• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Assignment of mouse Gfra1, the homologue of a new human HSCR candidate gene, to the telomeric region of mouse chromosome 19.

作者信息

Puliti A, Cinti R, Seri M, Ceccherini I, Romeo G

机构信息

Laboratory of Molecular Genetics, Gaslini Institute, Genova, Italy.

出版信息

Cytogenet Cell Genet. 1997;78(3-4):291-4. doi: 10.1159/000134675.

DOI:10.1159/000134675
PMID:9465906
Abstract

Glial cell line-derived neurotrophic factor (Gdnf) and its alpha receptor (Gfra1) interact with the Ret receptor triggering its tyrosine kinase activity. As Gdnf and Ret have been linked to the development of Hirschsprung disease (HSCR), it seems likely that Gfra1 could also be a susceptibility gene for HSCR. A further HSCR candidate gene is represented by the human homologue of the Dom (Dominant megacolon) mouse mutation, mapped to Chr 15, for which the gene has not yet been identified. In order to test if Gfra1 could be the Dom gene or if it represents a new possible HSCR locus we have undertaken the mapping of the mouse Gfra1. Using specific PCR primers on a somatic cell hybrid mapping panel and fluorescence in situ hybridization with an expressed sequence tag (EST) cDNA clone corresponding to the mouse Gfra1, we mapped the gene to mouse chromosome 19D2-D3, a region with known homology with human chromosome 10q24-->q26.

摘要

相似文献

1
Assignment of mouse Gfra1, the homologue of a new human HSCR candidate gene, to the telomeric region of mouse chromosome 19.
Cytogenet Cell Genet. 1997;78(3-4):291-4. doi: 10.1159/000134675.
2
Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility.人类胶质细胞源性神经营养因子受体α1:克隆、定位、基因组结构及作为先天性巨结肠易感性候选基因的评估
Genomics. 1998 Mar 15;48(3):354-62. doi: 10.1006/geno.1997.5191.
3
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.一名先天性巨结肠病患者中胶质细胞系源性神经营养因子(GDNF)和RET的种系突变。
Nat Genet. 1996 Nov;14(3):341-4. doi: 10.1038/ng1196-341.
4
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.RET配体GDNF的种系突变不足以导致先天性巨结肠症。
Nat Genet. 1996 Nov;14(3):345-7. doi: 10.1038/ng1196-345.
5
Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.家族性先天性巨结肠病:核苷酸序列研究揭示,在六个家族中的两个家族里,RET原癌基因存在点突变,而其他候选基因中未发现。
Am J Med Genet. 2000 Sep 4;94(1):19-27. doi: 10.1002/1096-8628(20000904)94:1<19::aid-ajmg5>3.0.co;2-k.
6
Assignment of the GDNF family receptor alpha-1 (GFRA1) to human chromosome band 10q26 by in situ hybridization.
Cytogenet Cell Genet. 1997;78(3-4):289-90. doi: 10.1159/000134674.
7
Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease.胶质细胞系源性神经营养因子对与2型多发性内分泌肿瘤综合征及先天性巨结肠相关的ret突变体具有不同的刺激作用。
Endocrinology. 1998 Aug;139(8):3613-9. doi: 10.1210/endo.139.8.6124.
8
Investigation of germline GFR alpha-1 mutations in Hirschsprung disease.先天性巨结肠症中种系GFRα-1突变的研究。
J Med Genet. 1999 Mar;36(3):217-20.
9
RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems.使用两种双重变性凝胶系统对先天性巨结肠患者进行RET和GDNF基因扫描。
Hum Mutat. 2000;15(5):418-29. doi: 10.1002/(SICI)1098-1004(200005)15:5<418::AID-HUMU3>3.0.CO;2-2.
10
Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease.人类GFRA2基因座的克隆与鉴定及该基因在先天性巨结肠病中的研究。
Hum Genet. 2001 May;108(5):409-15. doi: 10.1007/s004390100506.