腺嘌呤核苷酸

Objective To observe cataract incidence、characteristics、and conjunction with trinulceotide repeat,n,in the 3,-untranslated region of the myotonin protein kinase gene in twenty-five patients,consistent with typically or equivocally clinical and molecular diagnosis criteria of DM.

摘 要：目的观察强直性肌营养不良临床典型或可疑的患者并符合分子诊断标准的25例患者中白内障发病率、特点及与强直性肌营养不良蛋白激酶基因中CTG三核苷酸(C-胞嘧啶、T-胸腺嘧啶、G-乌嘌呤)重复次数的关系。

Objective To study the relationship between CTG repeat frenquency in MTPK gene and the change of ECG in patients with myotonic dystrophy.

目的 研究强直性肌营养不良症患者的肌强直蛋白激酶基因中胞嘧啶、胸腺嘧啶、鸟嘌呤CTG）三核苷酸重复次数与DM病人心电图改变的关系。

This kind of configuration suits the multi-nucleotide chain's purine pyrimidine alternate area. in 1989, the American scientists with scanning tunnel electron microscope law visual observation double helix DNA double helix DNA ︰ in 1952, Austrian lineage US biology chemist Zha Qiefu (E.chargaff,1905-) have determined in DNA 4 kind of basic group content, the discovery gland fat ling and thymine quantity are equal, the bird fat ling and cytosine quantity is equal.

这种构型适合多核苷酸链的嘌呤嘧啶交替区。1989年，美国科学家用扫描隧道电镜法直接观察到双螺旋DNA 双螺旋DNA︰1952年，奥地利裔美国生物化学家查伽夫（E.chargaff，1905—）测定了DNA中4种碱基的含量，发现其中腺膘呤与胸腺嘧啶的数量相等，鸟膘呤与胞嘧啶的数量相等。

The prestent invention discloses the cDNA sequnce of a new human reduced NADH: ubiquinone oxidoreductase 14 KDa subunit (NADH-CoQ14KDa subunit). The protein coded with the sequence is the homolog of ox's NADH-CoQB14.5b subunit.

本发明提供了一种新的人还原型烟酰胺腺嘌呤二核苷酸－辅酶Q氧化还原酶14千道尔顿亚基（NADH：ubiquinone oxidoreductase 14 kDa subunit，简称为&NADH－CoQ 14 kDa亚基&的cDNA序列，该序列编码的蛋白是牛NADH－CoQB14.5b亚基的同系物。

What would he tell Judith and the children?

他将怎样告诉朱迪丝和孩子们呢？

I this is at that time, the opinion with peacockish true girl is full of in a heart.

这就是当时的我，一个心中布满虚荣的女孩子真实的想法。