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1.
Brain Inj ; : 1-8, 2024 Feb 08.
Artigo em Inglês | MEDLINE | ID: mdl-38328943

RESUMO

OBJECTIVE: The LIMBIC Military and Tactical Athletic Research Study (MATARS) framework was established to confirm and extend understanding of concussion with initial studies driven by clinical data collected between 2015 and 2020 in a collegiate sports setting. The LIMBIC MATARS framework will be leveraged to apply gold-standard and innovative research designs to advance the science of concussion. This manuscript provides the background, methodology, and initial demographic data associated with the LIMBIC MATARS. METHODS: Consensus-based common data elements were used to conduct a retrospective chart review, specific to collegiate athletes diagnosed with concussions between 2015 and 2020 at 11 universities. RESULTS: A final sample of 1,311 (47.8% female) concussions were diagnosed during the five-year study period from athletes participating in a variety of National Collegiate Athlete Association (NCAA) sports. The LIMBIC MATARS demographic data, align with the NCAA and other pioneering multi-site concussion-related studies in terms of biological sex, race and ethnicity, and sport participation. CONCLUSION: This pragmatic, methodological approach was used to address several a priori hypotheses related to concussion, align with other multi-site studies of concussion, and establish a consortium for future investigations.

3.
Braz. j. med. biol. res ; 44(4): 283-290, Apr. 2011. ilus, tab
Artigo em Inglês | LILACS | ID: lil-581495

RESUMO

Insertional mutagenesis is an important tool for functional genomics in Drosophila melanogaster. The insertion site in the KG00562 mutant fly line has been mapped to the CG8709 (herein named DmLpin) locus and to the 3’ of kermit (also called dGIPC). This mutant line presents a high lethality rate resulting from a gain of function. To obtain some insight into the biological role of the mutated locus, we have characterized the mutation and its relation to the high mortality of the KG00562 fly line. In this mutant, we did not detect one of the DmLpin transcripts, namely DmLpinK, but we did detect an unusual 2.3-kb mRNA (LpinK-w). Further investigation revealed that the LpinK-w transcript results from an aberrant splicing between the untranslated first exon of DmLpinK and the mini-white marker gene. Lack of DmLpinK or LpinK-w expression does not contribute to lethality, since heterozygous KG00562/Def7860 animals presented lethality rates comparable to those of the wild type. In contrast, the overexpression of kermit was associated with lethality of the KG00562 fly line. Significantly higher levels of kermit were detected in the Malpighian tubules of KG00562/+ flies that presented higher lethality rates than wild-type or KG00562/Def7860 animals, in which the lethality was rescued. In agreement with a recently reported study, our data support the hypothesis that misexpression of kermit/dGIPC could interfere with Drosophila development, with further investigations being needed in this direction.


Assuntos
Animais , Proteínas de Transporte/genética , Proteínas de Drosophila/genética , Drosophila melanogaster/genética , Expressão Gênica/genética , Mutação/genética , Transcrição Gênica/genética , Proteínas de Transporte/metabolismo , Proteínas de Drosophila/metabolismo , Túbulos de Malpighi/química , Fenótipo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transformação Genética
4.
Braz. j. med. biol. res ; 34(7): 851-859, July 2001. ilus
Artigo em Inglês | LILACS | ID: lil-298677

RESUMO

We extended the characterization of the DNA puff BhB10-1 gene of Bradysia hygida by showing that, although its mRNA is detected only at the end of the fourth larval instar, BhB10-1 expression is not restricted to the salivary gland, the tissue in which this gene is amplified. Different amounts of BhB10-1 mRNA were detected in other larval tissues such as gut, Malpighian tubules, fat body, brain and cuticle, suggesting that this gene is expressed differentially in the various tissues analyzed. Analysis of transgenic Drosophila carrying the BhB10-1 transcription unit and flanking sequences revealed that the tested fragment promotes transcription in a constitutive manner. We suggest that either cis-regulatory elements are missing in the transgene or factors that temporally regulate the BhB10-1 gene in B. hygida are not conserved in Drosophila


Assuntos
Humanos , Feminino , Drosophila/genética , Expressão Gênica , Animais Geneticamente Modificados , Northern Blotting , Larva , RNA Mensageiro/genética
5.
Braz. j. med. biol. res ; 22(6): 675-81, June 1989. ilus
Artigo em Inglês | LILACS | ID: lil-75156

RESUMO

1. A white Brazilian woman not of Asian origin was found to have Hb H disease of moderate severity. 2. Gene mapping demonstrated that the disease was caused by the association of two abnormal alfa-globin gene clusters on chromosome 16: one with a deletion which removed the two function alfa genes and the other carryng the 3.7-Kb rightward deletion, which leaves functional alfa gene. 3. These data ilustrate the necessity for systematic molecular approaches to the diagnosis of this heterogeneous group of diseases


Assuntos
Pessoa de Meia-Idade , Humanos , Feminino , Deleção Cromossômica , Cromossomos Humanos Par 16 , Talassemia/genética
6.
Braz. j. med. biol. res ; 25(8): 777-80, 1992. tab, ilus
Artigo em Inglês | LILACS | ID: lil-113568

RESUMO

A recombinant clone carrying a 2-kb fragment was isolated from a mini-library of the B10 DNA puff of Bradysia hygida. This fragment was amplified in the salivary gland during the period of DNA puff formation. Amplification started when DNA puff anlage was formed and continued to increase, reaching a maximum of abouth 10-fold 28 h later. Northern blot hybridization experiments showed that this 2-kb fragment was complementary to two RNA species of about 1.3 kb and 1.1 kb, which are developmentally regulated in the salivary gland. Maximum amounts of these messages were present when the B10 puff is fully expanded


Assuntos
Clonagem Molecular , DNA , Drosophila , Amplificação de Genes , Glândulas Salivares , Transcrição Gênica
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