维普期刊资源整合服务平台（V6.5）

维普中文期刊产品整合服务

10篇 您的检索式：作者名="Moisan AM"

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

		题名	作者	年代	出处	被引量
	1	Structure of primate and rodent orthologs of the prostate cancer susceptibility gene ELAC2 显示文摘	Dumont M Frank D Moisan AM	2004	Biochimica et Biophysica Acta2004，1679，3：	1
	2	Role of eorticoste- roid binding globulin in the fast actions of glueocortieoids on the brain显示文摘	Moisan MP Minni AM Dominguez G	2014	Steroids2014，81，3：	1
	3	Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a mttlfistep testing approach in French-Canadian families with high risk of breast and ovarian cancer显示文摘	Simard J Dumont M Moisan AM	2007	J Med C enet2007，44，2：	1
	4	New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes 显示文摘	Moisan AM Ricketts ML Tardy V	1999	J Clin Endocrinol Metab1999，84，12：	1
	5	Effect of induced mild hy- pothermia on two pro-inflammatory cytokines and oxidative parame- ters during experimental acute sepsis 显示文摘	L6on K Moisan C Am rand A	2013	Redox Rep2013，18，3：	1
	6	A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta- hydroxysteroid dehydrogenase deficiency in 46, XX and 46,XY French- Canadians : evaluation of gonadal function after puberty 显示文摘	Alos N Moisan AM Ward L	2000	J Clin Endocrinol Metab2000，85，5：	1
	7	Structure of primate and rodent orthologs of the prostate cancer susceptibility gene ELAC2 显示文摘	Dumont M Frank D Moisan AM	2004	Biochimica et Biophysica Acta2004，1679，3：	1
	8	17α-hydroxylase/17,20-Lyase deficiency due to novel compound heterozygote mutations:treatment for tall stature in a female with male pseudohermaphroditism and spontaneous puberty in her affected sister显示文摘	Schwab KO Moisan AM Homoki J	2005	J Pediatr Endocrinol Metab2005，18，4：	1
	9	New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mu- tant enzymes 显示文摘	Moisan AM Ricketts ML Tardy V	1999	J Clin Endocrinol Metab1999，84，12：	1
	10	A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians:evaluation of gonadal function after puberty显示文摘	Alos N Moisan AM Ward L	2000	J Clin Endocrinol Metab2000，85，：	1

返回顶部每页显示：

共1页首页上一页第1页下一页末页 /1 跳转

goolge学术搜索-维普

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1　渝公网安备 50019002500403号　违法和不良信息举报中心

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