High-resolution genetic and physical mapping reveals a peanut spotted wilt disease resistance locus, PSWDR-1, to Tomato spotted wilt virus (TSWV), within a recombination cold-spot on chromosome A01. [PDF]
Wu D+11 more
europepmc +1 more source
Isolation and mapping of a polymorphic DNA sequence (pTHH37) on chromosome 14 [D14S16] [PDF]
Yusuke Nakamura+7 more
openalex +1 more source
Assessment and Mitigation of CRISPR‐Cas9‐Induced Nontargeted Translocations
Various inverted repeat elements are dispersed throughout genomes. This study reveals that these elements can cause significant chromosomal rearrangements when CRISPR editing occurs in their proximity. The risk can be mitigated by incorporating inverted repeat‐homologous segments into the CRISPR system, which represents a promising strategy for ...
Zhiyang Hou+6 more
wiley +1 more source
Evaluating Genome Assemblies for Optimized Completeness and Accuracy of Reference Gene Sequences in Wheat, Rye, and Triticale. [PDF]
Yan M+6 more
europepmc +1 more source
Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15 [Dl5S45]
E. Fujimoto+6 more
openalex +2 more sources
Isolation and mapping of a polymorphic DNA sequence (cTBQ12) on chromosome 10 [D10S29] [PDF]
T. Bragg+3 more
openalex +1 more source
This study shows that the classical secretory protein S100 calcium‐binding protein A9 (S100A9) can translocate to the nucleus upon de‐phosphorylation at Thr 113 in human amnion fibroblasts at parturition, where S100A9 induces heterochromatin erosion through segregation of the heterochromatin maintenance protein, resulting inLong Interspersed Nuclear ...
Fan Zhang+8 more
wiley +1 more source
Recombination and structural variation in a large 8-founder wheat MAGIC population. [PDF]
Shah R+7 more
europepmc +1 more source
Isolation and mapping of a polymorphic DNA sequence (pMHZ17) on chromosome 13 [D13S51] [PDF]
M. Hoff+7 more
openalex +1 more source
Direct Quantification of Protein–Protein Interactions in Living Bacterial Cells
Quantitative measurement of protein–protein interactions in living cells is vital for biotechnology applications. Fluorescence resonance energy transfer (FRET) signals in bacterial cells are often weak, leading to false‐positive. Quantitative FRET measurements are implemented to overcome the weak FRET signal.
Soojung Yi+12 more
wiley +1 more source