Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑和细胞毒活性。EGFR激酶抑
剂。有抗血管生成活性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑剂。诱导
。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激抑制剂。有抗血管生成活性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要对人类尿苷胞苷激
(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒。EGFR激酶抑制剂。有
血管生成
。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
雌激素。选择
PKC抑制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有肿瘤
,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定
菌
。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词
分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞长抑制和细胞毒
性。EGFR激酶抑制剂。有抗血管
性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌
性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动
,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有抗血管生成活性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC抑制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活JAK-STAT
号通路在内的多种促细胞有丝分裂
号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒。EGFR激酶抑制剂。有抗血管生成
。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择PKC抑制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌
。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词
分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞制和细胞毒活性。EGFR激酶
制剂。有抗血管
成活性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
抗雌激素。选择性PKC制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有抗肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一定抗菌活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿胞
激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互联网资源自动
成,部分未经过人工审
,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Displays cytostatic and cytotoxic activity. Inhibitor of EGFR kinase. Shows antiangiogenic activity.
显示细胞生长抑制和细胞毒活性。EGFR激酶抑制剂。有血管生成活性。
Antiestrogen. Selective protein kinase C (PKC) inhibitor. Induces apoptosis.
雌激素。选择性PKC抑制剂。诱导凋亡。
Altenusin was reported as myosin light chain kinase inhibitor and sphingomyelinase inhibitor.TAN-420E has antitumor activity.
TAN-420E曾报道有肿瘤活性,易氧化为Herbimycin A,后者是很好的除草剂,并具有一
活性。
Novel oncogene with kinase-domain (NOK) can activate multiple mitogenic signaling pathways including the janus kinases (JAK) and signal transducer and activator of transcription proteins (STAT).
摘要NOK能激活包含JAK-STAT信号通路在内的多种促细胞有丝分裂信号通路。
Uridine-cytidine kinase (UCK) (EC 2.7.1.48) is a pyrimidine ribonucleoside kinase that catalyzes the phosphorylation of uridine and cytidine to UMP and CMP.
在本论文的第一章中主要是对人类尿苷胞苷激酶(UCK,EC 2.7.1.48)基因进行的一系列研究。
声明:以上例、词性分类均由互
网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。