Results 211 to 220 of about 2,043,269 (377)

Isolation and mapping of a polymorphic DNA sequence (pTHH37) on chromosome 14 [D14S16] [PDF]

open access: green, 1988
Yusuke Nakamura   +7 more
openalex   +1 more source

Assessment and Mitigation of CRISPR‐Cas9‐Induced Nontargeted Translocations

open access: yesAdvanced Science, EarlyView.
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

Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15 [Dl5S45]

open access: green, 1988
E. Fujimoto   +6 more
openalex   +2 more sources

Nuclear Translocation of S100A9 Triggers Senescence of Human Amnion Fibroblasts by De‐Repressing LINE1 Via Heterochromatin Erosion at Parturition

open access: yesAdvanced Science, EarlyView.
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]

open access: yesG3 (Bethesda)
Shah R   +7 more
europepmc   +1 more source

Isolation and mapping of a polymorphic DNA sequence (pMHZ17) on chromosome 13 [D13S51] [PDF]

open access: green, 1988
M. Hoff   +7 more
openalex   +1 more source

Direct Quantification of Protein–Protein Interactions in Living Bacterial Cells

open access: yesAdvanced Science, EarlyView.
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

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