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1.
Rev Port Pneumol ; 10(4): 319-29, 2004.
Article in Portuguese | MEDLINE | ID: mdl-15492877

ABSTRACT

INTRODUCTION: Asthma, as a multifatorial disease, with high prevalence and frequent recurrence, attack people, independently of age, sex and geographical area. Because of lack of consensus about the definition of asthma, many questionnaires have been developed to standardize epidemiological criteria of suspicion and diagnosis. Among them, the European Community Respiratory Health Survey (ECRHS) is an important tool for prevalence studies on adults aged from 20 to 44 years old, that represented a methodological improvement of epidemiological surveys, turning them comparable about time and place. The objectives of this article are to comment the evolution of asthma concepts and its repercussion on epidemiological surveys, as well as to chronicle the tools used on these surveys, emphasizing the importance of ECRHS and presenting epidemiological data of asthma on 351 universitary hospital servers at Recife City -- Pernambuco -- Brazil.


Subject(s)
Asthma/epidemiology , Epidemiologic Research Design , Humans , Prevalence , Surveys and Questionnaires
2.
J Virol ; 75(10): 4705-12, 2001 May.
Article in English | MEDLINE | ID: mdl-11312342

ABSTRACT

It has previously been shown that the E7 protein from the cutaneous human papillomavirus type 1 (HPV1), which is associated with benign skin lesions, binds the product of the tumor suppressor gene retinoblastoma (pRb) with an efficiency similar to that of the E7 protein from the oncogenic HPV type 16. Despite this ability, HPV1 E7 does not display any activity in transforming primary cells. In addition, the two viral proteins differ in their mechanisms of targeting pRb. HPV16 E7 promotes pRb destabilization, while cells expressing HPV1 E7 do not show any decrease in pRb levels. In this study, we show that HPV1 E7, in contrast to HPV16 E7, has only a weak activity to neutralize the effect of cyclin-dependent kinase inhibitor p16INK4a. By generation of HPV1/16 E7 chimeric proteins, we have identified a central motif in the two E7 proteins, which determines their different abilities to overcome the p16INK4a-mediated cell cycle arrest. This motif is located downstream of the pRb-binding domain and comprises only three amino acids in HPV16 E7. Swapping this central motif in the two viral proteins causes an exchange of their activities involved in circumventing the inhibitory function of p16INK4a. Most importantly, our data show that the efficiency of the E7 proteins in neutralizing the inhibitory effect of p16INK4a correlates with their ability to promote pRb degradation.


Subject(s)
Cyclin-Dependent Kinase Inhibitor p16/metabolism , Oncogene Proteins, Viral/metabolism , Papillomaviridae/metabolism , Retinoblastoma Protein/metabolism , 3T3 Cells , Animals , Cell Division , Cyclin-Dependent Kinase Inhibitor p16/genetics , G1 Phase , Humans , Mice , Oncogene Proteins, Viral/genetics , Papillomaviridae/genetics , Papillomavirus E7 Proteins , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism
3.
Pediatr Neurol ; 13(3): 247-51, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8554663

ABSTRACT

A female patient with orofaciodigital syndrome type I associated with pachygyria, heterotopic gray matter, interhemispheric cyst, agenesis of the corpus callosum, and a Dandy-Walker anomaly is reported. Because some of these defects have been described in patients with different types of orofaciodigital syndromes, we recommend caution when using neuroradiologic criteria to separate these syndromes. Given the severe spectrum of brain abnormalities displayed by our patient, and considering their similarity with the brain defects formerly described in other X-linked dominant conditions with male lethality localized to Xp22, the use of DNA probes from Xp22 is advised in identifying the gene(s) causing orofaciodigital syndrome type I.


Subject(s)
Brain/abnormalities , Orofaciodigital Syndromes , Brain/pathology , Child , DNA Probes , Female , Humans , Male , Orofaciodigital Syndromes/classification , Orofaciodigital Syndromes/genetics , Orofaciodigital Syndromes/pathology
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