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1.
J Appl Psychol ; 108(12): 1903-1923, 2023 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-37498711

RESUMO

Many women experience psychological and emotional challenges during their transition to becoming a working mother. Postpartum depression (PPD) is one common, salient aspect of motherhood that can serve as a work-life shock event and profoundly shape women's work and nonwork lives yet has evaded discussion in the organizational sciences. Taking a grounded theory approach, we interviewed 41 women who experienced PPD as well as key informants who provided additional insights about PPD (e.g., an obstetrician, women working for organizations that support postpartum health). Our analysis highlights how being diagnosed with PPD activates a complex sensemaking process in which women process an imposing identity-a concept we introduce to the identity and work-family literatures reflecting an unexpected, undesirable identity that imposes upon existing (e.g., work) and/or provisional identities that may or may not be fully elaborated (e.g., motherhood), ultimately shifting how women think about the intersection of work and family. We also delineate how supports and antisupports (i.e., overt acts dismissive of women's PPD) shape the aforementioned processes. Combined, our research aims to advance the discussion of PPD within organizational scholarship, rendering significant implications for both theory and practice. (PsycInfo Database Record (c) 2023 APA, all rights reserved).


Assuntos
Depressão Pós-Parto , Feminino , Humanos , Depressão Pós-Parto/diagnóstico , Depressão Pós-Parto/psicologia , Emoções
2.
J Appl Psychol ; 107(2): 240-262, 2022 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-33844565

RESUMO

Gratitude plays an integral role in promoting helping behavior at work. Thus, cultivating employees' experiences of gratitude represents an important imperative in modern organizations that rely on teamwork and collaboration to achieve organizational goals. Yet, today's workplace presents a complex array of demands that make it difficult for employees to fully attend to and appreciate the various benefits they receive at work. As such, gratitude is difficult for employers to promote and for employees to experience. Despite these observations, the role of attention and awareness in facilitating employees' feelings of gratitude is largely overlooked in the extant literature. In this study, we examined whether one notable form of present moment attention, mindfulness, may promote helping behavior by stimulating the positive, other-oriented emotion of gratitude. Across two experimental studies, a semiweekly, multisource diary study, and a 10-day experience sampling investigation, we found converging evidence for a serial mediation model in which state mindfulness, via positive affect and perspective taking, prompts greater levels of gratitude, prosocial motivation, and, in turn, helping behavior at work. We discuss the theoretical and practical implications of our investigation, as well as avenues for the future research. (PsycInfo Database Record (c) 2022 APA, all rights reserved).


Assuntos
Comportamento de Ajuda , Atenção Plena , Emoções , Humanos , Motivação , Local de Trabalho
3.
J Thorac Cardiovasc Surg ; 141(1): 34-8, 2011 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21092993

RESUMO

OBJECTIVE: In the cancer population, pericardial effusions are a common and potentially life-threatening occurrence. Although decompression benefits most patients, paradoxical hemodynamic instability (PHI) develops in some, with hypotension and shock in the immediate postoperative period. This study examines paradoxical hemodynamic instability after pericardial window and identifies prognostic factors in patients with cancer who are treated for pericardial effusion. METHODS: Retrospective review of 179 consecutive pericardial windows performed for pericardial effusion in a tertiary cancer center over a 5-year period (January 2004 through March 2009). Demographic, surgical, pathologic, and echocardiographic data were analyzed for the end points of paradoxical hemodynamic instability (pressor-dependent hypotension requiring intensive care unit admission) and overall survival. RESULTS: The most common malignancies were lung (44%), breast (20%), hematologic (10%), and gastrointestinal (7%). Overall survival for the group was poor (median, 5 months); patients with hematologic malignant disease fared significantly better than the others (median survival 36 months; P = .008). Paradoxical hemodynamic instability occurred in 19 (11%) patients. These patients were more likely to have evidence of tamponade on echocardiogram (89% vs 56%; P = .005), positive cytology/pathology (68% vs 41%; P = .03), and higher volume drained (674 mL vs 495 mL; P = .003). Overall survival was significantly shorter in those in whom paradoxical hemodynamic instability developed (median survival 35 vs 189 days; hazard ratio = 3; P < .001), and the majority of them (11/19, 58%) did not survive their hospitalization. CONCLUSIONS: Postoperative hemodynamic instability after pericardial window portends a grave prognosis. Evidence of tamponade, larger effusion volumes, and positive cytologic findings may predict a higher risk of paradoxical hemodynamic instability and anticipate a need for invasive monitoring and intensive care postoperatively.


Assuntos
Hemodinâmica , Neoplasias/complicações , Derrame Pericárdico/cirurgia , Técnicas de Janela Pericárdica , Adulto , Idoso , Distribuição de Qui-Quadrado , Feminino , Mortalidade Hospitalar , Humanos , Hipotensão/etiologia , Hipotensão/fisiopatologia , Estimativa de Kaplan-Meier , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Neoplasias/mortalidade , Neoplasias/fisiopatologia , Cidade de Nova Iorque , Derrame Pericárdico/etiologia , Derrame Pericárdico/mortalidade , Derrame Pericárdico/fisiopatologia , Técnicas de Janela Pericárdica/efeitos adversos , Técnicas de Janela Pericárdica/mortalidade , Modelos de Riscos Proporcionais , Estudos Retrospectivos , Medição de Risco , Fatores de Risco , Choque/etiologia , Choque/fisiopatologia , Taxa de Sobrevida , Fatores de Tempo , Resultado do Tratamento
4.
Biol Blood Marrow Transplant ; 17(8): 1182-6, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21182974

RESUMO

Hematopoietic stem cell transplantation (HSCT) represents an extended period of physiologic stress. It is unknown whether patients with pre-existing coronary artery disease (CAD) may be poor transplant candidates. There are no data analyzing the risk of transplantation in this population. Sixty-nine patients with CAD who underwent 72 transplantations, autologous and allogeneic, were identified retrospectively. Fifty-five percent of these patients had prior percutaneous coronary intervention, 42% had verifiable history of myocardial infarction, and 23% had prior coronary artery bypass grafting. Outcomes were compared to 1109 patients without established CAD who underwent 1183 transplants during the same time period. Cancer diagnoses in the 2 groups were similar, predominantly lymphoma, multiple myeloma, and leukemia. There was no significant difference between the CAD group and the control group with respect to type of transplant (autologous 68% versus 64%, P = .612, myeloablative 86% versus 85%, P = .867). Treatment-related mortality was no different in the CAD group versus the control group (5.6% versus 4.9%, P = .777), nor were there differences in mortality at 1 year (15.3% versus 16.6%, P = .871), urgent intensive care unit admission (11.1% versus 9.9%, P = .686), or length of stay (25.5 days versus 28.4 days, P = .195). These findings suggest many patients with underlying coronary artery disease may be safely managed through hematopoietic stem cell transplantation.


Assuntos
Doença da Artéria Coronariana/fisiopatologia , Transplante de Células-Tronco Hematopoéticas , Ponte de Artéria Coronária/métodos , Doença da Artéria Coronariana/cirurgia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Resultado do Tratamento
5.
PLoS One ; 4(3): e4759, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19277212

RESUMO

Duchenne muscular dystrophy (DMD) is an incurable neuromuscular degenerative disease, caused by a mutation in the dystrophin gene. Mdx mice recapitulate DMD features. Here we show that injection of wild-type (WT) embryonic stem cells (ESCs) into mdx blastocysts produces mice with improved pathology and function. A small fraction of WT ESCs incorporates into the mdx mouse nonuniformly to upregulate protein levels of dystrophin in the skeletal muscle. The chimeric muscle shows reduced regeneration and restores dystrobrevin, a dystrophin-related protein, in areas with high and with low dystrophin content. WT ESC injection increases the amount of fat in the chimeras to reach WT levels. ESC injection without dystrophin does not prevent the appearance of phenotypes in the skeletal muscle or in the fat. Thus, dystrophin supplied by the ESCs reverses disease in mdx mice globally in a dose-dependent manner.


Assuntos
Blastocisto , Células-Tronco Embrionárias/transplante , Terapia Genética/métodos , Distrofia Muscular Animal/terapia , Animais , Quimera , Distrofina/genética , Distrofina/fisiologia , Proteínas Associadas à Distrofina/análise , Transferência Embrionária , Feminino , Óperon Lac , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos mdx , Microinjeções , Músculo Esquelético/química , Músculo Esquelético/patologia , Músculo Esquelético/fisiopatologia , Distrofia Muscular Animal/embriologia , Distrofia Muscular Animal/patologia , Distrofia Muscular Animal/fisiopatologia , Distrofia Muscular de Duchenne , Regeneração
6.
Science ; 306(5694): 247-52, 2004 Oct 08.
Artigo em Inglês | MEDLINE | ID: mdl-15472070

RESUMO

We report that Id knockout mouse embryos display multiple cardiac defects, but mid-gestation lethality is rescued by the injection of 15 wild-type embryonic stem (ES) cells into mutant blastocysts. Myocardial markers altered in Id mutant cells are restored to normal throughout the chimeric myocardium. Intraperitoneal injection of ES cells into female mice before conception also partially rescues the cardiac phenotype with no incorporation of ES cells. Insulin-like growth factor 1, a long-range secreted factor, in combination with WNT5a, a locally secreted factor, likely account for complete reversion of the cardiac phenotype. Thus, ES cells have the potential to reverse congenital defects through Id-dependent local and long-range effects in a mammalian embryo.


Assuntos
Embrião de Mamíferos/citologia , Cardiopatias Congênitas/terapia , Coração/embriologia , Transplante de Células-Tronco , Células-Tronco/fisiologia , Animais , Blastocisto , Divisão Celular , Células Cultivadas , Proteínas de Ligação a DNA/genética , Perda do Embrião , Feminino , Perfilação da Expressão Gênica , Regulação da Expressão Gênica no Desenvolvimento , Cardiopatias Congênitas/embriologia , Proteína 1 Inibidora de Diferenciação , Proteína 2 Inibidora de Diferenciação , Fator de Crescimento Insulin-Like I/genética , Fator de Crescimento Insulin-Like I/fisiologia , Troca Materno-Fetal , Camundongos , Camundongos Knockout , Miocárdio/citologia , Miocárdio/metabolismo , Miócitos Cardíacos/citologia , Análise de Sequência com Séries de Oligonucleotídeos , Pericárdio/embriologia , Pericárdio/metabolismo , Gravidez , Proteínas Proto-Oncogênicas/genética , Proteínas Proto-Oncogênicas/fisiologia , Proteínas Repressoras/genética , Fatores de Transcrição/genética , Proteínas Wnt , Proteína Wnt-5a
7.
Cell Cycle ; 3(7): 923-30, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15190203

RESUMO

Centrosome is the major microtubule organizing center in mammalian cells that plays a critical role in a variety of cellular events by the microtubule arrays emanating from it. Despite its significance, the molecular mechanisms underlying the structure and function of the centrosome are still not clear. Herein we describe the identification of three isotypes of human ninein by expression library screening with autoimmune sera from CREST patients. All three ninein isotypes exhibit centrosomal localization throughout the cell cycle when GFP-tagged fusion proteins are expressed transiently in mammalian cells. Construction of serial deletions of GFP-tagged ninein reveals that a stretch of three leucine zippers with a flanking sequence is required and sufficient for centrosomal targeting. Overexpression of ninein results in mislocalization of gamma-tubulin, recruiting it to ectopic (noncentrosomal) ninein-containing sites which are not active in nucleating microtubules. In these cells, nucleation of microtubules from the centrosome is also inhibited. These results thus suggest a regulatory role for ninein in microtubule nucleation.


Assuntos
Autoantígenos/imunologia , Síndrome CREST/imunologia , Centrossomo/imunologia , Proteínas de Ligação ao GTP/imunologia , Centro Organizador dos Microtúbulos/imunologia , Microtúbulos/imunologia , Animais , Autoanticorpos/sangue , Autoanticorpos/imunologia , Autoantígenos/sangue , Autoantígenos/química , Síndrome CREST/sangue , Síndrome CREST/fisiopatologia , Centrossomo/metabolismo , Proteínas do Citoesqueleto , Proteínas de Ligação ao GTP/sangue , Proteínas de Ligação ao GTP/química , Proteínas de Fluorescência Verde/metabolismo , Células HeLa , Humanos , Zíper de Leucina/fisiologia , Camundongos , Centro Organizador dos Microtúbulos/metabolismo , Microtúbulos/metabolismo , Mitose/fisiologia , Dados de Sequência Molecular , Proteínas Nucleares , Isoformas de Proteínas/imunologia , Isoformas de Proteínas/metabolismo , Homologia de Sequência de Aminoácidos , Fuso Acromático/imunologia , Fuso Acromático/metabolismo , Tubulina (Proteína)/metabolismo
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