期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
AZF microdeletions and partial deletions of AZFc region on the Y chromosome in Moroccan men 被引量:22
1
作者 Laila Imken Brahim El Houate +10 位作者 Abdelaziz Chafik Halima Nahili Redouane Boulouiz Omar Abidi Elbakkay Chadli Noureddine Louanjli Abdelouhab Elfath Mohammed Hassar ken mcelreavey Abdelhamid Barakat Hassan Rouba 《Asian Journal of Andrology》 SCIE CAS CSCD 2007年第5期674-678,共5页
Aim: To evaluate for the first time the frequency of Y chromosome microdeletions and the occurrence of the partial deletions of AZFc region in Moroccan men, and to discuss the clinical significance of AZF deletions. ... Aim: To evaluate for the first time the frequency of Y chromosome microdeletions and the occurrence of the partial deletions of AZFc region in Moroccan men, and to discuss the clinical significance of AZF deletions. Methods: We screened Y chromosome microdeletions and partial deletions of the AZFc region of a consecutive group of infertile men (n = 149) and controls (100 fertile men, 76 normospermic men). AZFa, AZFb, AZFc and partial deletions of the AZFc region were analyzed by polymerase chain reaction (PCR) according to established protocols. Results: Among the 127 infertile men screened for microdeletion, four subjects were found to have microdeletions: two AZFc deletions and two AZFb+AZFc deletions. All the deletions were found only in azoospermic subjects (4/48, 8.33%). The overall AZFc deletion frequency was low (4/127, 3.15%). AZF microdeletions were not observed in either oligoasthenoteratozoospermia (OATS) or the control. Partial deletions of AZFc (gr/gr) were observed in a total of 7 of the 149 infertile men (4.70%) and 7 partial AZFc deletions (gr/gr) were found in the control group (7/176, 3.98%). In addition, two b2/b3 deletions were identified in two azoospermic subjects (2/149, 1.34%) but not in the control group. Conclusion: Our results suggest that the frequency of Y chromosome AZF microdeletions is elevated in individuals with severe spermatogenic failure and that gr/gr deletions are not associated with spermatogenic failure. 展开更多
关键词 Y microdeletions HAPLOGROUPS gr/gr INFERTILITY bi-allelic markers
下载PDF
Transcriptional diversity of DMRT1(dsx-and mab3.related transcription factor1)in human testis
2
作者 Han Hua Cheng Ming Ying +3 位作者 Yi Hao Tian Yiqing Guo ken mcelreavey Rong Jia Zhou 《Cell Research》 SCIE CAS CSCD 2006年第4期389-393,共5页
在性决心的进化遗传的最近的进展显示到目前为止在数之中发现的性决心的那唯一的分子的类似在苍蝇之间两倍性,蠕虫 mab-3 和脊椎动物 DMRT1 (dsx 相关、 mab3 相关的抄写因素 1 )/DMY 基因。每这些因素编码 zinc-finger-like DNA 有约... 在性决心的进化遗传的最近的进展显示到目前为止在数之中发现的性决心的那唯一的分子的类似在苍蝇之间两倍性,蠕虫 mab-3 和脊椎动物 DMRT1 (dsx 相关、 mab3 相关的抄写因素 1 )/DMY 基因。每这些因素编码 zinc-finger-like DNA 有约束力的主题, DM 领域。进人的 DMRT1 基因的进化和函数的卓见能揭示性开发的进化机制。这里,我们在睾丸报导人的 DMRT1 的多重 isoforms 的鉴定和描述。这些抄本与 373, 275 和 175 氨基酸编码预言的蛋白质,他们被在 3' 区域的其他的拼接产生。DMRT1a 的表示水平比 DMRT1b 和 c 的那些高,并且 DMRT1c 表示在睾丸是最低的,基于从即时荧光灯的量的 RT-PCR 分析的吝啬的价值的比较。DMRT1b 和 c 源于 intronic 序列的 exonization,包括一个算术逻辑单元元素的 exonization。为在 DMRT1 基因以内的算术逻辑单元元素的进一步的搜索证明所有 99 个算术逻辑单元元素在两个方向上的非编码的区域之中是非随机分布式的。DMRT1 的这些新特征将在性发展机制的进化上有重要影响。 展开更多
关键词 睾丸组织 细胞分化 医学实验 DMRT1
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部