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1.
Physiol Plant ; 144(2): 161-8, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22084837

RESUMO

In plants and animals, the SCF-type ubiquitin protein ligases play an important role in many different physiological processes by regulating protein stability such as S-RNase-based self-compatibility, flower development, hormone responses and meiosis. This study identified an SlFbf gene in tomato that encodes 381 amino acid residues containing a typical F-box motif and an FBA_1 motif associated proteasome pathway; the transcripts of SlFbf was detected in all the tissues (root, stem, leaf, sepal, petal, stamen, pistil, green fruit, breaker fruit and red fruit), with the highest in stamen specifically during flowering stage; SlFbf responded to gibberellins, abscisic acid and light. Suppressed SlFbf leads to bigger pollen and less seeds showing that SlFbf might have an effect on fertilization through regulating stamen development. These findings provide more information about the functions of Fbf gene family.


Assuntos
Proteínas F-Box/genética , Genes de Plantas/genética , Proteínas de Plantas/genética , Solanum lycopersicum/genética , Sequência de Aminoácidos , Proteínas F-Box/química , Proteínas F-Box/metabolismo , Perfilação da Expressão Gênica , Regulação da Expressão Gênica de Plantas/efeitos dos fármacos , Regulação da Expressão Gênica de Plantas/efeitos da radiação , Íntrons/genética , Luz , Solanum lycopersicum/anatomia & histologia , Solanum lycopersicum/efeitos dos fármacos , Solanum lycopersicum/efeitos da radiação , Dados de Sequência Molecular , Especificidade de Órgãos/efeitos dos fármacos , Especificidade de Órgãos/genética , Especificidade de Órgãos/efeitos da radiação , Fenótipo , Reguladores de Crescimento de Plantas/farmacologia , Proteínas de Plantas/química , Proteínas de Plantas/metabolismo , Plantas Geneticamente Modificadas , Pólen/anatomia & histologia , Pólen/efeitos dos fármacos , Pólen/genética , Pólen/efeitos da radiação , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Sementes/efeitos dos fármacos , Sementes/crescimento & desenvolvimento , Sementes/efeitos da radiação , Supressão Genética/efeitos dos fármacos , Supressão Genética/efeitos da radiação
2.
Egypt J Immunol ; 18(2): 13-21, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-23082466

RESUMO

The number of patients with end stage renal disease (ESRD) is increasing considerably worldwide. The incidence of ESRD is likely to be higher than that reported from the developed world, with diabetic nephropathy, hypertension and chronic glomerulonephritis being the most common causes in Egypt. The aim of the present study is to investigate the Human leukocyte antigens [HLA-A,-B and -DRB1 antigens] as a risk factor for the primary diseases leading to ESRD in Egyptian patients. Our study included a total of 457 individuals comprising 207 ESRD patients and 250 healthy controls were enrolled into the study. Class I [HLA-A and-B] typing was performed by complement-dependent cytotoxicity (CDC) method, while class II HLA-DRB1 typing was performed by low resolution polymerase chain reaction (PCR)-sequence-specific oligonucleotide probe [PCR-SSOP]. We found that the most common primary disease groups leading to ESRD classified as Diabetic nephropathy, hypertensive nephrosclerosis and chronic glomerulonephritis. HLA-A2, -B8 and DRB1*3 and HLA-DRB1*11 significantly correlated with diabetic nephropathy, respectively. B8-DR3 haplotype is susceptible to DM. In, conclusion, determination of HLA-A,-B and -DRB1 as a risk factor for primary diseases leading to ESRD might be beneficial in preventing progression to ESRD and recurrence of the primary disease post-transplantation.


Assuntos
Antígenos HLA-A/sangue , Antígenos HLA-B/sangue , Cadeias HLA-DRB1/sangue , Falência Renal Crônica/imunologia , Adolescente , Adulto , Criança , Nefropatias Diabéticas/imunologia , Egito , Feminino , Glomerulonefrite/imunologia , Humanos , Modelos Logísticos , Masculino , Nefroesclerose/imunologia , Fatores de Risco , Adulto Jovem
3.
Clin Biochem ; 35(5): 369-75, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12270766

RESUMO

BACKGROUND: The role of cytokines and reactive oxygen species formation in the pathogenesis of chronic sinusitis is still not fully understood. This work was designed to determine if patients with chronic sinusitis demonstrate altered levels of serum IL-12 and/or tissue antioxidants. SUBJECTS AND METHODS: Mucosal biopsy specimens from the uncinate process of patients with chronic sinusitis were obtained from 52 patients using functional endoscopic sinus surgery. Normal mucosa samples were collected from 20 healthy controls. Patients' group was further classified according to computerized tomography findings into mild and severe subgroups. Serum IL-12 was estimated using enzyme immunoassay (EIA). The levels of tissue uric acid, and reduced glutathione were determined biochemically, alpha-tocopherol was measured by HPLC. Superoxide dismutase (SOD) activity was determined by spectrophotometry. RESULTS: A significant decrease in serum IL-12, tissue alpha-tocopherol and SOD in patient group was demonstrated (p < 0.05). Tissue uric acid and reduced glutathione showed primary increase in mild subgroup followed by significant drop in severe subgroup (p < 0.05). Negative significant correlation was observed between glutathione, uric acid, and SOD, and the severity of the disease (p < 0.05) independent of the cellularity of the biopsy. CONCLUSION: The presented data suggests a possible role of IL-12, and tissue antioxidants in development and progression of chronic sinusitis. Adjuvant antioxidant treatment may have role in achieving better prognosis of the disease.


Assuntos
Antioxidantes/análise , Interleucina-12/sangue , Sinusite/sangue , Sinusite/metabolismo , Cromatografia Líquida de Alta Pressão , Doença Crônica , Feminino , Glutationa/análise , Humanos , Masculino , Seios Paranasais/química , Seios Paranasais/enzimologia , Seios Paranasais/metabolismo , Espécies Reativas de Oxigênio/análise , Superóxido Dismutase/metabolismo , Ácido Úrico/análise , alfa-Tocoferol/análise
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