Assignment First

代寫論文:遺傳因素對乳腺有影響嗎

細胞顆粒存在於由DNA組成的染色體組成的基因中。DNA似乎由控制細胞結構和功能的粒子組成。它還展示了構成身體的細胞的結構和功能。這些基因被描述為指導手冊,使細胞生長和運作的過程。除此之外,在DNA中觀察到的異常被認為是導致細胞生長和功能缺陷的類型錯誤。這個基因上的錯誤是顯示相同的基因發生在家族祖先身上。

代寫論文:遺傳因素對乳腺有影響嗎

大多數遺傳性乳腺癌似乎與BRCA 1和BRCA 2這兩個異常基因有關。這兩種基因存在於每個人體內,該基因發揮的主要功能是修復細胞損傷,以及乳房、卵巢和其他細胞等身體部位的正常功能。由異常基因組成的基因似乎代代相傳。身體各部分的正常功能無法產生。10%的乳腺癌是由身體的異常功能引起的,在人類中很少觀察到(Alliot, 2006)。異常基因BRCA 1和BRCA 2提示乳腺癌的診斷,其結果在染色體的輔助下繼續發生突變。因此,該結構正被研究人員適當地傾斜關於另一部分染色體的突變,即SNP,它被證明與家族史有關。乳腺癌的發展似乎並沒有遺傳異常的乳腺癌,在這個病例中沒有家族史。

代寫論文:遺傳因素對乳腺有影響嗎

As the literature review is concerned, the topic describes the inherited breast cancers that are caused by the abnormal genes which are passed from the parent to the child. The cells particles are present in the genes that consist of the chromosomes which are made up of the DNA. The DNA seems to be consisting of the particles that control the structure and the function of the cells. It also shows the structuring and the functioning of the cells that makes up the body. The genes are depicted as the instruction manuals that enable the growth of the cells and enable the process of functioning. Apart from all these, the abnormalities observed in the DNA are indicated to be the typological errors that lead to the faulty cell growth and the functioning. The error in the gene is occurred with showing that the same gene occurs in the family ancestors.

代寫論文:遺傳因素對乳腺有影響嗎

Most of the inherited breast cancers are seemed to be associated with the two abnormal genes that are the BRCA 1 and BRCA 2. These two genes are present in each and every human being and the major function played by this gene is the repairing of the cell damage and the normal functioning of the body parts which are the breast, ovarian and the other cells. The genes consisting of the abnormalities are seemed to be passing on generation after the generations. The generation of the normal functioning of the body parts cannot be enabled. The 10% of the breast cancer is being accounted by the abnormal functioning of the body, and these are very rarely observed in the human beings (Alliot, 2006). The abnormal genes BRCA 1 and the BRCA 2 indicate the diagnosis of the breast cancers and the results are clearly illustrated from the mutations continued by the aid of chromosomes. Therefore, the structure is being appropriately leaned by the researchers regarding the mutations of the other piece of the chromosomes which is the SNP and it is illustrated to be linked with the family history. The development of the breast cancer does not seem to be inheriting the abnormal breast cancer and the no family history is being considered in this case.