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  1. ...contributions from sequencing data of plasma cfDNA (Fig. 1). The individuals studied were participants who had undergone screening for NPC (Chan et al. 2017, 2023). These subjects underwent plasma EBV DNA testing by real-time polymerase chain reaction (PCR) for NPC screening. The screening trial was conducted...
  2. ...of every single gene including primer design and synthesis, PCR, gel purification, and sequencing. Particularly, construction of UAS-cDNA/ORF plasmids for long cDNAs or ORFs by the recombinational (Gateway) cloning technique is truly problematic. Therefore, the technical difficulties of construction...
  3. ...attempted to exclude that off-target effects might account for the most unexpected mitotic abnormalities induced by siRNA-mediated knockdown of these genes. We therefore ectopically expressed siRNA-resistant cDNAs encoding PINK1 and TRIO in RPE cells and tested their ability to rescue the knockdown...
  4. ...%) was in accordance with the RNA-seq data set (Fig. 2C; Supplemental Fig. S3A). We next performed qRT-PCR with cDNA derived from germ cells, Sertoli cells, and Leydig cells to detect the expression pattern of the 20 candidate lncRNAs and observed that six candidate lncRNAs (1700027A15Rik, 1700006J14Rik, 1700052I22Rik...
  5. .... ↵ Quackenbush J. , Liang F. , Holt I. , Pertea G. , Upton J. ( 2000 ) The TIGR Gene Indices: Reconstruction and representation of expressed gene sequences. Nucleic Acids Res. 28 : 141 – 145 . ↵ Smith T.P.L. , Godtel R.A. , Lee R.T. ( 2000 ) PCR-based reaction setup for high-throughput cDNA library sequencing...
  6. ...created with PCR- and solid matrix–based technologies were only partially characterized and showed sequence redundancy similar to that of nonnormalized cDNA libraries used in ESTs projects. In addressing the normalization of full-length cDNAs, we felt that an aliquot of the mRNA initially used for the cDNA...
  7. ...Screening of Gene-Associated Polymorphisms by Use of In-Gel Competitive Reassociation and EST (cDNA) Array Hybridization Koshichi Gotoh 1 and Michio Oishi Human Gene 2, Kazusa DNA Research Institute, 2-6-7, Kazusa-Kamatari, Kisarazu, Chiba 292-0818, Japan...
  8. .... Microdissection We prepared full-length libraries from small tissues, including 71 microdissected tissues (Tables 1 and 3 ). To this end, we modified the Cap-Trapper for small quantities of total RNA, without PCR, which might skew representation, especially at expanses of long cDNAs and would affect...
  9. .... Trends Biotechnol. 19 : 511 – 518 . Piao Y. Ko N.T. Lim M.K. Ko M.S.H. ( 2001 ) Construction of long-transcript enriched cDNA libraries from submicrogram amounts of total RNAs by a universal PCR amplification method. Genome Res. 11 ( 9 ): 1553 – 1558 . Pruitt K.D. Maglott D.R. ( 2001 ) RefSeq and Locus...
  10. ...tool for cloning 5' ends of mRNAs and for constructing cDNA libraries by in vitro amplification. Nucleic Acids Res. 19: 5227-5232. 9. Troutt, A.B., M.G. McHeyzer-Williams, B. Pulendran, and G.J.V. Nossal. 1992. Ligation-an- chored PCR: A simple amplification technique with single-sided specificity...
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