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  1. ...Fluorescence Polarization in Homogeneous Nucleic Acid Analysis II: 5′-Nuclease Assay Sherif Latif 1 , 4 , Irma Bauer-Sardina 1 , 4 , Kostubh Ranade 2 , Kenneth J. Livak 3 , and Pui-Yan Kwok 1 , 5 1Division of Dermatology...
  2. .... Genome Res. 10 : 549 – 557 . ↵ Chen X. , Levine L. , Kwok P.Y. ( 1999 ) Fluorescence polarization in homogeneous nucleic acid analysis. Genome Res. 9 : 492 – 498 . ↵ Corder E.H. , Saunders A.M. , Strittmatter W.J. , Schmechel D.E. , Gaskell P.C. , Small G.W. , Roses A.D. , Haines J.L. , Pericak-Vance M...
  3. ..., , 468–470. . ↵ Chen X. , Levine L. , Kwok P.Y. ( 1999 ) Fluorescence polarization in homogeneous nucleic acid analysis. Genome Res. 9 : 492 – 498 . ↵ Germer S. , Holland M.J. , Higuchi R. ( 2000 ) High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR. Genome Res. 10...
  4. ...ligand unpaired (Upd) (Fig. 1B; Supplemental Fig. S1B). Hyperactivation of the JAK-STAT pathway in the testis results in overproliferation of both stem-cell types (Kiger et al. 2001; Tulina and Matunis 2001; Leatherman and DiNardo 2010), resulting in a more homogenous tissue composition for genomic...
  5. ...and survival; therefore, miRNA expression profiles may show inter-embryo variation. For this reason, we profiled individual embryos in proliferative (E4.5) and dormant states (in vivo and in vitro; see Methods). During in vivo diapause, dormancy progresses from the mural end of the embryo to the polar end over...
  6. ...-seq library constructionATAC-seq libraries were constructed following the Omni ATAC-seq protocol (Corces et al. 2017) with some modifications.Tissue homogenizationA cryopreserved tissue in a vial was quickly thawed in a water bath and transferred to an excess amount of ice-cold Dulbecco's phosphate buffered...
  7. ...(Supplemental Fig. S2A).View larger version: In this window In a new window Figure 1. Clustering and pseudotime analysis of single-cell germline transcriptomes. (A) FACS plot for sorting germ cells from embryonic homogenates of 0- to 8-h embryos with the GFP+ germ cells highlighted by a dotted circle. x...
  8. ...as a function of time. Experimentally, this is typically performed either by tracking single fluorescently labeled loci (Cabal et al. 2006) or by monitoring the dynamics of the nuclear local densities of stained histones (Zidovska et al. 2013) during ∼10–30 sec. From these experiments, trajectories...
  9. ...complex hindlimb duplication phenotypes with low penetrance (four out of 64 animals) (Fig. 4A–D). In one mouse at E18.5, one supernumerary hindlimbwith normal polarity was connected to an imperfectly duplicated pelvic girdle (Fig. 4A). The duplicated hindlimb showed a shortened femur, fibula, and tibia...
  10. ...expressed in yeast as GFP-fused proteins, which were then visualized under a fluorescence microscope. Of the 20 human genes, 16 genes induced the formation of protein aggregates when expressed in yeast. Protein aggregation was not observed for four genes: sodium channel epithelial 1 beta subunit; bone...
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