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1.
Chinese Journal of Medical Genetics ; (6): 742-744, 2013.
Article in Chinese | WPRIM | ID: wpr-254522

ABSTRACT

<p><b>OBJECTIVE</b>To report on a rare allele FGA-13 identified in Guangdong Han population.</p><p><b>METHODS</b>The rare allele was detected by PCR-STR and DNA sequencing.</p><p><b>RESULTS</b>The core repeat sequence of rare allele FGA-OL is [TTTC]₃[TTTT][TTCT][CTTT]₅ [CTCC][TTCC]₂, which has been determined as FGA-13.</p><p><b>CONCLUSION</b>The rare allele FGA-13 is also present in Guangdong Han population. This is significant for personal identification and paternity testing.</p>


Subject(s)
Female , Humans , Male , Alleles , Asian People , Genetics , Genotype , Tandem Repeat Sequences
2.
Journal of Forensic Medicine ; (6): 109-111, 2012.
Article in Chinese | WPRIM | ID: wpr-983722

ABSTRACT

OBJECTIVE@#To explore the forensic application value of detection of matrix metalloproteinase-11 (MMP-11) in menstrual blood by enhanced chemiluminescence method.@*METHODS@#Menstrual blood, vaginal swab, peripheral blood, saliva stain, urine stain and semen stain were collected to detect whether or not there were MMP-11 using enhanced chemiluminescence method. The specificity and reliability of the MMP-11 assay along with its sensitivity were evaluated.@*RESULTS@#The positive detection rate of MMP-11 in menstrual blood was 89.47%, whereas no MMP-11 was found in vaginal swab, peripheral blood, saliva stain, urine stain and semen stain. When 25 microL sample was added, the mass concentration of protein was 1.329 microg/microL, then MMP-11 could be detected. A positive detection rate of 89.58% was observed in MMP-11 positive menstrual blood samples after stored at 4 degrees C for 20 months.@*CONCLUSION@#Enhanced chemiluminescence method is sensitive and specific for detecting MMP-11, and can be applied to distinguish menstrual blood from common stain such as peripheral blood, vaginal fluid.


Subject(s)
Female , Humans , Biomarkers/blood , Blood Stains , Blotting, Western , Forensic Medicine/methods , Luminescent Measurements/methods , Matrix Metalloproteinase 11/blood , Menstruation , Reproducibility of Results , Saliva/chemistry , Sensitivity and Specificity , Urine/chemistry , Vagina/chemistry
3.
Journal of Forensic Medicine ; (6): 421-424, 2011.
Article in Chinese | WPRIM | ID: wpr-983692

ABSTRACT

OBJECTIVE@#To introduce the method of avuncular index (AI) calculation.@*METHODS@#Identity by decent coefficient, coancestry coefficient and AI law were employed in identification of uncle-niece relationship, when autosomal STR loci were detected to determine controversial uncle-niece relationship.@*RESULTS@#The results of AI calculation were coincidental using identity by descent coefficien, coancestry coefficient and AI law.@*CONCLUSION@#The results are coincidental using three methods in the different situations. AI index is higher with participation of children's mother.


Subject(s)
Female , Humans , Male , Algorithms , Alleles , Chromosomes, Human/genetics , Family , Forensic Genetics/methods , Genotype , Heterozygote , Models, Genetic , Paternity , Probability , Tandem Repeat Sequences/genetics
4.
Journal of Forensic Medicine ; (6): 118-122, 2009.
Article in Chinese | WPRIM | ID: wpr-983457

ABSTRACT

OBJECTIVE@#To investigate the application of ITO method and discriminant functions method in full sibling and half sibling identification.@*METHODS@#Five hundred pairs of full siblings (FS), 50 pairs of half siblings (HS) and 500 pairs of unrelated individuals (UR) were genotyped by PowerPlex 16 system. Full sibling index (FSI), half sibling index (HSI) and the FSI:HSI ratio were calculated with ITO method. Allelic matching of each pair of the three groups was compared. The locus numbers of no-allele sharing (x0), half-allele sharing (x1) and two-alleles sharing (x2) were calculated, respectively. The discriminant functions about full-siblings, half-siblings and unrelated individuals (UR) were established by SPSS 13.0 statistical software.@*RESULTS@#(1) Regard FSI > or = 19 or FSI < 1 as the standard of distinguishing full sibling from unrelated individual, the alternate correct percentage was 96.4%. Regard HSI > or = 19 or HSI < 1 as the standard of distinguishing half sibling from unrelated individual, the alternate correct percentage was 85.3%. Regard FSI:HSI > or = 1 or FSI:HSI < 1 as the standard of distinguishing full sibling from half sibling, the alternate correct percentage was 87.5%. (2) Four groups of discriminant functions were established. The alternate correct percentage of these discriminant functions were 84.4%-97.7%, with the highest one in full sibship-unrelated individual group.@*CONCLUSION@#Both ITO method and discriminant functions method are efficient in identification of full sibling or half sibling.


Subject(s)
Humans , Alleles , Discriminant Analysis , Forensic Genetics , Genetic Variation , Genomic Imprinting/genetics , Genotype , Paternity , Siblings , Tandem Repeat Sequences/genetics
5.
Journal of Shanghai Jiaotong University(Medical Science) ; (6): 869-872, 2009.
Article in Chinese | WPRIM | ID: wpr-634861

ABSTRACT

Objective To investigate the critical thinking ability of medical students and its related factors in order to provide evidence for higher medical education reform. Methods A total of 325 medical students were selected by cluster sampling method, and Critical Thinking Disposition Inventory-Chinese Version (CTDI-CV) was adopted for survery. Results The average total score of critical thinking ability of medical students was above 280, and 51.08% of students showed positive critical thinking ability. Among all the seven critical thinking dispositions, average scores of each item were all positive (>40) except that the significance of truth seeking (37.23) and systematicity (39.05) were indefinite. There were significant differences in critical thinking ability between medical students with different gender and academic years (P<0.05). Conclusion The critical thinking ability of medical students is positive, however, there still exist some shortages. An equal relationship between teachers and students should be established, the traditional course system be continuously reformed, a good environment for clinical training be created, and a variety of teaching methods be implemented to further strengthen the critical thinking ability of medical students.

6.
Journal of Forensic Medicine ; (6): 185-193, 2008.
Article in Chinese | WPRIM | ID: wpr-983379

ABSTRACT

OBJECTIVE@#To establish an accurate, simple, quick, specific and sensitive method for species identification by amplifying 12S rRNA gene with the same reaction system.@*METHODS@#Based on the downloaded 12S rRNA gene sequences of eleven species (human, chicken, duck, goose, pig, rabbit, rat, sheep, bull, dog and goat) from GenBank, a pair of universal primers to eleven species and three pairs of specific primers to human, chicken and duck were designed. The amplicons amplified with universal primers were used for internal controls, and the amplicons amplified with specific primers were used as identification of human, chicken and duck. DNA was extracted from various samples including blood stains, fresh or freezing muscles, heat-treated muscles and hairs. Both single DNA of human, chicken or duck and mixed DNA of any two kinds of them were amplified.@*RESULTS@#The lengths of universal amplicons were about 400 bp. The lengths of specific amplicons were 163 bp for human, 286 bp for chicken, and 374 bp for duck, respectively. No cross amplification was observed, indicating a high specificity of the specific primers. The identification rate was 100% for human, 99% for chicken, and 100% for duck, respectively. The detection sensitivity ranged from 2.5 pg to 200 pg of DNA concentration depending on species, even in mixtures of different species DNA without interference.@*CONCLUSION@#The method established could identify different species under the same reaction system.


Subject(s)
Animals , Cattle , Dogs , Humans , Rabbits , Rats , Blood , DNA/analysis , Forensic Genetics , Hot Temperature , Polymerase Chain Reaction/veterinary , Poultry/genetics , RNA, Ribosomal/genetics , Sheep , Species Specificity , Swine
7.
Journal of Forensic Medicine ; (6): 32-33, 2008.
Article in Chinese | WPRIM | ID: wpr-983349

ABSTRACT

OBJECTIVE@#To prove the feasibility of detecting menstrual blood as well as its cellular localization with rabbit-anti-human matrix metalloproteinase-11 (MMP-11) polyclonal antibody.@*METHODS@#MMP-11 in menstrual blood, peripheral blood, vaginal liquid, aged menstrual bloodstain, and endometrium sections were assayed with SAP immunohistochemistry.@*RESULTS@#MMP-11 was found only in menstrual samples within stroma and epithelium cells.@*CONCLUSION@#MMP-11 polyclonal antibody may be applied in the distinction between menstrual blood and venous blood.


Subject(s)
Adult , Female , Humans , Endometrium/pathology , Forensic Medicine/methods , Immunohistochemistry , Matrix Metalloproteinase 11/analysis , Menstrual Cycle/blood
8.
Chinese Journal of Pathology ; (12): 103-108, 2008.
Article in Chinese | WPRIM | ID: wpr-349964

ABSTRACT

<p><b>OBJECTIVE</b>To study the expression level and significance of glucose transporter 1 (Glut-1) in normal breast tissue, adenosis, adenoma and breast carcinoma.</p><p><b>METHODS</b>A total of 147 cases of female breast tissue samples, including 92 cases of invasive ductal carcinoma, 26 cases of breast fibroadenoma, 24 cases of breast adenosis and 5 cases of normal breast tissues, were collected for quantitative detection of the expression of Glut-1 protein by immunohistochemistry (EnVision method) and Western blot, and its mRNA by reverse transcriptase-polymerase chain reaction (RT-PCR).</p><p><b>RESULTS</b>In normal breast tissue and benign lesions of the breast, Glut-1 was undetectable or only weakly detectable in cytoplasm of ductal and acinar epithelia. In contrast, the intensity of Glut-1 staining was significantly higher in invasive ductal carcinomas (P = 0.0002) with protein expression predominantly in cellular membrane and lesser in cytoplasm. Western blot and RT-PCR analyses showed that the expression of Glut-1 protein and mRNA were significantly increased in invasive ductal carcinoma than fibroadenoma (P =0.001 for protein; P <0.05 for mRNA) and adenosis (P =0.001 for protein; P < 0.05 for mRNA). There was a significant difference among groups (P = 0.0002 for protein; P = 0.0001 for mRNA).</p><p><b>CONCLUSIONS</b>Glucose transport activity, as indicated by Glut-1 protein and its mRNA expression, significantly increases in breast carcinoma than non-cancerous lesions. The over-expression of Glut-1 in breast carcinoma is tightly coupled with tumor cell proliferation, invasion and metastasis, implying that Glut-1 may serve as a new marker in the early diagnosis and prognostication of breast malignancy as well as a new therapeutic target.</p>


Subject(s)
Female , Humans , Breast Neoplasms , Metabolism , Carcinoma, Ductal, Breast , Metabolism , Gene Expression Regulation, Neoplastic , Glucose , Physiology , Glucose Transport Proteins, Facilitative , Genetics , Metabolism , Glucose Transporter Type 1 , Genetics , Metabolism , Prognosis
9.
Chinese Journal of Rehabilitation Theory and Practice ; (12): 1161-1162, 2008.
Article in Chinese | WPRIM | ID: wpr-977671

ABSTRACT

@#Objective To explore the feasible of diagnosing ischemic cerebrovascular diseases by detecting central retina artery sclerosis(CRA) with color Doppler ultrasonography.Methods210 patients with ischemic cerebrovascular disease(420 eyes) and 80 healthy volunteers(160 eyes) were examined by color Doppler flow imaging(CDFI) to detect double sides blood frequency spectrum of CRA and hemodynamic parameters of CRA including peak systolic velocity(PSV),end of diastolic velocity(EDV)and resistant index(RI).ResultsThe blood frequency spectrum of CRA showed three apices and two vales or slanting triangle in healthy volunteers.But in patients with ischemic cerebrovascular disease,the blood frequency spectrum changed,and PSV and EDV were slower and RI increased compared with those in the healthy volunteers(PP<0.05~0.001).ConclusionIn patients with ischemic cerebrovascular disease,the blood flow of CRA is slower and RI increases compared with health individuals.The color Doppler ultrasonography can used for diagnosis of CRA sclerosis.

10.
Journal of Shanghai Jiaotong University(Medical Science) ; (6)2008.
Article in Chinese | WPRIM | ID: wpr-640995

ABSTRACT

Objective To explore status quo of Shanghai community health services based on the investigation of rural community doctors in Shanghai suburb,and to propose measures on training rural doctors. Methods Retrospective investigation was carried out in 114 rural community health service centers and 1 563 clinics.Primary investigation included the registration,distribution,age,academic titles and education background. Results The results showed insufficient number of human resources and inadequate investment in human capitals in the primary medical services of Shanghai suburbs,and there was a serious shortage of general practitioners.The other problems included older age,insufficient academic qualifications,and without professional titles. Conclusion We should improve the status and treatment of rural doctors.Job training and well-trained professional students should be encouraged for the primary health services.More and more doctors should be attracted to work in community health service centers.General practitioners' personnal information network and general medical training network should be established,and the general medical education system gets improvement.

11.
Journal of Shanghai Jiaotong University(Medical Science) ; (6)2006.
Article in Chinese | WPRIM | ID: wpr-640802

ABSTRACT

Objective To analyze the relationship between clinical competence of baccalaureate nursing students and its potential related factors,and investigate the results of curriculum reform of 4-year nursing undergraduate education.Methods The records of 263 baccalaureate nursing graduates were retrieved.Variables including age,years of college education,sex,college entrance examination scores,average scores of basic courses,average scores of public courses and average scores of professional courses were collected.Clinical competence was measured by the clinical practice tests at various clinical units.The linear regression analysis was performed to find out the influencing factors of clinical competence.Results The clinical competence was significantly related to sex,average scores of public courses and average scores of professional courses(P

12.
West China Journal of Stomatology ; (6): 148-152, 2006.
Article in Chinese | WPRIM | ID: wpr-288981

ABSTRACT

<p><b>OBJECTIVE</b>To observe and compare the luciferase activities of different length segments of human dentin matrix protein 1 promoter in human dental pulp stem cells (HDPSC), osteoblasts (OC) and Hela cells.</p><p><b>METHODS</b>The differentlength desired DNA segments were obtained from 2 195 bp Dmp1 promoter cloned by PCR method. The amplified promoter segments with different length were cloned into luciferase report gene vector pGL3-Basic, the correct orientation of those inserts was verified by cutting with two different restrict enzymes. The luciferase activity was observed after different pGL3-PDmp1 vectors were transfected transiently into those three different-type cells.</p><p><b>RESULTS</b>6 Dmp1 promoter segments with different-length were obtained successfully, and luciferase report gene vectors with different promoter segments were successfully constructed after identified by restriction enzymes cutting. They had different luciferase activities when they were transfected transiently into HDPSC, and the region of -505(-)-193 bp and -935(-)-505 bp could be regarded as the specific promoters of Dmp1 promoter for HDPSC and OC respectively, which could include the basic regulatory elements.</p><p><b>CONCLUSION</b>The correct clone of the upstream of human Dmp1 promoter segments with different length had been obtained, and they had strong luciferase activities in HDPSC and OC, but very low in Hela cell. These results will make an important basis for studying mineralized tissue-specific transcriptional regulation mechanisms of Dmp1.</p>


Subject(s)
Humans , Dentin , Extracellular Matrix Proteins , Gene Expression Regulation , Genetic Vectors , Phosphoproteins , Promoter Regions, Genetic , Transfection
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