当前位置:首页 » 翻译 
  • 匿名
关注:1 2013-05-23 12:21

求翻译:Fibroblast growth factor receptors (Fgfrs) consist of four signaling family members and one non-signaling "decoy" receptor, Fgfr-like 1 (Fgfrl1), all of which are expressed in the developing kidney. Several studies have shown that exogenous fibroblast growth factors (Fgfs) affect growth and maturation of the metanephric mesenchyme (MM) and ureteric bud (UB) in cultured tissues. Transgenic and conditional knockout approaches in whole animals have shown that Fgfr1 and Fgfr2 (predominantly the IIIc isoform) in kidney mesenchyme are critical for early MM and UB formation. Conditional deletion of the ligand, Fgf8, in nephron precursors or global deletion of Fgfrl1 interrupts nephron formation. Fgfr2 (likely the IIIb isoform signaling downstream of Fgf7 and Fgf10) is critical for ureteric morphogenesis. Moreover, Fgfr2 appears to act independently of Frs2α (the major signaling adapter for Fgfrs) in regulating UB branching. Loss of Fgfr2 in the MM leads to many kidney and urinary tract anomalies including vesicoureteral reflux. Thus, Fgfr signaling is critical for patterning of virtually all renal lineages at early and later stages of development.是什么意思?

待解决 悬赏分:1 - 离问题结束还有
Fibroblast growth factor receptors (Fgfrs) consist of four signaling family members and one non-signaling "decoy" receptor, Fgfr-like 1 (Fgfrl1), all of which are expressed in the developing kidney. Several studies have shown that exogenous fibroblast growth factors (Fgfs) affect growth and maturation of the metanephric mesenchyme (MM) and ureteric bud (UB) in cultured tissues. Transgenic and conditional knockout approaches in whole animals have shown that Fgfr1 and Fgfr2 (predominantly the IIIc isoform) in kidney mesenchyme are critical for early MM and UB formation. Conditional deletion of the ligand, Fgf8, in nephron precursors or global deletion of Fgfrl1 interrupts nephron formation. Fgfr2 (likely the IIIb isoform signaling downstream of Fgf7 and Fgf10) is critical for ureteric morphogenesis. Moreover, Fgfr2 appears to act independently of Frs2α (the major signaling adapter for Fgfrs) in regulating UB branching. Loss of Fgfr2 in the MM leads to many kidney and urinary tract anomalies including vesicoureteral reflux. Thus, Fgfr signaling is critical for patterning of virtually all renal lineages at early and later stages of development.
问题补充:

  • 匿名
2013-05-23 12:26:38
碱性成纤维细胞生长因子受体 (Fgfrs) 包括四个信号的家庭成员和非信号"假"受体 Fgfr 样 1 (Fgfrl1),所有这些都表示在肾脏发育中的一个。几项研究表明的增长和成熟后肾间质 (毫米) 和输尿管芽 (优美) 在体外培养的组织,也将影响外源性碱性成纤维细胞生长因子 (Fgfs)。在整个动物转基因和条件挖空方法表明,Fgfr1 和 Fgfr2 (主要是 IIIc 异构体) 在肾间质是早期的 MM 和优美形成的关键。配体 Fgf8,在肾单位前体或 Fgfrl1 全球删除条件删除中断肾单位形成。Fgfr2 (可能 iiib 部模拟信号下游的 Fgf7 和 Fgf10) 是输尿管形态发生的关键。此外,Fgfr2 似乎 Frs2α 独立行事 (Fgfrs 主要信号适配器) 调节优美分支。Fgfr2 MM 中损失导致包括膀胱输尿管反流的许多肾和尿路异常。因此,Fgfr 信号用于阵列的几乎所有肾宗族早期和后期阶段的发展至关重要。
 
 
网站首页

湖北省互联网违法和不良信息举报平台 | 网上有害信息举报专区 | 电信诈骗举报专区 | 涉历史虚无主义有害信息举报专区 | 涉企侵权举报专区

 
关 闭