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2009年论文发表
2010-01-20 00:00 检生学院 检生学院   (点击:)

论文题目 论文作者 杂志名称 发表时间
Mitochondrial Respiratory Complex I:Structure, Function and Implication in Human Diseases 吕建新(共同第1作者) Current Medicinal Chemistry 2009,16,1266-1277
Association of vitamin D receptor polymorphisms with the risk of prostate cancer in the Han population of Southern China 吕建新(通讯作者) BMC Medical Genetics 2009,10:125,1471-2350
Implications of mitochondrial DNA mutations and mitochondrial dysfunction in tumorigenesis. 吕建新(通讯作者) Cell Res. 2009 Jul;19(7):802-15.
Mitochondrial DNA mutations in the D-Loop region may not be frequent in cervical cancer: a discussion on pitfalls in mitochondrial DNA studies. 吕建新(通讯作者) J Cancer Res Clin Oncol. 2009, 135:649-651
Analysis of mitochondrial DNA mutations in D-Loop region in thyroid lesions. 吕建新(通讯作者) Biochimica et Biophysica Acta. Gen Subjects (2009),5
Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation. 管敏鑫(通讯作者) Biochim Biophys Acta. 2009 Sep 3.
Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation. 管敏鑫(通讯作者) Biochem Biophys Res Commun. 383(2009):286-292
Interaction of aminoglycosides with human mitochondrial 12S rRNA carrying the deafness-associated mutation. 管敏鑫(通讯作者) Antimicrob Agents Chemother. 2009 Nov;53(11):4612-8.
Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family. 管敏鑫(通讯作者) Hypertension. 2009,(7)329-337
Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae. 管敏鑫(通讯作者) Mitochondrion. 9(2009)180-185
Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree. 管敏鑫(通讯作者) Hypertension. 2009(7)1083-1090
Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family. 管敏鑫(通讯作者) J Genet Genomics. 36(2009)241-250
Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation. 管敏鑫(通讯作者)/梁敏(1) Biochem Biophys Res Commun. 2009,06,05,383(3),286-292
A Novel Immunotherapy for Superficial Bladder Cancer by Intravesical Immobilization of GM-CSF. 高基民(通讯作者) J Cell Mol Med. 2009 Jul 20
c-Jun/AP-1 pathway-mediated cyclin D1 expression participates in low dose arsenite-induced transformation in mouse epidermal JB6 Cl41 cells 高基民(共同通讯作者) Toxicol Appl Pharmacol 235(2009)18-24
The Death Domain of FADD Is Essential for Embryogenesis, Lymphocyte Development, and Proliferation 周晓辉(共同第1作者) THE JOURNAL OF BIOLOGICAL CHEMISTRYVOL. 2 10(2009)9917-9926
Evidence of Extensive Homologous Recombination in the Core Genome of Rickettsia 包其郁(通讯作者)/吴金雨(1) Comparative and Functional Genomics 2009.4.11
The Repertoire and Molecular Evolution Analysis of ABC Transporters in Cyanobacteria 吴金雨(通讯作者) Journal of Molecular Evolution 2009.9.16
PGA4genomics for comparative genome assembly based on genetic algorithm optimization 吴金雨(通讯作者) Genomics 2009.6.30
Protective effect of Sulfated Achyranthes bidentata polysaccharides on streptozotocin-induced oxidative stress in rats. 陈晓明(共同第1作者) Carbohydrate Polymers 2009; 75 (3): 415
IscA/SufA paralogues are required for the [4Fe-4S] cluster assembly in enzymes of multiple physiological pathways in Escherichia coli under aerobic growth conditions 丁焕根(通讯作者)/谭国强(1) Biochemical Journal 2009,420,463-472
Evidence of Extensive homologous recombination in the core genome of Rickettsia. Comparative and Functional Genomics 包其郁(通讯作者) Comparative and Functional Genomics (2009),10.1155/2009/510270
FlyPhy: a phylogenetic analysis platform for Drosophila genes and gene families. 包其郁(通讯作者)
BMC Bioinformatics 2009, 10:123
靶向IL18_EGF融合蛋白体内抗肿瘤活性研究 吕建新(1) 中国现代医学杂志 2009年第6期
线粒体基因组D-Loop区基因多态性与2型糖尿病的相关性 吕建新(通讯作者) 遗传 2009年第3期
Hearing loss and epilepsy may be associated with the novel mitochondrial tRNASer(UCN) 7472delC mutation in a Chinese family 吕建新(通讯作者) 遗传 2009年第12期
质粒介导KPC-2型碳青霉烯酶弗劳地柠檬酸盐杆菌的研究 王彩虹(1) 中华检验医学杂志 2009年第11期
问号钩端螺旋体ompA基因分析及其组表达产物的免疫学鉴定 楼永良(通讯作者) 中华微生物学和免疫学杂志 2009年第4期
定向表达COXⅠ功能性片段减轻叠氮钠所致线粒体功能障碍 吕建新(通讯作者) 细胞生物学杂志 2009年第6期
突变乙型肝炎病毒核心蛋白的克隆及表达 张洪勤(1) 中华传染病杂志 2009年第11期
尿液跨膜丝氨酸蛋白酶2基因和ETS转录因子家族成员相关基因融合体在前列腺癌诊断中的价值 陶志华(通讯作者) 中华检验医学杂志 2009年第8期
前列腺癌组织中多基因异常甲基化检测及临床意义 陶志华(通讯作者) 中华老年医学杂志 2009年第9期
靶向IL18_EGF融合蛋白的表达及其体外抗肿瘤活性的研究 吕建新(1) 科技通报 2009年第2期
同时产arr-3利福平核糖基化转移酶和PSE-1型超广谱β内酰胺酶的1株铜绿假单胞菌 李超(1) 中华检验医学杂志 2009年第2期
核修饰基因和线粒体DNA突变致耳聋及机制研究及其功能研究 管敏鑫(通讯作者) 听力学及言语疾病杂志 2009年第4期
Association study on the mitochondrial genome region np16181-16193 variation with type 2 diabetes mellitus 吕建新(1) 中国医学遗传学杂志 2009年第1期
SOLEXA测序法研究肺炎克雷伯菌质粒基因组的耐药基因 包其郁(通讯作者) 中华微生物学和免疫学杂志 2009年第12期

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