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1.
Journal of Experimental Hematology ; (6): 150-156, 2016.
Article Dans Chinois | WPRIM | ID: wpr-272487

Résumé

<p><b>OBJECTIVE</b>To investigate the common mutation spectrum of α- and β-thalassemia in Yunnan childbearing-aged population.</p><p><b>METHODS</b>The common mutation types of α- or β-globin genes were detected by multiple Gap-PCR and the PCR-reversed dot blotting, and the unknown mutation types were determined by DNA sequencing in DNA samples of hypochromic microcytic anemia patients and carriers who were confirmed to be positive by serologic screaning, then the mutation types of globin in Yunnan population were analyzed statistically.</p><p><b>RESULTS</b>A total of 40 kinds of mutation types were detected in 685 detected persons, among them the 3 commonest mutation types of α-globin genes were --(SEA)/αα (49.09%), -α(3.7)/αα (36.67%) and α(CS)α/αα (8.79%), the 3 commonest genetypes of β-globin gene were CD26(GAG>AAG)/N (43.78%), CD41-42(-CTTT)/N (20.1%) and CD17(AAG>TAG)/N (18.9%). There were 348 Han and 212 Dai ethnic persons in 685 cases, but their mutation of globin genes were different between these 2 ethnic groups. The results also showed that the gene mutation types were mostly concentrated in Dai ethnic individuals, since 28 of 38 detected α-β-thalassemia cases were Dai ethnic individuals.</p><p><b>CONCLUSION</b>The mutation spectrums of α- and β-globin genes in Yunnan childbearing-aged population are diverse and different from that in other areas of China.</p>


Sujets)
Humains , alpha-Globulines , Génétique , Anémie hypochrome , Ethnologie , Génétique , Asiatiques , Chine , Analyse de mutations d'ADN , Ethnies , Génétique , Dépistage génétique , Hétérozygote , Mutation , Réaction de polymérisation en chaîne , alpha-Thalassémie , Ethnologie , Génétique , Globines bêta , Génétique , bêta-Thalassémie , Ethnologie , Génétique
2.
Journal of Experimental Hematology ; (6): 157-161, 2016.
Article Dans Chinois | WPRIM | ID: wpr-272486

Résumé

<p><b>OBJECTIVE</b>To investigate the gene mutation spectrum of β-thalassemia in Dai ethnic population of 2 border region in Chinese Yunnan Province.</p><p><b>METHODS</b>The patients with β-thalassemia in Dai ethnic population of Dehong and Xishuangbanna autonamic prefecture were screened by using blood routine detection and capillary electrophoresis. The β-globin gene mutation in patients with β-thalassemia were detected by using PCR reverse dot-blot hybridization (PCR-RDB), the constitutive rate of gene mutation in patients with β-thalassemia of Dai ethnic population in two border regions was analyzed and compared.</p><p><b>RESULTS</b>A total of 186 patients with gene mutation of β-thalassemia were confirmed. Among them, 10 gene mutation were found, and the 5 main gene mutations were CD26 (62.56%), CD41-42 (18.97%), CD17 (14.36%), CD71-72 (2.05%) and IVS-II-654 (1.54%). Among Dai ethinic population in Dehong region, 4 gene mutations were found including CD26 (80.31%), CD17 (11.02%), CD41-42 (6.30%) and CD71-72 (2.36%). Among Dai ethinic population in Xishuangbanna region, 6 gene mutations were found, out of them the more common gene mutations were CD41-42 (42.64%), CD26 (29.41%) and CD17 (20.59%).</p><p><b>CONCLUSION</b>The gene mutations of β-thalassemia in Dai ethinic population of Yunnan province has been confirmed to be more genetic heterogenicity, the spectrums of β-thalassemia mutations in Dai ethinic population of different regions were significant different.</p>


Sujets)
Humains , Antigènes CD , Génétique , Asiatiques , Chine , Analyse de mutations d'ADN , Électrophorèse capillaire , Ethnies , Thérapie génétique , Mutation , Hybridation d'acides nucléiques , Réaction de polymérisation en chaîne , Globines bêta , Génétique , bêta-Thalassémie , Ethnologie , Génétique
3.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 886-888, 2009.
Article Dans Chinois | WPRIM | ID: wpr-242374

Résumé

<p><b>OBJECTIVE</b>To observe the expressions of tumor metastasis related factors (TMRF) in peripheral blood of patients with non-small cell lung cancer (NSCLC) for exploring the molecular mechanism for genesis of qi-deficiency and blood stasis (QDBS) syndrome in patients.</p><p><b>METHODS</b>Eighty selected NSCLC patients of stage II B/III were differentiated into the QDBS group and the non-QDBS group according to the Chinese medicine syndrome differentiation criteria, 40 in each group. The serum levels of vascular endothelial growth factor (VEGF), endostatin (ES) and soluble intercellular adhesive molecule-1 (slCAM-1) in patients were detected by ELISA, and the expression of adhesive molecule CD44 in peripheral blood was determined using flow cytometry.</p><p><b>RESULTS</b>Serum levels of VEGF (1002.78 +/- 312.08 ng/L), ES (120.88 +/- 20.00 microg/L), slCAM-1 (531.78 +/- 213.37 microg/L) and CD44 (136.65 +/- 29.60) were significantly higher in patients of QDBS group than in patients of non-QDBS group (653.18 +/- 318.99 ng/L, 98.29 +/- 23.92 microg/L, 409.36 +/- 167.65 microg/L and 98.46 +/- 20.64, respectively, P<0.01).</p><p><b>CONCLUSION</b>Objective inner links are found between the QDBS syndrome and TMRF in NSCLC patients; serum levels of VEGF, ES, slCAM-1 and CD44 can be served as the microcosmic basis for QDBS syndrome differentiation.</p>


Sujets)
Adulte , Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Carcinome pulmonaire non à petites cellules , Diagnostic , Anatomopathologie , Diagnostic différentiel , Endostatines , Sang , Antigènes CD44 , Sang , Molécule-1 d'adhérence intercellulaire , Sang , Tumeurs du poumon , Diagnostic , Anatomopathologie , Médecine traditionnelle chinoise , Méthodes , Métastase tumorale , Diagnostic , Anatomopathologie , Facteur de croissance endothéliale vasculaire de type A , Sang
4.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 440-443, 2008.
Article Dans Chinois | WPRIM | ID: wpr-343958

Résumé

<p><b>OBJECTIVE</b>To investigate the relationship between single dosage of 60Co radiation and the degree of radiation-induced skin ulcers, and to evaluate the curative effect of Heijiang Pill (HJP) on skin ulcer induced by various dosages of radiation in rats.</p><p><b>METHODS</b>Sixty-six Wistar female rats were randomly divided into three groups, the blank control group (n = 6) and the two radiation groups, each 30 rats, with their right hind leg exposed respectively to 60 Gy and 40 Gy of 60 Co radiation. The time of emergence and degree of skin ulcer were recorded. Then rats in the two radiation groups were subdivided into the HJP group, the Ethacridine group and the model group, 10 in each group, they received corresponding treatment after ulceration, and the incidence, pathology, cure rate and cure time of skin ulcer were observed in the 90 days of observation.</p><p><b>RESULTS</b>The incidence of skin ulcer was higher and occurred earlier in rats radiated with 60 Gy than that with 40 Gy (P < 0.05). In the same radiation dosage, the ulcer healing rate in rats treated with HJP was higher than that treated with Ethacridine (P <0.05), and in the subgroups of 40 Gy radiation, the mean cure time in the HJP group was shorter (P < 0.05). The local epithelial proliferation and repairing could be verified by pathological observation in the HJP group.</p><p><b>CONCLUSION</b>Larger dosage of radiation leads to earlier emergence and aggravation of ulcers. HJP can effectively cure radiation skin ulcer, and the effect is especially significant on the ulcer induced by low dose radiation.</p>


Sujets)
Animaux , Femelle , Rats , Relation dose-effet des rayonnements , Médicaments issus de plantes chinoises , Utilisations thérapeutiques , Lésions radiques expérimentales , Traitement médicamenteux , Rat Wistar , Ulcère cutané , Traitement médicamenteux , Comprimés
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