Assessment of homozygosity in gynogenetic diploid using microsatellite markers in scallop,Chlamys farreri;
微卫星评价栉孔扇贝雌核发育二倍体纯合性
Assessment of Homozygosity in Gynogenetic Diploid Using Microsatellite Markers in Japanese Flounder (Paralichthys olivaceus);
微卫星评价牙鲆雌核发育二倍体纯合性
Moreover, Junction PCR was emplyed to confirm the integration site and analyze zygosity.
据此,本实验主要研究了绿色荧光蛋白转基因猪及其子代中外源基因拷贝数和整合位点,并利用Junction-PCR对整合位点进行确定,同时进一步分析了整合位点的纯合性。
Transgene copy number and integration site were checked in transgenic pigs produced by somatic cell nuclear transfer (SCNT),moreover,Junction PCR was employed to confirm the integration site and analyze zygosity.
主要采用了绝对定量PCR和热不均一交错PCR(thermal asymmetric interlaced PCR,TAIL-PCR),检测了体细胞核移植技术生产的绿色荧光蛋白转基因猪中外源基因拷贝数和整合位点,并利用旁侧PCR(Junction PCR)对整合位点进行确定,同时进一步分析了整合位点的纯合性。
Detection of homozygous deletion and mutation of exon 5 and exon 8 of FHIT gene in differentiated thyroid carcinoma tissue;
分化型甲状腺癌组织中脆性组氨酸三联体基因外显子5、8纯合性缺失及突变检测
The homozygous deletion was detectyed by multiple PCR analysis and mutation by PCR-SSCP and DNA sequencing followed.
方法采用多重PCR、PCR-SSCP和DNA测序对62例胃癌、癌旁组织及10例正常胃黏膜标本中p16INK4a基因纯合性缺失和突变进行检测。
Aim: To investigate the frequencies of homozygous deletion of entire coding exons of fragile histidine triad (FHIT) gene in laryngeal squamous cell carcinoma (LSCC) tissue and its clinical significance.
目的:探讨喉鳞癌(LSCC)组织中脆性组氨酸三联体(FHIT)基因编码外显子纯合性缺失及其临床意义。
The Clinical Significance of the Detection of Homozygous Deletion of p16 Gene in Pleural Effusion;
胸水p16基因纯合性缺失的检测及其临床意义
A Simplified Approach for Detecting Homologous Deletion of SMN1 Genes in Spinal Muacular Atrophy
一种简化的检测SMN1基因纯合性缺失的方法
Homozygous Deletion, Methylation, Expression and Microsatellite Instability of FHIT Gene in Laryngeal Squamous Cell Carcinoma;
喉鳞癌中FHIT基因纯合性缺失、甲基化、表达及其微卫星不稳定性研究
Study on the Homozygous Deletion and Point Mutation of P16 Gene Exons of Keratinocytes in Psoriasis;
银屑病角质形成细胞p16基因外显子纯合性缺失与点突变的研究
Homozygous deletion of FHIT gene exon5,8 and the expression of FHIT protein in gastric carcinoma
胃癌中FHIT基因外显子5、8纯合性缺失及其蛋白表达的研究
Homozygous Deletions of Exon5, 8 and Protein Expression of the Tumor-suppressor Gene FHIT in Endometrial Carcinomas;
子宫内膜癌中抑癌基因FHIT第5和第8外显子纯合性缺失与蛋白表达的研究
The Study of Death-Associated Protein Kinase Alterations in Circulating DNA of Transitional Cell Carcinoma of the Bladder: Promoter Methylation and Homozygous Deletion;
膀胱移行细胞癌患者外周血循环DNA死亡相关蛋白激酶的甲基化与纯合性缺失的研究
Study on the Relationship between 22q11 Microdeletion and Simple Congenital Heart Disease;
单纯性先天性心脏病22q11微缺失的研究
On Fault after "Straightforwardness" and "Naivety"-More Discussion on Post 80 Writing Trend of Thought;
“率性”、“纯真”后的缺失——“80后”写作思潮再论
Prokaryotic Expression, Purification and Antibody Production of sp56-lost of Rat Sperm ZP3 Binding Protein sp56;
大鼠精子ZP3结合蛋白sp56缺失肽的原核表达、纯化及其抗体的制备
Frequency of 22q11 deletions in children with isolated conotruncal defects
单纯性圆锥动脉干畸形患者染色体22q11.2微缺失的研究
Experimental Study of Loss of Heterozygosity and Imprinting of CDKN1C on Laryngeal Squamous Cell Carcinoma;
喉鳞状细胞癌中CDKN1C基因杂合性缺失和印记缺失的实验研究
The Relationship between the Loss of Heterozygosity and Loss of Expression of p57~(kip2) mRNA
人肝癌p57~(kip2)基因表达缺失与杂合性缺失的关系研究
It also expounds Bahkin's discussion about three errors in formalism.
巴赫金从三个方面指出了形式方法的“纯技术（言）错误：本体化悖谬、美性缺失、新性丧失。
The Legitimacy Defect and Integration of the System of "Deferred Prosecution";
“暂缓不起诉”制度的合法性缺失及其整合
Study of the Combination of Acupuncture and Chinese Medicine in Treating Acute Ischemic Stroke Patients with Aphasia;
针药结合治疗急性缺血性中风失语症研究
Loss of Heterozygosity Analysis at 6q16-q23 in Pathogenesis of Non-Hodgkin Lymphomas;
6q16-q23杂合性缺失与NHL发病相关性的初步研究
Investigation of the Loss of the Heterozygosity to nm23-H_1 Gene and Its Association with the Biocharicteristics of Lung Cancer;
nm23-H_1基因杂合性缺失与肺癌生物学特性