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  • 匿名
关注:1 2013-05-23 12:21

求翻译:Lampreys are agnathans (vertebrates without jaws). They occupy a key phylogenetic position in the emergence of novelties and in the diversification of Kallmann syndrome (KS) is a clinically and genetically heterogeneous disorder that occurs in either an inherited or a sporadic manner. KS results from failed embryonic migration of GnRH-1 neurons from the nasal placode to the hypothalamus, due to the abnormal development of olfactory nerves and bulbs. Hypogonadotropic hypogonadism is related to GnRH deficiency, and anosmia is associated with the absence or hypoplasia of olfactory bulbs and tracts. KS patients can also present some non-reproductive or non-olfactory anomalies in addition to the above typical symptoms. For the high complexity of the molecular genetic mechanism of KS, to date, only 6 KS-related genes have been identified. The KAL1 gene is responsible for the X chromosome-linked recessive form of KS, while the fibroblast growth factor receptor 1 (FGFR1/KAL2) and fibroblast growth factor 8 (FGF8/KAL6) genes are related to the autosomal dominant form of the disease. However, the mutations in these 6 genes account for only about 25 - 30% of all KS cases, which suggests that other pathogenic genes involved in KS remain to be discovered. This article presents an overview on the studies of the pathogenic genes, clinical diagnosis and treatment of KS.是什么意思?

待解决 悬赏分:1 - 离问题结束还有
Lampreys are agnathans (vertebrates without jaws). They occupy a key phylogenetic position in the emergence of novelties and in the diversification of Kallmann syndrome (KS) is a clinically and genetically heterogeneous disorder that occurs in either an inherited or a sporadic manner. KS results from failed embryonic migration of GnRH-1 neurons from the nasal placode to the hypothalamus, due to the abnormal development of olfactory nerves and bulbs. Hypogonadotropic hypogonadism is related to GnRH deficiency, and anosmia is associated with the absence or hypoplasia of olfactory bulbs and tracts. KS patients can also present some non-reproductive or non-olfactory anomalies in addition to the above typical symptoms. For the high complexity of the molecular genetic mechanism of KS, to date, only 6 KS-related genes have been identified. The KAL1 gene is responsible for the X chromosome-linked recessive form of KS, while the fibroblast growth factor receptor 1 (FGFR1/KAL2) and fibroblast growth factor 8 (FGF8/KAL6) genes are related to the autosomal dominant form of the disease. However, the mutations in these 6 genes account for only about 25 - 30% of all KS cases, which suggests that other pathogenic genes involved in KS remain to be discovered. This article presents an overview on the studies of the pathogenic genes, clinical diagnosis and treatment of KS.
问题补充:

  • 匿名
2013-05-23 12:26:38
诺曼底是 agnathans (颌骨无脊椎动物)。他们占据关键的系统发育地位中出现的精品和多样化的功能低下综合症 (KS) 是发生在继承的一种临床和基因异构紊乱或零星的方式。KS 下丘脑,由于对嗅神经和灯泡的异常发展从鼻 placode GnRH 1 神经元失败胚胎迁移的结果。青少年是性腺激素释放激素缺乏与嗅觉障碍是缺乏或发育不全的嗅球和大片与相关联。KS 病人还可能会带来一些非生殖或非嗅的异常,除了上述的典型症状。高复杂性的分子遗传机制的 KS,到目前为止,已确定了只有 6 KS 相关基因。KAL1 基因是负责链接 X 染色体隐性形式 KS,同时碱性成纤维细胞生长因子受体 1 (FGFR1/KAL2) 和碱性成纤维细胞生长因子 8 (FGF8/KAL6) 的常染色体显性遗传的主导形式的疾病相关基因。不过,在这些 6 基因突变占仅约 25-30%的所有 KS 情况下,这表明其他致病基因的 KS 仍被发现。这篇文章的致病基因、 临床诊断和治疗的 KS 研究概述。
 
 
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