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1.
Journal of Sun Yat-sen University(Medical Sciences) ; (6): 731-738, 2019.
Artigo em Chinês | WPRIM | ID: wpr-817744

RESUMO

@# 【Objective】To summarize current situation of multiple sclerosis in South China and provide reference for MS diagnosis and treatment.【Methods】We selected patients of whom the first diagnosis was MS from 2011 to March 2019,and divided them into Adults group and Pediatrics group according to onset age above or below 14. We analyzed them from epidemiology,symptomatology,accessory examinations and treatment situation.【Results】296 patients were admitted into this research. The ratio of male to female was 1∶1.67. Median onset age was 26. Relapsing-remitting MS accounted for 63.2% of all patients. For initial episode,130 patients had motor symptoms(43.9%),118 patients showed sensory symptoms(39.9%),and 55 patients were accompanied with visual symptoms(18.6%). Statistical difference exists in sensory symptoms(114 vs. 4,Z = -2.155,P = 0.031)and paroxysmal symptoms(4 vs. 3,Z = -3.610,P = 0.000) of Adults group and Pediatrics group. For following episodes,the total relapsing time was 712,with motor symptoms relapsing 380 times(53.4%),sensory symptoms 265 times(37.2%)and visual symptoms 134 times(18.8%). Statistical difference existed in motor,sensory,visual,other ocular symptoms and paroxysmal symptoms. Positive rate of Oligoclonal bond was 45.5%. Positive rate of MOG-Ab was 16.7%. For brain MRI,periventricular lesions ≥ 9 accounted for 57.4% of all patients,with cortical & juxtacortical lesions 28.1% and infratentorial lesions 0.3%. Patients who had optic nerve lesions accounted for 63.2%. No statistical difference existed in them. For treatment,drugs they had used previously were glucocorticoid(79.7%),beta Interferon(15.9%)and azathioprine(13.9%).During the study,drugs they were using were glucocorticoid(15.5%),rituximab(9.1%),azathioprine(8.1%)and teriflunomide(8.1%).【Conclusions】For gender, age,symptomatology and accessory examinations,results of this research are similar to previous papers about multiple sclerosis in Asian. For treatment,the trend indicates that usage of new disease-modifying drugs goes up.

2.
Chinese Journal of Applied Physiology ; (6): 225-229, 2012.
Artigo em Chinês | WPRIM | ID: wpr-329902

RESUMO

<p><b>OBJECTIVE</b>To investigate whether cyclooxygenase-1 (COX-1) haplotype is associated, with aspirin resistance.</p><p><b>METHODS</b>The participants were 431 old Chinese Han patients with cardiovascular and cerebrovascular diseases who took aspirin. The 59 patients with aspirin resistance (AR) by light transmittance aggregation acted as the cases; the 372 aspirin-sensitive patients were the controls. The relationships between AR and 6 single nucleotide polymorphisms (SNPs) in COX-1 gene. rs1888943 (8759C/T), rs1330344 (1676A/G), rs3842787 (exon2, 50C/T, p.Pro17Leu), rs5787 (exon 4, 323G/A, p. ARg108Gln), rs5789 (exon7, 709C/A, p. Leu237Met) and rs5794 (exonl0, 1330G/A, p.Va1481Ile) were investigated by the USA Sequenom high-throughput single nucleotide polymorphisms (SNP) genotyping systems.</p><p><b>RESULTS</b>In this case-control trial, the frequency of mutant CGCGCC-haplotype in case was 0.48 (57/118) and in control was 0.39 (286/742), which was significantly higher than that of the control group (P < or = 0.05).</p><p><b>CONCLUSION</b>COX-1 haplotype is associated with aspirin resistance in old Chinese Han patients with cardio-cerebrovascular diseases, mutant CGCGCC-haplotype carriers of COX-1 has a significant significantly increased risk of AR.</p>


Assuntos
Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Povo Asiático , Genética , Aspirina , Farmacologia , Doenças Cardiovasculares , Genética , Estudos de Casos e Controles , Transtornos Cerebrovasculares , Genética , Ciclo-Oxigenase 1 , Genética , Resistência a Medicamentos , Genética , Genótipo , Haplótipos , Polimorfismo de Nucleotídeo Único
3.
Bulletin of The Academy of Military Medical Sciences ; (6): 577-579, 2009.
Artigo em Chinês | WPRIM | ID: wpr-642537

RESUMO

The liver is an important organ of the body,with an extraordinary capacity for responding to physical or chemical injuries by regenerating. The mechanisms behind liver regeneration are very complicated as hundreds of substances are involved.However,most of them are not liver-specific,such as HGF,EGF etc. We recently isolated a pure protein with hepatic stimulatory activity from the extract of a weanling calf liver and named its hepatopoietin Cn (HPPCn).This paper,with reference to our own work, mainly reviews the development and bioactivity about hepatic stimulator substance(HSS),augmenter of liver regeneration(ALR),hepassocin(HPS) and HPPCn,which are liver-specific biologically active peptides.

4.
Chinese Journal of Applied Physiology ; (6): 66-69, 2004.
Artigo em Chinês | WPRIM | ID: wpr-333714

RESUMO

<p><b>UNLABELLED</b>From large-scale sequence of human fetal liver cDNA library, we have obtained a full-length cDNA from an EST after further sequencing. It has been demonstrated by the alignment comparison with data base available that it is a novel member of Ubc family and got the number from GeneBank: UBF-F1 AF 294842.</p><p><b>AIM AND METHODS</b>To demonstrate its authenticity, UBF was amplified from the total RNA of human fetal liver and HL-60 cell line using RT-PCR, and the PCR products were further sequenced and compared with the original UBF sequence. To evaluate the expression level and subcellular location of UBF in human multiple tissues, in situ hybridization was carried out on the frozen section of human fetal multiple tissues and HL-60 cell line with DIG-labeled UBF cDNA probes.</p><p><b>RESULTS</b>The experimental results of RT-PCR and sequencing showed that the sequence of RT-PCR products were the same as the original UBF. The experimental results of in situ hybridization showed that UBF was expressed widely by human multiple fetal tissues and the expression level were very high in HL-60 cells.</p><p><b>CONCLUSION</b>It is suggested that the special structure of UBF is authentic, and the expression profiling research of UBF shows that UBF is expressed widely by human multiple fetal tissues and the expression level is very high in HL-60 cells, implying that UBF plays the important function in the developing tissues and leukemia cells. It is also suggested that UBF may be functionally related with the nucleic-involving cellular activities based on the results of sub-cellular localizations.</p>


Assuntos
Humanos , Sequência de Aminoácidos , Clonagem Molecular , Perfilação da Expressão Gênica , Células HL-60 , Dados de Sequência Molecular , Proteínas Pol1 do Complexo de Iniciação de Transcrição , Genética , Fases de Leitura , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Análise de Sequência de DNA , Enzimas de Conjugação de Ubiquitina , Classificação , Ubiquitinação
5.
Journal of Experimental Hematology ; (6): 177-182, 2002.
Artigo em Chinês | WPRIM | ID: wpr-337615

RESUMO

Hematopoietic stromal cells, being the essential ingredient of the hematopoietic microenvironment, play very important roles in the control and regulation of self-renewal, proliferation and differentiation of hematopoietic stem cells (HSC) via complex interactions of cell-cell, cell-humoral and cell-extracellular matrix. Evidence from in vivo experiment has proved that HSC derived from normal mice could reconstitute hematopoiesis of mice with HSC defects but failed to reconstitute hematopoiesis of those mice with microenvironment defects, showing the importance of hematopoietic microenvironment in the maintenance of hematopoiesis in vivo. A well-known long-term culture (LTC) system established by Dexter demonstrated in another way that stromal cell layer in the system could support ex vivo hematopoiesis for several months, even more than one year under the optimal conditions. It, however, has not been demonstrated that what is the key elements and in which way the ex vivo hematopoiesis could be maintained for so long time. As the inventions for the large-scale screening methodologies the suppression subtractive hybridization (SSH) was chosen for the screening differentially expressed genes expressed by LTC cultured stromal cells but not by the uncultured bone marrow cells (BMC). mRNA extracted from both cultured adherent cells (tester) and BMC (driver) were hybridized according to the protocol provided by CLONTECH. Total of 130 clones differentially expressed by cultured cells were randomly picked up and 106 ESTs were obtained after sequencing. They represent 26 identical or similar genes and 7 novel genes after the bioinformatics analysis. 5 of the novel genes with the entire open reading frame, without functional clues, have been cloned into the mammalian expression vectors and the functions of them in the control of proliferation and differentiation of HSC will be further exploring. The most interesting discovery is that 3 novel genes have signal peptides, implying the potential discovery of novel growth factors as 80% known growth factors have signal peptides. Our experimental results suggest that: (a) based on the results of subtractive efficiency, the SSH could be a reliable method to screen differentially expressed genes; (b) gene expression may be regulated by multiple factors, even conditioning-dependent, in this experiment the genes expressed by bone marrow stromal cells are LTC-cultivation inducible; (c) it is possible to find interesting genes or special gene after relatively large-scale screen.


Assuntos
Animais , Feminino , Masculino , Camundongos , Células Cultivadas , DNA Complementar , Genética , Metabolismo , Desoxirribonucleases de Sítio Específico do Tipo II , Metabolismo , Etiquetas de Sequências Expressas , Perfilação da Expressão Gênica , Células-Tronco Hematopoéticas , Biologia Celular , Metabolismo , Camundongos Endogâmicos BALB C , Reação em Cadeia da Polimerase , RNA Mensageiro , Genética , Metabolismo , Células Estromais , Biologia Celular , Metabolismo
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