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文章名     作者     期刊名     摘要     卷     期         如果没有找到您所需要的文献，请点击 ——此处申请     共32条记录   Transcriptome analysis of tree peony during chilling requirement fulfillment: Assembling, annotation and markers discovering [作者：Gai, SP; Zhang, YX; Mu, P; Liu, CY; Liu, S; Dong, L; Zheng, GS,期刊：Gene, 页码：256-262 , 文章类型： Article，,卷期：2012年497-2] Tree peony (Paeonia suffruticosa Andrews) is a well-known horticultural and medicinal plant. The flower buds must go through a period of endo-dormancy before bud sprouting in winter, but very little information concerned... Construction and validation of a GFP-based vector for promoter expression analysis in the fish pathogen Flavobacterium psychrophilum [作者：Gomez, E; Perez-Pascual, D; Fernandez, L; Mendez, J; Reimundo, P; Navais, R; Guijarro, JA,期刊：Gene, 页码：263-268 , 文章类型： Article，,卷期：2012年497-2] The study of the fish pathogen Flavobacterium psychrophilum has been drastically hampered by the difficulty to perform genetic manipulation of this organism. Although recent publications described the successful transfer... A new approach to touch down method using betaine as co-solvent for increased specificity and intensity of GC rich gene amplification [作者：Pratyush, DD; Tiwari, S; Kumar, A; Singh, SK,期刊：Gene, 页码：269-272 , 文章类型： Article，,卷期：2012年497-2] Tissue specific genes that contain high GC segments are difficult to amplify by standard PCR. We report an improved method for successful amplification of gene segment that has > 70% GC base pairs. This new method of tou... Paradoxical role of C1561T glutamate carboxypeptidase II (GCPII) genetic polymorphism in altering disease susceptibility [作者：Divyya, S; Naushad, SM; Addlagatta, A; Murthy, PVLN; Reddy, CR; Digumarti, RR; Gottumukkala, SR; Kumar, A; Rammurti, S; Kutala, VK,期刊：Gene, 页码：273-279 , 文章类型： Article，,卷期：2012年497-2] Glutamate carboxypeptidase II (GCPII) is predominantly expressed in brain, intestinal mucosa and prostate cancer in the form of three splice variants i.e. N-acetylated-alpha-linked acidic dipeptidase (NAALADase), folyl p... A major imprinted gene involved in hydatidiform mole is not located in 2q31.2-qter or 5q34-qter [作者：Lund, H; Nyegaard, M; Svarrer, T; Grove, A; Sunde, L,期刊：Gene, 页码：280-284 , 文章类型： Article，,卷期：2012年497-2] Introduction: Hydatidiform mole is an abnormal human pregnancy, characterised by absent or abnormal embryonic differentiation, vesicular chorionic villi and trophoblastic hyperplasia. Although the mole phenotype has here... LADA and T1D in Estonian population - Two different genetic risk profiles [作者：Kisand, K; Uibo, R,期刊：Gene, 页码：285-291 , 文章类型： Article，,卷期：2012年497-2] Aims/hypothesis: The aim of our study was to analyze combined impact of 17 polymorphisms at 8 gene regions previously shown to be associated with autoimmunity in diabetes. We hypothesized that the genetic predisposition ... Rapp-Hodgkin syndrome and SHFM1 patients: Delineating the p63-Dlx5/Dlx6 pathway [作者：Vera-Carbonell, A; Moya-Quiles, MR; Ballesta-Martinez, M; Lopez-Gonzalez, V; Bafalliu, JA; Guillen-Navarro, E; Lopez-Exposito, I,期刊：Gene, 页码：292-297 , 文章类型： Article，,卷期：2012年497-2] Rapp-Hodgkin Syndrome (RHS) is a genetic disorder resulting from mutations in the TP63 gene encoding p63 transcription factor. p63 is directly associated with a cis-regulatory element on chromosome 7q21 that controls the... Lack of common genetic factors for susceptibility to vascular dementia and Alzheimer's disease [作者：Kim, Y; Kong, M; Lee, C,期刊：Gene, 页码：298-300 , 文章类型： Article，,卷期：2012年497-2] Since vascular risk factors commonly act for susceptibility to Alzheimer's disease (AD) and vascular dementia (VaD) by declining cognitive abilities, we conducted a genetic association study to identify their common unde... Candesartan antagonizes pressure overload-evoked cardiac remodeling through Smad7 gene-dependent MMP-9 suppression [作者：Yu, H; Zhao, G; Li, H; Liu, XJ; Wang, SJ,期刊：Gene, 页码：301-306 , 文章类型： Article，,卷期：2012年497-2] The present study was designed to investigate the underlying molecular mechanism for Angiotensin II type 1 receptor blockers (ARBs) mediated cardio-protection against pressure overload-induced cardiac remodeling with a f... Genetic and transcriptional organization of the groEL operon containing trxA in Gemella morbillorum [作者：Hung, WC; Chen, HJ; Tseng, SP; Liaw, SJ; Tsai, JC; Hsueh, PR; Teng, LJ,期刊：Gene, 页码：307-313 , 文章类型： Article，,卷期：2012年497-2] Gemella morbillorum, a low G + C content Gram-positive bacterium, is considered to be a commensal organism in humans but occasionally causes endocarditis or other diseases. We determined the sequences of groESL, dnaK and... Impact of glutathione-S-transferase gene polymorphisms on enzyme activity, lung function and bronchial asthma susceptibility in Egyptian children [作者：Karam, RA; Pasha, HF; El-Shal, AS; Rahman, HMA; Gad, DM,期刊：Gene, 页码：314-319 , 文章类型： Article，,卷期：2012年497-2] Background: Asthma is a complex multifactorial disease with an obvious genetic predisposition. Polymorphisms of the glutathione-S-transferase (GST) genes are known risk factors for some environmentally-related diseases. ... A variant of unknown significance in the GLA gene causing diagnostic uncertainty in a young female with isolated hypertrophic cardiomyopathy [作者：Al-Thihli, K; Ebrahim, H; Hughes, DA; Patel, M; Tipple, M; Salvarinova, R; Gardiner, J; Vallance, H; Waters, PJ,期刊：Gene, 页码：320-322 , 文章类型： Article，,卷期：2012年497-2] Hypertrophic cardiomyopathy (HCM) is genetically heterogeneous, and largely caused by mutations in genes encoding sarcomere proteins. However, GLA mutations causing Fabry disease, an X-linked lysosomal storage disorder, ... SIRT3 gene expression: A link between inherited mitochondrial DNA variants and oxidative stress [作者：D'Aquila, P; Rose, G; Panno, ML; Passarino, G; Bellizzi, D,期刊：Gene, 页码：323-329 , 文章类型： Article，,卷期：2012年497-2] Signaling pathways between mitochondrial and nuclear genomes are activated to preserve cellular homeostasis, especially in the event of stress. Using cybrid cell lines, we investigated whether inherited mitochondrial DNA... Deep sequencing analysis of small non-coding RNAs reveals the diversity of microRNAs and piRNAs in the human epididymis [作者：Li, Y; Wang, HY; Wan, FC; Liu, FJ; Liu, J; Zhang, N; Jin, SH; Li, JY,期刊：Gene, 页码：330-335 , 文章类型： Article，,卷期：2012年497-2] The epididymis plays a crucial role in regulating the development of sperm motility and fertilizing capacity. Small non-coding RNAs (sncRNAs), especially microRNAs (miRNAs), can participate in the regulation of various p... Study on the age-dependent tissue expression of FUT1 gene in porcine and its relationship to E. coli F18 receptor [作者：Bao, WB; Ye, L; Zi, C; Su, XM; Pan, ZY; Zhu, J; Zhu, GQ; Huang, XG; Wu, SL,期刊：Gene, 页码：336-339 , 文章类型： Article，,卷期：2012年497-2] Escherichia coil (E. coli) that produces adhesin F18 is the main pathogen responsible for porcine post-weaning diarrhea and edema disease. The receptor for E. coli F18 has not been described in pigs, however the alpha (1... Stearoyl-CoA Desaturase 1 (SCD1) is a key factor mediating diabetes in MyD88-deficient mice [作者：Yokoyama, S; Hosoi, T; Ozawa, K,期刊：Gene, 页码：340-343 , 文章类型： Article，,卷期：2012年497-2] Saturated fatty acids, acting as ligands for toll-like receptor 4 (TLR4), induce inflammation and mediate the development of insulin resistance. Myeloid differentiation factor 88 (MyD88) is an adaptor protein for TLR4. P...