5篇
您的检索式：作者名="Ren Junguo"
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| 1 | Hydrogen production from diluted molasses by anaerobic hydrogen producing bacteria in an anaerobic baffled reactor (ABR)显示文摘 | Jianzheng Li Baikun Li Gefu Zhu Nanqi Ren Lixin Bo Junguo He | 2007 | International Journal of Hydrogen Energy2007，，15： | 1 |
| 2 | Anaerobic biohydrogen production from monosaccharides by a mixed microbial community culture显示文摘 | Jianzheng Li Nanqi Ren Baikun Li Zhi Qin Junguo He | 2007 | Bioresource Technology2007，，14： | 1 |
| 3 | STATIC SHAPE CONTROL OF LAMINATED PLATE CONTAINING PIEZOELECTRIC PATCHES显示文摘By applying the Heaviside function,the equations governing laminated plates possess-ing spatially distributed piezoelectric patches have been established.Based on these equations,staticshape control of laminated plates is discussed.By using a genetic and collocation algorithm,the opti-mal locations and scales of these piezoelectric patches have been selected.Numerical examples are pre-sented to illustrate the efficiency of the algorithm and the piezoelectric actuators. | Lin Xiqiang Ren Junguo | 1998 | Acta Mechanica Solida Sinica1998，11，2： | 1 |
| 4 | Anaerobic biohydrogen production from monosaccharides by a mixed microbial community culture显示文摘 | Li Jianzheng Ren Nanqi Li Baikun Qin Zhi He Junguo | | 0，，14： | 1 |
| 5 | Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome显示文摘Long QT syndrome(LQTS)is the prototype of the cardiac ion channelopathies,which cause syncope and sudden death.Inherited LQTS is represented by the autosomal dominant Romano-ward syndrome(RWS),which is not accompanied by congenital deafness,and the autosomal recessive Jervell and Lange-Nielsen syndrome(JLNS),which is accompanied by congenital deafness.The LQTS-causing mutations have been reported in patients and families from Europe,North America and Japan.Few genetic studies have been carried out in families with JLNS from China.This study investigates the molecular pathology in four families with LQTS(including a family with JLNS)in the Chinese population.Polymerase chain reaction and DNA sequencing were used to screen for KCNQ1,KCNH2,KCNE1,KCNE2 and SCN5A mutation.A missense mutation G314S in an RWS family was identified,and a single nucleotide polymorphism(SNP)G643S was indentified in the KCNQ1 of the JLNS family.In this JLNS family,another heterozygous novel mutation in exon 2a was found in KCNQ1 of the patients.Our data provide useful information for the identification of polymorphisms and mutations related to LQTS and the Brugada Syndrome(BS)in Chinese populations. | DU Rong TIAN Li YUAN Guohui LI Jin REN Faxin GUI Le LI Wei ZHANG Shouyan KANG Cailian YANG Junguo | 2007 | Frontiers of Medicine2007，1，3： | 0 |
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