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Early results of the integrative epigenomic-transcriptomic landscape of colorectal adenoma and cancer
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作者 You-Wang Lu Zhao-Li Ding +4 位作者 Rui Mao Gui-Gang Zhao Yu-Qi He Xiao-Lu Li Jiang Liu 《World Journal of Gastrointestinal Oncology》 SCIE 2024年第2期414-435,共22页
BACKGROUND Aberrant methylation is common during the initiation and progression of colorectal cancer(CRC),and detecting these changes that occur during early adenoma(ADE)formation and CRC progression has clinical valu... BACKGROUND Aberrant methylation is common during the initiation and progression of colorectal cancer(CRC),and detecting these changes that occur during early adenoma(ADE)formation and CRC progression has clinical value.AIM To identify potential DNA methylation markers specific to ADE and CRC.METHODS Here,we performed SeqCap targeted bisulfite sequencing and RNA-seq analysis of colorectal ADE and CRC samples to profile the epigenomic-transcriptomic landscape.RESULTS Comparing 22 CRC and 25 ADE samples,global methylation was higher in the former,but both showed similar methylation patterns regarding differentially methylated gene positions,chromatin signatures,and repeated elements.High-grade CRC tended to exhibit elevated methylation levels in gene promoter regions compared to those in low-grade CRC.Combined with RNA-seq gene expression data,we identified 14 methylation-regulated differentially expressed genes,of which only AGTR1 and NECAB1 methylation had prognostic significance.CONCLUSION Our results suggest that genome-wide alterations in DNA methylation occur during the early stages of CRC and demonstrate the methylation signatures associated with colorectal ADEs and CRC,suggesting prognostic biomarkers for CRC. 展开更多
关键词 Colorectal cancer Epigenomic alteration Transcriptome Methylation-regulated differentially expressed genes
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A survey on the status of semen analysis in 118 laboratories in China 被引量:31
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作者 Jin-Chun Lu Hong-Ye Zhang +2 位作者 Yu-An HU Yu-Feng Huang Nian-Qing Lu 《Asian Journal of Andrology》 SCIE CAS CSCD 2010年第1期104-110,共7页
收集实验室怎么表现测试的基线信息是一合理首先向为精液分析建立 intra 实验室和内部实验室的标准化和质量控制走。我们执行了执行在大陆中国测试的实验室的调查。一张问询表, 36 镇静询问盖住精液分析的所有方面,被设计,并且一个... 收集实验室怎么表现测试的基线信息是一合理首先向为精液分析建立 intra 实验室和内部实验室的标准化和质量控制走。我们执行了执行在大陆中国测试的实验室的调查。一张问询表, 36 镇静询问盖住精液分析的所有方面,被设计,并且一个拷贝对每 145 个实验室分布式。这些, 118 个实验室完成了问询表。调查结果证明那精液体积在 53.6% 视觉上被测量(59/110 ) 反应实验室,并且(73/103 ) 没有任何处理, 70.9% 不完全地分析的实验室液化了精液。另外,手册显微镜、帮助计算机的精液分析系统被使用分析精子集中,活动性和形态学。然而,超过五个方法在染色的平淡的精子被采用。连接酶的 immunosorbent 试金通常被使用决定 antisperm 抗体是否是在场的。几个精液的生物化学的标记被分析在仅仅 27.1%(32/118 ) 反应实验室。通常,为在对这调查作出回应的所有实验室的精液分析有 intra 实验室和内部实验室的质量控制措施的缺乏。在结论,精液分析和在调查实验室的测试结果的解释的方法显著地不同。特别地,许多实验室采用了除人的精液和 Spermcervical 粘液相互作用(1999 ) 的考试的世界健康组织实验室手册推荐的那些以外的方法。这些调查结果与可接受的质量控制为精液分析的标准化建议迫切需要让每个参数使结果可重复、有意义。 展开更多
关键词 实验室 精液 中国
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CETP polymorphism confer genetic contribution to centenarians of Hainan,south of China 被引量:1
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作者 Yun-Xia Zhang Ya Su +4 位作者 Li Tang Ze-Xing Yang Dai-Feng Zhou Yi-Min Qiu Wang-Wei Cai 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2016年第9期851-855,共5页
Objective:In this paper,we will discuss if the CETP polymorphism contributes to the centenarians in Hainan island.Methods:We tested the Taq IB and I405 V polymorphisms of CETP gene among 276 centenarians and 301 match... Objective:In this paper,we will discuss if the CETP polymorphism contributes to the centenarians in Hainan island.Methods:We tested the Taq IB and I405 V polymorphisms of CETP gene among 276 centenarians and 301 matched healthy individuals by AS-PCR and analyzed the data with SPSS software package(Version 19.0).Results:Our data indicated that allele B1 and V have the significant differences between centenarians and healthy control groups with P<0.001.Further analysis implied that genotypes B1B1(P<0.001,OR=0.148,95% CI=0.095-0.230) and VV(P<0.001 and OR=0.353,95% CI=0.237-0.525) were significantly different between centenarians and matched controls.The combination of B and V,such as B1B1-II(P<0.001,OR=0.128,95% CI=0.049-0.329),B1B1-IV(P<0.001,OR=0.115,95% CI=0.056-0.237),B1B2-VV(P<0.05,OR=0.534,95% CI=0.310-0.920),and B2B2-VV(P<0.001,OR=0.198,95% CI=0.086-0.453) have significant differences between centenarians and matched healthy individuals from Hainan.Conclusion:Our results implied that allele B1B1 and VV,as well as the combination B1B1-II,B1B1-IV,B1B2-VV and B2B2-VV may contribute to the longevity in centenarians of Hainan,south of China. 展开更多
关键词 CENTENARIANS POLYMORPHISMS of CETP Genetic CONTRIBUTION
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Small RNA sequencing revealed aberrant piRNA expression profiles in deciduas of recurrent spontaneous abortion patients
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作者 JIABAO WU XIAOHUA LIU +6 位作者 LU HAN HUA NIE YUAN TANG YUNGE TANG GE SONG LIXIN ZHENG WEIBING QIN 《BIOCELL》 SCIE 2022年第4期1013-1023,共11页
Piwi-interacting RNAs(piRNAs)is a novel class of non-coding RNAs.However,changes in piRNA expression profiles in recurrent spontaneous abortion(RSA)have not yet been investigated.The aim of this study was to identify ... Piwi-interacting RNAs(piRNAs)is a novel class of non-coding RNAs.However,changes in piRNA expression profiles in recurrent spontaneous abortion(RSA)have not yet been investigated.The aim of this study was to identify differentially expressed piRNAs in deciduas of RSA patients.Decidua tissues were collected by curettage from recruited RSA patients and normal early pregnant(NEP)women with their informed consent.Small RNA sequencing was used to evaluate the differences in piRNA expression profiles between RSA and NEP.The present results demonstrated that the counts of total piRNA reads in RSA samples were increased compared with those in NEP samples(0.21%vs.0.11%).Differential expression analysis identified 29 upregulated piRNAs and 18 downregulated piRNAs in RSA samples.RT-qPCR further confirmed that the expression levels of uniq-109625,uniq-89328,uniq-50651 and uniq-4569 were decreased in 8 RSA tissues,compared with 13 NEP tissues.Otherwise,pi-22628 and uniq-173406 were increased in 8 RSA tissues.Based on GO term and KEGG pathway analysis,we speculate that these piRNAs regulate RSA by targeting extracellular matrix component pathway,cell adhesion pathway and focal adhesion pathway.PiRNAs may be involved in RSA pathogenesis by target genes function on adhesion and extracellular matrix component. 展开更多
关键词 Recurrent spontaneous abortion Normal early pregnancy PIRNA RNA sequencing Expression profile
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Application of Nutritional Support in the Comprehensive Treatment of Gastric Cancer: A Case Report
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作者 Yue Li Zun Yue Zhang +3 位作者 Hua Wei Wang Jing Jiao Zhao Shi Tao Geng Kun Hua Wang 《Journal of Nutritional Oncology》 2020年第4期196-200,共5页
Objective To relieve long-term malnutrition caused by a malignant tumor affecting the pylorus and to prolong the patient survival.Methods A patient presented with complete pyloric obstruction due to pyloric tumors,and... Objective To relieve long-term malnutrition caused by a malignant tumor affecting the pylorus and to prolong the patient survival.Methods A patient presented with complete pyloric obstruction due to pyloric tumors,and achieved good therapeutic effects through nutritional support and effective chemotherapy.Results After about 40 days of treatment,all physiological indicators were improving.After chemotherapy,the pyloric tumor shrank and the complete obstruction was relieved.The patient was able to eat and drink normally.Conclusion Nutritional support,combined with chemotherapy,may effectively treat complete pyloric obstruction caused by advanced tumors. 展开更多
关键词 Nutritional support Gastric cancer Pyloric obstruction Advanced gastric cancer
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GnRH通过ERK途径来调控大鼠睾丸间质细胞类固醇激素的合成 被引量:5
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作者 Bing Yao Hai-Yan Liu +6 位作者 Yu-Chun Gu Shan-Shan Shi Xiao-Qian Tao Xiao-Jun Li Yi-Feng Ge Ying-Xia Cui Guo-Bin Yang 《Asian Journal of Andrology》 SCIE CAS CSCD 2011年第3期438-445,512,共9页
GnRH是由下丘脑神经元分泌,且在脊椎动物生殖功能中非常的必要。GnRH还被发现存在于脑以外的组织中,在睾丸间质细胞的炎阎醇激素合成过程中发挥了重要的作用。然而,信号通路对其的调节作用仍然不清楚。本研究我们主要检测MAPK信号通... GnRH是由下丘脑神经元分泌,且在脊椎动物生殖功能中非常的必要。GnRH还被发现存在于脑以外的组织中,在睾丸间质细胞的炎阎醇激素合成过程中发挥了重要的作用。然而,信号通路对其的调节作用仍然不清楚。本研究我们主要检测MAPK信号通路是否参与GnRH激动剂(GnRHa)诱导的雄激素的合成。我们建立了间质细胞的原代培养的方法。不同浓度GnRHa刺激间质细胞不同时间后3D—HSD和苇酮的量通过RT-PCR,Westernblot和RIA测定。在MAPK抑制剂PD-98059存在或不存在的情况下,我们也通过Westernblot的方法检测GnRHa对ERK1/2,JNK和p38的作用。结果显示GnRHa诱导睾酮的合成并且上调3β-HSDmRNA水平以及蛋A水平,同时也激活了ERK1/2水平,但是对JNK和p38的活化没有作用。虽然GnRHa最佳的浓度是100nmnol L-1,最佳时间是24h,但是GnRHa~]激细胞5min后ERK1/2活化作用达到最高水平,60min之内恢复到本地水平。而PD-98059则能完全阻滞ERKl/2活化,3β-HSD的上调以及睾酮合成。我们的数据显示GnRH通过ERK途径来调控大鼠睾丸间质细胞雄性激素的合成。GnRH对ERK1/2的活化诱导了3β—HSD基因和蛋白的表达,最终调节大鼠间质细胞类固醇激素的合成。 展开更多
关键词 3Β-HSD ERK1/2 GNRH JNK 睾丸间质细胞 p38
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Advantages and limitations of the parthenogenetic embryonic stem cells in cell therapy 被引量:1
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作者 Zhao-yang YU Bao-sheng HAN 《Journal of Reproduction and Contraception》 CSCD 2016年第2期118-124,共7页
Parthenogenetic embryonic stem cells(pE SCs), as "seed cells" for regenerative medicine, are an effective way to build patient-specific pluripotent stem cells, due to the fact that characteristics of self-re... Parthenogenetic embryonic stem cells(pE SCs), as "seed cells" for regenerative medicine, are an effective way to build patient-specific pluripotent stem cells, due to the fact that characteristics of self-renewal and pluripotent are similar to embryonic stem cells(ESCs). Parthenogenetic activation can be performed at meiosis I or meiosis II describing the embryos with distinct patterns of homozygosity and heterozygosity.Heterozygous pE SCs are expected to be used for autologous transplantation, while homozygous pE SCs enable to be used for allogeneic gene therapy in theory but is hampered by immunological barriers defined by the recognition of natural killer(NK)cells. In this review, we describe the mechanism of deriving heterozygous and homozygous pE SCs, and summarize the advantages and limitations of pE SCs in the area of cell therapy. 展开更多
关键词 胚胎干细胞 细胞治疗 PE公司 多向分化潜能 减数分裂 自然杀伤细胞 多能干细胞 再生医学
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Altered microRNA expression profiles of human spermatozoa in normal fertile men of different ages
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作者 Ming-Jia Zhao Yao-Nan Zhang +7 位作者 Yong-Ping Zhao Xian-Bing Chen Bao-Sheng Han Ning Ding Yi-Qun Gu Shu-Song Wang Jing Ma Mei-Ling Liu 《Asian Journal of Andrology》 SCIE CAS CSCD 2023年第6期737-744,共8页
MicroRNAs(miRNAs)are mediators of the aging process.The purpose of this work was to analyze the miRNA expression profiles of spermatozoa from men of different ages with normal fertility.Twenty-seven donors were divide... MicroRNAs(miRNAs)are mediators of the aging process.The purpose of this work was to analyze the miRNA expression profiles of spermatozoa from men of different ages with normal fertility.Twenty-seven donors were divided into three groups by age(Group A,n=8,age:20–30 years;Group B,n=10,age:31–40 years;and Group C,n=9,age:41–55 years)for high-throughput sequencing analysis.Samples from 65 individuals(22,22,and 21 in Groups A,B,and C,respectively)were used for validation by quantitative real-time polymerase chain reaction(qRT-PCR).A total of 2160 miRNAs were detected:1223 were known,937 were newly discovered and unnamed,of which 191 were expressed in all donors.A total of 7,5,and 17 differentially expressed microRNAs(DEMs)were found in Group A vs B,Group B vs C,and Group A vs C comparisons,respectively.Twenty-two miRNAs were statistically correlated with age.Twelve miRNAs were identified as age-associated miRNAs,including hsa-miR-127-3p,mmu-miR-5100_L+2R-1,efu-miR-9226_L-2_1ss22GA,cgr-miR-1260_L+1,hsa-miR-652-3p_R+1,pal-miR-9993a-3p_L+2R-1,hsa-miR-7977_1ss6AG,hsa-miR-106b-3p_R-1,hsa-miR-186-5p,PC-3p-59611_111,hsa-miR-93-3p_R+1,and aeca-mir-8986ap5_1ss1GA.There were 9165 target genes of age-associated miRNAs.Gene Ontology(GO)analysis of the target genes identified revealed enrichment of protein binding,membrane,cell cycle,and so on.The Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis of age-related miRNAs for target genes revealed 139 enriched pathways,such as signaling pathways regulating stem cell pluripotency,metabolic pathways,and the Hippo signaling pathway.This suggests that miRNAs play a key role in male fertility changes with increasing age and provides new evidence for the study of the mechanism of age-related male fertility decline. 展开更多
关键词 age FERTILITY MICRORNA SPERMATOZOA
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Gain of human telomerase RNA gene is associated with progression of cervical intraepithelial neoplasia grade Ⅰ or Ⅱ 被引量:11
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作者 LAN Yong-lian YU Lan +2 位作者 JIA Chan-wei WU Yu-mei WANG Shu-yu 《Chinese Medical Journal》 SCIE CAS CSCD 2012年第9期1599-1602,共4页
关键词 子宫颈癌 增益测量 RNA基因 端粒酶 上皮 生物标志物 3号染色体 基因探针
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Second pregnancy of trisomy 21 in a mother with mosaicism
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作者 CUI Ying-xia HAO Li-jun WANG Yun-hua XIA Xin-yi SHI Yi-chao LU Hong-yong YAO Bing HUANG Yu-feng 《Chinese Medical Journal》 SCIE CAS CSCD 2007年第14期1295-1296,共2页
In the case of a previous offspring with trisomy 21,recurrence risk for Down syndrome is about 1%.Itmay be due to chance,but the possibility of germlinemosaicism for trisomy 21 in one of the parents hasimportant impli... In the case of a previous offspring with trisomy 21,recurrence risk for Down syndrome is about 1%.Itmay be due to chance,but the possibility of germlinemosaicism for trisomy 21 in one of the parents hasimportant implications for the recurrence.Here we reporta young healthy mother,who has a second pregnancy oftrisomy 21. 展开更多
关键词 三体细胞21 镶嵌性 生物标记 妊娠
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Is serum sex hormone-binding globulin a dominant risk factor for metabolic syndrome? 被引量:6
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作者 Yi-Hong Yang Ming-Jia Zhao +6 位作者 Shan-Jie Zhou Wen-Hong Lu Xiao-Wei Liang Cheng-Liang Xiong Chang-Chun Wan Xue-Jun Shang Yi-Qun Gu 《Asian Journal of Andrology》 SCIE CAS CSCD 2015年第6期991-995,I0010,共6页
关键词 血清睾酮 代谢综合征 结合球蛋白 危险因素 性激素 Logistic回归分析 质量指数 置信区间
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Partial trisomy 4q:a case report 被引量:1
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作者 CUI Ying-xia WANG Yun-hua HAO Li-jun HOU Lin LI Wei HUANG Yun-feng 《Chinese Medical Journal》 SCIE CAS CSCD 2006年第13期1136-1139,共4页
acrocephaly,临床的调查结果经常包括象头小畸型那样的智力迟钝,发展延期和多重畸形在三染色体性 4q 症候群介绍了以及畸形的耳朵,高 / 宽广 / 沮丧的鼻音桥,牙齿和姆指异例。三染色体性 4q 被家庭平衡 translocation 或果汁饮料 no... acrocephaly,临床的调查结果经常包括象头小畸型那样的智力迟钝,发展延期和多重畸形在三染色体性 4q 症候群介绍了以及畸形的耳朵,高 / 宽广 / 沮丧的鼻音桥,牙齿和姆指异例。三染色体性 4q 被家庭平衡 translocation 或果汁饮料 novo 不平衡引起,这被建议了。我们与 46 的 karyotype 报导了三染色体性 4q 的一个新案例, XY, der (5 ) t (4; 5 )(q27; q35 ) 并且这 karyotye 第一次被报导。他的显型包括了严重智力迟钝,生长延迟,美容和姆指异例。由细胞发生的调查检测了,比较 genomic 杂交,在 situ 杂交的多色荧光,到 4qter 的从 4q27 的复制区域被证实。三染色体性 4q 是一稀罕临床的发现。到我们的知识,这是有复制碎片从 4q27 跨越到 4qter 的第八个案例。与以前描述的那些的 Comparingthe karyotypic 和 phenotypic 关联,我们与部分三染色体性 4q 报导了一个新案例症候群。 展开更多
关键词 染色体 遗传疾病 临床 治疗
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