cgg 中文意思是什麼

cgg 解釋
地球物理總公司
  1. In the normal population, the number of cgg repeats in fmr1 is highly polymorphic with the variation ranging from 6 to 54. such statistical data are obtained from caucasia people

    Fmri基因cgg重復次數在正常人中呈高度多態性，變異范圍n 6 sd ，這一變異在正常人群體中的分佈情況的統計數據主要來自高加索人群體。
  2. It excluded the expansion of cgg repeats in fmr1 gene to be the cause of the 7 patients of the xlmr families. the study on variable distribution of fmr1 cgg repeats in chinese people set up a simple and effective method for screening and gene diagnosis for fxs

    通過這一群體調查研究的進行，建立並穩定了對脆性x綜合征快速篩查和診斷的簡捷方法，並利用此方法對四個家系進行了快速基因診斷，排除7名患者的智力低下病癥由fmri基因cgg重復異常擴增所致。
  3. Fxs is mainly caused by a kind of dynamic mutation, the expansion of a cgg repeat located in the 5 ' - untranslated region ( 5 ' - utr ) of the fmr1 ( fragile x mental retardation ) gene

    該綜合癥由患者細胞中可見xq27 . 3的脆性位點fraxa而得名。絕大多數脆性x綜合征患者的發病是由於fmr1基因5端非翻譯區的三核苷酸cgg重復的不穩定擴增所致。
  4. Pcr - based analysis method was carried out in the following study. dna amplification by pcr in cgg repeats were performed on 154 people as normal control ( 73 males and 81 females ) and 23 members from four x - linked mental retardation ( xlmr ) families. after electrophoresed on a 6 % - denaturing polyacrylamide gel ( acr : bis = 19 : l ), genotypes of the objects were determined by analyzing pcr products

    本研究採用較以往更為簡便有效的pcr技術方法，對隨機抽取的154人的正常群體（男性73人、女性sl人）及來自四個智力低下家系的23名成員進行了fmr基因cgg重復序列的擴增，利用變性聚丙烯酸胺凝膠電泳技術對不同等位基因類型進行分離和統計。
  5. Unstable transmission within the cgg repeats less than 43 were found in the detection

    發現fm基因cgg重復次數在低於臨界值（ nm43 ）時也存在不穩定傳遞現象。
  6. Rt - pcr kit was from takara technology co. ltd. the sequence of the primer of pkb are shown below, together with all the sodn and saodn oligodeoxynucleotide were synthesized in takara technology co. ltd. pkb primers ; forward primer 5 ' cga gaa gcc gcg acc caa cac3 ' and reverse primer 5atg cac tac cgc cgg a3 "

    有絲分裂前， cdcz / cy山b 、組蛋白h ;激酶的活性通過被weel和myt激酶磷酸化cdcz的1卜巧和thr14殘基而抑制。在有絲分裂期mpf可以被cdc25活化，這兩個位點被去磷酸化， cdc25是蛋白水解酶，可以使cdcz的t打巧脫離磷酸化。
  7. The absence of the fmr1 gene product, fragile x mental retardation protein ( fmrp ), is believed to be responsible for the typical physical and mental characteristics of the fragile x syndrome. alleles with between 43 and 200 cgg repeats are called permutation. they are generally unmethylated with normal transcript and protein level, but are extremely unstable during transmission to next generation

    帶有前突變（ n = 43 200 ）的個體其fmr1基因通常不會甲基化，可以正常轉錄和翻譯產生fmrp ，故沒有臨床表型出現，但是，在向下一代傳遞的過程中卻是非常不穩定的，會從前突變擴增成為全突變。
  8. B - actin primers : forward 5tcc tat cgg cct cct cct ac 3 " and reverse 5aga atg tag tcc gcc agg tc 3 ", designed for 200bps. saodn oligodeoxynucleotide of pkb : stac agc ctg aga gga cct acc tg3 "

    在有絲分裂期， edc25經歷216位ser磷酸化同時其水解酶活性增強，活化的mpf磷酸化並活化edc25 ，形成正反饋，結果進一步活化mpf前體，活化的mpf促進細胞周期g2 / m期轉換。
  9. In most affected individuals, cgg repeats are massively expanded over 200 repeats ( full mutation ) and become abnormally h ypermethylated, w hich r esult i n t he s ilence o f t he fmr1 gene

    全突變患者cgg重復次數可達n 200 ，其fmr1基因的cgg重復區域本身及其附近的cpg島發生異常甲基化，引起基因關閉，而fmr1基因產物fmrp的缺乏，導致脆性x綜合征。
  10. Seeds, nursery service, organic fertilizers, biological pesticides and other agriculture accessories are available for sale in cgg office. please contact us for arrangement

    辦公室其他一般服務包括種子發售、種苗代育、有機肥料、生物農藥及其他有機農業用品發售，如欲購買請先來電查詢。
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