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1.
Genet Mol Res ; 15(1): 15017593, 2016 Mar 04.
Artigo em Inglês | MEDLINE | ID: mdl-26985938

RESUMO

The extracellular matrix (ECM) is the major macromolecule in skeletal muscle, which affects meat quality greatly. The remodeling of the ECM is mainly regulated by matrix metalloproteinases (MMPs). The expression patterns of MMP-1, -2, and -8 in longissimus dorsi muscle were explored using quantitative real-time polymerase chain reaction. The results show that the expression of MMP-1, -2, and -8 decreased significantly from 135 days of pregnancy to postnatal 30 months. While the expression of MMP-1, -2, and -8 showed no significant relationships with intramuscular fat contents, MMP-1 and -2 showed significant negative correlations with the shearing force of the longissimus dorsi muscle in cattle. The expression of MMP-1 also showed a significant negative correlation with cooking loss and a positive correlation with water holding capacity. The expression levels of MMP-1 and -2 were usually higher in fat than in skeletal muscle tissue. The expression of MMP-8 was significantly higher in the mammary fat pad and the longissimus dorsi muscle than in all other tissues. This study indicates that the remodeling of the ECM has important effects both on the development of postnatal skeletal muscle and on meat quality.


Assuntos
Qualidade dos Alimentos , Metaloproteinase 1 da Matriz/metabolismo , Metaloproteinase 2 da Matriz/metabolismo , Metaloproteinase 8 da Matriz/metabolismo , Músculos Paraespinais/metabolismo , Carne Vermelha , Animais , Bovinos , Desenvolvimento Fetal , Expressão Gênica , Metaloproteinase 1 da Matriz/genética , Metaloproteinase 2 da Matriz/genética , Metaloproteinase 8 da Matriz/genética , Músculos Paraespinais/embriologia , Músculos Paraespinais/crescimento & desenvolvimento , Reação em Cadeia da Polimerase em Tempo Real
2.
Genet Mol Res ; 14(4): 17281-8, 2015 Dec 17.
Artigo em Inglês | MEDLINE | ID: mdl-26681222

RESUMO

To investigate the expression of interleukin-24 (IL-24) in the children with acute leukemia (AL) and its effect on the apoptosis of bone marrow mononuclear cells (BMMNCs) in vitro. Four groups were assessed: acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), non-leukemia, and healthy groups, 20 children in each group. ELISA was used to measure IL-24 serum level. The bone marrow was taken from patients and controls. BMMNCs were isolated and the DNA was analyzed by glucose electrophoresis. Flow cytometry was used to determine BMMNC apoptosis. The serum level of IL-24 in the ALL and AML groups were significantly higher than in the other two groups. There was no statistical difference between ALL and AML groups, either between non-leukemia and healthy groups. BMMNCs were exposed to IL-24 for 48 h, and the apoptotic rate of the group treated with 50 ng/ml IL-24 was obviously higher than that of control group (0 ng/mL). The serum IL-24 level of AL children decreased comparing to non-leukemia and healthy children, indicating that IL-24 can induce BMMNCs apoptosis of AL children in vitro.


Assuntos
Células da Medula Óssea/metabolismo , Interleucinas/sangue , Leucemia Mieloide Aguda/metabolismo , Leucemia-Linfoma Linfoblástico de Células Precursoras/metabolismo , Adolescente , Apoptose/efeitos dos fármacos , Biomarcadores , Células da Medula Óssea/efeitos dos fármacos , Células Cultivadas , Criança , Pré-Escolar , Feminino , Humanos , Interleucinas/farmacologia , Leucemia Mieloide Aguda/sangue , Masculino , Leucemia-Linfoma Linfoblástico de Células Precursoras/sangue
3.
Genet Mol Res ; 14(4): 11745-51, 2015 Oct 02.
Artigo em Inglês | MEDLINE | ID: mdl-26436499

RESUMO

APC is a tumor suppressor gene that is involved in the processes of cell migration and adhesion, transcriptional activation, and apoptosis. The goal of this study was to evaluate the contribution of the APC rs383830 polymorphism to coronary heart disease (CHD) in Han Chinese. A total of 783 patients with CHD and 737 controls were tested in the current association study. Although our study did not identify an association between the APC rs383830 polymorphism and CHD, a breakdown analysis by gender indicated there was a significant contribution of the rs383830 T allele to the risk of CHD in males (P = 0.046, odds ratio = 1.267, 95% confidence interval = 1.004-1.598). In conclusion, our study suggested a male-specific association of the APC rs383830 polymorphism with CHD.


Assuntos
Proteína da Polipose Adenomatosa do Colo/genética , Alelos , Doença das Coronárias/genética , Predisposição Genética para Doença , Polimorfismo de Nucleotídeo Único , Idoso , Povo Asiático , Estudos de Casos e Controles , Doença das Coronárias/etnologia , Doença das Coronárias/patologia , Feminino , Expressão Gênica , Frequência do Gene , Estudo de Associação Genômica Ampla , Humanos , Masculino , Pessoa de Meia-Idade , Razão de Chances , Fatores de Risco , Fatores Sexuais
4.
Genet Mol Res ; 14(1): 1808-18, 2015 Mar 13.
Artigo em Inglês | MEDLINE | ID: mdl-25867326

RESUMO

We explored the associations of INSR and mTOR, 2 key genes in the insulin signaling pathway, and the susceptibility to type 2 diabetes mellitus and diabetic nephropathy. Three single-nucleotide polymorphisms (SNPs) (rs1799817, rs1051690, and rs2059806) in INSR and 3 SNPs (rs7211818, rs7212142, and rs9674559) in mTOR were genotyped using the Sequenom MassARRAY iPLEX platform in 89 type 2 diabetes patients without diabetic nephropathy, 134 type 2 diabetes patients with diabetic nephropathy, and 120 healthy control subjects. Statistical analysis based on unconditional logistic regression was carried out to determine the odds ratio (OR) and 95% confidence interval (95%CI) for each SNP. Combination analyses between rs2059806 and rs7212142 were also performed using the X(2) test and logistic regression. Among these 6 SNPs, 4 (rs1799817, rs1051690, rs7211818, and rs9674559) showed no association with type 2 diabetes mellitus or diabetic nephropathy. However, rs2059806 in INSR was associated with both type 2 diabetes mellitus (P = 0.033) and type 2 diabetic nephropathy (P = 0.018). The rs7212142 polymorphism in mTOR was associated with type 2 diabetic nephropathy (P = 0.010, OR = 0.501, 95%CI = 0.288- 0.871), but showed no relationship with type 2 diabetes mellitus. Combination analysis revealed that rs2059806 and rs7212142 had a combined effect on susceptibility to type 2 diabetes mellitus and diabetic nephropathy. Our results suggest that both INSR and mTOR play a role in the predisposition of the Han Chinese population to type 2 diabetic nephropathy, but the genetic predisposition may show some differences.


Assuntos
Antígenos CD/genética , Povo Asiático/genética , Diabetes Mellitus Tipo 2/genética , Nefropatias Diabéticas/genética , Polimorfismo de Nucleotídeo Único , Receptor de Insulina/genética , Serina-Treonina Quinases TOR/genética , Adulto , Idoso , Estudos de Casos e Controles , China , Feminino , Predisposição Genética para Doença , Genótipo , Técnicas de Genotipagem , Humanos , Masculino , Pessoa de Meia-Idade , Análise de Sequência de DNA
5.
Genet Mol Res ; 13(1): 1707-16, 2014 Mar 17.
Artigo em Inglês | MEDLINE | ID: mdl-24535896

RESUMO

Unveiling the genetic architecture of grain yield and yield-related traits is useful for guiding the genetic improvement of crop plants. Kernel row number (KRN) per ear is an important yield component, which directly affects the grain yield of maize. In this study, we constructed a set of 130 chromosome segment substitution lines (CSSLs), using Nongxi531 as the donor parent and H21 as recipient parent, by continuous backcrossing and selfing. In total, 11 quantitative trait loci (QTL) were detected for KRN by stepwise regression under 3 environmental settings, with 9.87-19.44% phenotypic variation being explained by a single QTL. All 11 QTL were also detected by single-factor ANOVA across the 3 environments tested. Of these 11 QTL, 4 were identified across more than 2 environments, indicating that they are authentically expressed under different environments to control the formation and development of KRN in female maize inflorescences. The CSSLs harbored a greater number of favorable alleles for KRN compared to the H21 line, and could be employed as improved H21 lines in maize breeding programs.


Assuntos
Mapeamento Cromossômico , Cromossomos/genética , Locos de Características Quantitativas/genética , Zea mays/genética , Cruzamento , Cruzamentos Genéticos , Grão Comestível/genética , Meio Ambiente , Fenótipo , Sementes/genética
6.
Genet Mol Res ; 9(2): 750-5, 2010 Apr 27.
Artigo em Inglês | MEDLINE | ID: mdl-20449807

RESUMO

The primary function of the human leukocyte antigen (HLA) system is to regulate the immune response. Because of its important role in the immune response and its high degree of polymorphism, the HLA system is associated with many diseases. We examined the polymorphisms of HLA-A, B and DRB1 alleles in 100 unrelated patients with lung carcinoma and in 438 unrelated normal controls of Han nationality from North China, using sequence-based typing and PCR with sequence-specific primers. We found that the frequencies of HLA-A*0201, A*2601, B*1518, B*3802, DRB1*0401, DRB1*0402, and DRB1*1201 were higher in the lung carcinoma group than in the normal control group. The P values were 0.035, 0.040, 0.001, 0.017, 0.014, 0.004, and 0.019, respectively, and the odds ratio values were 1.052, 3.513, 4.047, 3.054, 4.237, 19.397, and 2.128, respectively. The frequency of HLA-DRB1*1302 was lower in the lung carcinoma group than in the normal control group (P = 0.046, odds ratio = 0.168). We concluded that patients with lung cancer and healthy controls of Han nationality from North China differ in the frequencies of various HLA alleles.


Assuntos
Alelos , Povo Asiático/genética , Antígenos HLA-A/genética , Antígenos HLA-B/genética , Antígenos HLA-DR/genética , Neoplasias Pulmonares/genética , Adulto , Idoso , Estudos de Casos e Controles , China/etnologia , Feminino , Frequência do Gene/genética , Cadeias HLA-DRB1 , Humanos , Masculino , Pessoa de Meia-Idade
7.
Neuroepidemiology ; 8(2): 56-67, 1989.
Artigo em Inglês | MEDLINE | ID: mdl-2922099

RESUMO

Mortality attributed to multiple sclerosis (MS) was analyzed for 35 countries around the world using World Health Organization reports from 1965 to 1984. Trends were plotted for the United States and Canada, for various regions of Europe, Israel, South America, Asia, Australia and some Pacific countries. In general, MS mortality has declined steadily in North America and most of western Europe as well as in countries with a western culture but has remained stable or increased in eastern and northern Europe. Although several Mediterranean countries reported a recent increased frequency of MS, it was not (yet?) evident in mortality data. Intensive prospective surveillance of MS frequency trends in selected regions of the world will determine the validity of the trends based on mortality.


Assuntos
Saúde Global , Esclerose Múltipla/mortalidade , Ásia , Austrália , Canadá , Europa (Continente) , Humanos , Nova Zelândia , América do Sul , Estados Unidos
8.
Neurology ; 36(10): 1386-9, 1986 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-3762950

RESUMO

Migration from an area where MS is common to an area where it is rare (and vice versa) affects the risk of MS, provided migration occurs in childhood. A childhood infection might explain this effect. Therefore, the age pattern of infectious diseases in different regions was examined. A higher proportion of children showed positive titers to many viral diseases early in life in areas where MS is rare compared with those where MS is common. Also, mortality rates from a variety of infectious diseases correlated negatively with the MS mortality. Thus, infection early in life may "protect" against MS, and conversely, later infection, when the immune system has partially matured, may increase risk. MS may be an age-dependent, host-immune response to childhood infection.


Assuntos
Esclerose Múltipla/epidemiologia , Viroses/imunologia , Ásia , Pré-Escolar , Europa (Continente) , Gastroenteropatias/imunologia , Gastroenteropatias/mortalidade , Humanos , Lactente , Sarampo/mortalidade , Esclerose Múltipla/mortalidade , Ilhas do Pacífico , Doenças Respiratórias/imunologia , Doenças Respiratórias/mortalidade , Sorologia , América do Sul , Estados Unidos
9.
Neuroepidemiology ; 5(3): 148-58, 1986.
Artigo em Inglês | MEDLINE | ID: mdl-3785529

RESUMO

Comparison of stroke incidence in various parts of the world is difficult because differences in diagnostic criteria, medical facilities and age-sex distributions are often not taken into account. We calculated age-sex standardized incidence ratios (SIR) of stroke in 37 regions based on recent reports. The USA (1976) was taken as the standard population. In western countries SIRs varied from 0.8 to 2.1. In China and Japan, SIRs varied from 0.7 to 3.6. While the lowest and highest SIRs differed by a factor of 5, only 6 of the 37 studies yielded a SIR of more than 2.0 or below 0.75. Of these, 4 were from China and Japan. The highest ratios were based on a very intensive door-to-door survey and probably should not be compared to less intensive studies. We conclude that world-wide variation in age-sex adjusted stroke rates is relatively small.


Assuntos
Transtornos Cerebrovasculares/epidemiologia , Adulto , Fatores Etários , Idoso , Brasil , Canadá , China , Europa (Continente) , Feminino , Humanos , Japão , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Fatores Sexuais , Estados Unidos
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