential mechanisms that underlie female-specific biases in the incidence of PTSD.

Recalling important information about salient environmental cues is an integral part of how we navigate our world. Recalling too much, or too little, information about salient environmental cues is a part of the psychopathology of posttraumatic stress disorder (PTSD) (Milad and Quirk 2012). More specifically, the augmented recall of an association between an environmental cue and a traumatic event results in debilitating fear toward the cue, even in the absence of any threat. In contrast, impoverished recall of information that a cue, previously associated with trauma, is no longer a threat also results in debilitating fear toward the cue after it is no longer dangerous. Therefore, one way to mitigate debilitating fear that characterizes PTSD is to understand the neurobiological mechanisms underlying memory recall.Among many mechanisms, glucocorticoid action via signaling through glucocorticoid receptors (GRs) is an important neurobiological pathway that underlies the recall of salient information. When trauma-associated cues are encountered, the hypothalamic-pituitary-adrenal axis is activated and GR signaling is consequently triggered (McEwen et al. 1988; McEwen 1992; Lupien et al. 2009). Existing literature demonstrates that glucocorticoids and GRs do in fact influence learning, memory, and the recall of learning (Pugh et al. 1997; de Quervain et al. 1998, 2009, 2011, 2017, 2019; Roozendaal 2002, 2003; Conrad et al. 2004; Hui et al. 2004; Donley et al. 2005; Roozendaal and de Quervain 2005; Cai et al. 2006; Soravia et al. 2006; Yang et al. 2006; Roozendaal et al. 2009; Bentz et al. 2010; Blundell et al. 2011; Clay et al. 2011; Nikzad et al. 2011; Roesler 2012; Liao et al. 2013; Wislowska-Stanek et al. 2013; Arp et al. 2016; Reis et al. 2016; Dadkhah et al. 2018; Inoue et al. 2018; Scheimann et al. 2019; Lin et al. 2020). The relationship between glucocorticoids, GRs, learning and memory is complicated and within the literature cited above, one can find examples of GR action being facilitatory as well as inhibitory to learning and memory recall. As expansive as this research is, the influence of GRs on learning, memory, and recall of learning has mostly focused only on GR action in neurons or has ignored cell type specific contributions. While glia are approximately as common as neurons in the nervous system (von Bartheld et al. 2016; von Bartheld 2018), the role of GRs in glial cells on the recall of salient environmental cues has been neglected. More specifically, while astrocytes comprise a significant proportion of the glial cell population (von Bartheld et al. 2016) and express GRs (Vielkind et al. 1990; Bohn et al. 1991), the influence of GRs in astrocytes on memory recall remains largely unappreciated (for one exception, see the Discussion).Our goal in this study was to determine the influence of GRs in astrocytes on memory recall. To do so, we combined the robust and reliable experimental framework of classical fear conditioning in rodents (Santini et al. 2008; Dias et al. 2014; Bukalo et al. 2015; Keiser et al. 2017; Giustino and Maren 2018; Greiner et al. 2019; Gunduz-Cinar et al. 2019; Venkataraman et al. 2019) with molecular genetic manipulations in the prefrontal cortex (PFC), a brain region critical for the recall of memory (Morgan and LeDoux 1995; Quirk et al. 2000; Mueller et al. 2008; Quirk and Mueller 2008; Giustino and Maren 2015; Rozeske et al. 2015; Maren and Holmes 2016). We first trained mice to associate tone presentations with mild footshocks. After this auditory fear conditioning, we used a CRE-loxP strategy to specifically knock out GRs in astrocytes in the PFC (hereafter termed cortical astrocytes) of these trained mice. We then exposed animals to extinction training: 30 presentations of the tone in the absence of any footshocks. Finally, 1 d after the extinction training, we exposed animals to two presentations of the tone. This experimental timeline allowed us to ask how a lack of GRs in cortical astrocytes influences (1) the recall of the previous aversive association of the tone presentation with the footshock, (2) the extinction of fear that would typically occur during extinction training, and (3) the recall of extinction training allowing us to measure the influence of GRs in cortical astrocytes on the recall of extinction training. Broadly, our results demonstrate that knocking out GRs in cortical astrocytes disrupts fear memory recall in both male and female mice, while only disrupting extinction recall in female mice.  相似文献   
79.
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