p blood group 中文意思是什麼
p blood group
解釋
p血型-
Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel
結果如下：皮下包埋卜周者，無細胞真皮基質漸與周圍組織粘附，顏色由蒼白轉紅；皮下包埋3周者，無細胞真皮基質與周圍組織緊密枯附，盾晰葉辯；術后卜周，包埋的基質面積變化較包埋前無統計學差異o川0引，術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ） 。光鏡下術后卜周，宿主的淋巳組織細胞、成纖維細胞浸入生長，釉附在膠原纖維上，少量血管內皮細胞浸入基質；術后34周，無細胞真皮基質內較多的血管形成，故可認為無細胞真皮基質免疫原性低，能誘導宿主的成纖維細胞、巨噬細胞浸入生長，為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究， sd大鼠10隻，在其背部卜方造成全厚皮膚缺損的創面 -
The serum creatinine, blood urea nitrogen, triglyceride and low density lipoprotein decreased significantly in the jpqhr - treated group as compared with those in the control group ( p < 0. 05 ), while the number of erythrocyte rosette - forming cells increased significantly in the jpqhr - treated group as compared with those in the control group ( p < 0. 05 )
結果：健脾清化方組患者的臨床癥狀有明顯改善，血肌酐、尿素氮、甘油三酯和低密度脂蛋白均有下降，而紅細胞總花環有顯著增加，與對照組比較，有統計學意義（ p < 0 . 05 ） 。 -
Normal bn rats were vaccinated intraperitoneally with lctcv, ltcv and rpmi1640 culture buffer ( blank control ) respectively. one - way mixed lymphocyte reaction ( mlr ), flow cytometric analysis of the apoptosis of peripheral t cell and the rate of cd4 / cd8 in peripheral blood were performed before and after vaccination. results mlr showed that the immune response capability of bn rat spleen cells in lctcv group were suppressed significantly after vaccination ( p < 0. 01 )
于疫苗接種前和每次接種后第5天以被免疫bn大鼠的脾細胞作為反應細胞，以lou c大鼠的脾細胞作為刺激細胞（經絲裂黴素處理） ，進行單向混合淋巴細胞反應（ mlr ） ，同時對外周血t細胞凋亡和cd _ 4 ~ + 、 cd _ 8 ~ + t細胞亞群進行流式細胞分析。 -
There were significant differences rert0. 05 ) in number of cd4 + t cells in peripheral blood lymphocytes between group a and group d at l4, 47 and 54 days of pi, group a was higher than group d. there were sighficant differences ( prt0. 05 ) in number of cd4 + t cel1s in peripheral blood lymphocytes between group b and group d at 28 and 47 days of pi, group b was higher than group d. there were significant differences ( pwt0. 05 ) in number of cd4 + t ceils in peripherai blood lymphocytes between group c and group d at 28 days of pi, group c was higher than group d. there were significant differences ( prt0. 05 ) in number of cd8 + t cells in peripheral biood iymphocytes between group a and group d at l4 days of pi, group a was nigher than group d. there were significant differences ( p < 0. 05 ) in number of cd8 + t cells in peripheral b1ood lymphocytes between group b and group d at l4 days of p [, group b
C組與d組小員外周血cd4 ~ + t細胞數量在首免后28d與對照組比較，差異顯著（ p 0 . 05 ） ， c組小員外周血cd4 ~ + t細胞數量明顯高於d組。 a組與d組小鼠外周血cd8 ~ + t細胞數量在首免后第14d出現顯著差異（ p 0 . 05 ） ，博士學位論文豬輪狀病毒和傳染性胃腸炎病毒核酸免疫的研究2002年12月a組小鼠外周血cds 」 t細胞數量明顯高於d組。 b組與d組小鼠外周血cds 」 t細胞數量在首免后第14d出現顯著差異（ p 0 -
Results the frequency of discomfort, low blood pressure and arrhythmia in the treatment group is lower than that in control group ( p < 0. 01 ) but the density of kalemia in serum does not obvious change
結果高鉀透析組患者在不適癥狀、低血壓、心律失常發生率等方面均顯著低於對照組（ p < 0 . 01 ） ，而透析后血清鉀濃度無明顯改變。
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