开云app官网登录入口网页版-官方正版

#罕见遗传病#

12篇内容 | 1051人围观

关注话题

话题活跃用户

#插入话题

插入图片

最新最热

[GetTopicListResponse(id=2172481, encodeId=435621e24812a, content=<a href='/topic/show?id=211558456be' target=_blank style='color:#2F92EE;'>#新生儿#</a> <a href='/topic/show?id=617341813de' target=_blank style='color:#2F92EE;'>#基因筛查#</a> <a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a> <a href='/topic/show?id=22ff108130ac' target=_blank style='color:#2F92EE;'>#基因组测序技术#</a>, objectTitle=关注新生，预见未来 | 一次筛查超250种罕见遗传病，GUARDIAN项目将如何利用WGS改善新生儿筛查？, objectType=article, longId=803009, objectId=0cdb80300995, topicUrl=null, isHasObj=0, objectCover=https://img.medsci.cn/Random/young-people-on-medical-staff-meeting-ZFY96R4.jpg, objectUrl=/article/show_article.do?id=0cdb80300995, replyNumber=0, likeNumber=86, createdTime=2023-12-02, rootId=0, userName=梅斯管理员, userId=cade5395722, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=上海, moduleDTOList=[ModuleDTO(moduleId=0cdb80300995, moduleTitle=关注新生，预见未来 | 一次筛查超250种罕见遗传病，GUARDIAN项目将如何利用WGS改善新生儿筛查？, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=0cdb80300995)], followStatus=false, userIsMember=false, type=null, lengthMark=0), GetTopicListResponse(id=1968950, encodeId=1445196895020, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Nat Commun：全世界只发现了135名患者的罕见遗传病，被AAV基因治疗攻克了, objectType=article, longId=214187, objectId=497f21418e41, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=497f21418e41, replyNumber=0, likeNumber=0, createdTime=2022-02-05, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=497f21418e41, moduleTitle=Nat Commun：全世界只发现了135名患者的罕见遗传病，被AAV基因治疗攻克了, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=497f21418e41)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968948, encodeId=1ffc1968948f9, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=22年前他因基因治疗而死，整个行业因此停滞，如今，AAV基因治疗终于攻克了这种罕见遗传病, objectType=article, longId=211594, objectId=b3b6211594ce, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=b3b6211594ce, replyNumber=0, likeNumber=73, createdTime=2022-03-08, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=b3b6211594ce, moduleTitle=22年前他因基因治疗而死，整个行业因此停滞，如今，AAV基因治疗终于攻克了这种罕见遗传病, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=b3b6211594ce)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968949, encodeId=42521968949d3, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Nature Communications：不止疫苗，mRNA技术还能治疗罕见遗传病, objectType=article, longId=212114, objectId=f4e82121143f, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=f4e82121143f, replyNumber=0, likeNumber=83, createdTime=2022-04-11, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=f4e82121143f, moduleTitle=Nature Communications：不止疫苗，mRNA技术还能治疗罕见遗传病, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=f4e82121143f)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968945, encodeId=2e2c196894535, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Science：新方法有助于寻找罕见遗传病的病因, objectType=article, longId=181159, objectId=e70318115957, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=e70318115957, replyNumber=0, likeNumber=70, createdTime=2020-07-19, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=e70318115957, moduleTitle=Science：新方法有助于寻找罕见遗传病的病因, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=e70318115957)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968946, encodeId=895719689460e, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Science：罕见遗传病诊断——转录组分析技术再下一城, objectType=article, longId=181596, objectId=3f9118159668, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=3f9118159668, replyNumber=0, likeNumber=76, createdTime=2020-02-09, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=3f9118159668, moduleTitle=Science：罕见遗传病诊断——转录组分析技术再下一城, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=3f9118159668)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968947, encodeId=9d50196894ee9, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=FDA批准Alnylam的RNAi疗法givosiran治疗罕见遗传病——急性肝卟啉症, objectType=article, longId=183486, objectId=889518348636, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=889518348636, replyNumber=0, likeNumber=76, createdTime=2020-11-03, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=889518348636, moduleTitle=FDA批准Alnylam的RNAi疗法givosiran治疗罕见遗传病——急性肝卟啉症, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=889518348636)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968943, encodeId=393f19689432a, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Nature：罕见遗传病比我们想得更复杂！, objectType=article, longId=149963, objectId=f799149963d2, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=f799149963d2, replyNumber=0, likeNumber=94, createdTime=2019-05-15, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=f799149963d2, moduleTitle=Nature：罕见遗传病比我们想得更复杂！, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=f799149963d2)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968944, encodeId=e7ad196894461, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=英国NICE推荐Akice公司的反义寡核苷酸药物Tegsedi用于治疗罕见遗传病：转甲状腺素相关的淀粉样蛋白变性, objectType=article, longId=164501, objectId=d2851645017f, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=d2851645017f, replyNumber=0, likeNumber=58, createdTime=2019-05-18, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=d2851645017f, moduleTitle=英国NICE推荐Akice公司的反义寡核苷酸药物Tegsedi用于治疗罕见遗传病：转甲状腺素相关的淀粉样蛋白变性, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=d2851645017f)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968942, encodeId=41131968942df, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=国内首例MDT模式成功阻断罕见遗传病基因试管婴儿出生, objectType=article, longId=104133, objectId=112f10413358, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=112f10413358, replyNumber=0, likeNumber=69, createdTime=2017-08-20, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=112f10413358, moduleTitle=国内首例MDT模式成功阻断罕见遗传病基因试管婴儿出生, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=112f10413358)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968941, encodeId=1903196894189, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Nature：罕见遗传病的新疗法, objectType=article, longId=90181, objectId=b5de901812f, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=b5de901812f, replyNumber=0, likeNumber=0, createdTime=2017-05-21, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=b5de901812f, moduleTitle=Nature：罕见遗传病的新疗法, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=b5de901812f)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968940, encodeId=47f3196894063, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=NEJM：罕见遗传病---振动荨麻疹突变基因被发现, objectType=article, longId=63107, objectId=60e86310e74, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=60e86310e74, replyNumber=0, likeNumber=113, createdTime=2016-11-19, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=60e86310e74, moduleTitle=NEJM：罕见遗传病---振动荨麻疹突变基因被发现, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=60e86310e74)], followStatus=false, userIsMember=true, type=1, lengthMark=0), GetTopicListResponse(id=1968939, encodeId=eb7b1968939aa, content=<a href='/topic/show?id=893de9586ba' target=_blank style='color:#2F92EE;'>#罕见遗传病#</a>, objectTitle=Science：PI3Kδ基因突变导致呼吸道感染复发的罕见遗传病, objectType=article, longId=26744, objectId=650f26e445c, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=650f26e445c, replyNumber=0, likeNumber=80, createdTime=2014-01-05, rootId=0, userName=wangtianj2007@, userId=7d74253, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=650f26e445c, moduleTitle=Science：PI3Kδ基因突变导致呼吸道感染复发的罕见遗传病, moduleType=article, hrefUrl=//www.sandwebs.com/article/show_article.do?id=650f26e445c)], followStatus=false, userIsMember=true, type=1, lengthMark=0)] 风湿免疫小助手

罕见遗传病

2020-05-29

梅斯管理员 (审核中...)

前往app查看评论内容

#新生儿# #基因筛查# #罕见遗传病# #基因组测序技术#

关注新生，预见未来 | 一次筛查超250种罕见遗传病，GUARDIAN项目将如何利用WGS改善新生儿筛查？

2023-12-02发表于上海

(审核中...)

前往app查看评论内容

#罕见遗传病#

Nat Commun：全世界只发现了135名患者的罕见遗传病，被AAV基因治疗攻克了

2022-02-05

(审核中...)

前往app查看评论内容

#罕见遗传病#

22年前他因基因治疗而死，整个行业因此停滞，如今，AAV基因治疗终于攻克了这种罕见遗传病

2022-03-08

(审核中...)

前往app查看评论内容

#罕见遗传病#

Nature Communications：不止疫苗，mRNA技术还能治疗罕见遗传病

2022-04-11

(审核中...)

前往app查看评论内容

#罕见遗传病#

Science：新方法有助于寻找罕见遗传病的病因

2020-07-19

(审核中...)

前往app查看评论内容

#罕见遗传病#

Science：罕见遗传病诊断——转录组分析技术再下一城

2020-02-09

(审核中...)

前往app查看评论内容

#罕见遗传病#

FDA批准Alnylam的RNAi疗法givosiran治疗罕见遗传病——急性肝卟啉症

2020-11-03

(审核中...)

前往app查看评论内容

#罕见遗传病#

Nature：罕见遗传病比我们想得更复杂！

2019-05-15

(审核中...)

前往app查看评论内容

#罕见遗传病#

英国NICE推荐Akice公司的反义寡核苷酸药物Tegsedi用于治疗罕见遗传病：转甲状腺素相关的淀粉样蛋白变性

2019-05-18

(审核中...)

前往app查看评论内容

#罕见遗传病#

国内首例MDT模式成功阻断罕见遗传病基因试管婴儿出生

2017-08-20

(审核中...)

前往app查看评论内容

#罕见遗传病#

Nature：罕见遗传病的新疗法

2017-05-21

(审核中...)

前往app查看评论内容

#罕见遗传病#

NEJM：罕见遗传病---振动荨麻疹突变基因被发现

2016-11-19

(审核中...)

前往app查看评论内容

#罕见遗传病#

Science：PI3Kδ基因突变导致呼吸道感染复发的罕见遗传病

2014-01-05

科室
- - 订阅+
  - 更多科室
工具
服务