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1.
Traffic Inj Prev ; 21(2): 127-132, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32154732

RESUMO

Objective: The main aim of this survey study was to evaluate the relative persuasiveness of three newly developed and piloted public education messages aimed at monitoring/reading social interactive technology on a smartphone among young male and female drivers. In accordance with the Step Approach to Message Design and Testing, the messages were evaluated on a number of outcome measures and also explored the influence of self-reported involvement in the target behavior.Methods: Participants (N = 152; 105 F) were aged 17 to 25 years (Mage = 20.14 years, SD = 2.35) and were randomly allocated to either an intervention (one of the three messages) or control (no message) condition. The messages in the intervention group were assessed on acceptance (i.e., behavioral intention and message effectiveness), rejection, and the third person effect (TPE) differential score (i.e., the message is perceived to be more effective for others than for themselves).Results: Hierarchical regression analyses found that, compared to males, females reported: a) lower intention to monitor/read social interactive technology on a smartphone while driving, b) lower rejection; and, c) lower TPE likelihood, irrespective of message.Conclusions: These findings suggest that young male drivers and young female drivers require different message content to be effective and support the importance of including multiple outcome measures to explain the messages' persuasive effects.


Assuntos
Condução de Veículo/psicologia , Educação em Saúde/métodos , Smartphone , Adolescente , Adulto , Feminino , Humanos , Intenção , Masculino , Comunicação Persuasiva , Fatores Sexuais , Inquéritos e Questionários , Adulto Jovem
2.
Br J Ophthalmol ; 90(8): 955-6, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16774959

RESUMO

BACKGROUND/AIMS: Vitamin A deficiency, often presenting with nyctalopia, has been described in a number of patients with malabsorption as a result of intestinal bypass surgery and, more recently, bariatric surgery. In these reports vitamin A deficiency developed within several years of gastric or intestinal surgery. Three patients who developed decreased vision from vitamin A deficiency more than 18 years after their intestinal surgery are reported. METHODS: A retrospective review of the clinical findings of all patients diagnosed with vitamin A deficiency, as confirmed by serological testing, over the past year in a single neuro-ophthalmic practice. RESULTS: Four patients with vitamin A deficiency were seen, three of whom had intestinal surgery more than 18 years before the development of visual symptoms. CONCLUSION: The authors suggest that vitamin A deficiency should be suspected in patients with unexplained decreased vision and a history of intestinal surgery, regardless of the timing of the surgical procedure.


Assuntos
Derivação Jejunoileal/efeitos adversos , Síndrome do Intestino Curto/complicações , Deficiência de Vitamina A/etiologia , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Intestino Delgado/cirurgia , Masculino , Estudos Retrospectivos , Fatores de Tempo , Transtornos da Visão/etiologia
3.
Neuron ; 18(1): 29-42, 1997 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-9010203

RESUMO

The adult mammalian cortex is characterized by a distinct laminar structure generated through a well-defined pattern of neuronal migration. Successively generated neurons are layered in an "inside-out" manner to produce six cortical laminae. We demonstrate here that p35, the neuronal-specific activator of cyclin-dependent kinase 5, plays a key role in proper neuronal migration. Mice lacking p35, and thus p35/cdk5 kinase activity, display severe cortical lamination defects and suffer from sporadic adult lethality and seizures. Histological examination reveals that the mutant mice lack the characteristic laminated structure of the cortex. Neuronal birth-dating experiments indicate a reversed packing order of cortical neurons such that earlier born neurons reside in superficial layers and later generated neurons occupy deep layers. The phenotype of p35 mutant mice thus demonstrates that the formation of cortical laminar structure depends on the action of the p35/cdk5 kinase.


Assuntos
Córtex Cerebral/patologia , Córtex Cerebral/fisiopatologia , Quinases Ciclina-Dependentes , Neurônios/fisiologia , Proteínas Serina-Treonina Quinases/genética , Convulsões/genética , Animais , Córtex Cerebral/embriologia , Cruzamentos Genéticos , Quinase 5 Dependente de Ciclina , Desenvolvimento Embrionário e Fetal , Deleção de Genes , Biblioteca Genômica , Humanos , Camundongos , Camundongos Knockout , Camundongos Mutantes Neurológicos , Fases de Leitura Aberta , Reação em Cadeia da Polimerase , Proteínas Serina-Treonina Quinases/metabolismo , Recombinação Genética , Convulsões/patologia , Convulsões/fisiopatologia
4.
Nature ; 371(6496): 419-23, 1994 Sep 29.
Artigo em Inglês | MEDLINE | ID: mdl-8090221

RESUMO

Cyclin-dependent kinase 5 (Cdk5) was originally isolated through its structural homology to human Cdc2, a key regulator of cell-cycle progression. In tissue samples from adult mice, Cdk5 protein is found at the highest level in brain, at an intermediate level in testis, and at low or undetectable levels in all other tissues, but brain is the only tissue that shows Cdk5 histone H1 kinase activity. No equivalent kinase activity has been found in tissue culture cell lines despite high levels of Cdk5. This raised the possibility that a Cdk5 regulatory subunit was responsible for the activation of Cdk5 in brain. Here we describe the cloning and characterization of a regulatory subunit for Cdk5 known as p35. p35 displays a neuronal cell-specific pattern of expression, it associates physically with Cdk5 in vivo and activates the Cdk5 kinase. p35 differs from the mammalian cyclins and thus represents a new type of regulatory subunit for cyclin-dependent kinase activity.


Assuntos
Quinases Ciclina-Dependentes , Proteínas do Tecido Nervoso/metabolismo , Neurônios/enzimologia , Proteínas Serina-Treonina Quinases/metabolismo , Sequência de Aminoácidos , Animais , Sequência de Bases , Bovinos , Células Cultivadas , Sistema Nervoso Central/embriologia , Sistema Nervoso Central/enzimologia , Córtex Cerebral/citologia , Córtex Cerebral/enzimologia , Clonagem Molecular , Quinase 5 Dependente de Ciclina , DNA , Embrião de Mamíferos , Ativação Enzimática , Humanos , Camundongos , Dados de Sequência Molecular , Proteínas do Tecido Nervoso/genética , Proteínas Serina-Treonina Quinases/química , Proteínas Serina-Treonina Quinases/genética , Transfecção , Células Tumorais Cultivadas
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