维普期刊资源整合服务平台（V6.5）

27篇 您的检索式：作者名="Ferguson BM"

选中清除导出查看参考文献查看引证文献引用追踪共2页首页上一页第1页下一页末页 /2 跳转

	题名	作者	年代	出处	被引量
1	Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia显示文摘	Monreal AW Ferguson BM Headon DJ	1999	Nat Genet1999，22，4：	1
2	Cloning of Tabby,the murine homolog of the human EDA gene:evidence for a membrane-associated protein with a short collagenous domain显示文摘	Ferguson BM Brockdorff N Formstone E Ngyuen T Kronmiller JE Zonana J	1997	Hum Mol Genet1997，6，9：	1
3	Gene defect in ectodermal dysplasia implicates a death domain adapter in development显示文摘	Headon DJ Emmal SA Ferguson BM	2001	Nature2001，414，：	1
4	Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia显示文摘	Monreal AW Ferguson BM Headon DJ Street SL Overbeek PA Zonana J	1999	Nat Genet1999，22，4：	1
5	Crystal structure of inhibitor- bound human 5-1ipoxygenase-activating protein 显示文摘	Ferguson AD McKeever BM Xu S	2007	Science2007，317，5837：	1
6	Gene defect in ectodermal dysplasia implicates a death domain adapter in de- velopment 显示文摘	Headon DJ Emmal SA Ferguson BM	2001	Nature2001，414，：	1
7	Cloning of Tabby, the murine homolog of the human EDA gene : evidence for a membrane - associated protein with a short collagenous domain 显示文摘	Ferguson BM Brockdorff N Formstone E	1997	Hum Mol Genet1997，6，9：	1
8	Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia显示文摘	Monreal AW Ferguson BM Headon DJ		0，，：	1
9	Alpha-2 and imidazoline receptor agonists:their pharmacology and therapeutic role显示文摘	KHAN ZP FERGUSON CN JON ES BM	1999	Anesthesia1999，54，：	1
10	Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia 显示文摘	Monreal AW Ferguson BM Headon DJ	1999	Nat Genet1999，22，4：	1
11	Cloning of Tabby,the murine homolog of the human EDA gene:evidence for a membrane-associated proteinwith a short collagenous domain显示文摘	Ferguson BM Brockdorff N Formstone E		0，，：	1
12	Embryolog- ical and molecular investigations of parental imprinting on mouse chromosome 7 显示文摘	Ferguson - Smith AC Cattanach BM Barton SC	1991	Nature1991，351，6328：	1
13	Mediastinal pancreatic pseudocysts显示文摘	JAFFE BM FERGUSON TB HOLTZ S	1972	Am J Surgery1972，124，：	1
14	Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia 显示文摘	Monreal AW Ferguson BM Headon D J	1999	Nat Genet1999，22，4：	1
15	Gene defect inectoder- mal dysplasia implicates a death domain adapter indevelopment显示文摘	Headon DJ Emmal SA Ferguson BM	2001	Nature2001，414，：	1
16	Gene defect in ectodermal dysplasia implicates a death domain adapter in development显示文摘	Headon DJ Emmal SA Ferguson BM	2001	Nature2001，414，6866：	1
17	Gene defect in ectodermal dysplasia implicates a death domain adapter in development 显示文摘	Headon D J Emmal SA Ferguson BM	2001	Nature2001，414，6866：	1
18	Gene de- fect in ectodermal dysplasia implicates a death domain adapter in development显示文摘	Headon DJ Emmal SA Ferguson BM	2001	Nature2001，414，6866：	1
19	Parental- origin-specific epigenetic modification of the mouse H19 gene显示文摘	Ferguson Smith AC Sasaki H Cattanach BM		0，，：	1
20	Gene defect in ectodermal dysplasia implicates a death domain adapter in development显示文摘	Headon DJ Emmal SA Ferguson BM	2001	Nature2001，414，6866：	1

返回顶部每页显示：

共2页首页上一页第1页下一页末页 /2 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示