
ABL (gene) - Wikipedia
The ABL1 proto-oncogene encodes a cytoplasmic and nuclear protein tyrosine kinase that has been implicated in processes of cell differentiation, cell division, cell adhesion, and stress response such as DNA repair.
ABL1 Gene - GeneCards | ABL1 Protein | ABL1 Antibody
Mar 28, 2025 · ABL1 (ABL Proto-Oncogene 1, Non-Receptor Tyrosine Kinase) is a Protein Coding gene. Diseases associated with ABL1 include Congenital Heart Defects And Skeletal Malformations Syndrome and Leukemia, Chronic Myeloid.
浅谈白血病常见致病基因BCR、ABL1、BCR-ABL1、JAK2的意义
二、 abl1基因. 原癌基因,abl1蛋白的sh3结构域缺失会使abl1成为原癌基因,这种基因会常常和其他多种基因发生“不正当关系”,常见的就是与bcr基因融合成bcr-abl1,变异后的。 三、 bcr-abl1基因
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
Gene ID: 25, updated on 20-Feb-2025. This gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress.
【AmBeed简析】解读BCR-ABL1:从作用机制到抑制剂应用的探索
Jun 4, 2024 · Imatinib是一种TKI(酪氨酸激酶抑制剂),专门针对BCR-ABL1融合蛋白活性,显著改善了大多数CML患者的生存期和预后,目前这种药物被认为是标准疗法。 Imatinib 与ATP竞争 BCR-ABL1 激酶的ATP 结合口袋,从而抑制其进一步磷酸化。 在 Imatinib 之前,新确诊的CML 患者的中位存活率为 3-5 年,而在2015年,CML患者的10年生存率大于80% [2,4]。 虽然Imatinib非常成功,但患有BCR-ABL1白血病的CML病例中,有一部分要么在规定时间内对Imatinib不敏 …
ABL1 gene - MedlinePlus
The ABL1 gene provides instructions for making a protein involved in many processes in cells throughout the body. The ABL1 protein functions as a kinase, which is an enzyme that changes the activity of other proteins by adding a cluster of oxygen and phosphorus atoms (a phosphate group) at specific positions.
ABL 原癌基因 1,非受体酪氨酸激酶(ABL1)基因 | MCE
该基因是一种原癌基因,编码参与多种细胞过程的蛋白酪氨酸激酶,包括细胞分裂、粘附、分化和应激反应。 该蛋白的活性受其 SH3 结构域的负调控,因此删除编码该结构域的区域会导致致癌基因。 普遍表达的蛋白质具有受 CDC2 介导的磷酸化调节的 DNA 结合活性,表明细胞周期功能。 已发现该基因与各种白血病中的多种易位伙伴基因融合,最显着的是导致与断点簇区域基因 5' 端融合的 t (9;22) 易位 (BCR; MIM:151410) .该基因的可变剪接导致两个转录本变体,其中包含可 …
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase [Homo sapiens ...
Mar 26, 2025 · Title: Human ABL1 deficiency syndrome (HADS) is a recognizable syndrome distinct from ABL1-related congenital heart defects and skeletal malformations syndrome. Characteristics and literature review of ETV6::ABL1 fusion gene-positive acute myeloid leukemia.
Structure, Regulation, Signaling, and Targeting of Abl Kinases in ...
The Abl family of cytoplasmic tyrosine kinases consists of 2 members, Abl and Arg (Abl-related gene), encoded by the ABL1 and ABL2 genes in humans, and has important roles in various biological processes. 1,2 Abl kinases share a central SH2-kinase domain unit with the majority of other cytoplasmic kinases 3 and have a long C-terminal tail ...
ABL1基因的功能与作用机制解析 - 八方基因
Dec 29, 2024 · abl1基因是一个多功能的非受体酪氨酸激酶,通过调控多个信号通路来影响细胞的多种生物学过程。 它的异常与多种癌症的发生密切相关,特别是通过形成BCR-ABL融合基因导致的慢性髓性白血病。