بدائل البحث:
cell decrease » cell disease (توسيع البحث), mean decrease (توسيع البحث), cell release (توسيع البحث)
fold decrease » fold increase (توسيع البحث), fold increased (توسيع البحث)
euploid cell » myeloid cell (توسيع البحث)
cell decrease » cell disease (توسيع البحث), mean decrease (توسيع البحث), cell release (توسيع البحث)
fold decrease » fold increase (توسيع البحث), fold increased (توسيع البحث)
euploid cell » myeloid cell (توسيع البحث)
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21
Raw data Fig 3 Western Blot densitometry.
منشور في 2024"…Initial, large-scale genomic alterations like aneuploidies and loss of heterozygosity eventually resolved, as populations gained small-scale mutations. …"
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22
Raw data Fig 4 pH2-8 AUC calculation.
منشور في 2024"…Initial, large-scale genomic alterations like aneuploidies and loss of heterozygosity eventually resolved, as populations gained small-scale mutations. …"
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23
Raw data Fig D in S1 Text growth curves.
منشور في 2024"…Initial, large-scale genomic alterations like aneuploidies and loss of heterozygosity eventually resolved, as populations gained small-scale mutations. …"
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24
SNARE proteins rescue impaired autophagic flux in Down syndrome
منشور في 2019"…Based on our previous observations of PN disruption in DS, we investigated possible dysfunction of the autophagic machinery in human DS fibroblasts and other DS cell models. Following induction of autophagy by serum starvation, DS fibroblasts displayed impaired autophagic flux indicated by autophagolysosome accumulation and elevated p62, NBR1, and LC3-II abundance, compared to age- and sex-matched, euploid (CTL) fibroblasts. …"
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25
Virtual-Partition Digital PCR for High-Precision Chromosomal Counting Applications
منشور في 2021"…This demonstration assaytested on 432 samples contrived from sheared cell-line DNA at multiple input concentrations and simulated fractions of euploid or trisomy-21 “fetal” DNAis analyzed using both traditional dPCR thresholding and VPdPCR. …"
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26
Genome instability in STRIPAK complex mutants.
منشور في 2024"…<p>(A) Read depth analyses from whole-genome sequencing of the WT/WT (CnLC6683) parental diploid strain and heterozygous mutant diploid strains. The WT/WT genome is euploid, while <i>PPH22/pph22</i>Δ and <i>MOB3/mob3</i>Δ strains exhibit multiple instances of segmental and whole chromosome aneuploidy, with dark blue and orange highlighting regions/chromosomes with increased and decreased read depth, respectively. …"