[2]An R, Li Y Q, Lin Y L, et al. EZH1/2 as targets for cancer therapy[J]. Cancer Gene Therapy, 2023, 30(2): 221-235.
Siah1/2-dependent gene expression analysis confirms an ER stress signature.Marzia ScortegagnaHyungsoo KimJianLiang LiHang YaoLaurence M. BrillJaeseok HanEric LauDavid BowtellGabriel HaddadRandal J. Kaufman
The new mutation of dync2h1 gene leads to short costal thoracic dysplasia with or without polydactyly syndrome type 3 Wang Junxia Wang Fangna Li Juan Shi Zijia Cheng Qingqing Zheng Zongpeng Chu Wei Gao Jian Authors Info & Affiliations Published: 2022 -03 -05 · DOI: 10.3760/cma...
品系全名 C57BL/6Smoc-Tph1em2Smoc 目录号 NM-KO-231220 品系状态 胚胎冻存 导出PDF 基因信息 基因名 Tph1 基因曾用名 Tph NCBI ID 21990 MGI ID 98796 Ensembl ID ENSMUSG00000040046 Pubmed Tph1 人类同源基因 TPH1 品系描述 The exon4 of Tph1 gene was deleted to generate Tph1 knockout mouse. ...
这个基因编码一个大的细胞质动力蛋白,它参与纤毛的逆行运输,并在鞭毛内运输中发挥作用,这是纤毛/鞭毛组装所必需的过程。该基因的突变引起与原发性纤毛功能改变有关的异质性疾病谱,常涉及多指畸形、骨骼发生和多囊肾。选择性剪接导致编码不同蛋白质的多个转录变体。 This gene encodes a large cytoplasmic dynein ...
geneH1-0 id3005 aliasesHBP geneSLBP id7884 genbank_ids mutation namemTurquoise2-SLBP(18-126)-IRES-H1-mMaroon1 shRNA_sequence size3043 species 9606 Homo sapiens 100 Synthetic tags resistance markers : 1358 tags : High Copy more info or order: ...
这个基因编码一个大的细胞质动力蛋白,它参与纤毛的逆行运输,并在鞭毛内运输中发挥作用,这是纤毛/鞭毛组装所必需的过程。该基因的突变引起与原发性纤毛功能改变有关的异质性疾病谱,常涉及多指畸形、骨骼发生和多囊肾。选择性剪接导致编码不同蛋白质的多个转录变体。[由RefSeq提供,2010年1月]This gene encodes a larg...
This gene encodes a large cytoplasmic dynein protein that is involved in retrograde transport in the cilium and has a role in intraflagellar transport, a process required for ciliary/flagellar assembly. Mutations in this gene cause a heterogeneous spectrum of conditions related to altered primary ciliu...
Entrez Gene ID:(Human) 11221 功能 phosphoprotein phosphatase activityprotein tyrosine phosphatase activityphosphatase activityMAP kinase tyrosine/serine/threonine phosphatase activityMAP kinase phosphatase activityprotein phosphatase 参与通路 inactivation of MAPK activityregulation of adaptive immune responseprotein dep...
DYNC2H1gene and clinical phenotypes were consistent with the diagnosis of short rib-thoracic dysplasia typeⅢ,which was verified by Sanger.In this case,the mutation was inherited from the parents who had normal clinical phenotype.The homozygous mutation of c.4267C>T of the DYNC2H1gene is the ...