GeneZhang Y, Han QL, Li CY, et al. Genetic analysis of the TBX1 gene promoter in indirect inguinal hernia[J]. Gene, 2014, 535(2): 290-293.Zhang Y, Han Q, Fan H et al (2014) Genetic analysis of the TBX2 gene promoter in indirect inguinal hernia. Hernia 18:513-517. doi:...
Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] [中文简述(自动翻译):] 这个基因是共享一个公共的DNA结合结构域,所述T-box基因的系统发育保守的家族的??一个成员。 T-box基因编码参与发育过程的调控的转录因子。
关键词TBX1基因;常染色体显性;多囊肾病中图分类号R692.12文献标志码A文章编号0258—4646(2014)08—0673—04网络出版地址http:///kcms/detail/21.1227.R.20140721.1701.016.htmlExpressionandSignificanceofTBX1GeneinKidneyTissuesinPatientswithAutosomalDominantJIANGHong—kun,GUOYan-ping,LILei2,JIANGHong,BAIYing—long3(1...
Objective To investigate the mutations of TBX1 gene in Chinese patients with congenital heart defects(CHD),and study the relationship between mutations of TBX1 gene and nonsyndromic CHD. 目的检测中国先天性心脏病患者TBX1基因突变以探讨TBX1基因突变与非综合征心脏畸形发生的相关性。 更多例句>> 2) ...
Mutations of TBX1 Gene in Chinese Patients with Congenital Heart Defects 中国先天性心脏病患者TBX1基因突变的研究 2. Researches on TBX1 Gene with Human Simple Conotruncal Heart Malformation; TBX1基因与人类单纯性心脏圆锥动脉干畸形的相关研究 3. The Regulatory Mechamisms of Zebrafih Tbx1 in Cardi...
中国先天性心脏病患者TBX1基因突变的研究 华中科技大学 硕士学位论文 中国先天性心脏病患者TBX1基因突变的研究 姓名：黄莹 申请学位级别：硕士 专业：儿科 指导教师：金润铭 20070501
More gene data Compare Top validated antibodies antibodies-online ABIN2842819 4 references Polyclonal WB ICC IHC LSBio LS-B10717 Polyclonal WB ICC IHC Abnova Corporation PAB17338 3 references Polyclonal WB ICC NovoPro Bioscience Inc. 138527 Polyclonal WB EL ICC IHC Abgent AP9383b ...
结论 Tbx1基因可能为上述综合征中某一发育异常的致病基因,与心脏圆锥干畸形致病基因的关系有待于无杂合性缺失患者的突变检测。[关键词] 心脏缺失,先天性;Tbx1基因;基因缺失;杂合子[中图分类号]R541;Q554 [文献标识码]A [文章编号]1008-1372(2003)09-1160-02HeterozygosityMicrodeletionofTbx1Geneat22q1112...
Tbx1 GeneTbx1 ExpressionPharyngeal morphogenesis is a complex process involving precise coordination of multiple cell types and transcription networks.TBX1heterozygous mutation causes DiGeorge Syndrome, a typical disorder of pharyngeal development. In mice, loss of function ofTbx1causes severe disruption ...
In vertebrates, the inner ear is comprised of the cochlea and vestibular system, which develop from the otic vesicle. This process is regulated via inductive interactions from surrounding tissues. Tbx1, the gene responsible for velo-cardio-facial syndrom