調節同調序列 的英文怎麼說
中文拼音 [diàojiétóngdiàoxùliè]
調節同調序列
英文
adjusted homology sequence-
The two single - pass transmembrane proteins, delta and serrate, have been identified as notch ligands. the transcription factor suppressor of hairless [ su ( h ) ] is the major downstream effector of notch signaling pathway. rbp - j, the mammalian homolog of su ( h ), recognizes the core sequence ( c / tgtgggaa ) of dna
Rbp - j是果蠅促神經發生基因su （ h ） （ suppressorofhairless ）在哺乳動物的同源物，它通過其識別序列（ c tgtgggaa ）結合於受調控基因的啟動子區，在轉錄激活因子的驅動下調節細胞分化和個體發育相關基因的表達。The essence of edid is to set up a normal behavior fuzzy sub collection a on the basis of watching the normal system transfer of the privilege process, and set up a fuzzy sub collection b with real time transfer array, then detect with the principle of minimum distance in fuzzy discern method the innovation point of this paper is : put forward the method of edid, can not only reduce efficiently false positive rate and false negative rate, also make real time intrusion detection to become possibility ; have independent and complete character database, according to the classification of monitoring program, design normal behavior and anomaly behavior etc., have raised the strongness of ids ; use tree type structure to preservation the character database, have saved greatly stock space ; in detection invade, carry out frequency prior principle, prior analysis and handling the behavior feature of high frequency in information table, have raised efficiency and the speed of detection, make real time intrusion detection to become possibility ; have at the same time realized anomaly intrusion detection and misuse intrusion detection, have remedied deficiency of unitary detection method
這種方法的實質是在監控特權進程的正常系統調用基礎上建立正常行為模糊子集a ，用檢測到的實時調用序列建立模糊子集b ，然後用模糊識別方法中的最小距離原則進行檢測。本文的創新點是：通過對特權進程的系統調用及參數序列的研究，提出了基於euclidean距離的入侵檢測方法edid ，不僅能有效降低漏報率和誤報率，而且使實時入侵檢測成為可能；設計有獨立而完整的特徵數據庫，根據被監控程序的類別，分別設計正常行為、異常行為等，提高了檢測系統的強健性和可伸縮性；特徵數據庫按樹型結構存儲，大大節省了存儲空間；在檢測入侵時，實行頻度優先原則，優先分析和處理信息表中的高頻度行為特徵，提高檢測的速度和效率，使實時入侵檢測成為可能；同時實現了異常入侵檢測和誤用入侵檢測，彌補了單一檢測方法的不足。In order to study the expression of 3 - defensins in liver as acute phase response proteins, a murine systemic acute phase responsive model was established by intraperitoneal injection o f lipopolysaccharide ( lps ) in our study. the mbd3 cdna sequence ( 145 - 169 bp ) was labled with [ - 32p ] atp as a probe to detect mbd3 mrna in different tissues by northern blot and analyze the time - and dose - dependant expression caused by lps. the 5 " flanking sequence ( - 167 - 179 bp ) of the mbd3 gene was designed as the probe and labled with [ - 32p ] dctp to investigate the binding of transcriptional factors to this region by electrophoretic mobility shift assay ( emsa ) and south - western blot
以小鼠mbd3基因145 ? 169bpcdna序列合成探針，經[ - ~ （ 32 ） p ] atp標記后通過northernblot方法檢測mbd3在肝臟中的表達，同時分析了mbd3基因誘導表達的組織特異性，劑效和時效關系；結合mbd3基因啟動子區序列分析，以- 164 ? - 179bp雙鏈dna序列合成探針，經[ - ~ （ 32 ） p ] dctp標記后通過電泳遷移率改變實驗（ emsa ）和south ? westernblot方法對參與mbd3在肝臟中誘導表達調節的轉錄因子進行分析。After analyzed the basic principle of optimized noise reduction on tyre pattern, summarized three approaches to noise reduction. the first is trying to reduce size of single block or socket to reduce noise amplitude on time domain, the second is to adjust stripes sorting order and their interlace value to avoid noise - made by every single block - peak values on time domain overlayed and the last is to adjust ratio of blocks and sockets, ratio of stripe interval and stripe sorting order to avoid noise periodical distribution and abnormal high peak values in some frequency strip
論文第四章分析了輪胎花紋優化降噪的基本原理，總結出三條降噪途徑：在允許范圍內盡量減小單個塊或槽的大小、刻刀槽軟化花紋塊來減小噪聲時域波幅度；調整節距排列順序、花紋條之間的錯位值，使各發聲單元發出的聲壓時域波形的同向峰值錯開，避免同向峰值疊加；調整花紋塊和槽比例、節距比例、節距排列順序，盡量避免周期性分佈，使輪胎所發出的噪聲趨于白噪化，避免某些頻段的異常高峰值。Traditional delay estimation based on ica requires the trail sequences to initialize the receiver, but the new algorithm based on ica does not need the trail sequences. it is based on the channel character of downlink, using the ica algorithm to estimate the multi - path mixture matrix, then, find the delay information which is embodied by the column vector of the mixture matrix. the simulation results show that it does enhance the performance of traditional detector without wasting the invaluable frequency resource
傳統的通道估計演算法需要訓練序列使接收端的參數調整到理想狀態，而本文提出的基於ica的通道估計的多用戶檢測演算法不需要訓練序列，它是利用下行通道的固有特點，用ica的盲源分離法估計出多徑通道的卷積矩陣，從而從中提取出通道的延遲信息，模擬實驗結果證明這種方法在節省了頻譜資源的同時取得較好的估計效果，使得傳統的接收機的誤碼性能得到了很大的提高。By combining the information from the cdna sequences with functions of their homologs, we suggest that two kinds of hormones may play important roles during flower regeneration in a few ways : ( i ) proteolytic system of ubiqutin / 26s proteosome complex, ( ii ) actin - dependent vesicular cycling of auxin efflux carrier, ( iii ) regulating transcription of genes, ( iv ) phosphorylation and dephosphorylation
經過進一步的篩選，結合序列特徵和同源基因的功能信息對這些基因功能進行了初步分析。認為兩種外源激素可能通過泛素26s蛋白酶體復合體對調節蛋白的降解機制，生長素運輸載體肌動蛋白依賴的小泡運輸，基因轉錄調節，磷酸化和去磷酸化等調節過程誘導風信子花分生組織的再生。Usted homology sequence
調節同調序列Blastn analysis showed that each of the 10 sequences had no homology with the structural genes or regulatory genes in the anthocyanin biosynthesis. it was suggested that there were some limitations to isolate the specific ast gene by ddrt - pcr
Blastn分析表明，這10個差異表達的cdna片段與數據庫中花青苷生物合成途徑中的結構基因和調節基因序列沒有同源性，表明用ddrt - pcr的方法克隆特定的ast基因有一定的局限性。Its well established pkb play an important role in cellular processes such as glucose metabolism, cell proliferation, apoptosis, and transcription and cell migration. there are recent indications that pkb could have a wide spread function in cell cycle regulation, but little is known about the effect of pkb on the regulation of mammalian cell cycle, especially the mouse fertilized eggs
Pkb akt的氨基酸序列測定揭示了它的c末端1 - 147位是調節區，稱為ah結構域，其中1 - 106位是ph結構域，這個區域包含約100個氨基酸，是血小板中pkc底物同源序列，且在pkb akt ， rasgtp ， msos和- spectrin中均被發現。We divided all stpks into 5 subfamilies according to their own structure characterizes. stk - i only possess regions similar to the typical catalytic domain of stpks, stk - ii contain wd40 repeats, stk - iii contain all kinds of regulator domain in their c - terminal region, stk - iv have their catalytic domains located in the n - terminal region, while hstk - i also have a his kinase domain of two - component system
按照stpks結構的不同可劃分為五個亞類： stk -亞類只含有一個催化區域； stk -亞類的c端含有wd40重復序列； stk -亞類的c端含有不同的調節區域； stk -亞類的催化區域位於c端， hstk -亞類則既含有絲氨酸蘇氨酸激酶的催化區域，又含有組氨酸激酶催化區域。分享友人