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A+P一体化5G设备的使用探讨
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作者 谢涵 《电信快报》 2021年第8期29-33,共5页
随着5G时代的到来,各地5G基站的建设如火如荼,同时5G网络建设存在工程投资大、5G天线部署需要关注覆盖性能及部署周期等问题。文章针对在利旧基站建设过程中存在的天面空间受限、5G低挂高、铁塔风荷载受限等问题,对A+P(Combination of a... 随着5G时代的到来,各地5G基站的建设如火如荼,同时5G网络建设存在工程投资大、5G天线部署需要关注覆盖性能及部署周期等问题。文章针对在利旧基站建设过程中存在的天面空间受限、5G低挂高、铁塔风荷载受限等问题,对A+P(Combination of active and passive antennas)一体化设备在中国电信和中国联通的5G基站建设中的使用方式提出一些建议,根据A+P设备在不同建设场景来进行工程建设、投资分析,说明A+P一体化设备的较高实用性。 展开更多
关键词 5G覆盖 天线 基站天面空间 A%pLUS%p(Combination of active and passive antennas)
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ANALYSIS OF HUMAN PLACENTA BY ^(31)P NUCLEAR MAGNETIC RESONANCE AND THIN-LAYER CHROMATOGRAPHY SCANNING COMBINED WITH THE CORRECTIVE METHOD OF ABSORBANCE PROPORTIONAL COEFFICIENT
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作者 Rong GUO Jian wei CHEN Yi Min XU AiHua ZHANG Nanjing College of Traditional Chinese Medicine,Nanjing 210029 《Chinese Chemical Letters》 SCIE CAS CSCD 1993年第12期1081-1084,共4页
Five phospholipids in human placenta were determined by phosphorus 31 nuclear magnetic resonance(^(31)P NMR)spectroscopy and thin-layer chromatography(TLC) scanning combined with the corrective method of absorbance pr... Five phospholipids in human placenta were determined by phosphorus 31 nuclear magnetic resonance(^(31)P NMR)spectroscopy and thin-layer chromatography(TLC) scanning combined with the corrective method of absorbance proportional coefficient. The NMR spectrometer used this investigation was a Bruker AM-500 spectrometer operating at 202.4 MHz for ^(31)P chemical shifts are relative to 85% phosphoric acid. TIC was carried out by silica gel H plate developed in chloroform-methanol-glacial acetic acid-ethanol-water(25:4:6:2:0.5),with Vaskovsky reagent as colour -developing agent of phospholipids. 展开更多
关键词 p NUCLEAR MAGNETIC RESONANCE AND THIN-LAYER CHROMATOGRApHY SCANNING COMBINED WITH THE CORRECTIVE METHOD OF ABSORBANCE pROpORTIONAL COEFFICIENT ANALYSIS OF HUMAN pLACENTA BY LpC TLC
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USH2A mutation and specific driver mutation subtypes are associated with clinical efficacy of immune checkpoint inhibitors in lung cancer
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作者 DEXIN YANG YUQIN FENG +6 位作者 HAOHUA LU KELIE CHEN JINMING XU PEIWEI LI TIANRU WANG DAJING XIA YIHUA WU 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2023年第2期143-156,共14页
This study aimed to identify subtypes of genomic variants associated with the efficacy of immune checkpoint inhibitors(ICIs)by conducting systematic literature search in electronic databases up to May 31,2021.The main... This study aimed to identify subtypes of genomic variants associated with the efficacy of immune checkpoint inhibitors(ICIs)by conducting systematic literature search in electronic databases up to May 31,2021.The main outcomes including overall survival(OS),progression-free survival(PFS),objective response rate(ORR),and durable clinical benefit(DCB)were correlated with tumor genomic features.A total of 1546 lung cancer patients with available genomic variation data were included from 14 studies.The Kirsten rat sarcoma viral oncogene homolog G12C(KRAS^(G12C))mutation combined with tumor protein P53(TP53)mutation revealed the promising efficacy of ICI therapy in these patients.Furthermore,patients with epidermal growth factor receptor(EGFR)classical activating mutations(including EGFRL858Rand EGFRΔ19)exhibited worse outcomes to ICIs in OS(adjusted hazard ratio(HR),1.40;95%confidence interval(CI),1.01-1.95;P=0.0411)and PFS(adjusted HR,1.98;95%CI,1.49-2.63;P<0.0001),while classical activating mutations with EGFR^(T790)Mshowed no difference compared to classical activating mutations without EGFR^(T790)Min OS(adjusted HR,0.96;95%CI,0.48-1.94;P=0.9157)or PFS(adjusted HR,0.72;95%CI,0.39-1.35;P=0.3050).Of note,for patients harboring the Usher syndrome type-2A(USH2A)missense mutation,correspondingly better outcomes were observed in OS(adjusted HR,0.52;95%CI,0.32-0.82;P=0.0077),PFS(adjusted HR,0.51;95%CI,0.38-0.69;P<0.0001),DCB(adjusted odds ratio(OR),4.74;95%CI,2.75-8.17;P<0.0001),and ORR(adjusted OR,3.45;95%CI,1.88-6.33;P<0.0001).Our findings indicated that,USH2A missense mutations and the KRAS^(G12C)mutation combined with TP53 mutation were associated with better efficacy and survival outcomes,but EGFR classical mutations irrespective of combination with EGFR^(T790)Mshowed the opposite role in the ICI therapy among lung cancer patients.Our findings might guide the selection of precise targets for effective immunotherapy in the clinic. 展开更多
关键词 Immune checkpoint inhibitor(ICI) Lung cancer Usher syndrome type-2A(USH2A)missense mutation Kirsten rat sarcoma viral oncogene homolog G12C(KRAS^(G12C))mutation combined with tumor protein p53(Tp53)mutation Epidermal growth factor receptor(EGFR)mutation
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